Clinical research coordinator jobs in Phoenix, ArizonaCreate job alerts

Job Description ESSENTIAL FUNCTIONS • Reviews potential protocols to evaluate their feasibility and advises on implementation within standard clinical practices, • Recruits study participants by referrals from clinical sites; schedules appointments, interviews and evaluates potential participants to ensure they meet eligibility requirements; instructs participants concerning protocol and obtains informed consent, • Monitors and participates in research activities including data collection, data entry and analysis for a research project, • Schedules and/or coordinates the scheduling of required laboratory tests and/or radiographic exams, • Assists in developing patient educational materials and provides patient and/or family members with instructions on investigational drug/device administration and other pertinent information related to study participation, • Assists in preparing forms for submission to appropriate oversight/regulatory committees, • Is the primary resource to clinical and support staff within the scope of the study; ensures adherence to clinical and imaging protocols, scheduling study visits within protocol windows, appropriate sites of service for study activities, • Prepares and submits study related reports to sponsors, institutional review boards and other parties as required, • Hosts sponsor visits for qualification, initiation, and monitoring of sponsored studies, • Completes case report forms for study participants and documents applicable data in study records/databases., • Inventories and requisitions research study supplies and equipment, • Works with research accounting to ensure appropriate billing of research activities, • Knowledge of the principles, practices and techniques of clinical care, • Knowledge of clinic policies and procedures, • Knowledge of computer systems and applications, including but not limited to Microsoft Office and Electronic Data Capture systems, • Knowledge of medical practices, terminology, • Knowledge of organizational policies and procedures, • Skill in planning and organizing clinical trials, • Skill in evaluating effectiveness of existing methods and procedures, • Ability to communicate clearly and effectively, • Ability to set priorities among multiple projects, • Normal office environment., • Work in clinical and hospital environments, • Requires sitting and standing associated with a normal office environment., • Some bending and stretching required.

Job Description Job Summary: We are seeking a highly organized and motivated Entry Clinical Research Coordinator (CRC) to join our research team. The CRC will coordinate and support all aspects of clinical trials and research studies, including subject recruitment, data collection, regulatory compliance, and specimen handling. Candidates with current Phlebotomy certification or Medical Assistant (MA) certification are strongly preferred, as this role may include specimen collection and basic clinical procedures. Key Responsibilities: • Coordinate day-to-day clinical research activities to ensure study protocols are followed., • Recruit, screen, and enroll study participants., • Obtain informed consent and ensure ethical conduct in all study interactions., • Collect, process, and ship biological specimens per protocol (e.g., blood draws, urine samples)., • Perform basic clinical procedures as permitted by certification (e.g., vital signs, EKGs)., • Maintain accurate and timely documentation in case report forms and electronic databases., • Communicate with sponsors, monitors, and IRBs regarding study progress and compliance., • Schedule participant visits and follow-ups; ensure visit windows are met., • Ensure proper storage, handling, and accountability of investigational products, if applicable., • Bachelor's degree in a health-related field or equivalent experience., • At least 1–2 years of experience in clinical research preferred., • Phlebotomy certification or MA certification preferred., • Knowledge of Good Clinical Practice (GCP) and regulatory guidelines., • Excellent organizational skills and attention to detail., • Strong interpersonal and communication skills., • Proficiency in Microsoft Office and electronic data capture systems (e.g., REDCap, EDC platforms)., • Experience working in clinical trials, especially in a hospital or academic setting., • Familiarity with IRB processes and clinical trial documentation., • Bilingual skills (depending on patient population) may be a plus.

Job DescriptionDescription: Named a Top Workplace in Arizona, Arizona Arthritis & Rheumatology Associates, P.C. is the largest private Rheumatology practice in the United States. The practice has over 60 providers, 15 sites and over 300 employees providing assessment and treatments for rheumatological, podiatric, and electromyography patients. Our providers work together to keep patients healthy, and are recognized for excellence in medicine and for being pioneers in new treatments, ably supported by our Research department. Our vision is to provide the best Rheumatology care, anywhere and, to balance sustainable operation with the highest possible level of patient care. We are a seeking an ambitious, friendly, positive, and compassionate Billing Coordinator to join our billing department at our business office located in Glendale. The Billing Coodinator is responsible for the proactive management of assigned payer/patient accounts, driving ownership, accountability, and results. This role serves as the primary steward of assigned AR buckets, collaborating with offshore teams, identifying trends, resolving barriers, and ensuring consistent progress toward financial targets. Through leadership, analysis, and communication, the Lead AR Coordinator directly supports the department’s goal of maintaining a strong, efficient, and patient-centered revenue cycle. Responsibilities: • Own and manage an assigned payer bucket, ensuring full accountability for accounts receivable performance., • Analyze AR trends, denial patterns, and payer-specific issues; escalate findings to leadership with recommended actions., • Assign, monitor, and follow up on offshore team tasks via NextGen, ensuring timely account touches and resolution., • Maintain clear communication and performance oversight with assigned offshore team members, holding them accountable to quality standards., • Proactively identify changes in payer policies, trends in claim denials, and operational barriers impacting AR performance., • Collaborate with leadership on process improvements, payer escalations, and financial reconciliation., • Participate in monthly reporting cycles by providing updates on payer performance, expected collections, barriers, and success metrics., • Assist with offshore and onsite team education and operational support to ensure consistency in account handling., • Collaborate with clinic staff and managers to support, train, educate, inform, with anything related to patient inquiries, balances, registration, or any RCM related support., • Engage in professional development opportunities including obtaining billing certifications and leadership training., • Maintain compliance with departmental adjustment policies, regulatory guidelines, and documentation standards., • Deliver exceptional service through timely, respectful, and solution-oriented communication with patients., • Perform other duties as assigned. Learn more about AARA on our website at Requirements: Qualifications: Required High School diploma or equivalent required Exceptional customer service skills and extensive experience Medical collections, medical billing or payment experience required, 2 years Demonstrated knowledge of state & federal collections guidelines, 2 years Preferred Clinical Billing and Collections experience in a large healthcare practice, 2 years Associate’s degree or advanced education specific to business administration NextGen PM system, 1 year. Bilingual

Job Description Overview As a Junior Clinical Research Coordinator, you are responsible for assisting with the management and coordination of all aspects of conducting clinical trials within s RII, surgery centers, both clinically and administrative/regulatory. Responsibilities • Acts as a representative of clinical research and as liaison between investigators, other study staff, primary care providers, IRB and sponsor., • Screens, consents, enrolls and follows study subjects ensuring protocol compliance and close monitoring while subjects are on study utilizing Research Nurses’ oversight for help with clinical decision making., • Responsible for all data and source documentation, and adverse experience reporting, • Responsible for following departmental policies, • Responsible and for assuring proper billing for research subjects. Assures that charges for tests and treatments are appropriately communicated and processed., • Assists as needed in preparing study for submission to IRB and ensures all regulatory documents are completed., • Attends study-related meetings as appropriate., • Travels between RCA research offices as needed for patient and business needs., • Develops screening/enrollment/follow up mechanisms., • Ensure adherence to protocol requirements., • Schedules and performs patient procedures, assessments, evaluations and testing as required by the protocol, including but not limited to blood sample collection, processing and shipping, ECG, vital signs, etc., as applicable., • Organizational maintenance of all aspects of the trial, including but not limited to timeliness in completing CRFs, reporting adverse events, managing caseload and study files., • Responsible for quality data entry into sponsor’s database (electronic data capture systems or paper CRFs) and query resolution., • Ensures proper study drug administration, compliance and accountability, including receipt and , storage and dispensing., • Ensures patient safety and ensures coordination of patient care as needed., • Assists with maintenance of regulatory documents, IRB reporting and submissions of amendments, renewals, etc., • Assists with study initiation visits, monitoring visits, closeout visits and audit visit, ensuring all study documentation and study issues are addressed., • Communicates regularly with the Manager of Clinical Research at RII and Principal Investigators about study related issues., • Ensures compliance with department standards and all federal regulations and international guidelines of good clinical practice., • Maintain job related certifications (IATA, Human subjects, subjects’ protection training, GCP, and protocol specific required training)., • Active in acquiring professional growth by obtaining CRC certification when eligible and joining a professional association such as SOCRA or ACRP., • Performs other duties and responsibilities as required., • Promotes a positive work environment and works to be an integral member of the team, • Encourage a team-oriented environment supporting the AVP Mission, Vision and Core Values., • Participate in on-going training and continuing education., • Show respect and deal appropriately with co-workers, patients, and visitors., • Perform any and all duties assigned. Qualifications • Associate or Bachelor’s Degree or working toward one, • Clinical experience in Retina or other optical care, • Prior research experience, • Current IATA, Human Subjects’ protection training or GCP training highly desirable, • Certificates, Licenses, Registrations:, • Specialty certification such as CCRC preferred

Job Description About Us: Arizona Liver Health (ALH) is dedicated to driving high standards of care and advancing medical innovation through leading clinical trials, ensuring patient safety and regulatory compliance, and generating high-quality clinical data. Our network of multiphase, multitherapeutic research, standard of care, and VEN Centers sites is staffed by skilled providers, research, clinic, pharmacy, and patient outreach professionals. ALH operates state-of-the-art facilities and programs to meet the evolving needs of clinical research and overall patient treatment. Title: Marketing Campaign Strategist Status: Full-time, Exempt Salary: $75,000 - $85,000 annually, depending on experience Job Summary: The Marketing Communications Coordinator plays a central role in crafting and delivering clear, compelling, and brand-aligned messaging across digital and offline channels for ACT, ALH, and VEN. This individual is responsible for content development, communications strategy, campaign coordination, and marketing support for events and digital channels. This role requires strong writing, project management, and cross-functional collaboration skills. The role involves close collaboration with the marketing manager and creative team to align messaging and ensure consistent brand representation. Essential job functions/duties Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions. Patient Recruitment Campaigns: • Plan, develop, and manage targeted recruitment campaigns for clinical trials across paid media, social, email, and community outreach., • Assist in the creation and editing of visual content (graphics, short videos, etc.) using tools like Canva or Adobe Suite for paid advertising, • Collaborate with study teams to understand protocol criteria, target demographics, and site-specific needs., • Collaborate with the BD team on outreach campaigns to sponsors and CROs, including email sequences, LinkedIn ads, and conference activations., • Lead campaign planning, execution, and reporting using platforms such as Meta Ads Manager, Google Ads, and Monday.com., • Develop performance dashboards to monitor KPIs across recruitment and BD campaigns., • Manage campaign budgets, vendor relationships, and ensure alignment with branding and compliance standards., • Strong understanding of paid media platforms (Meta, Google, YouTube, LinkedIn, X) and CRM tools (Monday.com preferred)., • Excellent copywriting skills with the ability to adjust tone for patient or industry audiences., • Demonstrated success in managing campaign timelines, budgets, and vendor relationships., • Bachelor's degree in marketing, communications, life sciences, or a related field., • Familiarity with HIPAA and IRB (Institutional Review Board) marketing compliance., • Prior experience in patient recruitment or clinical trial marketing., • Knowledge of feasibility tools, trial databases, or sponsor/CRO marketing strategies., • Meta Ads Manager, Google Ads, YouTube Ads, • Canva, Adobe Creative Cloud, • Must be able to reliably commute or plan to relocate before starting, • Able to lift at least 15 lbs., • Able to sit for long periods (at least 50%), • Some interoffice travel may be required with use of company vehicle or mileage reimbursement Must have valid documentation and authorization to work in the U.S. Affirmative Action/EEO statement It is the policy of the Institute for Liver Health DBA Arizona Liver Health and Arizona Clinical Trials to provide equal employment opportunities without regard to race, color, religion, sex, national origin, age, disability, marital status, veteran status, sexual orientation, genetic information or any other protected characteristic under applicable law. This policy relates to all phases of employment, including, but not limited to, recruiting, employment, placement, promotion, transfer, demotion, reduction of workforce and termination, rates of pay or other forms of compensation, selection for training, the use of all facilities, and participation in all company-sponsored employee activities. Provisions in applicable laws providing for bona fide occupational qualifications, business necessity or age limitations will be adhered to by the company where appropriate. Other duties Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Other responsibilities may be communicated directly by the reporting manager/supervisor. Duties, responsibilities, and activities may change at any time with or without notice. Notice to Staffing Agencies: It is our policy that any and all contact with third party staffing or recruitment vendors come through our Talent Acquisition Team directly. We have an established and preferred network of contracted partners that we engage if and when we deem it necessary. We request that staffing agencies refrain from repeatedly contacting our hiring managers or employees directly. Unsolicited resumes, onsite solicitations, and inquiries will not be considered or responded to. Overly persistent or forceful inquires may also be blocked across our network at the domain level as spam. Thank you for your understanding.

Job DescriptionSalary: TL;DR Northwest Valley & Phoenix Locations As a Clinical Research Coordinator, you have mastered the art of multitasking, prioritizing, and efficiency. Your acute attention to detail has all your peers asking you to proofread their work (which you love doing!). You thoroughly enjoy dissecting and internalizing large amounts of information. When faced with a challenge, you pull from your experience, grab your tools, and execute a plan. You consider yourself a rule follower, but able to pivot if the situation calls for it. When given an assignment, you are the project manager, set your own deadlines, AND crush them. Patient care and excellent bedside manner is a top priority for you. Your hobbies include reading, checking things off your to-do list, and creative projects. Youre not afraid to think outside the box or work outside of your comfort zone. As a Clinical Research Coordinator, you see yourself further developing your skills to grow your career in a patient-facing setting because you care about the community in which you serve. You have a minimum of 1 year previous clinical research experience. Fluency in English and Spanish required. Bachelor's degree required. What you will own & improve • Coordinate patient visits. You will be responsible for independently conducting complex interventional & therapeutic protocols in compliance with FDA regulations and ICH-GCP guidelines. You may coordinate at each of our 5+ offices we work in throughout the Phoenix valley., • Patient acquisition. You will be responsible for meeting enrollment goals for studies in which you are assigned as lead by means of chart review, lunch-and-learns, and other community outreach activities., • Cultivate positive relationships. Develop and maintain strong connections with all of our customers (Sponsor/CRO & Physician Specialists)., • Adhere to strict safety parameters. You will be responsible for identifying, documenting, and reporting adverse events, protocol deviations, and other unanticipated problems. Duties may include liaising with laboratories regarding findings. All the while consulting with the Principal Investigator and patient in order to assess patient eligibility into the trial and throughout their participation., • Drug records and dispensing. You are responsible for maintaining detailed records regarding drug receipt, dispensing, and maintenance. This includes patient education and monitoring adherence to study rules, • Assessments and exams. You are responsible for obtaining training, certification, and maintaining credentials to perform various tasks as defined by study protocols., • Process important study information. You will be responsible for reading and internalizing incoming information from study bulletins, newsletters, and memos. This information may require you to update documents and relay this information to the team by utilizing a project management platform, Basecamp., • Vitals, phlebotomy and laboratory. You will be responsible for collecting patient vitals, drawing labs, as well as processing and shipping samples. What you already know • You have a minimum of 1 year clinical research experience, so you already know the basics. For example, you can rattle off these acronyms in your sleep: EDC, GCP, ICF, SIV/IMV/COV, AE/SAE, and DOA., • You have experience reviewing patient charts in order to assess eligibility for enrolling trials. Youre not afraid to pick up the phone to screen a patient for a new study and by the time youre done the two of you are BEST buds., • How to effectively manage your time when there is a lot on your plate. Youve got tried and true techniques to keep you on tasks, meeting your own deadlines, and setting yourself up for success., • Previous experience in or passion for ophthalmology is a major plus! What you will learn • As the project manager of the studies you are assigned as lead, you will learn to execute timely study start-up, develop source documents, and manage monitoring visits., • You will learn how to perform quality assurance checks and audit patient source and regulatory files., • Regulatory tasks such as file maintenance, start-up document execution and collection, and IRB reporting guidelines. About the Team This role reports to our Director of Clinical Research. Local travel is required Benefits at DocTrials Competitive salary Health insurance Dental & vision Paid time off Bonus structure Retirement plan Flexible schedule Company adventures Values at DocTrials Align Your Daily Priorities Roll Out the Red Carpet Be obsessed about learning Show Up Ready What Can We Do? Dont Panic Dont Work in a Bubble Recognize the Gray Have a positive purpose About Us DocTrials' culture is guided by our values and behavior. Our success depends on how much we care for each other, our customers, and our community. DocTrials is an alliance of physician sites specializing in the conduct of clinical studies within their private practices. Sites in the alliance work under DocTrials' core standard operating procedures and quality control measures that provide a methodology ensuring the highest quality control and best practice utilization across sites. This provides assurance and confidence to sponsors that they will achieve quality data in the most efficient and timely manner. DocTrials was founded with the primary goal of connecting patients and physicians with clinical trials across the US; aiding in the process to discover new therapies, bring hope, and find new treatment for disease.

Job Description About Us: Arizona Liver Health (ALH) is dedicated to driving high standards of care and advancing medical innovation through leading clinical trials, ensuring patient safety and regulatory compliance, and generating high-quality clinical data. Our network of multiphase, multitherapeutic research, standard of care, and VEN Centers sites is staffed by skilled providers, research, clinic, pharmacy, and patient outreach professionals. ALH operates state-of-the-art facilities and programs to meet the evolving needs of clinical research and overall patient treatment. Job Summary: Arizona Liver Health/Arizona Clinical Trials is looking for qualified candidates for the TEMPORARY Clinical Research Coordinator II position in Peoria. Title: TEMPORARY -- Clinical Research Coordinator II (CRC2) Compensation: $35-$40 per hour, depending on experience Status: Full-time, 3-Month Contract (eligible for overtime) Work Schedule: Monday-Friday, 7am-4pm (set schedule) Start date: ASAP Essential job functions/duties: Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions. • Under the direction of the Principal Investigator or sub-investigator, manage the conduct of clinical research activities., • Responsible for coordinating and implementing assigned protocols in compliance with FDA CFR, GCP and company SOPs., • Collects and records clinical research data, assists in patient assessments, scheduling, maintain study files, study supplies and study medication accountability., • Develop management systems and prepare for study initiation, • Review with the Principal Investigator the inclusion/exclusion criteria, overall structure and requirements of each protocol, • Review the protocol summary sheet and the Informed Consent Form for accuracy and clarity about these protocols to staff and patients., • Responsible for the recruitment and screening of potential participants, which includes chart review of patients and schedules, contacting leads from outside recruitment efforts, and following up on referrals from all sources., • Responsible for meeting recruitment goals for each study., • May assume primary responsibility in the implementation and management of new clinical trials in a knowledgeable and collaborative manner., • Performs all functions according to established policies (SOPS), procedures, regulatory and accreditation requirements, as well as applicable professional standards., • Provides educational information to subjects. Serves as a resource and support person for subjects and families by being a consistent person they can contact within the clinical research program., • Provides all employees and research subjects with an excellent service experience by consistently demonstrating professional decorum., • Serves as a liaison to all physicians, employees, and third-party vendors., • Record data and study documentation, • Keep the clinical trial management system updated with newly recruited subjects, tracking completed visits and stipends for the participants and investigators and ensuring status of each patient is accurate., • Assign patient stipend pay card at screening, • Document reason for screen-fail in real time, • Plans, prepares and performs tasks required by protocol, which may include, but not limited to the following:, • Record data as directed using the appropriate media or platform, • Follow procedures for access and security for electronic data entry, • Review keyed data for accuracy as needed, • Send data to the data collection center on a timely basis, • Maintain source documentation for all data entered, including clinic chart visit notes, lab data and procedure reports, • Develop and/or edit source as needed independently or with Quality Assurance / Quality Control team to, • Ensure compliance with protocol and EDC., • Correct and edit data as directed and as appropriate., • Informed Consent, • Obtaining patient medical history and medication lists, • Phlebotomy and basic laboratory tests, • Processing & shipping labs for central and local labs, • Patient education and training, • ECG, • Administer questionnaires and assessments, • Vital signs, • Collect information for adverse event reporting, • Assist with efficacy assessments, • Data Entry and Query Resolution, • Study drug administration, including injections, • Tracking study supply inventory and reordering when necessary, • Schedule patient visits in appropriate electronic systems, • Documenting all patient visits and communications in progress notes, • Document and record all AEs and SAEs as outlined in protocol, • Monitor and report adverse events, • Triages adverse events and communicates with the research physician regarding the occurrence of adverse and serious adverse events within 24 hrs. Follow-up with the subject and collaborate information as needed., • Responsible for administrative duties including filing documents related to subject's participation in research, regulatory, lab results, receipts, invoices, calibration reports, etc., • Ensure W-9 and medical release forms are signed by subjects annually., • Management of site activities during audits and inspections, • Management of ancillary staff as assigned, • Train and supervise support staff (e.g., CRC I), • Mentor for externs, • Train newly hired employees as either Research Assistant and/or CRC, • Prepare for quality assurance audits and regulatory inspections as needed, • Act as contact person before, during and after audits and inspections, • Provide all required documentation to auditors, • Make all appropriate corrections as requested by auditors, • Coordinate site response to audit/inspection findings., • Participates in monitoring visits from sponsor provided appointees, ensures monitors are able to meet/speak with PI and ensures all concerns are addressed in a timely manner., • Minimum (3) years of experience working previously as a Clinical Research Coordinator for late phase clinical trials., • Experience and training in the conduct of clinical research (specific experience and/or training in clinical research, including IRB submissions, reporting and source documentation, trial management)., • A thorough understanding of regulatory requirements, principles of GCP and biomedical research ethics., • Interpersonal and communication skills—interact effectively with professional, administrative staff, sponsor and regulatory representatives, patients, potential subjects and referral sources., • Possess a sound and in-depth understanding of each protocol that has been assigned as a primary responsibility protocol deviations, serious adverse events and other reporting requirements., • Able to perform all Job duties listed for Job Description for Phlebotomist, • Associates or Bachelor's degree in healthcare, clinical research management, or related required., • Master's degree or study-specific training preferred, • GCP certification required at hire., • Experience and training in the conduct of clinical research and basic knowledge of medical terminology., • Experience and training in the conduct of clinical research (specific experience and/or training in clinical research recruitment, including IRB submissions and trial enrollment management), • 5 days Sick Time EEO statement It is the policy of the Institute for Liver Health DBA Arizona Liver Health and Arizona Clinical Trials to provide equal employment opportunities without regard to race, color, religion, sex, national origin, age, disability, marital status, veteran status, sexual orientation, genetic information or any other protected characteristic under applicable law. This policy relates to all phases of employment, including, but not limited to, recruiting, employment, placement, promotion, transfer, demotion, reduction of workforce and termination, rates of pay or other forms of compensation, selection for training, the use of all facilities, and participation in all company-sponsored employee activities. Provisions in applicable laws providing for bona fide occupational qualifications, business necessity or age limitations will be adhered to by the company where appropriate. Notice to Staffing Agencies: It is our policy that any and all contact with third party staffing or recruitment vendors come through our Talent Acquisition Team directly. We have an established and preferred network of contracted partners that we engage if and when we deem it necessary. We request that staffing agencies refrain from repeatedly contacting our hiring managers or employees directly. Unsolicited resumes, onsite solicitations, and inquiries will not be considered or responded to. Overly persistent and pushy inquires may also be blocked across our network as spam. Thank you for your understanding and cooperation.

Job DescriptionSalary: $20 - $30 Depending on Experience Axsendo Clinical Research is seeking a motivated and detail-oriented Clinical Research Coordinator to join our team on a part-time/prn basis. This position offers the potential for a transition to full-time employment based on performance and project needs. The ideal candidate will have a strong interest in clinical research and be comfortable with some travel within the Phoenix area. Key Responsibilities: • Assist in the planning, execution, and monitoring of clinical trials., • Coordinate and manage study-related activities, including patient recruitment and scheduling., • Ensure compliance with regulatory requirements and study protocols., • Collect, maintain, and manage study data and documentation., • Collaborate with investigators, sponsors, and study team members., • Participate in training and orientation of new staff and study volunteers., • Conduct site visits and assist with patient follow-ups as needed., • Prepare and administer IP, • Previous experience in clinical research or a healthcare setting is a plus., • Strong organizational and multitasking skills., • Excellent communication and interpersonal abilities., • Proficient in Microsoft Office and data management software., • Opportunity for professional growth and development., • Potential for transition to a full-time role based on project needs and performance.

Job Description Position Title: Clinical Research Coordinator (CRC) Location: Arizona Veterans Research and Education Foundation is based on the Phoenix VA Medical Center Campus in Phoenix, Arizona. Schedule: Full-time (40 hours/week) Minimum Contract Obligations: 1 year, grant funded Salary: Commensurate with experience and qualifications; range $50,000 to $73,000 Join a great team working with our military veterans! We are a non-profit medical research organization based in Phoenix, Arizona. At Arizona Veterans Research and Education Foundation (AVREF), we offer our team members the opportunity to work on impactful research that benefits veterans’ health, while enjoying a competitive salary, generous benefits, a collaborative environment, and flexible scheduling. About Us: Arizona Veterans Research and Education Foundation (AVREF) uniquely partners with the Phoenix Veterans Administration Health Services, universities, and pharmaceutical/ device companies to conduct research benefiting military veterans. Our Research makes a difference! We bring cutting-edge research opportunities to veterans, improving their lives. The Position: We’re looking for a Clinical Research Coordinator (CRC). The CRC will recruit, screen, and enroll eligible participants, implement protocol procedures, monitor follow-up visits, and oversee regulatory and administrative details as needed. The salary range reflects industry standards, and we offer a robust benefits package, including health, vision, and dental insurance, life insurance, short and long-term disability benefits, a Simple IRA with matching funds (immediate vesting), vacation, and sick leave. This position is contingent uponapproval from the Veterans Affairs Administration and may be rescinded ifapproval is not granted. Approval can take anywhere from 2-4 months. Position start date will be given once approval is acquired. Study Types: We are recruiting CRCs to work as part of a team on a research project investigating cancer to improve veterans’ health. The study is stable, funded, and ongoing. Flexibility to work as part of a team, is essential. Requirements: • Prior successful clinical research experience, • Knowledge of medical terminology, • Excellent understanding of project management and clinical research processes, • Willingness to cross-train in other roles as needed, • Detail-oriented, self-directed, and able to work within a team environment, • Personable, collaborative, and cooperative, • Comfortable with or willing to learn minimally invasive medical procedures, • Ability to pass a background check, • Proficient in technology: email, Microsoft Office, teleconferencing, and Electronic Medical Record (EMR) systems, • Ability to draw blood and process laboratory samples to include aliquoting, • Know how to analyze, collect, and store data from EMR, • Medical background, • ACRP or CCRP certification, • Daily administration and conduct of research projects, • Interact with Principal Investigators, Sub-Investigators, Research Committee Coordinators, laboratory staff, and clinical staff from various departments, • Provide direct coordinator services/procedures/consultation and participate in site visit activities from a sponsor or granting agency, • Work with other team members to recruit study participants, • Complete study visits activities, • Coordinate study activities with other study sites and central laboratories, • Assist in the preparation of the study, review documents, and correspondence with the Research Committees, • Screen, recruit, and enroll qualified subjects into clinical trials and monitor their status, • Comply with all SOPs, Federal regulations, and good clinical and ethical practices, • Ensure accurate clinical assessment, source documentation, data collection, regulatory file composition, and trial communications with subjects, investigators, and caregivers, • Prepare and submit trial-specific information to the IRB and others, as assigned

Job Description Clinical Research Nurse Coordinator This role involves conducting study activities as delegated by the Principal Investigator and in compliance with study protocols, GCP, and FDA regulations. Key Responsibilities: • Administer prescribed study and concomitant medications, • Perform phlebotomy and handle the collection, processing, and shipment of biological samples, • Perform ECGs, monitor vital signs, and carry out other specialized nursing procedures, • Valid State of Arizona RN license, • Minimum 3 years of Clinical Research Nurse Coordinator experience, • CPR/ACLS certified, GCP, phlebotomy, and IATA trained, • Bachelor’s degree in Nursing from an accredited institution The pay range for this position is $85000.00 - $100000.00/yr. Benefits. Benefits. Benefits. Benefits. Benefits. Benefits. Benefits. Benefits. Benefits. Benefits. Benefits. Benefits. Workplace Type This is a fully onsite position in Phoenix,AZ. Application Deadline This position is anticipated to close on Oct 24, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email for other accommodation options.

Job DescriptionSalary: $27 - $34 Hourly About Us At Axsendo Clinical Research, we believe that successful clinical trials are built on true partnerships. We are deeply invested in the journey from discovery to delivery, with a singular focus on advancing life-changing medical therapies. Every aspect of our work centers around peoplethe patients we serve, the teams we support, and the processes we refine. Through this compassionate and dedicated approach, we aim to transform the landscape of medical treatment and access to healthcare. Position Overview We are seeking an experienced Clinical Research Coordinator (CRC) to join our team. The ideal candidate will have at least 3 years of clinical research experience, strong organizational and leadership skills, and a demonstrated commitment to patient care and research integrity. This is an exciting opportunity to play a vital role in advancing clinical research while working closely with patients, investigators, sponsors, and cross-functional teams. Key Responsibilities • Recruit, screen, consent, and enroll study participants while maintaining accurate and confidential records., • Collect, process, and manage study data and specimens in compliance with study protocols and GCP., • Support regulatory submissions (IRB applications, amendments) and assist compliance with required documentation., • Coordinate daily study activities, including scheduling, monitoring visits, and ensuring protocol adherence., • Collaborate with investigators, sponsors, and internal teams to ensure seamless study execution., • Assist with audits, monitoring visits, and quality checks to ensure ongoing regulatory compliance. Qualifications • Bachelors degree in a health-related field preferred., • Minimum 3 years of clinical research experience required., • CCRC or ACRP certification preferred., • Strong organizational and communication skills., • Phlebotomy experience required. Skills • Proficiency in phlebotomy and specimen handling techniques., • Experience with CTMS (CRIO preferred but not required)., • Strong organizational and time-management skills with the ability to manage multiple priorities., • Excellent verbal and written communication abilities., • Proficiency in Microsoft Office Suite and clinical research software., • Ability to work independently and collaboratively within a multidisciplinary team., • Detail-oriented with a strong commitment to accuracy, compliance, and research integrity., • Prior experience in Pulmonology, Podiatry, or Cardiology preferred. Other Requirements • Valid drivers license and reliable transportation for travel between local offices., • Flexibility to adjust work hours MondayFriday as protocol or subject visits require. Benefits • Competitive pay with opportunities for advancement., • Paid time off and company holidays.

Job Description GENERAL STATEMENT OF DUTIES Coordinates and oversees clinical or field operation of research projects involving human subjects. Leads in assessing, planning, implementing clinical research study protocols/designs. Is responsible for subject consenting, data collection, and regulatory compliance in clinical research studies. ESSENTIAL FUNCTIONS • Assists with protocol development and/or reviews potential protocols to evaluate their feasibility and implementation within standard clinical practices, • Generates forms and prepares applications for regulatory approvals (e.g. Institutional Review Board), manages regulatory processes and documentation for assigned studies, • Recruits study participants by referrals or by placing advertisements on television, radio, or in newspapers, • Schedules study appointments; screens and evaluates potential participants to ensure they meet eligibility requirements; obtains informed consent to participate in studies., • Manages, monitors and participates in research activities including data collection, data entry, and analysis for a research project., • Completes case report forms for study participants and documents applicable data in study records/databases., • Schedules and/or coordinates the scheduling of required laboratory tests, imaging studies, and/or exams, • Evaluates and/or develops patient educational materials and provides patient and/or family members with instructions on investigational drug/device administration and other pertinent information related to study participation., • Trains coordinates and educates patient care team in the conduct of study protocols, • Inventories and requisitions research study supplies and equipment; arranges for repair and maintenance of equipment, • Coordinates and participates in monitoring visits with sponsors and regulatory agencies, • Four plus years experience in the health care field or an equivalent combination of education and experience., • Knowledge of the principles, practices, and techniques of clinical care, • Knowledge of clinic policies and procedures, • Knowledge of computer systems and applications, • Knowledge of medical practices, terminology, • Knowledge of organizational policies and procedures, • Skill in planning and organizing clinical trials, • Skill in evaluating the effectiveness of existing methods and procedures, • Ability to communicate clearly and effectively, • Ability to set priorities among multiple projects, • Normal office environment., • Work in clinical and hospital environments., • Some travel within the community., • Requires sitting and standing associated with a normal office environment., • Some bending and stretching are required.

Job DescriptionCRC Operations Lead Job DetailsJob Location: AUUA Glendale - Glendale, AZ Position Type: Full Time Job Shift: Day Description POSITION SUMMARY: The CRC/Operations Lead is a senior team member responsible for conducting clinical trials while also serving as a go-to resource for operational questions, training, and workflow support. In addition to managing their own study protocols, this individual provides guidance to staff on all site study protocols, site policies, and documentation practices. The CRC/Operations Lead supports training and onboarding, helps troubleshoot day-to-day challenges, and assists with administrative oversight, including timecard reviews. KEY RESPONSIBILITIES: • Manage assigned clinical trials end-to-end, including participant visits, data collection, source documentation, and sponsor relations., • Able to manage multiple studies with varying indications., • Leads complex trials, ensuring compliance with protocol and regulatory requirements., • Develops effective strategies for promoting/recruiting research participants and retaining participants in long term clinical trials., • Demonstrations understanding of Urology America and key stake holders to ensure continuing of patient care., • Work to build the research department in scope, size, reputation, and professionalism., • Serve as a study resource for CRCs and support personnel., • Provide day-to-day operational support, helping staff interpret study protocols, procedures, and SOPs., • Maintain certifications in, and continually update knowledge of, FDA, GCP, ICH, federal and state regulations, etc., • Attend all site SIVs and other sponsor meetings to ensure smooth study start-up and expedited enrollment., • Support study feasibility activities alongside Investigators and site managers., • Train and mentor new and existing CRCs, including shadowing, skills checks, and protocol-specific training., • Ensures good Investigator relations and manages trainings, schedules, and other communications/processes needed for Investigator support., • Assist in creating and updating training materials and onboarding workflows., • Support the Clinical Research Manager with administrative oversight, such as reviewing timecards, study/office supply needs, or visit scheduling concerns., • Participate in site audits or monitoring visits, helping staff with compliance preparation., • Act as a liaison between individual market operations and leadership, elevating staffing, policy, or workflow concerns as needed., • Ensure study conduct is compliant with GCP, IRB, SOPs, and ALCOA-C documentation standards., • Act as the point person to the local market clinic and leadership teams., • Work with the EMR and data management systems to complete EDC, eCRFs, find patients, maintain records., • Support vendor management and vendor set up., • Ensures CTMS compliance and completion., • Partner with finance to ensure local site CTMS completion and proper invoicing. Qualifications ERFORMANCE REQUIREMENTS: Knowledge • Knowledge of health care field; medical practice clinical and administrative systems, departments, and practices, including clinical financial policies and reimbursement payment requirements., • Ability to use multi-line phone systems and basic computer systems., • Interpersonal communication with internal staff and external customers., • Skill in evaluating and implementing study protocols and budgets., • Skill in reading medical chart terminology., • Ability to communicate effectively with patients, staff, and external contacts via phone, in person, and through electronic mail., • Elicit appropriate information for patients to clinic staff., • Ability to read and understand information and ideas presented in writing., • Physical demands: Involves sitting approximately 90 percent of the day, walking or standing for the remainder. Work may require stooping and bending to access files, supplies, mobility to complete errands, and lifting up to 20 pounds., • 2–5 years of experience as a Clinical Research Coordinator., • Proven knowledge of GCP, FDA regulations, and site-level clinical research operations., • Strong leadership, mentorship, and interpersonal communication skills., • Experience training or mentoring others preferred., • Detail-oriented and able to manage multiple responsibilities with minimal supervision., • Urology therapeutic area experienced preferred. PI0a05dc12de99-25405-38546384

Job DescriptionSalary: TL;DR Northwest Valley & Phoenix locations Full & part time available As a Clinical Research Assistant, you love to-do lists, organization, and are a master of administrative tasks. You have pronounced attention to detail and are obsessed with learning. As a lifelong seeker of knowledge you read everything! Patient care and excellent bedside manner is a top priority for you. When faced with a challenge, you take a breath, grab your resources, and make a plan! Preparation, agendas, and crushing tasks are your jam. You are an eager self-starter who wants to develop a strong foundation to grow as a Clinical Research Coordinator. You may or may not have some previous clinical research experience and/or ophthalmology experience. Fluency in English and Spanish required. Bachelor's degree preferred. What you will own & improve • Patient acquisition: You will be responsible for reviewing patient charts for enrolling trials, creating telephone screening sheets, and conducting recruitment calls. You may also schedule and support with lunch n learn and other community outreach activities., • Patient chart maintenance: You will be responsible for scanning, filing, and completing tasks within Clinical Trial Management Software (CTMS)., • Process important study information. Relay information from study bulletins, newsletters, and memos to the team by utilizing a project management platform, Basecamp., • Site organization and upkeep. Manage study supplies, inventory, prepping, and ordering., • Vitals and laboratory. You will be responsible for collecting patient vitals and performing laboratory assessments., • Clinic flow. Like a clinic ninja, you will manage the task of quickly and efficiently moving patients through protocol assessments. What you already know • How to engage with patients, deliver excellent customer service, and roll out the red carpet!, • You know your way around a computer, printer, scanner the basics. You also consider yourself tech savvy and pick up on new platforms quickly., • How to make the most out of any space; no matter how small. You consider organizing a hobby and probably have a personal label maker., • Previous experience in the medical field (ophthalmology or other) is a major plus! What you will learn • You will establish a strong foundation of skills to grow as a Clinical Research Coordinator in order to conduct complex interventional & therapeutic protocols in compliance with FDA regulations and ICH-GCP guidelines., • How to conduct patient acquisition to meet and exceed enrollment goals., • How to cultivate a positive working relationship with all of our customers (Sponsor/CRO & Physician Specialists). About the Team This role reports to our Director of Clinical Research. Local Travel required. Benefits at DocTrials Competitive salary Health insurance Dental & vision Paid time off Retirement plan Flexible scheduling Company adventures Values at DocTrials Align Your Daily Priorities Roll Out the Red Carpet Be obsessed about learning Show Up Ready What Can We Do? Dont Panic Dont Work in a Bubble Recognize the Gray Have a positive purpose About Us DocTrials' culture is guided by our values and behavior. Our success depends on how much we care for each other, our customers, and our community. DocTrials is an alliance of physician sites specializing in the conduct of clinical studies within their private practices. Sites in the alliance work under DocTrials' core standard operating procedures and quality control measures that provide a methodology ensuring the highest quality control and best practice utilization across sites. This provides assurance and confidence to sponsors that they will achieve quality data in the most efficient and timely manner. DocTrials was founded with the primary goal of connecting patients and physicians with clinical trials across the US; aiding in the process to discover new therapies, bring hope, and find new treatment for disease.

Job Title: Lead Clinical Research Coordinator (CRC) Location: Phoenix, Arizona 85050 Schedule: Monday–Friday, 9:00 AM–5:00 PM (On-site) Type: Contract-to-Hire, 6 month Pay: $35-$45/hour Overview We are seeking an experienced and driven Lead Clinical Research Coordinator to help build and lead a brand-new research department from the ground up. This individual will serve as both a hands-on coordinator and a leader, managing all aspects of clinical trials while guiding a new physician and eventually mentoring a team of CRCs. This is a unique opportunity for someone eager to take ownership, grow into a management role, and be the backbone of a developing clinical research program. Key Responsibilities • Serve as the primary point of contact for all clinical research activities at the site., • Perform end-to-end study coordination, from startup and recruitment through closeout., • Prepare and manage study documentation, including regulatory binders, source documents, and eSource/CTMS data entry., • Conduct participant visits, including consent, assessments, and procedures such as phlebotomy and EKGs as needed., • Oversee participant recruitment using EMR systems and community outreach initiatives., • Ensure all studies are conducted in compliance with FDA, ICH-GCP, and sponsor requirements., • Maintain meticulous documentation and quality control across all studies to ensure audit readiness., • Collaborate with and train a new physician principal investigator (PI), providing guidance on research processes and best practices., • Lead and mentor future CRC hires, delegating tasks, conducting quality reviews, and maintaining workflow balance., • Manage investigational product accountability and study supply inventory., • Prepare for and participate in sponsor, CRO, and FDA monitoring visits or audits., • Over time, assume expanded responsibilities such as budget negotiations and contract management. Typical Day Breakdown • Morning: Prepare for participant visits, review eSource systems, greet and consent participants, and perform study procedures., • Midday: Manage regulatory files, recruitment activities, and communication with the PI and site staff., • Afternoon: Conduct quality control reviews, mentor newer staff, and meet with sponsors or prepare for audits., • End of Day: Log activities in CTMS, organize documentation, and plan for upcoming study visits. Qualifications (Must-Have) • Minimum of 3 years of experience as a Lead Clinical Research Coordinator., • Proven ability to manage complex protocols independently from startup to closeout., • Strong regulatory knowledge, including IRB submissions, essential documents, and FDA/ICH-GCP compliance., • Fully comfortable in an on-site role (Monday–Friday)., • Exceptional organizational skills and attention to detail. Preferred Skills (Nice-to-Haves) • Phlebotomy and EKG experience., • Prior experience supporting sponsor or FDA audits., • Experience training or working with research-naïve PIs., • Familiarity with rating scales such as MADRS, SETS, CGI, CSSRS, or MOAA/S. Why This Role Is Exciting • Opportunity to lead and build a new clinical research program from the ground up., • Direct mentorship from a physician PI who values work-life balance and flexibility., • Clear career growth trajectory into a Research Manager role with team-building responsibility., • Supportive and human-centered work environment—understanding that life happens. This role is ideal for an experienced CRC who thrives in dynamic settings, loves taking initiative, and wants to grow into leadership.

We are seeking an experienced and driven Lead Clinical Research Coordinator to help build and lead a brand-new research department from the ground up. Collaborate with and train a new physician principal investigator (PI), providing guidance on research processes and best practices. Lead Clinical Re

Job Description Flight Coordinator: As an Air Ambulance Medical Flight Coordinator Case Manager, your primary responsibility will be to coordinate all aspects of patient transfer, by air or ground, to ensure continuity of patient care in all phases of each Air Ambulance transport. These may include, but are not limited to, transfers to a higher or specialized level of care for acute patients i.e. rehab, cancer, transplant, pediatric, end-of-life, emergency out-of-country evacuations and commercial medical escort flights. This position requires on-site office duties as well as work from home. Salary will be determined based on experience related to this position. Medical Flight Coordinator Case Manager Responsibilities Receiving and qualifying emergent and non-emergent requests for patient transfer, via air or ground ambulance, from Hospital Case Managers, Transfer Centers, Commercial Insurance Carriers, Corporate Partners and Private Families. Quoting, negotiating and coordinating day-to-day flight operations in accordance with all Federal and company regulations and requirements. Understanding Aircraft specifications, capabilities and aviation terminology to assist Operations in the scheduling of Aircraft and pending flights. Understanding medical conditions, terminology and flight physiology to appropriately communicate information to Clinical Manager and Medical Director in establishing patient transport status and coordination of transfer. Understanding Crew Resources and capabilities, both medical and flight. Briefing Flight and Medical Crews on all aspects of flights Fulfilling all special requests or notifications from Flight or Medical Crews. Monitoring the progress of all phases of transport and flight follow from departure through arrival. Updating All parties at each phase of the transport and providing a “high touch” experience for Case Managers, Corporate Partners, and Private Patient Families by being available to answer questions, address concerns and establish a level of comfort and trust. Implementing company safety procedures and policies, departmental procedures, and policies, as well operational standards and procedures. Conducting periodic market research to determine competitive industry position. Utilizing CRM for collecting, organizing and analyzing key market information, opportunities and client data to promote company brand and services. Reporting directly to Flight Coordination Supervisor Friday thought Monday. Four Ten hour shifts always worked consecutively.

Key Responsibilities: * Administer prescribed study and concomitant medications * Perform phlebotomy and handle the collection, processing, and shipment of biological samples * Perform ECGs, monitor vital signs, and carry out other specialized nursing procedures * Ensure accurate implementation of

Clinical Coordinator – Inpatient Wound Care RN (Day Shift). Are you an experienced RN with a passion for wound healing and leadership? Abrazo Arrowhead Campus is seeking a Clinical Coordinator for Inpatient Wound Care to lead and support our specialized team. Coordinate daily clinical operations o

Ensure quality patient care while maintaining cost-effective clinical operations in accordance with all legal, compliance, and regulatory requirements and programs. Minimum of 12 months of nursing experience, plus 6 months of specialized experience providing clinical nursing care to dialysis patien

RN Cardiac Clinical Coordinator Full Time Days Position Summary. THE RN CARDIAC CLINICAL COORDINATOR FULL TIME DAYS CANDIDATE WILL POSSESS THE FOLLOWING EDUCATION, LICENSE/CERTIFICATIONS, AND EXPERIENCE. Two years relevant clinical nursing experience and for Level II EQ Only: A minimum of two years

The Clinical Coordinator is responsible for assisti ng with management and operation of clinic. Growth: Assist with clinical and operational processes to improve patient health and minimize hospitalizations and missed treatments. Must have basic computer skills, including Microsoft Office (Word, Exc

Tenet-AZ Region is seeking a Registered Nurse (RN) Clinical Coordinator, Cardiology for a nursing job in Phoenix, Arizona. Clinical Coordinator Cardiac Progressive Care Unit/ Tele Position Summary. THE CLINICAL COORDINATOR CARDIAC CANDIDATE WILL POSSESS THE FOLLOWING EDUCATION, LICENSE/CERTIFICATION

DocCafe has an immediate opening for the following position: Physician Assistant - Academic/Faculty/Research in Arizona.

We are seeking an experienced and results-driven Construction Project Manager to oversee and manage multiple commercial construction projects nationwide.The ideal candidate will have a strong background in commercial construction management, a proven ability to lead teams and seamlessly work with su

The Operations Project Manager – Consumer Packaged Goods will oversee and manage full item life cycle(s) processes, coordinating timelines with cross-functional project teams.This includes but is not limited to item commercialization, sales analytics, inventory management, and demand planning, wit

We are looking for a detail-oriented and professional Front Desk Receptionist to support Arizona’s Safety Division.In this role, you will answer calls from the public and document critical safety incidents involving railroad and pipeline systems.Record safety incident reports.Review inspection and

Administrative Assistant / Receptionist.I wanted to share the details with you:.Administrative Assistant – Receptionist.E Camelback Rd, Phoenix, AZ 85016.Monday – Friday, 8:00 AM to 5:00 PM.Greet and assist walk-in members.Respond to basic member inquiries.Log incoming/outgoing mail and record c

Diamond Peak Recruiting is seeking experienced MEP Project Managers to lead high-profile data center projects for top-tier GCs.You'll oversee mechanical, electrical, and plumbing installations for hyperscale facilities powering AI and cloud computing, driving the industry's 12% annual growth.This in

Perform clinical tracers and report findings and plans for improvement if needed to Clinical Quality Management. Responsible for monitoring clinical supply policies and procedures, provide continuing education, preparation for The Joint Commission, Infection Control, Safety Procedures, Emergency Pre

Senior Project Manager – Transmission | Grid Planning & System Studies – Phoenix, AZ.Are you ready to lead critical transmission planning projects that will define the reliability and resilience of the U.Do you want to shape how utilities and system operators manage renewable integration, pl

Stanley Consultants is an award-winning and industry-leading global consulting engineering firm, with an unmatched commitment to culture, values, and ethics.We are dedicated to client experience and solve the most complex challenges to create a sustainable, connected, and enriched world for all.As t

Are you a quality-driven project leader who can effectively communicate and interact with internal and external stakeholders? Do you thrive on taking ownership from the design-build stage through close-out? Are you looking for a company that recognizes that the reason we work is to support the peopl

Ninyo & Moore Geotechnical & Environmental Consultants has an immediate opening for a Construction Services Project Manager in Phoenix, Arizona.The successful candidate will manage construction and material testing projects, including managing project budgets and meeting and interacting with

Required Skills: Strong Agile fundamentals with technical acumen required.Required to manage scrum ceremonies for two or more agile teams.Finalize commitments, sprint plans with Tech teams from a tech perspective PI Readiness Works within and across team(s) to anticipate, track, and resolve risks an

Senior Project Manager - Mechanical.We are seeking a highly skilled Senior Project Manager - Mechanical to oversee and manage complex mechanical projects from inception to completion.The ideal candidate will have a strong background in construction and mechanical systems, including HVAC, plumbing, a

Successful Project Coordinators should have a few years of experience in inventory control, excellent time-management skills, and knowledge of organizational techniques. Waahe Capital is looking for a highly motivated Project Coordinator with Inventory Management experience to join our Ops team. Pro

Come work as a construction Project Account Manager with a growing company.Project Account Managers are in charge of assisting our Reconstruction Project Managers in organizing our ongoing projects, as well as managing insurance carriers or third party administrators.This position involves new job i

Company is a worldwide provider of legal services, serving law firms, corporations, financial institutions and government agencieshelping them streamline the administration of business operations.Its scalable, flexible technology is designed to help you quickly and efficiently turn huge amounts of d

Join Our Team as a Water Resources Lead in Phoenix, AZ!.Are you a passionate and experienced.Do you thrive on leading complex projects, mentoring talented engineers, and making a real impact on community resilience? If so, we want you on our team in sunny Phoenix, AZ!.As our Water Resources Lead, yo

Come work as a construction Project Account Manager with a growing company.Project Account Managers are in charge of assisting our Reconstruction Project Managers in organizing our ongoing projects, as well as managing insurance carriers or third party administrators.This position involves new job i

At Agate Software, we are building a better world by revolutionizing how government agencies and nonprofits manage their grant processes.Our solutions empower our customers to maximize their resources, drive compliance, and focus on their core missions of distributing millions of dollars in funding

Rebuild Project Manager – Restoration Services.W Todd Dr Ste 103, Tempe, Arizona 85283.Commission % based on Overall Monthly Profitability.Right Restoration Partners is revolutionizing the emergency restoration industry.Backed by private equity, we’ve rapidly expanded since our launch in 2024 by

Keyser is a nationally recognized, full-service commercial real estate brokerage firm that exclusively represents tenants.Known as The Commercial Real Estate Disruptor by USA Today, Keyser provides clients with a comprehensive approach to commercial real estate strategy.The firm focuses solely on th

Company is a worldwide provider of legal services, serving law firms, corporations, financial institutions and government agencieshelping them streamline the administration of business operations.Its scalable, flexible technology is designed to help you quickly and efficiently turn huge amounts of d

We are actively looking for a Project Coordinator.

Provide assistance to the team as needed; research, data entry, etc.

Project Coordinator (DoD SkillBridge Internship). As a Project Coordinator in the Preferred Banking Division you'll play a vital role in aiding the successful execution of enterprise projects to realize enterprise goals and objectives.