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Clinical Records Supervisor
2 months ago
Position Overview:
As a key player in the management of clinical research documentation, you will oversee the records management process at the AbbVie Clinical Pharmacology Research Unit (ACPRU). Your role is essential in ensuring compliance with all regulatory standards and AbbVie’s internal protocols.
Key Responsibilities:
1. **Records Management:** Take charge of the organization and maintenance of clinical trial records, ensuring accuracy and accessibility.
2. **Regulatory Compliance:** Ensure that all documentation meets the required regulatory and AbbVie standards.
3. **Collaboration:** Work closely with clinical research teams to support their documentation needs and facilitate smooth operations.
Qualifications:
Ideal candidates will possess a strong background in business operations and records management, with a focus on clinical research environments.
