Our client is a renowned full-service clinical research organization (CRO) recognized for its expertise in clinical operations, data management, biostatistics, medical writing, and pharmacovigilance. With a deep commitment to advancing medical innovations, they serve a diverse clientele comprising national and international biopharmaceutical and medical device companies.
Responsibilities :
Supervise and lead a team of Clinical Data Managers (CDMs).
Oversee the execution of each project assigned to the team.
Conduct quality checks on all deliverables before submission to internal or external stakeholders.
Prepare and deliver individual performance evaluations.
Provide mentorship to DM staff and devise solutions for complex issues.
Support staff in their interactions with sponsors and management of vendors.
Keep supervisors informed of study progress and team management through regular meetings.
Cultivate a positive, proactive management approach and foster effective communication within the team.
Develop and update data management SOPs and training manuals.
Conduct data management and study-specific training for CDMs and study teams.
Offer insights from a data management perspective during clinical trial protocol design.
Oversee the creation and maintenance of study-specific documentation.
Manage data review, query generation procedures, and medical term coding.
Define and perform SAE reconciliation processes.
Collaborate with DM leads and DB programmers to design (e)CRFs and edit checks in the EDC system.
Ensure the completion of UAT for EDC system and modules.
Supervise DM lead to ensure efficiency and quality of electronic data receipt, integration, and reconciliation.
Review queries and trends to ensure data completeness and integrity.
Develop training materials and user guides for EDC data collection tools and deliver user training.
Participate in client and team meetings, offering insights on best practices.
Provide input to cross-functional study timelines and resource requirements.
Deliver regular status updates to cross-functional study teams, management, and sponsors.
Implement technical solutions, introduce new tools, and drive process improvement strategies.
Lead large and complex projects and identify project scope changes.
Present at sales and marketing meetings for prospective clients.
Offer strategic input to departmental and company goals.
Lead key departmental goals and initiatives.
Education :
Bachelor's degree in a scientific or health-related field or equivalent qualification.
Experience :
Minimum of 10 years' experience in Clinical Data Management.
Minimum of 2 years' supervisory experience required.
Skills :
Proficiency in GCPs and regulatory agency guidelines.
Familiarity with medical terminology.
Expertise in data management software applications, particularly Medidata RAVE.
Exceptional organizational and time management skills.