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Manager, Clinical Data Management
Manager, Clinical Data ManagementIntePros Consulting • Cambridge, Massachusetts, US
Manager, Clinical Data Management

Manager, Clinical Data Management

IntePros Consulting • Cambridge, Massachusetts, US
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Manager, Clinical Data Management

Client Overview :

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.
  • Strong collaboration and leadership abilities.
  • Excellent oral and written communication skills.
  • Outstanding interpersonal skills.
  • #LI-DR2

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    Clinical Data Manager • Cambridge, Massachusetts, US

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