Research Compliance Analyst
Healthcare/Medical | Hybrid in Los Angeles, CA | Full Time, Contract, and Temporary | From $35.00 to $35.00 per hour
Job Description
Research Compliance Analyst 2880534
One of the most prestigious and well-known universities seeks a Research Compliance Analyst. The successful candidate will be responsible for staffing, administering, or managing research oversight and compliance committee activities related to research activities such as human subjects, animal use and care, conflict of interest, and export control. The company offers a great work environment!
Research Compliance Analyst Pay and Benefits:
- Hourly pay: $35/hr
- Worksite: Los Angeles, CA 90095 - Hybrid
- W2 Employment, Group Medical, Dental, Vision, Life, Retirement Savings Program, PSL
- 40 hours/week, 6 Month Assignment
Research Compliance Analyst Responsibilities:
- Apply research compliance professional concepts to review research protocols to ensure that all regulatory criteria are met, as well as policies and/or regulations from the organization, the state, and systemwide.
- Under general supervision, participate in pre-review and follow-up of full board committee protocols.
- Determine the appropriate level of review in triage.
- Under general supervision, issues formal communications to funding agencies and other regulatory organization units.
- Communicate with researchers and provide guidance on how to resolve particular issues of concern and meet the requirements of external regulatory bodies,s and to properly document these actions in accordance with all applicable laws, regulations, policies, and procedures.
- Generate and analyze reports of review and approval activities.
- Communicate directly with investigators to resolve all concerns as identified during the review process.
- Participate in the training of individuals and departments on relevant compliance processes, forms, and policies.
- Participate in the development and revision of standard operating procedures and guidelines.
Research Compliance Analyst Qualifications:
- 2+ years of clinical research regulatory experience.
- Bachelor’s Degree in a related area.
- Experience submitting to local and external IRBs.
- Experience working with industry sponsors and handling monitor visits.
- Working knowledge of regulatory documents (DOA, financial disclosures, 1572s, inform consent documents, etc.).
- Knowledge of relevant Federal and State regulations and policies.
- Excellent customer service skills, pleasant, helpful, and patient.
Shift:
- 08:00 am - 05:00 pm.