Research Associate, Clinical Research
Listed on 2026-01-15
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Healthcare
Clinical Research
Parexel Early Phase Clinical Unit supports the development of innovative new medicines which are vital for public health, improving outcomes, and saving lives. The early phase and first‑in‑human trials are the first step in testing these novel treatments in humans.
At the Parexel Glendale, CA unit our highly trained and skilled Research Associates are crucial to ensuring the successful completion of Phase I trials. This is a great role for anyone who aspires to be an enrollment specialist, clinical research coordinator, or eventually manager. Parexel provides a great system of support to help you grow and advance your career internally.
Parexel provides an extensive induction program and ongoing training while following your individual career path.
ScheduleShift: Flex – predominantly work the day shift but must be able to flex to work evening shifts starting after 3:00 pm when business requires. 2 to 3 weekend shifts required.
Responsibilities- Understand study protocols and be able to complete required medical procedures.
- Recruit study participants by calling the database, attending company‑sponsored community events, posting flyers in schools, senior centers, supermarkets, and other establishments.
- Enter study participants in the study participant tracking system and study logs, maintain appointment calendars, and operate company information systems and computer programs.
- Conduct screening visits and study protocol‑specific study participant visits, assist staff physicians in assessment of concomitant medications, adverse events, lab results, and other test results.
- Prepare/monitor study supplies and stock levels in clinic/hospital.
- Label, inventory, and send plasma samples.
- Problem‑solve study participant issues as they arise.
- Ensure basic study participant safety is provided.
- Assist with monitor visits (i.e., room set‑up, etc.).
- Identify issues that need sponsor approval and bring these to the attention of the CRC.
- Maintain and update knowledge of Clinical Operating Guidelines and their proper application.
- Assume appropriate role with study participants and caregivers.
- Assure quality and accuracy of source and CRF documentation.
- Comply with Quality Management (QM) department guidelines and perform corrections for QM, CRC and Monitor/Sponsor Representative in a timely manner.
- Customer service experience in a fast‑paced environment.
- Clinical Research experience or patient experience is required.
- B.S. or higher in a related life science field OR HS diploma or GED with experience.
- Comfortable standing and walking for a prolonged period of time.
- Certified Phlebotomy Technician I License is required.
Base Pay Range: $20.00 to $26.00 per hour. Actual salaries may vary within the range based on several factors including, but not limited to, education, training, experience, professional achievement, and location.
In addition to base salary, some roles may be eligible for participation in Parexel’s annual performance‑based bonus plan, annual salary review and additional total rewards incentives.
Eligible employees receive market‑leading benefit programs including paid time off, 401(k) match, life insurance, health insurance, and other benefits in accordance with the terms of applicable plans.
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