Roche

Medical Director – CVM

Roche

full-time

Posted on:

Location Type: Office

Location: Shanghai • 🇨🇳 China

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Job Level

Lead

Tech Stack

Google Cloud Platform

About the role

  • Participates in development of the CD plan for assigned molecule(s)/indication(s)
  • Gathers and analyzes data and information necessary to create the CD plan
  • Works with other CST members and relevant sub-teams to develop CD plan components (e.g., analytics/data strategy, KOL development, publications strategy, etc.)
  • Works with CST and other relevant teams to develop and provide information and input for budget/resource requirements necessary to implement and execute the CD plan
  • Stays abreast of internal and external developments, trends and other dynamics relevant to the work of CD to maintain, at all times, a fully current view and perspective of internal/external influences and/or implications for the assigned therapeutic and disease area(s)
  • As appropriate, participates in competitive intelligence and/or other market/industry assessment activities and projects
  • Maintains the highest standards and levels of scientific and clinical knowledge in the specific therapeutic and disease area(s)
  • Collaborates with a variety of internal and external partners and stakeholders, such as clinical investigators, clinicians, scientists and key opinion leaders (KOLs), as well as multidisciplinary internal groups, including other groups in PD, research, business development, commercial operations, legal, etc.
  • May participate in meetings, reviews, discussions and other interactions regarding early development/Phase I studies to provide clinical science input and guidance.
  • Includes reviewing and providing late stage input into Phase I and II protocols
  • Supports internal partners in transitioning new drugs/indications into Medical Affairs (MA) studies, including providing CD input for MA study protocol development.

Requirements

  • M.D. Required
  • Therapeutic knowledge within metabolism, obesity, and diabetes with relevant clinical, scientific, and clinical trial/development experience required
  • Academic/teaching background is a plus
  • Experience working with the principles and techniques of data analysis, interpretation, and clinical relevance
  • Experience publishing results of a scientific study in a peer-reviewed journal is preferred
  • Knowledge of medical aspects of GCP (Good Clinical Practice), ICH (International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use), FDA, EMA, and other relevant guidelines and regulations is preferred
  • 2 or more years of post-graduate academic or clinical experience
Benefits
  • Roche is an Equal Opportunity Employer.
  • Local/Global Communities Visible in the local site community, e.g. contributes to scientific discussion in the community.
  • Able to provide study/program updates to the wider community.

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard skills
data analysisclinical trial experiencescientific publishingclinical relevanceclinical science inputprotocol developmentbudget/resource managementcompetitive intelligenceanalytics strategyKOL development
Soft skills
collaborationcommunicationinterpersonal skillsorganizational skillsleadership
Certifications
M.D.