Manager, Clinical Data Management

Worldwide Clinical Trials•Sacramento, CA
•$99,000 - $196,000

About The Position

This role provides management and leadership oversight of assigned teams and projects within the Data Management department for study execution and budget management. The position supports the development and implementation of Worldwide processes and initiatives. The company is a global, midsize CRO that focuses on innovation and pioneering approaches to find cures for diseases. They employ over 3,500 experts worldwide and aim to change the way the world experiences CROs. Their mission is to improve lives through passionate and purposeful work, fostering an inclusive and equitable environment where professionals can thrive.

Requirements

  • Bachelor’s degree or higher in biomedical sciences, life sciences, computer science or related discipline — or equivalent relevant experience.
  • Min of 9 years of experience in clinical data management or a related role within the pharmaceutical, biotechnology, or medical device industries.
  • 2-4 years of line management experience.

Nice To Haves

  • Excellent attention to detail.
  • Excellent written and verbal communication skills.
  • Expert knowledge of data management best practices & technologies as applied to clinical trials.
  • Excellent communication and interpersonal skills to collaborate with cross-functional internal and external teams.
  • Advanced understanding of clinical trial process and protocols documents (protocols, statistical analysis plans, CRFs, study reports) and processes.
  • Independent analytical and problem solving skills.
  • Strong project management skills and experience managing data management teams and projects for operational and budget oversight.
  • Line management experience including recruitment, career development and performance reviews.

Responsibilities

  • Provide management and leadership oversight of teams and projects within Data Management department for study execution and budget management.
  • Act as the primary point of contact for any study specific escalations (internal or external).
  • Represent the company at sponsor governance meetings.
  • Manage assigned departmental personnel ensuring staff are allocated to projects appropriately and according to their abilities/competencies, appropriate oversight, training and mentoring is provided, projects within the team are appropriately resourced, operational or budget risks are discussed and addressed, any performance related escalations for team member are managed and handled appropriately, and upcoming availability is highlighted to DM Management to ensure continuity of utilisation.
  • Define and monitor objectives for individual team members, ensuring there are opportunities for career and personal development.
  • Provide support to Business Development staff by participating in preparation of proposals and presentations to sponsors.
  • Participate as necessary in sponsor audits, regulatory authority inspections and other third party meetings. Ensure than any recommendations are discussed and that solutions are incorporated.
  • Perform the role of Subject Matter Expert for a specific DM process, including ongoing review to ensure the process is effective and efficient, acting as a central point of contact for any related questions from the team, providing ongoing training to all team members, taking ownership of any related Quality Issues identified, ensuring root cause analysis and CAPAs as required, and ownership and regular updates of related QMDs or other guidance documents.
  • Provide mentorship to other members of the DM department.
  • Lead and manage departmental initiatives for process improvement and efficiencies as defined by the DM Departmental leadership.
  • Perform other duties as assigned.

Benefits

  • Competitive benefits package depending on location.
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