Job Summary
A company is looking for a Contract CRA to support their Phase 2/3 trials.
Key Responsibilities
- Support Sr CTM on clinical study activities from study start-up to closeout
- Oversee study management and vendors, ensuring effective site management and CRO monitoring activities
- Contribute to the development of critical study documents and support overall study-wide activities
Required Qualifications
- Minimum Bachelor's degree in a relevant scientific discipline
- Minimum 2 years of CRA experience within the pharma or biotech industry
- Global experience required
- Phase II/III trial experience
- Cardiovascular, Diabetes, or Metabolic experience highly preferred
Comments