International Clinical Program Leader, Clinical Operations
vor 1 Tg.
  • Job facts
  • We are offering an exciting opportunity to join our Medical Affairs Clinical Operations team within Pharma Development Clinical Operations (PDG).

    Our team is providing strategic input, operational oversight and delivery of clinical studies to support the Integrated Evidence Plan for programs in Global Medical Affairs.

    As an International Clinical Program Leader (ICPL) you provide strategic input and oversight to the development of the medical plans for Global Medical Affairs studies.

    You line manage several International Clinical Trial Managers (ICTMs), providing leadership to deliver clinical studies within a designated therapy area (TA) in accordance with appropriate quality standards. For this purpose :

  • You make broad contribution at a strategic level including input into risk management plans, business value assessment and TA indication expertise.
  • You contribute to the development of integrated evidence and medical plans and establish the operational plan for new studies, providing innovative and flexible solutions and options.
  • You review the operational plan with the TA leadership for alignment within the TA and communicate initial budget, timelines, and changes to review bodies as appropriate.

  • You are accountable for meeting all operational deliverables in the medical plan in accordance with time, cost, and quality commitments.
  • You are a team player who builds strong relationships, collaborates and communicates effectively with internal and external stakeholders, ensuring alignment of the operational program and deliverables.
  • You build and provide leadership to high performing study teams with clear roles, responsibilities and accountabilities to deliver studies as outlined by the medical plan.
  • You identify and manage resource needs through proactive planning and effective recruitment.
  • You provide leadership and support the development and training of your direct reports in order to optimize their capability to successfully contribute to project deliverables.
  • You lead by example to create a positive work environment by encouraging mutual respect, innovation and accountability on a functional and project level.
  • You provide technical / scientific / functional expertise to the function and TA.
  • What else are we offering?

    We are dedicated to support our staff in development of their knowledge and skills and offer further career opportunities locally and globally where people demonstrate talent and aptitude.

    Who are we looking for?

    We are seeking a committed individual who holds a University degree in a Scientific, Medical or Healthcare subject. Further qualification, e.

    g. PhD or MBA is advantageous. You have extensive experience in pharmaceutical industry and drug development complemented with substantial experience in organization, implementation, and delivery of global clinical study programs.

    In addition, you bring :

  • Broad experience of clinical study management including vendor / CRO management, ICH-GCP, leading / working as part of a team and coordinating study level activities to deliver quality data.
  • Demonstrated leadership, influencing, communication and strategic project management skills, experience in managing direct reports and ability to engage and inspire others.
  • Meaningful analytical skills, including previous experience with forecasting and analyzing benchmarking research results.
  • Ability to analyze complex activities and information to arrive at reasonable conclusions. Proficient computer skills across multiple applications.

  • Ability to work independently with appropriate consultation as needed.
  • Fluency in spoken and written English.
  • Other information

    You will be based at either our Swiss (Basel) or UK (Welwyn Garden City) office

    Some international travel will be required (

    Ready to apply?

  • Who we are Our UK Pharmaceutical head office is situated in Welwyn garden City, Hertfordshire, with beautiful country side surrounding the area.
  • Supported by major motorways & airports as well as being a 30 minute train ride to London, access is easy. With over 1400 people occupying our site in Welwyn, you can expect opportunities in Early Development (pRED), Product Development (PD), Commercial (Rx) and of course our corporate function.

    Roche is an equal opportunity employer and strictly prohibits unlawful discrimination based upon an individual’s race, color, religion, gender, sexual orientation, gender identity / expression, national origin / ancestry, age, mental / physical disability, medical condition, marital status, veteran status, or any other characteristic protected by law.

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