Senior Clinical Data Manager Position
Psi CRO
Take charge as a Senior Clinical Data Manager, overseeing critical data management operations for clinical trials. Contribute your expertise to ensure flawless execution and compliance in data collection and reporting.
You will be responsible for data management activities from study document reviews to database locks across various clinical projects. This role emphasizes communication with project teams and clients, ensuring all data processes meet rigorous standards. Your insights will drive the development of data management plans, collaborate with the Document Center, and facilitate training sessions for junior team members.
Key Responsibilities: - Direct all data management tasks for clinical trial projects - Liaise with project teams and clients regarding data management issues - Create and validate data management plans for studies - Conduct quality control checks and manage audit preparations - Provide training on CRF procedures for the clinical team
Requirements: - Bachelor's degree or similar relevant qualification - Minimum 3 years of experience in data management for EDC studies - Proficient in EDC/CDM systems, ideally Medidata Rave or Oracle Inform - Background in project data management is beneficial - Strong organizational and management skills
Enhance your clinical research career by applying your data management expertise in impactful trial projects.#J-18808-Ljbffr
You will be responsible for data management activities from study document reviews to database locks across various clinical projects. This role emphasizes communication with project teams and clients, ensuring all data processes meet rigorous standards. Your insights will drive the development of data management plans, collaborate with the Document Center, and facilitate training sessions for junior team members.
Key Responsibilities: - Direct all data management tasks for clinical trial projects - Liaise with project teams and clients regarding data management issues - Create and validate data management plans for studies - Conduct quality control checks and manage audit preparations - Provide training on CRF procedures for the clinical team
Requirements: - Bachelor's degree or similar relevant qualification - Minimum 3 years of experience in data management for EDC studies - Proficient in EDC/CDM systems, ideally Medidata Rave or Oracle Inform - Background in project data management is beneficial - Strong organizational and management skills
Enhance your clinical research career by applying your data management expertise in impactful trial projects.#J-18808-Ljbffr
Vacancy posted 2 hours ago
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