Medical Director, CVM

Roche

Medical Director responsible for clinical development planning and execution for Roche's therapeutic programs. Collaborating with cross-functional teams and stakeholders in the field of metabolism, obesity, and diabetes.

Posted 6/2/2026full-timeShanghai • 🇨🇳 ChinaLeadWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

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
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
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
May participate in meetings, reviews, discussions and other interactions regarding early development/Phase I studies to provide clinical science input and guidance
Supports internal partners in transitioning new drugs/indications into Medical Affairs (MA) studies, including providing CD input for MA study protocol development
Participates in design, development, and execution of clinical studies
Collaborates with others in the development of product safety profiles
Includes reviewing and providing late stage input into Phase I and II protocols
Supports other CST members to ensure correct medical/scientific data interpretation for interim and final study reporting
Acts as a medical monitor for assigned studies
Participates as standing or ad hoc member of sub-teams relevant to assigned molecule(s)/indication(s)

Requirements

What you’ll need

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
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
Up to 30% global travel

Benefits

Comp & perks

🌐 Worldwide ❌ Jobs You've Hidden ⭐️ Saved Jobs ✅ Applied Jobs ✉️ Email Alerts 👤 Account Roche Website LinkedIn All Job Openings 10,000+ employees Founded 1896 ⚕️ Healthcare Insurance 💊 Pharmaceuticals 🧬 Biotechnology Healthcare Insurance
Pharmaceuticals
Biotechnology Roche is at the forefront of technological advancements in healthcare. The company emphasizes the importance of diversity, equity, and inclusion across its global workforce of over 101,000 employees. Roche is particularly focused on research and development, digital innovation, and creating sustainable collaborations to benefit patients worldwide. With a strong culture of rewarding employee performance, Roche provides a diverse range of career opportunities in areas such as tech, manufacturing, and business strategy, encouraging innovation to transform global healthcare. The company also offers various programs for students and graduates, and operates in several countries, including Germany, Austria, and Switzerland. Medical Director, CVM 🔥 33 minutes ago 🏢 Shanghai – Onsite ⏰ Full Time 🔴 Lead 👨‍⚕️ Medical Director Apply Now Find Hiring Managers Customize resume + cover letter Report problem ☆ Save ☑️ Mark as applied ❌ Hide 📋 Description
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
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
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
May participate in meetings, reviews, discussions and other interactions regarding early development/Phase I studies to provide clinical science input and guidance
Supports internal partners in transitioning new drugs/indications into Medical Affairs (MA) studies, including providing CD input for MA study protocol development
Participates in design, development, and execution of clinical studies
Collaborates with others in the development of product safety profiles
Includes reviewing and providing late stage input into Phase I and II protocols
Supports other CST members to ensure correct medical/scientific data interpretation for interim and final study reporting
Acts as a medical monitor for assigned studies
Participates as standing or ad hoc member of sub-teams relevant to assigned molecule(s)/indication(s) 🎯 Requirements
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
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
Up to 30% global travel Apply Now 📊 Check your resume score for this job Improve your chances of getting an interview by checking your resume score before you apply. Check Resume Score Similar Jobs Associate Medical Director, Oncology 🕒 May 8 IQVIA 10,000+ employees ⚕️ Healthcare Insurance 🧬 Biotechnology 🤖 Artificial Intelligence Website LinkedIn All Job Openings Global Medical Advisor providing medical advice and support on Oncology projects. Collaborating with project leaders and teams in clinical research settings with extensive medical review responsibilities. 🏢 Shanghai – Onsite 💰 $1G Post-IPO Debt on 2023-05 ⏰ Full Time 🔴 Lead 👨‍⚕️ Medical Director Medical Director – Oncology 🕒 May 8 IQVIA 10,000+ employees ⚕️ Healthcare Insurance 🧬 Biotechnology 🤖 Artificial Intelligence Website LinkedIn All Job Openings Medical Director (Oncology) overseeing medical monitoring and strategic advisory for clinical projects. Leading global and regional medical advisor initiatives while ensuring patient safety across studies. 🏢 Shanghai – Onsite 💰 $1G Post-IPO Debt on 2023-05 ⏰ Full Time 🔴 Lead 👨‍⚕️ Medical Director View More Medical Director Jobs 🌐 Worldwide Built by Lior Neu-ner. I'd love to hear your feedback — Get in touch via DM or support@remoterocketship.com Search Search Jobs by country Search jobs by city Search jobs by job title Search entry-level jobs Search junior-level jobs Search senior-level jobs Search jobs by tech stack Search jobs by contract type Search remote internships Search remote part-time jobs Remote jobs Anywhere in the World Companies Hiring Anywhere in the World Companies Hiring Sales People Anywhere in the World Companies Hiring Software Engineers Anywhere in the World Resources Advice Tips for finding remote jobs Interview questions and answers Resume examples Cover letter examples Post a job Affiliates Privacy policy Terms of service Job board SEO course AI Apply Copilot OpenClaw job finder Jobs by Country Remote jobs anywhere in the world (Worldwide remote jobs) Remote jobs United States Remote jobs Australia Remote jobs Brazil Remote jobs Canada Remote jobs France Remote jobs Ireland Remote jobs Germany Remote jobs Netherlands Remote jobs Spain Remote jobs UK Popular Jobs Remote data analyst jobs Remote customer support jobs Remote executive assistant jobs Remote marketing jobs Remote product designer jobs Remote product manager jobs Remote project manager jobs Remote recruiter jobs Remote sales jobs Remote software engineer jobs Jobs by Type Remote full-time jobs Remote part-time jobs Remote contract jobs Remote internship jobs Remote entry-level jobs Remote jobs with no experience required Remote junior jobs (1-3 years of experience) Digital nomad jobs Remote jobs with no degree required Freelance remote jobs Temporary remote jobs Remote jobs hiring now Stay at home mom jobs

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Hard Skills & Tools

data analysisclinical trial developmentclinical study designmedical monitoringscientific publishingclinical relevance interpretationbudget/resource managementcompetitive intelligencesafety profile developmentprotocol development

Soft Skills

collaborationcommunicationinterpersonal skillsorganizational skillsleadershipscientific knowledgeadaptabilityteamworkproblem-solvingstakeholder engagement

Certifications

M.D.