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Sr Clinical Program Lead

  • Penzberg, Bavaria DE, Germany, 82377
  • Full Time

The Sr. Clinical Program Lead, in Clinical Operations and Data Management, provides comprehensive operational support for FMI’s participation in clinical trials sponsored by BioPharma partners, Academic partners, and FMI led trials. This position strategically manages a portfolio of studies independently and efficiently. The Sr. Clinical Program Lead is not only responsible for developing, implementing, and monitoring the execution plans for the clinical studies they support from initial study intake through final project deliverables, but are also responsible for contributing to the design of partner and FMI sponsored research. Activities include: proactive, clear, and customer-centric communication, day to day project management, as well as, operational excellence and oversight of clinical trials. The Sr. Clinical Program Lead will work collaboratively with internal and external stakeholders across functions to manage samples, timelines, resource plans, and critical path activities directly impacting the successful implementation and on-going execution of clinical studies. 

 

Strategically represent Clinical Operations in governance sub-committees (Clinical Subteam of LCT).

  • Study Planning and Start-Up:
    • Lead study intake process with partner/collaborator, evaluate feasibility of study with internal stakeholders, and obtain FMI approval to support clinical trials (via CSP, SRC, or PRORECO meeting) with finalized SOW.
    • Communicate decisions to external partners/collaborators.
    • Contribute to the design of the study.
    • Lead internal FMI study start-up activities including contracting, IRB submission and approval, finalization of study materials including manuals, study specific requisition forms/kits, project specific plans, and sample processing guidelines.
    • Collaborate with partner to establish working approach, including optimization of communication and sharing of tools.
    • Develop and deliver study start-up training with partner, internal stakeholders, and external clinical trial sites as required

Trial Operations:

  •  Manage the implementation, on-time execution, and conduct of FMI support of clinical studies; including the management of milestones, timelines and deliverables, development and management of budget/finances, sample forecasting and invoicing, and management of resources.
  • Oversight of cross-functional study team members to ensure initiation and execution of the clinical program within approved budget and timelines.
  • Understand how to support and deliver the trial endgame, which is the data and reports.
  • Work and collaborate closely with Clinical Program Leads, laboratory teams, and Process Specialists to ensure sample tracking and chain of custody is maintained from accessioning through data/report delivery.
  • Partner with Data Management and Data Reporting Team to ensure timely delivery of a quality data product in line with Partner expectations and contractual deliverables.
  • Identify and mitigate against study risks, escalating as necessary.
  • Engage in problem solving as needed related to sample receipt, accessioning, tracking, genomic analysis, report generation, and dissemination.
  • Effectively track and communicate program/study progress to Partners with ability to create and update detailed dashboards and trackers.
  • Provide study updates across partner portfolio and escalate as needed to FMI leadership, including Clinical Operations and Data Management, Alliance Management, and Clinical Development
  • Ensure timely documentation and communication of decisions and updates on timelines and deliverables.
  • Support Laboratory Operations and Process Specialists with sample return and destruction process for Partner/Collaborator samples.
  • Support Partner/Collaborator and internal process audits.
  • Contribute to study close-out reports and close studies within FMI systems.
  • Communication/Other:
    • Maintain documentation on key study contacts (internal and external).
    • Build and maintain relationships with internal and external stakeholders and provide study updates as needed to Medical and BioPharma leadership.
    • Lead partner-facing study meetings.
    • Awareness of competitive landscape, changing regulations, and guidance with ability to assess the impact on clinical projects and make modifications as necessary.
    • Ability to creatively approach challenges and problem resolution to optimize the conduct of clinical trials.
  • Process Oversight and Study Compliance:
    • Lead Clinical Operations initiatives to improve clinical operations and data management processes.
    • Serve as an FMI resource regarding clinical trial regulations.
    • Track, resolve, and communicate NCRs/process deviations with direct impact to clinical trials to partners.
    • Initiate CAPAs in conjunction with Process and Training Leads and QA to correct and prevent issues from reoccurring.

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Internal applicants, please use your FMI email address.

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Foundation Medicines European subsidiary is located within the Roche Campus in Penzberg, Germany, just a couple of miles south of Munich. Roche Penzberg is one of Europe’s largest biotechnology centers, employing around 6,200 people from over 50 nations.

In addition to laboratory operations, the site functions as hub for internal collaborations and partnerships. The central location in Europe and within the Penzberg campus allow for a strong synergy between Foundation Medicine, various national and international partners and Roche. 

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The Foundation Medicine team in Penzberg consists of several groups, such as Laboratory Operations, Client Services & Accessioning, Computational Biology, Quality Assurance, Automation Engineering, Project management, Finance and IT. Many of the Roche amenities on campus can also be used by Foundation Medicine employees, such as the gym, canteen, and bus services.

Learn more about our German location from our Project Manager, Barbara.