Job Summary
The Clinical Research Associate I will play a pivotal role in supporting the execution of clinical trials, ensuring compliance with regulatory standards, and fostering collaborations between various stakeholders. This position is essential in monitoring the progress of clinical studies, maintaining data integrity, and ensuring the safety and efficacy of investigational products. The role provides a unique opportunity to engage in the dynamic field of clinical research, making significant contributions to advancing medical knowledge.
Responsibilities
- Monitor clinical trials and ensure adherence to protocols and regulations.
- Conduct site visits and maintain relationships with study sites.
- Verify case report forms and manage data discrepancies.
- Assist in preparing study documentation and regulatory submissions.
- Facilitate communication between project managers, investigators, and sponsors.
- Support participant recruitment and retention efforts.
Qualifications
- A bachelor’s degree in life sciences or a related field.
- Strong organizational skills and attention to detail.
- Excellent communication and interpersonal abilities.
- Ability to work collaboratively in a team environment.
- Familiarity with clinical trial processes and regulatory requirements is preferred.
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.
