Clinical Research Associate (Senior)
Company: Proforma Health
- Location: Durham, United States
- Seniority: Senior
- Employment type: Full-time
- Posted: 9 days ago
- Offer language: English
Job description
Role: Clinical Research Associate responsible for leading site monitoring activities and ensuring protocol compliance in clinical trials.
Key Responsibilities
- Conduct site monitoring visits, including selection, initiation, routine, and close-out activities.
- Build and maintain strong relationships with investigative sites to enhance performance and recruitment.
- Ensure adherence to protocols, data integrity, and high-quality study execution.
- Monitor study progress by tracking regulatory approvals, enrollment, and data quality.
- Identify risks, resolve issues, escalate concerns, and maintain accurate documentation.
Qualifications & Skills
- Bachelor’s degree in life sciences, healthcare, or related field.
- At least 1.5 years of on-site monitoring experience.
- Solid knowledge of GCP, ICH, and regulatory standards.
- Strong communication, problem-solving, and organizational abilities.
- Ability to manage multiple priorities in a fast-paced environment.
