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The In-house Clinical Research Associate (CRA) works closely with the Project Manager and clinical team, providing support for general clinical trial execution including tracking project progress, preparing and organizing study site documentation, maintaining the Trial Master File, assisting with site identification and management, and managing Clinical Trial Material and other site supplies. The In-house CRA acts as a contact for the clinical team for designated project communications, and performs administrative tasks to support team members with clinical trial execution as needed. The In-house CRA may conduct monitoring visits, under the direction of an experienced CRA or independently after appropriate training.
Preferred qualifications:
• BS in scientific discipline or pharmacy, RN, or BSN degree or equivalent experience
• Clinical trial experience and/or completion of a Clinical Trial Certificate program is required
• Basic understanding of GCP/ICH Guidelines is required
• Oncology background or experience is preferred
• Effective written communication skills and computer skills are required
• Clinical Monitoring experience is a plus
• The In-house CRA must possess the ability to work closely with all disciplines within a small company, displaying innovative thinking, a strong sense of responsibility, accountability, and integrity
- Compensation: Competitive compensation package commensurate with experience. Participation in Employee Stock Ownership Plan.
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