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Associate Clinical Development Medical Director

Entreprise
Novartis Pharma AG
Lieu
BASEL
Date
29.09.2025
Référence
182062

Position Overview

This role encompasses crucial responsibilities related to the clinical and medical aspects of ongoing programs and trials at a country level. The focus is on delivering strategic and tactical leadership in clinical operations while facilitating successful implementation of clinical studies.

Key Responsibilities

  • Provide expert clinical development insights specific to the country, collaborating closely with the clinical trial operations team to ensure high-quality execution of trials within established timelines.
  • Assess the feasibility of clinical trial protocols and make informed decisions based on medical practices and competitive analysis.
  • Supply clinical and medical expertise to team members and site personnel regarding Institutional Review Boards (IRB) and Ethics Committees (EC).
  • Develop appropriate content for Informed Consent Forms (ICFs) ensuring clarity and patient-friendly language.
  • Engage with external experts, including Regulatory Authorities and Patient Advocacy groups, providing scientific and clinical input.
  • Formulate clinical trial plans by considering the broader ecosystem to enhance implementation success, including robust training on indications, compounds, and protocols.
  • Optimize recruitment strategies leveraging insights from investigators and stakeholders to overcome challenges.
  • Ensure adherence to safety standards and the quality of clinical data, supporting the resolution of trial-related scientific issues.
  • Facilitate communication with global teams regarding clinical/medical protocol deviations and other safety concerns.
  • Support innovative study designs by analyzing country-specific datasets relevant to clinical trials.

Qualifications

  • Medical degree (MD/DO) or equivalent, with a preference for training in cardiology.
  • Knowledge of siRNA and clinical training desirable.
  • Proficient understanding of clinical trial protocols, regulatory requirements, and relevant country regulations.

Why Join Us?

Being part of this team means engaging with a community dedicated to advancing patient care and innovative science. Collaboration, support, and inspiration are at the core of our work culture, driving breakthroughs that profoundly impact patient lives.

Diversity and Inclusion

We are committed to establishing an inclusive work environment that reflects the diverse communities we serve. We believe a diverse workforce enriches our perspective and enhances our ability to serve patients effectively.

Benefits and Rewards

Explore a variety of programs and resources designed to foster your personal and professional growth. We are dedicated to providing a supportive atmosphere where you can thrive.

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