Senior Medical Director

vor 2 Wochen

Basel, Basel-Stadt, Schweiz Coopers Group AG Vollzeit CHF 180'000 - CHF 300'000 pro Jahr

We are looking for an Integrated Product Medical Lead (m/f/d).

About the Role

The
Integrated Product Medical Lead (IPML)
plays a pivotal role in advancing an innovative
oncology early development portfolio
. In this position, you will make a significant impact through the successful progression of global development programs and the strategic expansion of the pipeline.

You will set the
medical vision and strategic direction
for assigned programs, ensuring a scientifically sound, end-to-end clinical development strategy across multiple modalities, biologies, and indications — spanning from preclinical stages through handover to late-stage development.

Acting as the
clinical leader
within cross-functional program teams, you will define, execute, and deliver clinical strategies that maximize the value and success of early oncology assets. You will also contribute to the evaluation of novel assets and innovation initiatives, helping shape the next generation of oncology therapies.

Key Responsibilities

  • Serve as the
    clinical leader and primary medical representative
    for global early development programs.
  • Develop and execute the
    clinical vision and strategy
    addressing unmet medical needs, grounded in scientific rationale.
  • Ensure timely milestone delivery, proactively identifying and mitigating roadblocks to execution.
  • Support
    preclinical evaluation and validation
    of new oncology assets in collaboration with research teams.
  • Guide the transition from preclinical to clinical development, enabling informed go/no-go decisions.
  • Review and approve core study documents, ensuring alignment with the clinical development plan and target product profile.
  • Maintain deep knowledge of the
    scientific, clinical, and regulatory landscape
    to drive cutting-edge precision oncology development.
  • Build and maintain relationships with
    academic and industry partners, key opinion leaders, health authorities, and patient advocacy groups
    .
  • Lead strategic initiatives supporting organizational excellence and innovation in early clinical development.
  • Foster a culture of
    collaboration, empowerment, and accountability
    across self-directed matrix teams.

Who You Are

  • M.D.
    with at least
    5 years of direct patient care
    and
    board certification in oncology/hematology
    or a closely related subspecialty.
  • Proven scientific excellence demonstrated by
    peer-reviewed publications
    or academic contributions.
  • 3–5 years of drug development experience
    , including
    2+ years in early-phase clinical development
    .
  • Broad expertise across
    varied therapeutic modalities
    , including small and large molecules.
  • Experience engaging with
    global health authorities
    and understanding regulatory processes.
  • Ability to
    design and implement medical strategies
    independently and mentor others in doing so.
  • Exceptional
    leadership, communication, and strategic thinking skills
    .
  • Strong motivation, sense of ownership, and a proactive, solution-oriented mindset.
  • Fluency in English
    required; proficiency in another major European language (especially German) is an advantage.

Why Join

This is a rare opportunity to influence the trajectory of breakthrough oncology assets in early development, working within a
highly collaborative, global environment
that encourages innovation, autonomy, and scientific excellence.

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