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Job summary
A research management firm located in West Sacramento is seeking an experienced professional to coordinate clinical trials. The successful candidate will manage relationships with sponsors and ensure trial progress while adhering to regulations. Responsibilities include maintaining study logs, resolving issues, and developing SOPs. Candidates must have at least AA or BS degree and 2 years of relevant experience in clinical research or study coordination.
Qualifications
AA or BS degree is required.
Minimum of 2 years of clinical research or study coordination experience.
Experience in regulated environments required.
Responsibilities
Serve as primary contact for clinical trial testing.
Coordinate assigned trials under Lead PM guidance.
Maintain study logs and provide updates.
Resolve issues and expand critical items.
Develop SOPs as needed.
Skills
Strong Excel and computer skills
Excellent communication and customer service
Knowledge of GCP, HIPAA, and medical terminology
Detail-oriented
Organized
Adaptable
Education
AA or BS degree
Job description
Serve as primary contact for clinical trial testing, managing sponsor/client relationships and trial progress
Coordinate assigned trials under Lead PM guidance; communicate with clinical/regulatory teams
Maintain study logs, metrics, and provide updates
Resolve issues and expand critical items
Develop SOPs as needed
Perform QC on deliverables and support secondary QC
Train staff as required
Qualifications
AA or BS degree
2+ years clinical research/study coordination experience (CRO, university, or medical setting)
Experience in regulated environments; familiarity with CAP/CLIA/CDx