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Clinical Sciences Trial Leader/Senior Clinical Sciences Trial Leader, Translational Medicine

Novartis
Full-time
Remote friendly (Cambridge, MA)
United States
$119,700 - $222,300 USD yearly
Clinical Research and Development

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Role Summary

Clinical Sciences Trial Leader/Senior Clinical Sciences Trial Leader, Translational Medicine position located in Cambridge, MA or Basel, Switzerland. Up to 5% travel. You will support or lead the clinical science and operations of planning and executing translational medicine clinical trials, collaborating across a global network and partnering with physicians and scientists to design patient-centric trial strategies.

Responsibilities

  • Operationally and scientifically lead complex clinical studies
  • Drive and deliver aspects of global clinical trial execution from study design, setup, and recruitment to final reporting
  • Lead the matrix-management of global clinical trial teams, collaborating across the organization and externally with service providers/investigator sites
  • Drive the development of clinical study protocols, clinical operations execution plans and other required documents
  • Ensure quality conduct and document standards across the clinical trial lifecycle
  • Lead clinical data review (Sr. Clinical Sciences Trial Leader) and support clinical data review (Clinical Sciences Trial Leader)
  • Contribute to project/program level plans (Sr. Clinical Sciences Trial Leader)
  • May mentor junior team members
  • Support optimization of standard methodologies in clinical trial operations and promote an open learning environment
  • Leverage data and digital technologies within clinical studies

Qualifications

  • A minimum of BSc in life sciences required; MSc, PharmD or PhD desired
  • Clinical Sciences Trial Leader: 2β€šΓ„Γ¬4 yearsβ€šΓ„Γ΄ experience; Sr. Clinical Sciences Trial Leader: 4+ yearsβ€šΓ„Γ΄ experience in clinical trial management/operations
  • Leadership potential for the CL role; demonstrated leadership for the Sr. CL role
  • Track record of collaboration and building strong partnerships
  • Strong project management, planning, prioritization, and multitasking abilities
  • High change agility and proactive learning; accountable and adaptable
  • Clear written and verbal communication

Skills

  • Study design and protocol development/writing experience desirable

Education

  • Required: BSc in life sciences
  • Preferred: MSc, PharmD or PhD

Additional Requirements

  • Travel up to 5% as defined by the business
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