Sr Mgr Clin Study Lead Contract

East Coast, NJ - Pharmaceutical & Biotech - Remote - Full time

Date Posted: 5/20/2024

Contract Sr. Manager Clinical Study Lead
Remote Position (NY/NJ, East Coast)

Will lead the cross-functional study team responsible for the global execution of large, complex clinical trials from study design through study close out. These responsibilities apply to both internally sourced studies and studies outsourced to CROs, so we need a Temp SCSL who has experience managing Third-Party Vendors.

Responsibilities:
Leading all aspects of and contributing to the development of study specific documentation e.g. case report forms (CRF), data management plan, monitoring plan, monitoring oversight plan, project specific training plan, data review plan, statistical analysis plan, etc. Supervising set-up and maintenance of study systems such as Clinical Trial Management System (CTMS), Trial Master File (TMF) etc. Ensuring compliance with the clinical trial registry requirements. Providing input into baseline budget and timeline development and managing the study against planned budget, timeline and results. Leading risk assessment and identifies risk mitigation strategies at the study level. Managing feasibility assessment to select relevant regions and countries for the study. Conducting site evaluation and selection, leading investigator meeting preparation and execution. Monitoring progress for site activation and monitoring visits and acts on any deviations from plan, and develop/implement patient recruitment and retention strategies. Overseeing and providing input to the study drug and clinical supplies forecasting, drug accountability and drug reconciliation. Ensuring data quality including regular review of data metrics and listings, protocol deviations, eligibility violations, dosing deviations, and suspected serious non-compliance by sites. Ensuring clinical project audit and inspection readiness through the study lifecycle and contributing to CAPAs as required. Supervising study close-out activities and contributing to clinical study report writing and review. Directly supervising Clinical Trial Management staff.

Requirements:
Must have direct management experience with demonstrated results building and developing outstanding teams along with the capacity to understand and implement the strategic direction and guidance for respective clinical studies. Can take a proactive and self-disciplined approach to managing projects with a developed ability to meet deadlines and prioritize. Have a history of effectively leading and negotiating with vendors. Have a data-driven approach to planning, executing and problem solving. Operate with a high degree of cross-functional agility using exceptional influencing and interpersonal skills. Have the innate ability to rally disparate groups to accomplish lofty shared goals.

To be considered for this opportunity you must possess a Bachelors’ degree with a minimum of 8 years of relevant industry experience. Advanced degrees may be considered in lieu of relevant experience. Direct experience managing global clinical trial operations is a must, including experience developing protocols and key study documents. You will also need technical proficiency trial management software and MS applications to be considered.

Please contact Darren Gutowski at dgutowski@clarkdavis.com




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