Lead Medical Director

TN United Kingdom; Plymouth; On-site; USD 233,000 - 434,000; Full time

Job summary

An established industry player is seeking a Lead Medical Director specializing in Haematology/Oncology to spearhead clinical development efforts. This role involves crafting and executing clinical strategies for late-stage drug development while working closely with diverse teams and ensuring alignment with strategic objectives. Candidates should possess a strong clinical background, particularly in Hematology/Oncology, with proven leadership and analytical skills. Join a forward-thinking organization committed to advancing science and enhancing patient quality of life through innovative therapies.

Qualifications

• 3+ years clinical experience in Hematology/Oncology.
• 5+ years in pharma/biotech late-stage clinical development.

Responsibilities

• Develop and execute clinical strategies for late-stage drug development.
• Collaborate with multidisciplinary teams and support regulatory filings.

Skills

Leadership Skills

Analytical Skills

Collaboration Skills

Education

MD/MBBS

MD/PhD

Job description

Below is a refined version of the job description with improved formatting and focus:

Job Title: Lead Medical Director - Haematology/Oncology

Company Overview: We advance science to enable more quality time with loved ones.

The Opportunity: Support the development and implementation of the Clinical Development Plan (CDP) for assigned molecules/indications, collaborating with internal and external partners, providing clinical science input, and contributing to regulatory submissions.

Responsibilities include:

1. Developing and executing clinical strategies for late-stage (Phase II-III) drug development.
2. Collaborating with multidisciplinary teams, including research, commercial, legal, and external stakeholders.
3. Reviewing and providing input on early and late-phase clinical trial protocols.
4. Supporting regulatory filings and developing labeling and packaging language.
5. Ensuring alignment of the CD plan with strategic objectives and developing components like data strategies and publication plans.

Location: South San Francisco, CA; Welwyn, UK; Basel, CH. (Relocation benefits not offered)

Qualifications:

• MD/MBBS, MD/PhD, with 3+ years clinical experience; Board Certified in Hematology/Oncology.
• 5+ years in pharma/biotech late-stage clinical development.
• Experience in non-malignant hematology, hemostasis, thrombosis, hemophilia, or gene therapy is preferred.
• Strong analytical, leadership, and collaboration skills.

Compensation: Salary range $233,500 - $433,600, plus potential bonuses, based on experience and location.

Genentech is an equal opportunity employer committed to diversity and inclusion. For accommodations, contact us using the provided form.