Roche
Lead Medical Director, Product Development, Hematology
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Roche’s Clinical Development organization
Roche’s Clinical Development organization is structured by therapeutic area and is responsible for developing and executing the late development (Phase II – III) clinical strategies and plans that deliver medically-differentiated therapies that provide meaningful improvement to patients.
The Lead Medical Director
The Lead Medical Director leads or makes major contributions to development of the Clinical Development (CD) strategy and plan and is responsible for effective and efficient execution for the assigned molecule(s)/indication(s).
Responsibilities
- Support the development and implementation of the Clinical Development Plan (CDP) for assigned molecule(s)/indication(s).
- Gather and analyze data and information necessary to create the CD plan.
- Collaborate with a variety of internal/external partners & stakeholders, as well as multidisciplinary internal groups, including business development, research, commercial, legal, etc.
- Participate in meetings, reviews, discussions and other interactions regarding early development/Phase I studies to provide clinical science input & guidance.
- Take an active role with other CST members, regulatory and other internal partners/stakeholders in the completion and submission of regulatory filings and other regulatory documentation.
- Ensure strategic and operational alignment of the CDP with the relevant CD strategy, strategic and annual LCP.
- Work with other CST members and relevant sub-teams to develop CDP components (e.g., analytics/data strategy, KOL development, publications strategy, etc.)
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Location
This position is based on-site in Boston, MA (US), San Francisco, CA (US), Basel, CH or Welwyn, UK. Relocation support will not be provided for this position.
Who You Are
Required
- Board Certified/Board Eligible (or its equivalent) MD (MBBS), MD(MBBS)/PhD physician in Oncology & Hematology
- 5+ years of post-grad relevant clinical/scientific research and/or clinical trial experience.
- 3 or more years of experience in biopharmaceutical clinical development with experience in late stage drug development.
- 3+ years of medical monitoring experience within the life sciences space.
- 2+ years of experience engaging with clinical sites, PIs, KOLs etc.
- Solid understanding of Phase II – III drug development.
- Demonstrated ability to foster and promote a highly productive and inclusive team-based culture in fast-paced clinical and/or research settings.
- Significant experience working with the principles and techniques of data analysis, interpretation and clinical relevance.
- Demonstrated experience in scientific writing.
- Demonstrated communication skills in both long-form scientific presentation and short-form communication of complex scientific topics.
Preferred
- Disease area of focus is Lymphoma.
- Strong interpersonal skills: Outstanding interpersonal, verbal, and written communication and influencing skills.
- Demonstrated experience working with various clinical trial designs, including outcome trials.
- Sound knowledge of the pharma/biotech industry, the multiple functions and roles involved in the drug development process.
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Compensation and Benefits
- The expected salary range for this position based on the primary location of Boston, MA is $213,000 - $396,000.
- Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.
- A discretionary annual bonus may be available based on individual and Company performance.
- This position also qualifies for the benefits detailed at the link provided below.
Equal Opportunity Employer
Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.
If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.
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