Roche
Healthcare
MedicalDirector(CVM)
Neural analysis suggests this role is
optimal for Director candidates.
“Medical Director (CVM) at Roche. Skills: Clinical development, Therapeutic knowledge, Medical affairs. Participate in development of CD plan. Gather and analyze data”
Industry & Context.
Data analysis; Data interpretation; Decision Making
Up to 30% global travel
What They're Looking For.
Must Have
M. D. Required, Therapeutic knowledge metabolism, obesity, diabetes, Clinical, scientific, clinical trial/development experience, 2 or more years post-graduate academic or clinical experience
Nice to Have
Academic/teaching background is a plus, Experience publishing results of a scientific study in a peer-reviewed journal, Knowledge of medical aspects of GCP, Knowledge of ICH, Knowledge of FDA, Knowledge of EMA, Knowledge of other relevant guidelines and regulations
What You'll Do.
Participate in development of CD plan
Gather and analyze data
Develop CD plan components
Develop and provide input for budget/resource requirements
Stay abreast of internal and external developments
Participate in competitive intelligence
Maintain scientific and clinical knowledge
Collaborate with internal and external partners
Provide clinical science input and guidance
Review and provide late stage input into Phase
Support transition of new drugs/indications into Medical Affairs
Participate in design
execution of clinical studies
Collaborate in development of product safety profiles
Collaborate in development of clinical sections of investigator
Collaborate in development of presentations
Guide and advise others in identification and selection
Participate in development and implementation of communications strategies
Participate in development and delivery of key presentations
Present at advisory boards
Collaborate in development of study analytics
Collaborate in development of data management plans
Participate in ongoing reviews of medical/safety data
Measure and monitor study progress
Proactively communicate issues
Ensure timely completion of interim study reporting
Close-out clinical studies
Complete study reporting
Support correct medical/scientific data interpretation
Act as a medical monitor for assigned studies
Participate in relevant Clinical Science Team (CST)
Support cross-functional integration
coordination and alignment
Support training of new CST members
Support sub-teams in assigning and training new team
Support development of briefing packages
Support development of responses to HA questions
Participate in health authority (HA) interactions
Support completion and submission of regulatory filings
Provide clinical science information and input for regulatory
Develop label and packaging language
Contribute to scientific discussion in the community
Provide study/program updates to the wider community
How You'll Work.
Team & Collaboration
Cross-functional integration; Cross-functional coordination; Cross-functional alignment; Internal and external partners; Multidisciplinary internal groups; Clinical investigators; Clinicians; Scientists; Key opinion leaders (KOLs); Other groups in PD; Research; Business development; Commercial operations; Legal; Study Management Teams
Communication Scope
Verbal communication; Written communication; Presentation skills; Business presentation; Interpersonal skills
Full Job Description
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. ### ### The Position **EXPERIENCE AND QUALIFICATIONS:** * **Academic/Scientific/Clinical:** * * 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** * **Regulatory:** 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** * **Duration of Experience:** 2 or more years of post-graduate academic or clinical experience * Up to 30% global travel ** _Key Skills and Behaviours_** * **Ethics:** Has impeccable ethics. Demonstrates, or proven ability to demonstrate, Roche Values * **Attention to detail:** Outstanding attention to detail * **Business Acumen:** Has working knowledge of the pharma/biotech industry, the multiple functions and roles involved in the drug development process. Regularly leads development of disease strategies and plans * **Organization:** Can prioritize multiple tasks and goals on time, on target, and within budget * **Interpersonal skills** : Good interpersonal, verbal communication and influencing skills: can influence without authority
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