Clinical research coordinator jobs in Irving, TexasCreate job alerts

Hours of Work : 40 Days Of Week : Work Shift : 8X5 Day (United States of America) Job Description : Your Job: In this highly visible, fast-paced, and challenging position, you'll collaborate with multidisciplinary team members to provide the very best care for our patients. The primary purpose of the Pathology Technical Coordinator position is to provide timely and accurate lab results and ensure compliance with all regulatory agencies for an assigned area. Your Job Requirements: • Bachelor's Degree in Chemical, Physical, Biological, Clinical Laboratory Science or Medical Technology, • MT(ASCP) or equivalent Your Job Responsibilities: • Communicate clearly and openly, • Build relationships to promote a collaborative environment, • Be accountable for your performance, • Always look for ways to improve the patient experience, • Take initiative for your professional growth, • Be engaged and eager to build a winning team Methodist Dallas Medical Center is one of North Texas’ best places to work. And it keeps getting better. The flagship hospital of Methodist Health System, Methodist Dallas is a 595-bed acute care teaching and referral hospital. It is home to the only adult Level I Trauma Center in southern Dallas, the first and only Certified Comprehensive Stroke Center in southern Dallas, and the newly renovated Linda and Mitch Hart Breast Center. Celebrating more than 90 years of service, we strive to have a diverse workforce that reflects the communities we serve and welcomes the skills and talents of all groups. Our reputation as an award-winning employer shows in the distinctions we’ve earned: • Magnet®-designated hospital, • 150 Top Places to Work in Healthcare by Becker’s Hospital Review, 2023, • Top 10 Military Friendly® Employer, Gold Designation, 2023, • Top 10 Military Spouse Friendly® Employer, 2023, • Level III Neonatal Intensive Care Unit, • Liver, kidney, and pancreas transplantation programs

WHY UT SOUTHWESTERN? With over 75 years of excellence in Dallas-Fort Worth, Texas, UT Southwestern is committed to excellence, innovation, teamwork, and compassion. As a world-renowned medical and research center, we strive to provide the best possible care, resources, and benefits for our valued employees. Ranked as the number 1 hospital in Dallas-Fort Worth according to U.S. News & World Report, we invest in you with opportunities for career growth and development to align with your future goals. Our highly competitive benefits package offers healthcare, PTO and paid holidays, on-site childcare, wage, merit increases and so much more. We invite you to be a part of the UT Southwestern team where you'll discover a culture of teamwork, professionalism, and a rewarding career! Exceptional Benefits That Support You – Personally and Professionally At UT Southwestern, we believe in taking care of the people who take care of others. As a full-time employee, you’ll enjoy a comprehensive benefits package designed to support your health, career growth, and work-life balance: • Free Medical Insurance – A free insurance plan tailored to your needs, • $10,000 Sign-On Bonus – A warm welcome to our team, half paid after 6 and the remainder after 12 months, • Teacher Retirement System (TRS) Contributions – Secure your future with state-supported retirement, • Tuition Reimbursement – Advance your education with financial support for continued learning, • Certification Pay & Referral Bonuses – Earn more for your expertise and help grow our team, • Clinical Ladder Program – Boost your earnings by up to $6,000/year based on your professional development, • Onsite Childcare – Convenient, high-quality care for your little ones while you work, • Exclusive Employee Discounts – Save on hotels, gym memberships, cellphone plans, and more, • Generous Paid Time Off – Enjoy holidays and vacations with a flexible PTO package To explore all the benefits UT Southwestern offers, visit: Our Benefits | UT Southwestern Medical Center Careers Nursing Opportunities to Follow your Heart About the Inpatient Float Pool Team ·The Inpatient Float Pool at UT Southwestern is a high-impact, system-level nursing team that ensures safe, responsive, and flexible staffing across both Clements University Hospital and Zale Lipshy Pavilion. Float Pool RNs and PCTs are cross-trained to support more than 30 inpatient units—including multiple critical care areas, med/surg, oncology, telemetry, progressive care, rehabilitation, and complex specialty services—adapting in real time to fluctuations in census, acuity, and staffing demands. · More than a coverage model, the Float Pool is a strategic clinical resource that partners with inpatient leadership, Central Staffing, and Hospital Administration to sustain safe care delivery and support hospital-wide operations. ESSENTIAL FUNCTIONS Job Duties • Performs and accurately documents physical, psychosocial, and emotional assessments. All assessments take into consideration age specific criteria (children, adolescents, adults and older adults)., • Actively anticipates patient's and/or patient's family needs and expectations and utilizes these in conjunction with the assessment to develop an appropriate plan of care for the patient., • Utilizes critical thinking skills in planning and prioritizing nursing care. Maintains and utilizes competencies per unit expectation. Identifies and implements appropriate nursing interventions based on the completed assessment., • Completes accurate and timely documentation of these interventions. Active coordinator of the interdisciplinary plan of care., • Confers with all members of the health care team in a collaborative fashion, sharing information and observations of the patient and/or patient's family in a manner that contributes to optimal patient care., • Appropriately prioritizes nursing interventions based upon completed assessment. Promptly identifies changes in condition as evidenced by nursing assessment, labs, x-rays, etc. Reports changes, takes follow-up action as appropriate., • Evaluates implemented interventions and modifies care according to the evaluation. Documents interventions and modifications to the plan of care in an accurate and timely manner., • Adheres to appropriate hospital and/or Department of Nursing policies, procedures, clinical pathways and nationally accepted standards of nursing practice while delivering nursing care to patients., • Suggests practices to enhance Nursing care based on current literature and research. Provides appropriate and timely answers and/or education to patient's and/or patient's families., • Completes accurate and timely documentation of all education provided. Obtains feedback/evaluation of understanding from patient/family, i.e., have we helped you? Patient/family verbalizes comfort with after discharge care., • Demonstrates effective communication with children, adolescents, adults and older adults. Welcomes and orients patient/family to the unit. Encourages patient/family participation in care. Required Education • (BLS) BASIC LIFE SUPPORT course accredited by the American Heart Association (AHA) or American Red Cross (ARC) Upon Hire and, • (ACLS) ADV CARDIAC LIFE SUPPORT course accredited by the American Heart Association (AHA) or American Red Cross (ARC) Upon Hire, • (RN) REGISTERED NURSE Current Texas RN license Upon Hire or (NLC) NURSING LICENSURE COMPACT-BNE Current Texas (or BNE Compact State) RN license Upon Hire and, • (NIHSS) Natl Inst Health Stroke Scale Certification Upon Hire and, • 3 years of nursing experience in an ICUKnowledge, Skills and Abilities, • Responds to all reasonable requests in an appropriate and timely manner and communicates in a concise and positive manner. Consistently maintains control of feelings, emotions, body language., • Maintains patient confidentiality in accordance with University Medical Center policy. Presents constructive feedback regarding system or process failures and participates in resolution in a proactive and positive manner., • Bending/Leaning Over, • Lifting, • Pulling, • Pushing, • Standing, • Stooping, • Clinical Setting EEO Statement UT Southwestern Medical Center is committed to an educational and working environment that provides equal opportunity to all members of the University community. As an equal opportunity employer, UT Southwestern prohibits unlawful discrimination, including discrimination on the basis of race, color, religion, national origin, sex, sexual orientation, gender identity, gender expression, age, disability, genetic information, citizenship status, or veteran status. BenefitsUT Southwestern is proud to offer a competitive and comprehensive benefits package to eligible employees. Our benefits are designed to support your overall wellbeing, and include: • PPO medical plan, available day one at no cost for full-time employee-only coverage, • 100% coverage for preventive healthcare – no copay, • Paid Time Off, available day one, • Retirement Programs through the Teacher Retirement System of Texas (TRS), • Paid Parental Leave Benefit, • Wellness programs, • Tuition Reimbursement, • Public Service Loan Forgiveness (PSLF) Qualified Employer, • Learn more about these and other UTSW employee benefits!

Job Description Overview: At Alliance Clinical Network we're people with a purpose, dedicated to advancing medical innovation and healing technology through groundbreaking research. We bring our energy and our passion to improving patient lives every day. Summary: Provide administrative and clinical support to research site by performing tasks such as assisting the front desk, taking vital signs, preparing exam rooms, etc. This is a temporary position for approximately 6 months. Essential Duties and Responsibilities: • Previous clinical research experience highly preferred, • Previous phlebotomy experience preferred, • Comfortable in a fast-paced clinical setting, • Perform study procedures such as EKG, vital signs, nasal swabs, and protocol specific procedures, • Accurately documenting patient information in health records, • Administer questionnaires and monitor patient compliance, • Acknowledge study patients' needs and tend to them appropriately, • Completion of accredited healthcare certification program, required., • 2 years’ experience in running research protocols, required., • 2 years’ experience in FDA regulations and GCP, required., • 2 years’ experience in phlebotomy and EKG, required., • Exceptional attention to details and organization., • Must possess excellent verbal and written communication skills., • Excellent customer service skills with internal and external stakeholders.

Job Description JOB LOCATION/SCHEDULE: Monday – Friday / on-site / LOCATION HERE COMPANY OVERVIEW: Alliance Clinical Network we’re people with a purpose, dedicated to advancing medical innovation and healing technology through groundbreaking research. We bring our energy and our passion to improving patient lives every day. SUMMARY: The ACRC will assist in the execution of clinical trials in compliance with study protocols, regulatory guidelines, and Good Clinical Practice (GCP). This position is ideal for individuals looking to grow their career in clinical research and contribute to advancing medical science. ESSENTIAL DUTIES AND RESPONSIBILITIES: • Assist in screening and recruiting study participants according to protocol eligibility criteria., • Schedule and coordinate participant visits, including study procedures, assessments, and follow-ups., • Collect and record study data accurately in case report forms (CRFs) and electronic data capture (EDC) systems., • Maintain study documentation, including source documents, regulatory files, and participant records., • Support informed consent discussions by ensuring participants understand study requirements., • Assist in monitoring participants for adverse events and report findings to the CRC or Principal Investigator (PI)., • Coordinate specimen collection, processing, and shipment per protocol requirements., • Ensure compliance with study protocols, institutional policies, and regulatory requirements (FDA, IRB, ICH-GCP)., • Prepare study materials, including study kits, lab supplies, and regulatory binders., • Communicate effectively with investigators, study sponsors, monitors, and other research staff., • Perform administrative duties related to research studies, such as data entry, filing, and appointment reminders., • Draw labs from study participants as required by protocol., • Process laboratory samples, including centrifugation, aliquoting, and storage per protocol specifications., • Ship biological samples following regulatory guidelines and sponsor instructions. QUALIFICATION REQUIREMENTS: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. EDUCATION AND EXPREIENCE: • Bachelor’s degree in a health-related field (e.g., Biology, Nursing, Public Health, or related discipline) preferred. Equivalent experience may be considered., • Certified Phlebotomy Technician (CPT) certification required., • Prior experience in healthcare, research, or clinical settings is a plus but not required., • Basic knowledge of clinical research processes and regulations (GCP, FDA, IRB) is a plus., • Strong organizational skills and attention to detail., • Excellent communication and interpersonal skills to interact with patients, staff, and external stakeholders., • Ability to work both independently and collaboratively in a fast-paced environment.

Job Description 60% Travel is Required for this Position ESSENTIAL DUTIES AND RESPONSIBILITIES: • Partner with Regional Site Director to ensure compliance and productivity of all clinical site staff and operations., • Manage, train and support clinical site staff., • Review, comprehend and communicate study protocols., • Oversee Site Initiation Visit (SIV), Pre-Study Validation Visit (PSV) and Interim Monitoring Visit (IMV)., • Assist CRC team as requested to facilitate research and business needs., • Conduct and manage clinical trials in accordance with the study protocol guidelines and internal SOP’s., • Ensure all data is entered into sponsor’s data portal and all queries are resolved in a timely manner., • Work closely with CRO/CRA and IRB., • Perform administrative tasks such as ordering supplies and equipment for the study., • Manage all required study start up documentation, training and timelines on assigned study protocols. QUALIFICATION REQUIREMENTS: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. EDUCATION AND EXPREIENCE: • Associate’s degree and/or completion of accredited healthcare certification program, required., • Comfortable stepping into a leadership role., • 4+ years’ experience in clinical research, required., • 4+ years’ experience working as a Clinical Research Coordinator, preferred., • Comprehensive knowledge of FDA, GCP & confidentiality., • Exceptional attention to detail and organization., • Excellent written and communication skills. TRAVEL INVOLVED: 60% BENEFITS: • 401 (k) Retirement Plan, • Medical, Dental, and Vision Insurance, • Paid Time Off (PTO), • Floating Holidays, • And more!

Job Description Summary: The Clinical Research Coordinator (CRC) manages and coordinates clinical research studies, ensuring they are conducted efficiently, ethically, and in compliance with regulatory requirements. The role involves working with principal investigators, research staff, and study participants to oversee all aspects of trials, including recruitment, data management, regulatory compliance, and monitoring participant progress. Duties and Responsibilities: The Clinical Research Coordinator: • Performs study subject., • Screens and recruits’ subjects., • Doses and administers study drugs and/or implements study methodologies., • Accounts for study drugs., • Communicates with subjects and medical group providers, including the Principal Investigator and any Sub-Investigators., • Accounts for study drugs., • Communicates with subjects and medical group providers, including the Principal Investigator and any Sub-Investigators., • Collects, labels, stores, and ships specimens collected from subjects in connection with a clinical research trial., • Enters patient and research data in systems designated by the company., • Maintains patient charts and resolves research queries., • Monitors study activities to ensure compliance with study protocols and with applicable federal, state, and local regulatory and site requirements., • Maintains required records of study activity including case report forms, drug dispensation records, and regulatory forms., • Tracks enrollment status of subjects and documents dropout information, such as dropout causes and subject contact efforts and communicates this information as directed., • Assess eligibility of potential subjects through methods such as screening interviews, reviews of medical records, and discussions with physicians and other health care professionals., • Oversees subject enrollment to ensure that informed consent is properly obtained and documented., • Records adverse events and side effect data and confers with Investigators regarding the reporting of events to oversight agencies., • Prepares for or participates in quality assurance audits conducted by study sponsors, federal agencies, or designated review groups., • Creates source documents as assigned, such as regarding protocols, memos, patient participation., • Prepares study-related documentation such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, and progress reports., • Reviews proposed study protocols to evaluate factors such as sample collection processes, data management plans, and potential subject risks., • Instructs research staff in scientific and procedural aspects of studies including standards of care, informed consent procedures, or documentation procedures., • Collaborates with Investigators and Company Management to prepare presentations or reports of clinical study procedures, results, and conclusions., • Communicates with laboratories or investigators regarding laboratory findings., • Reviews scientific literature, participates in continuing education activities, and/or attends conferences and seminars to maintain knowledge of clinical research., • Orders drugs or devices necessary for study completion., • Documents findings and events in the Company’s research CTMS platform and in other binders and platforms as directed., • Occasional travel to Company sites, Principal Meetings, and/or Company meetings. Requirements: Minimum high school diploma required. • Bachelor's degree in Life Sciences, Nursing, or a related field (preferred)., • Previous Psychiatric experience required., • Previous experience in clinical research or a related role., • Familiarity with Good Clinical Practice (GCP) and regulatory guidelines (FDA, ICH)., • Certification as a Clinical Research Coordinator (e.g., ACRP, SOCRA) is a plus., • Strong organizational and time management skills., • Excellent attention to detail and ability to maintain accurate records., • Effective communication skills, both written and verbal., • Ability to work independently and collaboratively in a team environment., • Prolonged periods of sitting at a desk and working on a computer, • Must be able to lift 20 pounds at a time., • Travel to our Houston, Texas site is required.

Job Description SUMMARY: The Sr Central Services Coordinator oversees the daily function of multi-site clinical research programs on required protocols. The Sr Central Services Coordinator works virtually with the central services team, on-site clinical staff, and patients to ensure protocols are met. ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. 1)Comply with all company policies, procedures, and conduct. 2)Strictly adhere to confidentiality and compliance standards. 3)Lead the Central Services team in virtual clinical research coordination of study subjects and quality study protocol adherence. 4)Oversee quality standards of the Central Services processes and protocols. 5)Train and oversee Central Service Coordinators and Central Service Coordinator JRs. 6)Communicate the efficiency and productivity results of the team to management and actively source solutions for improvements. 7)Virtually communicate effectively and courteously with study patients via tele-health platform. 8)Demonstrate a caring and pleasant demeanor toward patients and their families. 9)Acknowledge study patients' needs and tend to them appropriately. 10)Collects patient medical history and conditions. 11)Conduct study visits across all sites via tele-health platform. 12)Ensure Informed Consents are obtained by on-site staff. 13)Participant study visit review and completion. 14)Ensure data quality. 15)Collect and evaluate medical records for compliance. 16)Conduct A/E and SAE assessments. 17)Maintain and update regulatory files. 18)Ensure accuracy of data collected. 19)Review study e-source documents to comply with study protocol. 20)Manage all required study documentation, training, and timelines on assigned study protocols. 21)Participate in CRO/Sponsor/Audit interactions. 22)Meet deadlines and goals as assigned. QUALIFICATION REQUIREMENTS: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. EDUCATION and EXPERIENCE: 1)Associate’s degree in healthcare or related field, preferred. 2)4+ years experience working in Clinical Research, required. 3)4+ years experience in leading clinical teams. 4)2 years experience in healthcare, required. 5)2 years experience in FDA regulations and GCP. 6)Comprehensive knowledge of FDA, GCP and HIPAA as applied to clinical research. 7)Knowledge of current studies being conducted. 8)Comprehensive knowledge of company's SOPs, policies and Confidentiality agreements. 9)Knowledge of safety hazards and procedures that establish a safe work environment.t 10Skilled in computer and data collection software 11)Excellent customer service skills with internal and external stakeholders. 12)A proven ability to multi-task in a rapidly changing environment. BENEFITS: • 401 (k) Retirement Plan, • Medical, Dental, and Vision Insurance, • Paid Time Off (PTO), • Floating Holidays, • And more! WORK LOCATION: Irving, Texas

Job Description Summary: The Clinical Research Compliance Specialist supports clinical research studies by monitoring protocol and regulatory compliance, reviewing research data for accuracy, managing documentation and milestones, auditing essential documents, writing monitoring reports, and developing risk monitoring plans and study-related documents. Essential Duties and Responsibilities: • Conduct SOP/GCP/Compliance Training with coordinators at site., • Ensure sites are adhering to ACN’ s policies and procedures., • Perform on-site and remote audits as a quality assurance tool that is used to evaluate compliance and to ensure human subject protection and data integrity., • Ensure valid findings from the audit/inspection report are managed effectively by the organization, and in accordance with our procedures. Escalate significant findings to CTNx Management., • Coach and Support CRCs and PIs on a continuous basis based upon audit findings., • Monitor the protocol and regulatory compliance of clinical research studies (with low —to high-risk research designs) in multiple treatment areas., • Review research data from source documentation for accuracy, completeness, and timeliness., • Collaborate with the offshore compliance team and the onsite study team to effectively address critical findings., • Strictly adhere to confidentiality and compliance standards., • Collect, review, maintain, and audit essential documents, • Assist with developing documents and implementing study-specific risk monitoring plans., • Support ongoing communication with study teams regarding trial qualification, initiation, monitoring, remote monitoring, and close-out activities., • Serves as the main point of contact in compliance audits and interim monitoring visits., • Read and comprehend new research protocols as well as amended protocols., • Meet assigned targets, goals, and completion deadlines., • Utilize analytical, problem-solving, and critical thinking., • Utilize precise attention to detail., • Perform other duties as assigned to meet the goals and objectives of the department and institution, • Comply with all company policies, procedures, and conduct. Qualification Requirements: To perform this job successfully, an individual must be able to satisfactorily perform each essential duty. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform essential functions. Education and Experience: • An associate degree in healthcare or a related field is preferred., • At least two (2) years of clinical research experience as a Clinical Research Coordinator (CRC) or one (1) year of experience as a Clinical Research Associate (CRA) is required., • Proficient in Microsoft Word, Excel and Adobe Acrobat., • Working knowledge of medical and/or clinical trial terminology., • Working knowledge in relevant scientific fields., • Strong attention to detail., • Must be able to prioritize competing demands., • Must possess excellent verbal and written communication skills., • A proven ability to multi-task in a rapidly changing environment. Special Skills, Knowledge, and Abilities: • Understands the task at hand, seeks out information, and draws conclusions from available data to deliver outcomes., • Adapts quickly to changing priorities to perform as needed in his/her role., • Remains calm when faced with changes to (and in) his/her work., • Effectively relays understanding of diverse perspectives., • Can handle communication upwards and downwards as needed., • Presents information in a clear, well-thought-out way and tailored to the audience., • Shows support for the new direction even when the details have not been finalized., • Spots early indications of underperformance and takes corrective actions. Celebrates successes., • Works with partners inside his/her function to find the best solutions that align with functional priorities. Is easy to work with to find solutions., • Supports the creation/implementation of data management plans by understanding site/study data sourcing techniques and overall compilation., • Independently assists data management tasks/processes in line with study-related data plans., • Identifies and resolves data queries and requirements based on knowledge of the origin, flow, and management of data through a clinical study., • Ensures compliance with SOPs related to data quality within assigned studies., • Contributes to study management and research procedures by consistently executing assigned tasks in compliance with GCP guidelines, with minimal supervision, • Applies understanding of clinical study/site operations to address requirements (e.g., study selection and set-up, clinical monitoring, risk mitigation support)., • Shows awareness of basic safety, ethical, and HPP considerations, and regulatory requirements in terms of documentation and study conduct., • Assists in the development of relevant technical, study, and/or regulatory materials to ensure compliance with regulatory, safety, & ethical requirements. Certificates, Licenses, Registrations: Maintain GCP certification and other on-the-job certifications as required. Travel Required: 5-10% Physical Demands and Working Conditions: The physical demands described here are representative of those that an employee must meet to successfully perform the essential functions of this job. • Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions., • While performing the duties of this job, the employee is regularly required to stand, walk, sit, kneel, use hands to finger, handle, or feel, and talk or hear., • The employee must occasionally lift and/or move up to 25 pounds., • This job requires Specific vision abilities, including close vision, depth perception, and the ability to adjust focus., • The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job., • Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions., • An essential function of the job is to be able to comply with all applicable federal, state and local safety and health regulations that would apply to this job., • The employee must move about the workspace to access work surface and shelves, cabinets, drawers, and equipment that are at, below or above the work surface., • Nothing in this job description limits management’s right to assign or reassign duties and responsibilities to this job at any time as business needs dictate. This job description reflects management’s assignment of essential functions; it does not proscribe or restrict the tasks that may be assigned. The information contained herein is not intended to be an all-inclusive list of the duties and responsibilities of the job, nor is it intended to be an all-inclusive list of the skills and abilities required to do the job. While every attempt has been made to outline the basic job responsibilities, adjustments in the process may change and expand the job duties. In addition, employees may be asked to perform duties outside of this description at the discretion of the Executive Management Team.

Job Description ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. 1. Comply with all company policies, procedures, and conduct., 2. Strictly adhere to confidentiality and compliance standards., 3. Communicate effectively and courteously with study patients regarding study objectives and ongoing instructions., 4. Administer questionnaires and monitor participant compliance., 5. Acknowledge study patients' needs and tends to them appropriately., 6. Collect patient medical history and conditions., 7. Obtain Informed Consent., 8. Study drug dispensation records, accountability., 9. Liaison with laboratories to ensure timely participant testing, 10. Collect and evaluate concomitant medication., 11. Collect and evaluate medical records for compliance., 12. Conduct A/E and SAE assessments., 13. Perform EKG, vital signs, nasal swabs and protocol specific procedures., 14. Evaluate clinical lab reports., 15. Maintain office site regulatory files., 16. Verify accuracy of data collected., 17. Assist with the recruitment and engagement of study subjects as needed., 18. Document temperatures for IP stored on-site., 19. Develop study e-source documents to comply with study protocol., 20. Manage all required study startup documentation, training, and timelines on assigned study protocols., 21. Meet all study protocol requirements and deadlines., 22. Manage and adhere to study budgets., 23. Participate and support IMV (interim monitoring visits) and site initiation visits. QUALIFICATION REQUIREMENTS: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. EDUCATION and EXPERIENCE: 1. Associate’s degree in healthcare or related field, preferred., 2. 4 years’ experience in Clinical Research and knowledge of protocols and procedures, required., 3. 4 years’ experience in FDA regulations and GCP., 4. 2 years’ experience in phlebotomy and EKG, required., 5. Proven track record of analytic reasoning skills., 6. Exceptional attention to details and organization., 7. Must possess excellent verbal and written communication skills., 8. Excellent customer service skills with internal and external stakeholders., 9. A proven ability to multi-task in a rapidly changing environment. WORK LOCATION: Dallas, Texas BENEFITS: • 401 (k) Retirement Plan, • Medical, Dental, and Vision Insurance, • Paid Time Off (PTO), • Floating Holidays, • And more!

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

The Project Manager is responsible for the day-to-day oversight and coordination of construction activities.Project Managers are responsible for managing each project from inception to completion.This includes the initial estimation of a project, the buying-out of commitments, preparation of master

This position is responsible for providing project management systems and technical direction to EPC projects teams for the purpose of delivering safe, cost-effective and quality execution of small to medium scale electric substation, transmission, and distribution projects and/or client accounts.Th

We are looking for a proactive and ambitious Project Manager who is able to successfully run a project that is completed to exceed the expectations of the client.This candidate will plan and supervise all construction activities from inception to completion.They will work closely with other members

Project Manager- Commercial General Contractor.Ground-Up Commercial Construction.Our client, a well-established General Contractor with a strong reputation in the Dallas market, is seeking an experienced Project Manager to join their team.Specializing in ground-up commercial projects, including groc

A prestigious architecture and design firm is looking to hire a Project Coordinator/Office Manager to work closely with the executives and project managers. Collaborate with Office Coordinators in other offices.

My client is searching for a full-time licensed.The candidate should have a high-level of design and leadership ability to help the clients achieve their workplace goals and objectives and to mentor other employees.The candidate shall be both highly organized and collaborative, as well as, high-perf

Looking for candidates in both the Magnolia, Tomball, Conroe, Spring, The Woodlands area OR Austin, Roundrock, Hutto area.MBA Energy & Industrial, LLC (mba-nrg.Magnolia, Texas, north of Houston is immediately hiring an energetic and experienced Project Manager for managing Oil and Gas Process Facili

Project Managers with experience in.The selected candidate will be responsible for the end-to-end leadership of project delivery and client development, ensuring operational excellence, strict adherence to safety protocols, and financial accountability from project initiation to closeout.Provide com

About Dovetail Custom Wood & Metal.Dovetail is one of the leading architectural fabrication firms in the U.Our work spans luxury high-rise hotels, premier restaurants, elite residential towers, and iconic public venues.We thrive on complexity, detail, and craftsmanship.When others say it can’t be

Ready to lead high-impact projects and grow into firm ownership?.This is a unique opportunity to join a respected structural engineering firm as a Senior Project Manager and technical lead, with a clear path to Principal in an employee-owned company.This established and design-focused structural eng

Bi-Annual Bonus, Vehicle, 401k, Insurances, Progression.Are you a Senior Project Manager with concrete, tilt wall experience looking to make your mark on Texas’s landmark projects?.Are you looking to lead a team and manage some of the largest concrete construction projects in the country?.This is

SSARCO of TX, PLLC has an immediate opening for an experienced.This is an IN-OFFICE position, Monday through Friday, from 8:00 a.Qualified applicants will send cover letter, resume, references, and portfolio to is a Dallas-based commercial architecture firm focused on building s

Senior Project Manager - Structural Engineering (Dallas, TX).Lead impactful work in a firm built on trust, mentorship, and long-term growth.A respected structural engineering firm in Dallas is seeking a.With a strong pipeline of work arriving in the next few weeks, they're looking for a.The firm has

Senior Electrical Project Manager (Healthcare).Must commute into Dallas, TX (Willing to pay relocation).Salary Range: $170,000 - $200,000.All relevant experience needs to be within the last 6 years (recent healthcare facility project work).Minimum 5 years of experience as an electrical project manag

The Senior Construction Project Manager (CPM) plays a ‘hands-on’ role as the primary point of contact for commercial projects globally.This position is responsible for executing projects, developing project schedules and budgets, managing trades and ensuring successful, on-time and on-budget (ma

Water/Wastewater Construction (Dallas Area).I’m partnering with a well-established heavy civil contractor in the Dallas Area region that is actively growing its team and works on Projects in the range of $40 - 200M.Water & Wastewater Treatment Plants.We are looking to identify strong talent in the

Project Manager – Land Development.I'm partnered with a top civil engineering and land development firm in Dallas, which is looking for an experienced Project Manager to join their growing Dallas office.This is an outstanding opportunity for a senior-level civil engineer who thrives in leadership,

THIS IS NOT A TECH POSITION – MUST HAVE KNOWLEDGE OF COMMERCIAL HVAC AND PLUMBING SYSTEMS.Way Mechanical is seeking a Project Manager to join our team! Way Mechanical is one of the nation’s largest and most experienced mechanical contractors.We specialize in commercial air conditioning, plumbing

Supports the Project Manager in planning and executing self-perform drywall projects, ensuring quality, budget, and schedule goals are met.Assists with cost tracking, documentation, coordination, and communication across field and office teams.POSITION RESPONSIBILITIES AND DUTIES:.Able to perform al

Ventana is seeking a well-rounded Project Managers for insulated metal panel (IMP).The PM will oversee installation, project.Manage scope, schedule, and budget for insulated metal panel projects.Coordinate with internal teams, subcontractors, and vendors to meet project requirements.Review and inter

My client is seeking a highly skilled and experienced Project Manager to join their team in Dallas.This role is perfect for someone with 7+ years of experience in land development, with at least 1-2 years as a Project Manager.Experience in single-family residential projects is preferred.Lead and man

Jamail & Smith stands as a beacon of excellence in construction, committed to unparalleled customer service and pioneering operational standards.Since our founding in 1982, we have proudly delivered over 7,900 projects with precision and efficiency, earning the trust of more than 80 public entities

Founded in 2007, Ward Getz & Associates LLC (WGA) is a Texas based professional consulting firm that has steadily grown in a competitive market by consistently delivering exceptional quality and service.Our success is rooted in the belief that creative design drives successful projects and that stro

Compensation: $100,000-$140,000, Bonus, Truck, Full Benefits, and Company Stock.One of the premier Healthcare General Construction companies is adding a Project Manager to their Healthcare team due to company growth.This GC is 100% employee-owned and offers a lucrative employee stock option plan (ES

Senior Project Manager – Concrete Construction - Dallas, TX Region.Are you a seasoned concrete construction leader ready to take the reins on high-profile concrete projects across Texas? This is your opportunity to join a respected, forward-thinking concrete subcontractor with a strong pipeline an

Join a team where your leadership directly impacts the next generation, design and deliver inspiring educational spaces for students and communities.A well-established and respected engineering consultancy is seeking a.Dallas office, leading complex structural projects across a diverse range of sect

Project Manager - Commercial Construction.Bonus + Auto Allowance + Excellent Health Insurance + 401(k).This is a standout opportunity for a proven construction leader to step into a high-impact role with one of the most respected General Contractors in Texas.Our client is a powerhouse in commercial

Healthcare | Industrial | Data Center | Commercial Construction.Are you an experienced Electrical Project Manager ready to take the lead on high-value, complex projects? One of Texas' premier electrical contractors is expanding its Dallas team and looking for a driven professional to manage a divers

Austin team! This role is perfect for someone who thrives in the fast-paced world of construction and wants to play a key role in bringing projects to life.You’ll work alongside experienced project leaders to oversee and drive all phases of construction projects — from planning to execution.You�

The purpose of this position is to provide advanced administrative and clerical support to a respective department, managerial staff and/or director.This is accomplished by providing customer service to the agency membership, public and staff, processing information; organizing committee, public, an

Corporate Interior Project Manager/Estimator - North Dallas.Blayze Recruitment is partnering with a.With a reputation for precision and style and more than.Lead estimating and project management for.Manage contracts, budgets, procurement, subcontractor negotiations, and change orders.Oversee the ent

Senior Project Manager | Dallas, TX.My client is seeking a versatile Project Manager to join their Dallas-based land development team within a well-established civil and environmental consulting firm.With nearly 30 years in business and offices across multiple states, the company is known for delive

CapX Project Manager – Leading Projects That Shape Communities.Location: Irving, TX (corporate office), Up to 60% travel required.MUST have distressed property renovation and value add experience!.Knowledge in structural repairs, foundation work, exterior systems, HVAC, site work, value-add renova

We are currently hiring a Project Coordinator for our office in Dallas, Texas, just northwest of the downtown area. The primary responsibilities of a Project Coordinator include:.

We are seeking a highly experienced.This role is with a well-established general contractor that has been consistently recognized as one of the.About the Company (Highlights).A Texas-based builder with more than.Recognized for its strong culture of collaboration, integrity, and long-term employee de

The Senior Project Manager will organize, manage, and plan complex projects for the organization and ensure that goals and objectives are accomplished within the timelines set forth in the contract.Oversees a team to ensure projects are completed on time and to specifications.Delegates work and assi

The ideal candidate will oversee projects from bidding to execution.You will work with senior management and act as the point of contact for clients.Oversee all stages of project life cycle.Provide timely status reports to stakeholders.Strong organizational and project management skills.Industry kno

We are representing multiple leading Electrical and MEP contractors in the Dallas / DFW area who are seeking experienced Project Managers at all levels to join their growing teams.Roles range from Project Manager through Senior Project Manager to Project Executive, offering exciting opportunities to