Lead Clinical Scientist, Hematology/Oncology

Genentech; Plymouth; On-site; USD 141,000 - 262,000; Full time

Job summary

A leading company in the pharmaceutical industry is seeking a Lead Clinical Scientist in Hematology/Oncology to oversee clinical science aspects of late-stage clinical strategies. This role involves leading study teams, contributing to clinical documentation, and ensuring compliance with regulations. Candidates should possess an advanced degree and relevant experience in clinical development.

Qualifications

• 3+ years of experience in early or late-stage clinical development, especially in onco-hematology.
• Knowledge of global clinical trial regulations and guidelines.

Responsibilities

• Independently carry out study conduct responsibilities.
• Lead execution of Medical Data Review Plans, data interpretation, and study reporting.
• Design trials, write protocols/ICFs, and coordinate CRFs.

Skills

Communication

Stakeholder Management

Education

Advanced degree (e.g., PhD, PharmD, MSN, MPH) in relevant life sciences

Job description

Lead Clinical Scientist, Hematology/Oncology

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Position Overview

The PDC (Pharmaceutical Development Clinical) organization is responsible for developing and executing late-stage (Phase 2-3) clinical strategies to deliver innovative therapies that significantly benefit patients. The Lead Clinical Scientist oversees clinical science aspects related to study teams and may lead studies or projects to support the Clinical Development Plan (CDP) for specific molecules or indications. Responsibilities include contributing to CDP strategy, clinical documentation, representing the CDP in forums, leading site training, acting as a primary contact, conducting safety reviews, and providing clinical science input into reports.

Key Responsibilities

1. Independently carry out study conduct responsibilities.
2. Lead execution of Medical Data Review Plans, data interpretation, and study reporting.
3. Design trials, write protocols/ICFs, and coordinate CRFs.
4. Develop and contribute to scientific presentations, posters, manuscripts, and external communications.
5. Contribute to regulatory interactions, submissions, and responses.
6. Collaborate with internal and external stakeholders, including early development teams.
7. Support and guide Clinical Science Fellows and Scientists.
8. Engage with Therapeutic Area Experts, partners, and academic institutions.
9. Ensure compliance with applicable laws, regulations, and guidelines such as GCP, ICH, FDA, EMA.

Location

Based in Basel, Switzerland; Boston, MA; South San Francisco, CA; or Welwyn, UK. No relocation benefits offered.

Qualifications

Required:

• Advanced degree (e.g., PhD, PharmD, MSN, MPH) in relevant life sciences.
• 3+ years of experience in early or late-stage clinical development, especially in onco-hematology.
• Knowledge of global clinical trial regulations and guidelines.
• Strong communication and stakeholder management skills.

Preferred:

• Ability to work independently and within cross-functional teams.
• Experience with regulatory submissions and clinical trial design.

Compensation and Benefits

Salary range for San Francisco, CA: $141,000 - $262,000, plus discretionary bonus and benefits. Exact pay depends on experience and location.

Additional Information

Genentech is an equal opportunity employer. Accommodations are available for applicants with disabilities.