Job Summary
The Senior Clinical Research Associate plays a critical role in managing interactions with clinical sites and investigators. This position involves ensuring the protection of subjects’ rights, safety, and well-being while facilitating effective communication within clinical research environments.
Responsibilities
- Establish and nurture relationships with clinical sites and research investigators.
- Prioritize and advocate for the rights, safety, and welfare of study subjects.
- Serve as a primary communicator between clinical sites and the research team.
- Oversee the compliance and integrity of clinical trials.
- Contribute to the development of study protocols and ensure adherence to regulatory requirements.
Qualifications
- Proven experience in clinical research and monitoring.
- Strong understanding of GCP and regulatory guidelines.
- Excellent organizational and communication skills.
- Ability to work independently and collaboratively in a remote setting.
- Relevant educational background in life sciences or a related field.
PSI CRO 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.
