Job Summary
The Senior Clinical Research Associate (CRA) plays a vital role in enhancing global health through the execution of clinical trials and ensuring compliance with regulatory standards. This position is essential for driving clinical research efforts effectively and supporting site teams, including Principal Investigators, Study Coordinators, and Pharmacists.
Responsibilities
- Collaborate with site teams to ensure smooth clinical trial operations.
- Monitor trial progress and ensure adherence to regulatory requirements.
- Assist in data collection, management, and reporting for clinical studies.
- Provide support to Principal Investigators and Study Coordinators during trials.
- Engage in activities that promote patient safety and data integrity throughout the research process.
Qualifications
- Bachelor’s degree (BA/BS) in a related field or a nursing degree.
- A graduate degree in life sciences or a health-related discipline may be advantageous.
- Experience in clinical research, particularly with hands-on trial management.
- Strong understanding of regulatory requirements in clinical trials.
- Effective communication and interpersonal skills to work in a team-oriented environment.
Parexel 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.
