Senior Clinical Research Associate - US
University degree in medical/life sciences or nursing; 3+ years independent clinical trial monitoring (oncology preferred); strong ICH GCP knowledge; computer proficiency; excellent communication and negotiation; valid reputed company’s license.
Key Responsibilities
- performing monitoring
- managing sites
- reviewing CRFs
Job Details
- Category: Research and Development (R&D)
- Seniority: Mid Level
- Commitment: Full Time
- Workplace: Remote — Philadelphia, Pennsylvania, United States
- Languages: English
Benefits
- Generous reputed company time off
- Tuition reimbursement
- Retirement plan
About Optimapharm
A mid-sized global contract research organisation delivering patient-reputed company clinical development and trial management services. — Industry: Research and Development
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