Lead Medical Director, Product Development, Hematology

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)

• You are a Board Certified/Board Eligible (or its equivalent) MD (MBBS), MD(MBBS)/PhD physician in Oncology & Hematology.
• You have 5+ years of post-grad relevant clinical/scientific research and/or clinical trial experience; You have 3 or more years of experience in biopharmaceutical clinical development with experience in late stage drug development.
• You have 3+ years of medical monitoring experience within the life sciences space; you are able to support the senior team members with this responsibility.
• You have 2+ years of experience engaging with clinical sites, PIs, KOLs etc.
• You have a solid understanding of Phase II – III drug development (e.g. trials across different stages of development, or formal education/qualifications in pharmaceutical medicine or drug development); have made significant contributions to an organization’s drug development (whether at Roche or another organization); have identified and created clinical development strategies that have led to label-enabling outcomes.
• You have demonstrated the ability to foster and promote a highly productive and inclusive team-based culture in fast-paced clinical and/or research settings.
• You have significant experience working with the principles and techniques of data analysis, interpretation and clinical relevance, and demonstrated experience in scientific writing (e.g. manuscripts, grants, scientific protocols, health authority documents).
• You have demonstrated communication skills in both long-form scientific presentation and short-form communication of complex scientific topics.

Preferred:

• Your disease area of focus is Lymphoma.
• You have strong interpersonal skills: Outstanding interpersonal, verbal, and written communication and influencing skills: have built and cultivated important relationships both inside an organization and externally.
• You have the 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.
• You have demonstrated experience working with various clinical trial designs, including outcome trials.
• You have sound knowledge of the pharma/biotech industry, the multiple functions and roles involved in the drug development process.

Compensation

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.

Benefits

Equal Employment Opportunity

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.