Roche

Healthcare

MedicalDirector(CVM)

$1500–2500k ~AI est. Shanghai, China FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Director candidates.

The Brief

“Medical Director (CVM) at Roche. Skills: Clinical development, Therapeutic knowledge, Medical affairs. Participate in development of CD plan. Gather and analyze data”

Industry & Context.

Healthcare
Problems you'll solve

Data analysis; Data interpretation; Decision Making

Eligibility Requirements

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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