Clinical Research Associate II/III - US
University degree pref. medical/life sciences or nursing; 2+ years independent clinical trial monitoring; strong knowledge of ICH GCP and regulatory requirements; computer proficiency; excellent communication and negotiation skills; valid reputed company’s license.
Key Responsibilities
- performing monitoring
- managing sites
- negotiating budgets
Job Details
- Category: Research and Development (R&D)
- Seniority: Entry Level
- Commitment: Full Time
- Workplace: Remote — Philadelphia, Pennsylvania, United States
- Languages: English
Benefits
- Generous reputed company time off
- Retirement plan
About Optimapharm
A mid-sized global contract research organisation delivering patient-reputed company clinical development across phases I–IV. — Industry: Research and Development
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