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.
Fortrea provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
