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Lead clinical scientist, hematology/oncology

Plymouth
Genentech
Clinical scientist
€60,000 - €80,000 a year
Posted: 28 May
Offer description

Lead Clinical Scientist, Hematology/Oncology

Join to apply for the Lead Clinical Scientist, Hematology/Oncology role at Genentech.


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.

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