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Apidel Technologies is seeking a local contract nurse RN Clinical Coordinator, Research / Clinical Research for a local contract nursing job in Newport Beach, California. Job Description & Requirements • Specialty: Research / Clinical Research, • Discipline: RN, • Start Date: ASAP, • Duration: 13 weeks, • 40 hours per week, • Shift: 8 hours, days Key Responsibilities • Manage Phase I–IV clinical trials (industry-sponsored, government-funded, investigator-initiated), • Ensure compliance with GCP, FDA, NIH, and OHRP regulations, • Perform protocol review, study start-up, and site initiation activities, • Lead informed consent process and patient education, • Conduct subject recruitment, screening, and eligibility assessments, • Perform clinical assessments and sample collection (IATA compliant), • Maintain regulatory binders, source documentation, and study files, • Complete case report forms (CRFs) and resolve data queries, • Monitor and report adverse events (AE/SAE), • Enter and validate data in clinical research databases (EDC systems), • Participate in monitoring visits, audits, and study meetings, • Support budgeting, cost analysis, and financial tracking of studies, • Mentor junior CRCs and support team development Required Qualifications • Active Registered Nurse (RN) license – California, • BLS Certification, • Minimum 2+ years of clinical research experience, • Proficiency in Microsoft Office (Word, PowerPoint) Apidel Technologies Job ID #API1798. About Apidel Technologies At Apidel Technologies LLC, we specialize in delivering high-impact healthcare staffing solutions that empower organizations to maintain operational excellence and deliver exceptional patient care. With our headquarters in Illinois and regional offices in New Jersey, California, and Georgia, we offer both nationwide reach and local insight to support the dynamic workforce needs of healthcare providers across the U.S. We deliver unmatched expertise in placing top-tier healthcare professionals, including Registered Nurses, Licensed Practical Nurses/Licensed Vocational Nurses, Certified Nursing Assistant/Certified Medical Assistant, and Nurse Practitioners, Medical Laboratory Scientist, Phlebotomist, Histologists, across a diverse spectrum of care settings such as hospitals, clinics, rehabilitation centers, long-term care facilities, correctional institutions, and more. Our deep talent network and sector-specific understanding position us as a valuable partner to client platforms, enabling a scalable and seamless workforce experience for healthcare employers and job seekers. Since our founding in 2012, Apidel has earned the trust of Fortune 500 healthcare organizations, mid-sized providers, and government agencies at the county and state levels. We provide end-to-end staffing services, contingent workforce solutions, direct hire, temp-to-hire, and executive search, designed to align with your clinical and operational objectives. As a certified WBENC firm, we are committed to Diversity, Equity, Inclusion & Belonging (DEI&B) and take a client-centric approach that combines industry insight, agile delivery models, and culturally competent staffing to help our clients thrive in today’s fast-evolving healthcare Benefits • 401k retirement plan, • License and certification reimbursement, • Medical benefits, • Dental benefits, • Vision benefits, • Referral bonus, • Sick pay

Pride Health is hiring a Clinical Research Coordinator RN! (Full time, ON-SITE) Schedule: Monday-Friday (8:30am-5pm) Type: Permanent, full time Pay Rate: $55-75/hour Specific Duties: • Manages complex clinical research trials, including industry-sponsored, government-funded, and investigator-initiated studies., • Ensures compliance with Good Clinical Practice, FDA regulations, and human subject protection standards., • Coordinates overall study operations, including protocol review, study initiation, and informed consent., • Conducts subject recruitment, screening, and eligibility assessments., • Collects, processes, and documents laboratory samples in compliance with IATA standards., • Completes protocol-required clinical assessments and procedures., • Collects, enters, and maintains accurate study data; completes case report forms and resolves data queries., • Monitors and reports adverse events per protocol and regulatory requirements., • Maintains regulatory documentation and study binders., • Participates in study meetings and site initiation visits. Must have qualifications/experience: • Active RN License, • Two or more years of experience performing clinical research duties or equivalent experience and training, • Knowledge of Good Clinical Practices, protection of human subjects, and FDA regulatory guidelines, • Working knowledge of FDA, NIH, and OHRP regulatory requirements., • Working knowledge of ICH Good Clinical Practice guidelines., • Understanding of clinical trial methodologies., • Experience filing Institutional Review Board documentation Apply for this role with Pride Health! “Pride Global offers eligible employee’s comprehensive healthcare coverage (medical, dental, and vision plans), supplemental coverage (accident insurance, critical illness insurance and hospital indemnity), 401(k)-retirement savings, life & disability insurance, an employee assistance program, legal support, auto home insurance, pet insurance, and employee discounts with preferred vendors."

Job Description SUMMARY OF POSITION: The Product Coordinator supports the planning, development, and execution of a defined product line within our equipment category. This role is ideal for someone who is passionate about sports, detail-oriented, and eager to learn how high-performance products are brought to life—from concept to market. Work closely with cross-functional teams, helping manage product data and timelines, assisting in market and consumer analysis, and ensuring the successful execution of product launches. ESSENTIAL FUNCTIONS: • Product Support & Development: Assist in the creation of product briefs, specifications, and documentation for new product concepts. Support cross-functional teams (Design, R&D, Sourcing) throughout development stages. Help track prototypes, testing feedback, and product samples. Maintain accurate product information, SKU setup, and updates in product management systems., • Market & Consumer Insights: Conduct basic category research, competitive scans, and trend analysis. Gather athlete and consumer feedback to support product decision-making. Help analyze sales and performance data to identify opportunities and gaps., • Project Coordination: Assist in managing product timelines, calendars, and key milestone deliverables. Coordinate sample requests, product meetings, and cross-functional communication. Support the development and preparation of presentations for line reviews and product updates., • Go-to-Market Support: Collaborate with Marketing on launch materials, product stories, and asset needs. Work with Sales to prepare assortment tools, product decks, and account support materials. Help review packaging copy, instructions, and product information for accuracy., • This is a full-time position, • Typical work hours and days are Monday – Friday, 8:30 a.m. to 5:00 p.m., • This position is based out of the Fountain Valley, CA office, • Some travel may occur (usually less than 10%), domestic or international., • The Company is committed to fair, equitable, and transparent compensation. Final compensation will be determined by various factors such as your relevant work experience, education, certifications, skills, and geographic location., • The salary range for this role in Fountain Valley, CA is $65,000 - $78,000., • Bachelor’s degree in Business, Marketing, Product Design, or a related field., • 0–2 years of experience in product management, merchandising, marketing, or relevant internships (sporting goods/outdoor preferred)., • Strong organizational skills and attention to detail., • Comfortable working with data and basic analytics., • Effective communicator with the ability to work cross-functionally., • Passion for sports, fitness, and innovative athletic equipment. PHYSICAL DEMANDS/WORK ENVIRONMENT: Candidate must be able to successfully perform the essential functions of this job with ability to: be in a stationary position 50% of the time; occasionally move about inside the office to access fine cabinets, office machinery (such as a calculator, copy machine, printer, etc.); constantly operate a computer; occasionally ascend/descend stairs; constantly position self to maintain files in file cabinets; the ability to communicate information and ideas so others will understand; must be able to exchange accurate information in these situations; the ability to observe details at close range (within a few feed of the observer); and frequently move boxes weighing up to 15 pounds across office for various needs. Ability to work in outdoor weather conditions if projects/opportunities arise. The noise level in the work environment is usually moderate. This job specification should not be construed to imply that these requirements are the exclusive standards of the position. Incumbents will follow any other instructions and perform any other related duties as may be required by their supervisor. Reasonable accommodations may be offered to enable individuals with disabilities to perform the essential functions. The requirements listed are representative of the knowledge, skill, and/or ability required. United Sports Brands is an Affirmative Action and Equal Employment Opportunity (EEO) employer.

Job DescriptionNational Institute of Clinical Research, a research organization serving the pharmaceutical and biotech industries, is searching for a highly experienced Medical assistant with Phlebotomy experience to assist our research coordinators in clinical trials. The Research Assistant will be responsible for assisting the Research Study Coordinator in recruiting subjects for assigned clinical trials and coordinating the research activities and visits for the subjects enrolled in research projects. Essential functions include scheduling research visits for subjects enrolled in clinical trials, the performance of EKG, routine phlebotomy, other lab assessments such as vital signs, and obtaining necessary lab results for the subjects. The research assistant will also be responsible for assisting the study coordinator in reviewing and requesting medical records. Must have experience with PC software applications including word processing. The ability and willingness to learn new software programs is also required. QUALIFICATIONS Medical assistant / Phlebotomist with at least one to two years of clinical experience (certification preferred) or a laboratory technician with at least one to two years of clinical experience. Bilingual proficiency in English and Arabic preferred Location: Huntington Beach, CA Employment Type • Full-Time, • This is not a remote position Benefits: • Medical Insurance, Dental Insurance, Vision Insurance, 401k, PTO

Job Description Real Estate Coordinator Costa Mesa, CA Boardwalk Investments Group, LLC ("Boardwalk") is a privately held commercial real estate investment company. Headquartered in Costa Mesa, California, the Firm currently manages a commercial real estate portfolio comprised of retail, mixed-use, office and multifamily assets located primarily in Orange County, California. Since 2012, Boardwalk's investment strategy is to actively acquire, stabilize, and manage commercial real estate located in core, coastal markets in California. The Real Estate Coordinator supports the site selection, evaluation, and leasing process by coordinating research, documentation, and communication across brokers, landlords, internal teams, and vendors. ESSENTIAL DUTIES AND RESPONSIBILITIES • Lead the research and identification of potential office locations within Orange County aligned with operational, technical, and budget requirements, • Serve as a primary point of coordination with brokers, property managers, and leasing contacts to obtain complete and accurate property information, • Evaluate prospective locations against required criteria including size, power capacity, connectivity options, zoning, parking, and building infrastructure, • Coordinate, schedule, and attend property tours; independently document findings, photos, utilities, and rental details for internal review, • Develop and maintain detailed tracking systems, spreadsheets, and comparison tools to support site selection decisions, • Proactively manage follow-ups with brokers and landlords to clarify specifications, request supplemental documentation, and confirm site feasibility, • Prepare clear internal summaries, comparison analyses, and recommendations to support leadership decision-making, • Support the real estate and operations teams throughout the site selection, due diligence, and expansion process, ensuring timelines and deliverables are met REQUIRED QUALIFICATIONS • Bachelor’s degree in real estate, Business, Finance, or a related field, or equivalent professional experience, • 1+ years of experience in real estate coordination, commercial leasing, property management, or a related role preferred, • Strong attention to detail with the ability to evaluate, compare, and summarize multiple property options and data points, • Highly organized and self-directed, with the ability to manage multiple priorities and conduct independent research, • Proficiency in Microsoft Office Suite, particularly Excel for tracking, analysis, and comparison reporting The above is intended to describe the general content of and requirements for the performance of this job. It is not to be construed as an exhaustive statement of duties, responsibilities or requirements. Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time. Boardwalk is an equal opportunity employer (Minorities/Females/Disabled/Veterans) PM22

The position is responsible for managing complex clinical research trials including drug, device, and biologic studies across Phase I, II, III, and IV clinical trials, government-funded research, and investigator-initiated studies while ensuring compliance with Good Clinical Practice standards, huma

The position is responsible for managing complex clinical research trials including drug, device, and biologic studies across Phase I, II, III, and IV clinical trials, government-funded research, and investigator-initiated studies while ensuring compliance with Good Clinical Practice standards, huma

Social Media Coordinator Job Duties: Research audience preferences and discover current trends Create engaging text, image and video content Design posts to sustain readers' curiosity and create buzz around new

Job Description & RequirementsSpecialty: Research / Clinical ResearchDiscipline: RNStart Date: ASAPDuration: 13 weeks40 hours per weekShift: 8 hours, daysEmployment Type: Local ContractPosition SummaryThe Clinical Research Coordinator RN II (CRC RN-II) manages complex clinical trials (Phase I–IV)

Job Description Top Reasons to Work with Us: OptionWide is a newly formed, technology-driven mortgage lender offering our unique Non-QM mortgage products in the state of California with planned expansions in other states nationwide. With over 100 years of combined lending experience in management, we are an organization comprised of top professionals in our industry offering rapid growth potential to all team members. We offer a great working environment with our corporate headquarters located conveniently at the newly renovated Met Office Building Campus in Costa Mesa. Be a part of a team that offers a great culture, stability, quality training, and great upward potential in the lending industry! About the Position: Social Media Coordinator/Specialist Experience Required: 1 Year Minimum If you are passionate about technology, marketing, and digital media this is a career for you! You have the opportunity to reach and influence millions of people in how they perceive your creative ideas. What we are looking for is individuals with a strong sense of self-motivation and the willingness to learn and grow with us. We are an organization that promotes within and we are looking for individuals that are looking for long-term career opportunities with us. Duties & Responsibilities • Build and execute social media strategy through competitive research, benchmarking, messaging the audience., • Web analytics & social media reporting daily/weekly/monthly, • Monitor campaigns daily and suggest immediate changes when lead activity decreases., • Closely monitor monthly ad spend, media budgets and report on activity., • Assist with any other marketing projects or tasks, as needed such as email, social media, and offline campaigns., • Improve lead generation and general discovery of content by target groups, • Generate, edit, publish and share daily content (original text, images, video) that builds meaningful connections and encourages community members to take action., • Continuously improve by capturing and analyzing the appropriate social data/metrics, insights and best practices, • Remains abreast of new ideas, practices, principals, and techniques in social media marketing and shares and implements new practices in campaigns., • Experience in Google Ads, Facebook Ads, 3rd Party Media Sources, Analytics Software, Landing Page Creation, • Excellent project/time management skills, • Working knowledge of photography and graphic design Salary: $15.00 to $17.00 /hour

A healthcare staffing company is seeking a full-time Clinical Research Coordinator RN in Newport Beach, California. Candidates must possess an active RN license and have at least two years of clinical research experience. This role involves managing complex clinical research trials and ensuring comp

Job Description Full Time Perm Required Education : High School Diploma. Preferred Education: Bachelor of Science in Nursing (BSN) Degree or higher. Required Certifications & Licensure: Current licensure in good standing as a Registered Nurse in the State of California. Basic Life Support (BLS) Certification. Company DescriptionLanceSoft is rated as one of the largest staffing firms in the US by SIA. Our mission is to establish global cross-culture human connections that further the careers of our employees and strengthen the businesses of our clients. We are driven to use the power of our global network to connect businesses with the right people, and people with the right businesses without bias. We provide Global Workforce Solutions with a human touch.LanceSoft is rated as one of the largest staffing firms in the US by SIA. Our mission is to establish global cross-culture human connections that further the careers of our employees and strengthen the businesses of our clients. We are driven to use the power of our global network to connect businesses with the right people, and people with the right businesses without bias. We provide Global Workforce Solutions with a human touch.

We are seeking a detail-oriented and motivated Clinical Research Coordinator (CRC) to support the planning, execution, and management of clinical trials. This role is ideal for candidates with foundational to intermediate experience in clinical research who are looking to grow their careers in a fas

Job Title: Part-Time Clinical Research Coordinator Hours: Hybrid - 15 per week (Monday-Friday) Contract duration: Until December 2026 Start date: ASAP Job Description We are seeking an experienced individual with a clinical research experience to serve as the Clinical Research Coordinator for a

Previous clinical research experience required. Requires understanding and application of regulations and standards applied in clinical research areas and medical devices/combination products. Senior Clinical Research Associate.

We are working with an exciting clinical trial site organization with over 25 locations, dedicated to advancing innovative therapies and improving lives by making clinical research more efficient and accessible.

We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day.We are an equal opportunity/affirmative action employer that believes everyone matters.Qualified candidates will receive consideration for employment regard

We are working with an exciting clinical trial site organization with over 25 locations, dedicated to advancing innovative therapies and improving lives by making clinical research more efficient and accessible.

Under the direction of the Principal Investigator and the Clinical Research Coordinator, the incumbent will assist in the setup, execution, and data collection of clinical studies. The campus has produced five Nobel laureates and is known for its academic achievement, premier research, innovation an

Under supervision of the Clinical Research Manager, the Assistant Research Data Coordinator (ARDC) supports the clinical research efforts of the CFCCC by providing comprehensive data management for a research portfolio of Phase I-IV cancer-related protocols according to Good Clinical Practices (GCP)

Independently or under the supervision of the Clinical Research Manager and the Assistant Director of Clinical Research Operations, the incumbent is responsible for coordinating clinical trials in the UCI Center for Clinical Research (CCR). A minimum of 3 years of related work experience as a clinic

TemporaryFull-TimeClinical Research Coordinator. Knowledge of clinical research processes, including trial coordination and human subject research regulations. Effective communication and organizational skills to coordinate with research teams and study participants.

A healthcare organization is seeking a Clinical Research Coordinator in Orange, California. This position involves overseeing multiple clinical research studies and ensuring compliance with protocols. The ideal candidate will have completion of a Medical or Phlebotomy training program and relevant c

Under supervision of the Clinical Research Manager, the Research Data Coordinator (RDC) supports the clinical research efforts of the Chao Family Comprehensive Cancer Center by providing comprehensive data management for a research portfolio of Phase I-IV cancer-related protocols according to Good C

A leading clinical research services provider in California is seeking a Finance Support Specialist to assist with financial operations within clinical research settings.

Under supervision of the Clinical Research Manager of the Clinical Trials Unit, the Assistant Clinical Research Coordinator supports the clinical research efforts of the Cancer Center by providing comprehensive coordination and data management of multiple Phase II-IV cancer-related protocols accordi

Under the supervision of the Medical Office Administrator, the Clinical Research Coordinator oversees the day to day functions of multiple clinical research studies. F02 AMG Clinical Trials: Required to have College Degree Upon hire: Phlebotomy Certificate (for department SJuHMG Clinical Trials) 2 y

Responsibilities This recruitment is for Temporary Full-Time Clinical Research Coordinator positions through UCI's internal temporary staffing service. Qualifications Required: Knowledge of clinical research processes, including trial coordination and human subject research regulations. The cam

A healthcare organization in Orange, California, is seeking a Clinical Research Coordinator to oversee multiple clinical research studies. Applicants should have completed an accredited Medical or Phlebotomy training program, with preferred experience in a Clinical Research setting.

A healthcare organization in California seeks a Clinical Research Coordinator to manage day-to-day clinical research functions. Required qualifications include completion of a medical training program and experience in a clinical research setting.

Description Under the supervision of the Medical Office Administrator, the Clinical Research Coordinator oversees the day to day functions of multiple clinical research studies. Job Category: Research Job Function: Clinical Support Job Schedule: Full time Job Shift: Multiple shifts available Career

Responsibilities Under the supervision of the Medical Office Administrator, the Clinical Research Coordinator oversees the day‑to‑day functions of multiple clinical research studies. Two years experience in a clinical research setting; three years preferred.

The Consumer Insights Division of our organization is expanding its nationwide research team. No previous market research or industry experience required. Participate in nationally recognized research initiatives.

This job is with Jabil, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community.Please do not contact the recruiter directly.At Jabil (NYSE: JBL), we are proud to be a trusted partner for the world's top brands, offering comprehensive engineeri

The Senior Clinical Research Scientist will join the Clinical Science & External Research (CSER) Team responsible for global evidence dissemination of scientific findings from investigator led clinical trials and registries sponsored by Johnson & Johnson MedTech Electrophysiology. Support and coordi

This job is with JLL, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community.Please do not contact the recruiter directly.JLL empowers you to shape a brighter way.Our people at JLL are shaping the future of real estate for a better world by co