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As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and ... We're flexible-we're open to part-time or full-time commitments with flexible schedules. Why Join ...
As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and ... We're flexible-we're open to part-time or full-time commitments with flexible schedules. Why Join ...
Clinical Trial Associate Part Time information
See salary details
$17.31 - $22.12
4% of jobs
$22.12 - $26.92
8% of jobs
$26.92 - $31.73
12% of jobs
$31.88 is the 25th percentile. Wages below this are outliers.
$31.73 - $36.54
26% of jobs
$36.54 - $41.35
18% of jobs
$43.02 is the 75th percentile. Wages above this are outliers.
$41.35 - $46.15
19% of jobs
$46.15 - $50.96
6% of jobs
$50.96 - $55.77
2% of jobs
$55.77 - $60.58
1% of jobs
$60.58 - $65.38
1% of jobs
$65.38 - $70.19
2% of jobs
$17
$39
$70
How much do clinical trial associate part time jobs pay per hour?
What are the key skills and qualifications needed to thrive as a Clinical Trial Associate Part Time, and why are they important?
What does a Clinical Trial Associate Part Time do?
What are some typical responsibilities of a part-time Clinical Trial Associate, and how do they balance workload with limited hours?
What is the difference between Clinical Trial Associate Part Time vs Clinical Trial Coordinator?
| Aspect | Clinical Trial Associate Part Time | Clinical Trial Coordinator |
|---|---|---|
| Credentials | Bachelor's degree, relevant certifications often preferred | Bachelor's degree, experience in clinical research |
| Work Environment | Part-time, office and clinical sites | Full-time, primarily office-based with site visits |
| Employer & Industry | Pharmaceutical companies, CROs, biotech firms | Research institutions, hospitals, pharmaceutical companies |
| Common Search & Comparison | Yes | Yes |
The main difference between a Clinical Trial Associate Part Time and a Clinical Trial Coordinator lies in their work hours and scope. The part-time associate typically works fewer hours and focuses on specific trial tasks, while the coordinator manages broader trial activities full-time. Both roles require similar educational backgrounds and are integral to clinical research teams.

Full-time, Part-time
Medical, Dental, Vision, Life, Retirement
Posted 7 days ago
Saint Peter's University Hospital rating
8.0
Based on 14 frontline employees who took The Breakroom Quiz
130th of 1,020 rated hospitals
Job description
MFM Clinical Study Grant
The Clinical Research Associate - Part Time will:
- Serve as the organizational appointee for assigned MFM research projects, maintaining the relationship and oversight of study procedures.
- Initiation / implementation of the observational or clinical research projects assigned including: Maintenance of Investigator and Research Staff CVs, Licensure and Training Records, Drafting and updating the Informed Consent Form with CIRB Boilerplate, Completion of Institutional Review Board (IRB) modifications with supporting documentation.
- Maintain oversight of designated research project study activities including performing the following functions: Subject recruitment, Consenting and Enrollment/Randomization, Perform study procedures/assessments in accordance with clinical trial guidelines, Complete Data Entry into Case Report Forms and Query Resolution, Process/Ship Specimens per trial requirements, Maintain Regulatory files including delegation logs, FDA form 1572, training logs and other trial documents in compliance with federal and local regulations, Process IRB amendments, annual renewals, closures, etc, Attend regular meetings with members of the project at partnering institutions and sponsors to report on study progress.
- Maintain financial records including Accounts Receivable Report, Check remittance with back-up details and assist with the annual A-133 audit.
- Serve as a liaison between investigators, research staff, hospital staff, the IRB and sponsors.
- Maintain and utilize research's Clinical Trial Management System (CTMS).
- Maintain strict patient confidentiality including restricted access to clinical trial files.
- Attend and participate in research meetings and report on study progress.
- Perform other tasks as assigned by leadership.
- Comply with all SPUH policies, procedures, objectives, quality assurance, safety, environmental and infection controls.
Requirements:
- Bachelor's Degree in science or healthcare field preferred.
- Two years of experience in healthcare and/or research.
- Ability to work independently as well as in a team environment.
- Proficient in Microsoft Office Suite.
- Certified Clinical Research Professional (CCRP) or other similar research accreditation preferred.
- Previous Phlebotomy experience or certification preferred.
Salary Range: 24.33 - 38.93 USD
We offer competitive base rates that are determined by many factors, including job-related work experience, internal equity, and industry-specific market data. In addition to base salary, some positions may be eligible for clinical certification pay and shift differentials.
The salary range listed for exempt positions reflects full-time compensation and will be prorated based on employment status.
Saint Peter's offers a robust benefits program to eligible employees that will support you and your family in working toward achieving and maintaining secure, healthy lives now and into the future. Benefits include medical, dental, and vision insurance; savings accounts, voluntary benefits, wellness programs and discounts, paid life insurance, generous 401(k) match, adoption assistance, back-up daycare, free onsite parking, and recognition rewards.
You can take your career to the next level by participating in either a fully paid tuition program or our generous tuition assistance program. Learn more about our benefits by visiting our site at Saint Peter's.
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About Saint Peter's Healthcare System
Sourced by ZipRecruiter
Industry
Health care and social assistance
Company size
1,001 - 5,000 Employees
Headquarters location
New Brunswick, NJ, US
Year founded
1907