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: Therapeutic knowledge, Clinical development, Data analysis. Participate in development of the CD plan. Gather and analyze data and information”

Industry & Context.

Healthcare
Problems you'll solve

Data interpretation; Decision making

Eligibility Requirements

Up to 30% global travel

What They're Looking For.

Must Have

M. D. Required, 2 or more years of 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 is preferred, Knowledge of medical aspects of GCP, ICH, FDA, EMA, and other relevant guidelines and regulations is preferred

What You'll Do.

Participate in development of the CD plan

Gather and analyze data and information

Develop CD plan components

Develop and provide information for budget/resource requirements

Stay abreast of internal and external developments

Participate in competitive intelligence activities

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 internal partners in transitioning new drugs/indications

Participate in design

and execution of clinical

Collaborate in development of product safety profiles

Guide and advise others in identification and selection

Participate in development and implementation of communications strategies

Participate in development and delivery of key presentations

Collaborate in development of study analytics and data

Participate in ongoing reviews of medical/safety data

Collaborate to measure and monitor study progress

Collaborate to ensure timely completion of interim study

Collaborate to close-out clinical studies

Support members to ensure correct medical/scientific data interpretation

Act as a medical monitor for assigned studies

Participate in the 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 local site

Provide study/program updates to the wider community

How You'll Work.

Team & Collaboration

Cross-functional integration; Cross-functional alignment; Internal and external partners; Multidisciplinary internal groups; Clinical investigators; Scientists; Key opinion leaders (KOLs)

Communication Scope

Verbal communication; Written communication; Business presentation

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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