Pfizer
Director of Site Management and Monitoring (DSMM)
Pfizer, Los Angeles, California, United States, 90079
Director of Site Management and Monitoring (DSMM)
Join to apply for the
Director of Site Management and Monitoring (DSMM)
role at
Pfizer . Position Summary
Supporting Pfizer Oncology, in partnership with the Director of Clinical Site Operations (DCSO), you will ensure appropriate Site Care Partners (SCP) are in place to deliver end-to-end study start-up, site management, and monitoring activities in line with study milestones for the United States. You will oversee the job functions of the Site Care Partner and support the DCSO in ensuring overall operational site management, patient safety, and quality of study execution in accordance with laws, Good Clinical Practice, and Pfizer standards. You will collaborate cross-functionally with teams involved in Study Start Up, Site Activation, Clinical Trial Assistance, Investigator Contracts, Monitoring, Analytics, Recruitment, and Study Management to facilitate site and country selection, and support regulatory approvals. Additionally, you will execute investigator site/recruitment strategies, lead strategic initiatives, and shape the clinical development environment in the U.S. to meet Pfizer’s development goals. Position Responsibilities
Line management of Site Care Partners (team of approximately 15 colleagues and FSPs). Lead and coach resources within assigned regions. Ensure growth and development of the Site Operations organization. Oversee job functions and ensure compliance with training requirements. Perform joint site visits to assess performance where required. Resolve site, country, and regional issues to maintain quality and investigator relationships. Contribute to country/site selection, study design, and start-up processes. Provide feedback on site decisions to stakeholders. Ensure timely and quality site activation and mitigate deficiencies in trial conduct. Identify and enable virtual monitoring sites as applicable. Share issues and trends with stakeholders. Manage resources across portfolios to ensure balanced allocation. Minimum Requirements
Relevant PhD with at least 5 years of clinical research experience, or Relevant Masters with at least 7 years, or Bachelor’s degree with at least 8 years of experience. Extensive knowledge of clinical trial methodologies and experience managing high-quality trials. Leadership experience managing diverse teams in a matrix environment. Experience engaging with senior stakeholders and cross-functional support teams. Availability to travel up to 20%. Strong learning agility. Preferred Qualifications
Understanding of Pfizer People Experience (PX) procedures and policies. Additional Information
This is a remote position within the U.S. with a salary range of $169,700 - $282,900. It includes bonuses, benefits, and potential relocation assistance. The position requires compliance with Pfizer’s policies and U.S. employment laws. Pfizer is an equal opportunity employer and participates in E-Verify. Work authorization in the U.S. is required.
#J-18808-Ljbffr
Join to apply for the
Director of Site Management and Monitoring (DSMM)
role at
Pfizer . Position Summary
Supporting Pfizer Oncology, in partnership with the Director of Clinical Site Operations (DCSO), you will ensure appropriate Site Care Partners (SCP) are in place to deliver end-to-end study start-up, site management, and monitoring activities in line with study milestones for the United States. You will oversee the job functions of the Site Care Partner and support the DCSO in ensuring overall operational site management, patient safety, and quality of study execution in accordance with laws, Good Clinical Practice, and Pfizer standards. You will collaborate cross-functionally with teams involved in Study Start Up, Site Activation, Clinical Trial Assistance, Investigator Contracts, Monitoring, Analytics, Recruitment, and Study Management to facilitate site and country selection, and support regulatory approvals. Additionally, you will execute investigator site/recruitment strategies, lead strategic initiatives, and shape the clinical development environment in the U.S. to meet Pfizer’s development goals. Position Responsibilities
Line management of Site Care Partners (team of approximately 15 colleagues and FSPs). Lead and coach resources within assigned regions. Ensure growth and development of the Site Operations organization. Oversee job functions and ensure compliance with training requirements. Perform joint site visits to assess performance where required. Resolve site, country, and regional issues to maintain quality and investigator relationships. Contribute to country/site selection, study design, and start-up processes. Provide feedback on site decisions to stakeholders. Ensure timely and quality site activation and mitigate deficiencies in trial conduct. Identify and enable virtual monitoring sites as applicable. Share issues and trends with stakeholders. Manage resources across portfolios to ensure balanced allocation. Minimum Requirements
Relevant PhD with at least 5 years of clinical research experience, or Relevant Masters with at least 7 years, or Bachelor’s degree with at least 8 years of experience. Extensive knowledge of clinical trial methodologies and experience managing high-quality trials. Leadership experience managing diverse teams in a matrix environment. Experience engaging with senior stakeholders and cross-functional support teams. Availability to travel up to 20%. Strong learning agility. Preferred Qualifications
Understanding of Pfizer People Experience (PX) procedures and policies. Additional Information
This is a remote position within the U.S. with a salary range of $169,700 - $282,900. It includes bonuses, benefits, and potential relocation assistance. The position requires compliance with Pfizer’s policies and U.S. employment laws. Pfizer is an equal opportunity employer and participates in E-Verify. Work authorization in the U.S. is required.
#J-18808-Ljbffr