Job description

JOB SUMMARY:

Interview Type: TEAMS w/onsite visit if offered assignment

Required Qualifications:
Bachelor’s degree
3+ years in the field of clinic research

Demonstrated experience on:
*Writing research correspondence to IRB and study sponsors.
*Submitting continuations and amendments to regulatory bodies.
*Tracking regulatory documents (including lab certifications, CV’s, IRB compliance and correspondence letters, medical licenses, FDA Forms, Delegation of Authority Forms, Serious Adverse Event submissions, etc.)

Knowledge of and ability to answer questions regarding:
*FDA Good Clinical Practice (GCP) and Good Laboratory Practice (GLP) as well as Local Institutional Review Board (IRB) regulatory requirements.

Preferred Qualifications:
1+ years oncology experience
CCRP certification

Job Types: Full-time, Contract

Pay: $40.00 - $45.00 per hour

Benefits:

• 401(k)
• Dental insurance
• Flexible spending account
• Health insurance
• Paid time off
• Vision insurance

Schedule:

• 8 hour shift
• Day shift

Ability to commute/relocate:

• Los Angeles, CA 90025: Reliably commute or planning to relocate before starting work (Required)

Education:

• Bachelor's (Required)

Experience:

• Project management: 3 years (Preferred)
• Clinic research: 3 years (Preferred)

License/Certification:

• CCRP (Required)

Work Location: In person

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