The TMF Manager provides advanced leadership in Trial Master File (TMF) strategy and operations independently guiding complex studies and ensuring excellence in TMF management. This role serves as a key escalation and decision-making point between study teams and TMF Operations driving alignment and timely resolution. The TMF Manager strengthens organizational capability by fostering proactive issue management and promoting cross-functional collaboration to support the successful delivery of clinical studies.
Key Role Responsibilities
Responsible for the strategic oversight and management of Trial Master File (TMF) operations across one or more complex clinical studies or programs.
Serves as the primary TMF operations lead for complex studies providing strategic oversight and proactive issue resolution across study teams.
Demonstrates strong expertise in eTMF management systems processes and compliance requirements ensuring inspection readiness and operational excellence throughout the study lifecycle. Key experience to look for would be experience within multiple eTMFs (either multiple systems or Veeva eTMF across multiple companies)
Partners effectively with cross-functional study management teams and external stakeholders to anticipate challenges drive solutions and maintain high-quality documentation.
Provides mentorship and guidance to Senior TMF Associates fostering capability development and consistency across studies.
Partner with study and program teams to define TMF strategies governance and milestones aligned with study timelines.
Qualifications
68 years of experience in clinical documentation or TMF operations within a CRO sponsor or pharma environment.
Proven experience managing or leading TMF activities for complex global or late-phase clinical studies.
*Accommodations are available for applicants with disabilities upon request throughout the recruitment lifecycle
We may use artificial intelligence (AI) tools to support parts of the hiring process such as reviewing applications analyzing resumes or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed please contact us.
Required Experience:
Manager
The TMF Manager provides advanced leadership in Trial Master File (TMF) strategy and operations independently guiding complex studies and ensuring excellence in TMF management. This role serves as a key escalation and decision-making point between study teams and TMF Operations driving alignment and...
The TMF Manager provides advanced leadership in Trial Master File (TMF) strategy and operations independently guiding complex studies and ensuring excellence in TMF management. This role serves as a key escalation and decision-making point between study teams and TMF Operations driving alignment and timely resolution. The TMF Manager strengthens organizational capability by fostering proactive issue management and promoting cross-functional collaboration to support the successful delivery of clinical studies.
Key Role Responsibilities
Responsible for the strategic oversight and management of Trial Master File (TMF) operations across one or more complex clinical studies or programs.
Serves as the primary TMF operations lead for complex studies providing strategic oversight and proactive issue resolution across study teams.
Demonstrates strong expertise in eTMF management systems processes and compliance requirements ensuring inspection readiness and operational excellence throughout the study lifecycle. Key experience to look for would be experience within multiple eTMFs (either multiple systems or Veeva eTMF across multiple companies)
Partners effectively with cross-functional study management teams and external stakeholders to anticipate challenges drive solutions and maintain high-quality documentation.
Provides mentorship and guidance to Senior TMF Associates fostering capability development and consistency across studies.
Partner with study and program teams to define TMF strategies governance and milestones aligned with study timelines.
Qualifications
68 years of experience in clinical documentation or TMF operations within a CRO sponsor or pharma environment.
Proven experience managing or leading TMF activities for complex global or late-phase clinical studies.
*Accommodations are available for applicants with disabilities upon request throughout the recruitment lifecycle
We may use artificial intelligence (AI) tools to support parts of the hiring process such as reviewing applications analyzing resumes or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed please contact us.