Global Clinical Trial Lead

vor 1 Woche

Lausanne, Waadt, Schweiz Debiopharm Vollzeit

Debiopharm_ is an independent biopharmaceutical company based in Switzerland with an ongoing commitment to research in oncology and infectious diseases in order to improve patient outcomes and quality of life.

Our main activities include drug development, drug manufacturing and digital health investment. Debiopharm International SA aims to develop innovative therapies that target high unmet medical needs.

Our unique "development only" business model allows us to act as a bridge between disruptive discovery products and patient access in international markets.

We first identify high-potential compounds for in-licensing, clinically demonstrate their safety and efficacy and then select large pharmaceutical commercialization partners to maximize patient access globally.

_

  • At Debiopharm you will be at the forefront of the fight against cancer and infectious diseases, and you will have the opportunity to work on new innovative medicines for patients. Efficiency is our mode of action, saving lives our collective target._
Are you a dedicated and experienced Clinical Trial Lead with a passion for advancing oncology research, leading and innovating in the field of oncology clinical trials? Join our team as

Global Clinical Trial Lead


You will lead a cross-functional Clinical Trial Team, oversees the outsourced activities to ensure trial progress as planned and drives achievement of milestones to timelines, budget, and quality standards.


Your responsibilities will be but not limited to:

  • Leads and facilitates cross-functional interfaces and interactions within the Clinical Trial Team and external partners (i.e., CRO and other vendors).
  • Provides direct input to protocol development and other essential triallevel documents to ensure efficient and effective delivery of trial objectives and in accordance with the relevant Standard Operating Procedures.
  • Develops, executes, and maintains operational Risk Management Plan highlighting potential risks and actions.
  • Creates and drives trial level milestones and timelines. Oversees trial level performance against the agreed plans (including global recruitment and projection plan), milestones and key performance indicators.
  • Ensures all trialrelated documents and systems (e.g., clinical database, IRT etc.) required for Ethics/Regulatory submissions and trial initiation are developed by the Clinical Trial Team and CRO/vendors within the specified timelines.
  • Ensures selection of clinical trial sites which meet protocol requirements, and all essential documents are in place for approval of site initiation and release of Investigational Medicinal Products to the sites.
  • Ensures CRO/vendors contracted at trial level are performing to contractual obligations and timelines/budget and that oversight is documented and any issues are escalated appropriately.
  • Responsible for trial budget, reforecasting after initial budget estimate and for management through the trial lifecycle and provide budget process report including any financial risks and mitigation plans.
  • Ensures clinical trial is inspectionready at all time and Trial Master File (TMF) completion including TMF plan is in place and ongoing QC activities are performed to always ensure TMP completeness.

Requirements:

  • Bachelor's Degree/Master's Degree in Science or Healthcare
  • 58 years of relevant clinical experience in pharmaceutical industry including 23 years of project management experience
  • Excellent knowledge of Good Clinical Practice, regulatory process, and clinical development process
  • Experience with health authority inspections (FDA/EMA) and audits preferred
  • Strong critical thinking and problemsolving skills
  • Strong team leadership and project management skills with ability to collaborate across function in a matrix environment
  • Excellent communication, interpersonal and conflict management skills with ability in establishing and maintaining effective working relationships with internal and external team members and stakeholders
  • Ability to work under pressure and managing competing priorities
  • Demonstrated ability to effectively forecast and manage trial budget
  • Fluent in English (French and another European language are an asset)

Benefits

  • International, highly dynamic environment with a long term vision.
  • Crossfunctional collaboration at the forefront of the most advanced scientific developments in oncology and antibacterial industry
  • Exposure to a wide variety of areas and functions within clinical development and the pharmaceutical industry
  • Participation in a company where innovation, people and entrepreneurship are the fundamental keys to success.
  • Proud to be an Equal-Pay certified, we ensure offering to all our employees the same opportunities
  • Submission of unsolicited resumes in advance of an agreement between the Human Resources Department and the external staffing agency or recruiter does not create any implied obligation on the part of Debiop

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