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Roche

Senior Medical Director, Product Development, Neurology

Welwyn
$253.7k – $471.1k/yr
Posted 1 day ago
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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.

Senior Medical Director

The Senior Medical Director leads development of the Clinical Development (CD) strategy and plan and is responsible for ensuring effective and efficient execution for the assigned molecule(s)/indication(s). Senior Medical Directors are expected to perform their responsibilities independently, and effectively lead multiple projects.

Responsibilities

  • Lead, delegate, and be responsible for the development and implementation of the CD strategy and/or plan for assigned molecule(s)/indication(s).
  • Represent CD for the assigned molecule(s)/indication(s) to other internal Roche groups.
  • Ensure cross-functional integration, coordination, and alignment to enable effective and efficient CD plan execution.
  • Collaborate with a variety of internal and external partners and stakeholders, such as clinical investigators, clinicians, scientists, key opinion leaders (KOLs), and multidisciplinary internal groups.
  • Participate in meetings, reviews, discussions, and other interactions regarding early development/Phase I studies to provide clinical science input and guidance.
  • Lead health authority (HA) interactions, including the development of briefing packages.
  • Lead role with other CST members, regulatory, and other internal partners/stakeholders in the completion and submission of regulatory filings and other regulatory documentation.
  • Provide clinical science information and input for regulatory submissions and other regulatory processes.
  • Be accountable for training new CST members.

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Location

This position is based on-site in San Francisco, CA (preferred); Boston, MA; Basel, CH; Welwyn, UK. Relocation benefits are not being offered for this position.

Who You Are

Required

  • Board Certified/Board Eligible (or its equivalent) MD (MBBS), MD(MBBS)/PhD trained Neurologist.
  • 6+ years of pharma/biotech R&D experience and/or recognized as an expert in your field; effectively contribute to pipeline strategy and lead cross-functional teams.
  • Late stage experience within the Neurology space and have worked with various health authorities.
  • Demonstrated ability to work with pharma partnering on relevant acquisitions, joint ventures, or other strategic partnerships.
  • Significant experience designing and conducting clinical trials.
  • Demonstrated experience in late stage development; ability to use sophisticated analytical thought, identify innovative approaches, and act as a mentor.
  • 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, and demonstrated experience in scientific writing.
  • Outstanding communication skills in both long-form scientific presentation and short-form communication of complex scientific topics.
  • Demonstrated ability to collaborate with relevant team members to measure and monitor study progress against objectives and plans, including any variances, and proactively communicate any issues, challenges, and potential strategies to resolve.
  • Experienced working with various clinical trial designs.

Preferred

  • Demonstrated clinical experience within multiple sclerosis.
  • Leadership experience.
  • Strong interpersonal skills: Outstanding interpersonal, verbal, and written communication and influencing skills; have built and cultivated important relationships both inside and outside of the organization and externally; have proven abilities to influence internal partners and stakeholders, thought leaders, national advocacy organizations, national standard-setting bodies, and other relevant external parties.
  • Proven ability to use sophisticated analytical thought, identify innovative approaches, and act as a mentor.
  • Demonstrated abilities to influence internal partners and stakeholders, thought leaders, national advocacy organizations, national standard-setting bodies, and other relevant external parties. Seamlessly collaborates with colleagues/other parts of the organization.

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Salary

The expected salary range for this position based on the primary location of South San Francisco, CA is $253,700 - $471,100. 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.

Benefits

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.

Accommodations

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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Skills

Clinical development
Neurology
Clinical trial design
Regulatory strategy
Health authority interactions
Cross-functional leadership
Scientific writing
Data analysis
Clinical strategy
Stakeholder management
Mentorship
Pipeline strategy
Regulatory filings
Clinical science
Strategic partnerships

Location

Basel, Basel-City, Switzerland

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