Job Summary
Fortrea is looking for a skilled Senior Clinical Research Associate who possesses over three years of experience in clinical monitoring, particularly with a focus on Phase I trials. This position is based in Durham, North Carolina, and requires a dedicated individual to ensure the smooth execution of clinical studies.
Responsibilities
- Conduct thorough monitoring of clinical trial sites to ensure compliance with the protocol.
- Oversee the integrity of data collected throughout the study.
- Verify adherence to clinical trial protocols and regulatory requirements.
- Monitor adverse event reporting and ensure that safety protocols are followed.
Qualifications
- Minimum of 3 years of experience in clinical monitoring, especially in Phase I trials.
- Strong understanding of clinical research regulations and Good Clinical Practice (GCP).
- Excellent communication and organizational skills.
- Ability to work collaboratively within a team-focused environment.
