Clinical Research Associate (CRA) – Pharmaceutical
Company: Atharv LLC
- Location: Raleigh, United States
- Employment type: Full-time
- Posted: 2 days ago
- Offer language: English
Job description
This Clinical Research Associate (CRA) position involves supporting clinical trial monitoring, reviewing research documentation, and coordinating with clinical research sites to support study activities.
Key Responsibilities
- Monitor clinical trial activities according to study protocols.
- Review research documentation and study records.
- Coordinate communication with clinical research sites and study teams.
- Support site initiation, monitoring, and closeout activities.
- Identify and document protocol deviations and other study issues.
- Follow applicable Good Clinical Practice (GCP) standards and research procedures.
Qualifications
- Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or a related discipline, or equivalent relevant experience.
- Relevant clinical research or trial monitoring experience.
- Knowledge of Good Clinical Practice (GCP) guidelines.
- Strong organizational and documentation skills.
- Ability to communicate effectively with clinical research teams.
- Willingness to travel when required by the assignment.
How to Apply
Submit your updated resume highlighting clinical research experience, therapeutic areas, relevant qualifications, and availability through Atharv LLC.
