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Clinical Research Training Jobs (NOW HIRING)

Winaxis

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Fresh graduates with relevant internships or clinical research training are encouraged to apply. Key Responsibilities Coordinate and manage clinical research studies in compliance with study ...

Winaxis

Clinical Research Coordinator

Jersey City, NJ · On-site

$25.25 - $33.75/hr

Fresh graduates with relevant internships or clinical research training are encouraged to apply. Key Responsibilities Coordinate and manage clinical research studies in compliance with study ...

Winaxis

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Fresh graduates with relevant internships or clinical research training are encouraged to apply. Key Responsibilities * Coordinate and manage clinical research studies in compliance with study ...

Pinnacle Clinical Research

WI · On-site

$60 - $80/hr

Clinical Research Coordinator Full Time Houston, TX, US 23 days ago Requisition ID: 1074 Summary ... Training to be provided * Must have basic life support (BLS) training, provided during onboarding

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How much do clinical research training jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for clinical research training in the United States is $24.09, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $24.76 per hour, depending on experience, location, and employer.

What is clinical research training?

A Clinical Research Training job involves developing, organizing, and delivering educational programs for clinical research professionals. This role ensures that researchers, coordinators, and other staff understand regulatory requirements, ethical considerations, and best practices in clinical trials. Responsibilities may include creating training materials, conducting workshops, and maintaining compliance with industry standards. It is essential for ensuring the integrity and effectiveness of clinical research studies.

What does a typical day look like for someone working in clinical research training?

A typical day in Clinical Research Training often involves developing and delivering training materials for research staff, conducting onboarding sessions for new team members, and ensuring all participants meet regulatory and protocol requirements. Trainers may collaborate closely with investigators, study coordinators, and regulatory teams to assess learning needs and update curricula as guidelines evolve. The role also includes monitoring training records, organizing workshops or seminars, and providing support for staff questions on GCP and compliance. This dynamic work environment offers opportunities for continuous professional development and direct impact on the success and integrity of clinical research projects.

What are the key skills and qualifications needed to thrive in clinical research training?

To excel in Clinical Research Training, you typically need a background in life sciences or healthcare, familiarity with clinical trials, and strong organizational abilities. Experience with learning management systems (LMS), Good Clinical Practice (GCP) certification, and proficiency in relevant regulatory documentation tools is highly beneficial. Outstanding soft skills include excellent communication, instructional ability, attention to detail, and adaptability to evolving protocols. These competencies are crucial for effectively educating clinical staff, ensuring compliance, and maintaining high-quality research standards.

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Clinical Research Training jobs near you
Infographic showing various Clinical Research Training job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 18% Part Time, and 1% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $50,108 per year, or $24.1 per hour.

Clinical Research Coordinator

Winaxis

Dallas, TX • On-site

$24 - $32/hr

Full-time

Medical, PTO

Re-posted 23 days ago

Job description

Job Title : Clinical Research Coordinator (CRC) Experience : 0–3 Years Location : Dallas, Texas Employment Type : Full-time Job Summary:- We are looking for a motivated and detail-oriented Clinical Research Coordinator to support the planning, execution, and management of clinical research studies. The ideal candidate should have 0–3 years of experience in clinical research and a strong understanding of Good Clinical Practice (GCP), ICH guidelines, and regulatory requirements. Fresh graduates with relevant internships or clinical research training are encouraged to apply. Key Responsibilities Coordinate and manage clinical research studies in compliance with study protocols, ICH-GCP guidelines, and applicable regulations. Screen, recruit, and enroll study participants. Obtain informed consent from study participants. Schedule and coordinate patient visits and follow-up appointments. Collect, verify, and maintain accurate study documentation and source data. Enter clinical data into Electronic Data Capture (EDC) systems. Maintain Trial Master File (TMF), Investigator Site File (ISF), and essential study documents. Report adverse events and serious adverse events according to protocol and regulatory requirements. Coordinate with investigators, sponsors, CROs, and ethics committees. Prepare for monitoring visits, audits, and regulatory inspections. Ensure protocol compliance and participant safety throughout the study. Assist with study start-up, close-out activities, and regulatory submissions. Required Qualifications Bachelor's or Master's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Microbiology, or a related field. 0–3 years of experience in clinical research or clinical trial coordination. Knowledge of ICH-GCP, FDA, and local regulatory guidelines. Familiarity with EDC systems and Microsoft Office. Strong organizational, communication, and documentation skills. Ability to work independently and as part of a multidisciplinary team. Preferred Qualifications GCP Certification. Clinical Research certification is an added advantage. Experience with site coordination or patient recruitment. Knowledge of clinical trial documentation and regulatory submissions. Key Skills Clinical Trial Coordination ICH-GCP Compliance Patient Recruitment Informed Consent Process Source Documentation Electronic Data Capture (EDC) Trial Master File (TMF) Regulatory Documentation Adverse Event Reporting Data Management Communication & Coordination Attention to Detail Time Management Benefits Competitive salary Health insurance Performance-based incentives Training and career development opportunities Paid leave and holidays Exposure to global clinical research projects How to Apply Interested candidates can submit their updated resume along with a cover letter highlighting their clinical research experience, certifications, and relevant skills.