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Roche

Early Development Lead Medical Director, Non-oncology

Roche is hiring an Early Development Lead Medical Director, Non-oncology in Shanghai, China. Level rates it ; you can apply on Roche.

Level's read on this job

  • Little AI ●○○○ is how Level rates this role: aI is not part of the work.
  • The posting mentions clinical development, medical monitoring and drug development among its tools and skills.
  • Level classes it as a lead role.
  • Roche has 1,200+ other open roles on Level.

AI in this role

Leading early clinical development programs and trial strategies as an Early Development Lead Medical Director in China.

clinical-developmentmedical-monitoringdrug-developmentclinical-trials

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

The Position

In Roche’s China Early Development (ED) Center of Excellence (CoE), we play a critical role in accelerating the global early development of transformative medicines for patients in order to tackle some of the world’s toughest unmet healthcare needs. We are a strategic partner to global early development teams of Roche Pharma Research and Early Development (pRED), Genentech Research and Early Development (gRED), and pharma Product Development (PD) to integrate China into the global early development programs. Together, we bring forward extraordinary life-changing innovation at speed.

This position is located in the clinical science function of Roche Product Development China, home of the China ED CoE. This position is dedicated to leading and driving early development programs in therapeutic areas of immunology, neurology, CVRM, and ophthalmology as a clinical lead.

The Opportunity

This role will have the opportunity to shape global early development strategy and CDP, to drive innovative early development trial design, to make significant impacts to the efficiency and success of our early development programs in therapeutic areas of immunology, neurology, CVRM, and ophthalmology, and contribute to the China drug development innovation ecosystem.

In your role, you will:

  • Contribute to and influence global asset strategy and early development CDP as a member of the global asset teams
  • Proactively identify opportunities of accelerating and optimizing global ED CDP leveraging expertise, experience, speed, and scale in China
  • Lead the China cross-functional team to evaluate opportunities of China joining global ED programs or China-first trials from strategic, scientific, regulatory, and operational perspectives
  • Drive innovative trial design and trial conduct in close partnership with global early development functional experts on China-first clinical trials
  • Being the Medical Monitor for China ED clinical trials
  • Scientifically engage China TAEs, Roche internal and external stakeholders
  • Serve as a scientific point of contact to global early development asset teams of non-oncology therapeutic areas (immunology, neurology, CVRM, ophthalmology)
  • Mentor junior medical directors to further build capability and capacity of ED CoE

Who you are

  • You hold a MD, or a Bachelor/Master of Clinical Medicine with at least 3 years of post-graduation clinical practice; clinical expertise in immunology preferred
  • You have a minimum of 5 years of experience in biopharmaceutical industry and extensive early development experience, early development experience in immunology preferred
  • You have hands-on experience in developing early development CDP, designing and running early development clinical trials, interacting with Health Authorities, collaborating with investigators and clinical research sites, and interpreting early development clinical trial data
  • You have a very good understanding of global development guidelines and regulations, including CDE, FDA and EMEA
  • You are an effective communicator: Excellent written and verbal English communication skills, with the ability to present complex concepts to global cross functional teams, governance committees and key stakeholders in a logical and succinct manner
  • You are a great team player; highly collaborative, good interpersonal and influencing skills, can influence without authority

Who we are

A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.


Let’s build a healthier future, together.

Roche is an Equal Opportunity Employer.

How we rate this

Early Development Lead Medical Director, Non-oncology at Roche rates 0 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.

Classification

Little AI. AI is not part of the work.

  1. ●●●● Builds AI80 to 100
  2. ●●●○ Works on AI60 to 79
  3. ●●○○ Uses AI40 to 59
  4. ●○○○ Little AI0 to 39

Levels come from how often the tools, models and workflows of the role are named in the posting itself. Read the description and count the AI tools, models and workflows it names.

Prepare for this job

Built from this posting and from similar jobs on Level.

Skills and AI tools this role asks for

Clinical DevelopmentMedical MonitoringDrug DevelopmentClinical Trials

Questions you could be asked

  1. Tell me about a project where clinical development was part of your work. What did you do?
  2. Tell me about a project where medical monitoring was part of your work. What did you do?
  3. Tell me about a project where drug development was part of your work. What did you do?
  4. Tell me about a project where clinical trials was part of your work. What did you do?

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  • List these exact terms on your resume: Clinical Development, Medical Monitoring, Drug Development, and Clinical Trials. An applicant tracking system matches the wording, not the idea.
  • Attach one line of real, concrete experience to at least one of them. A tool named with nothing behind it rarely survives a human read.

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