Director, Clinical Scientist

Summit Therapeutics, Inc.; United Kingdom; Remote; GBP 120,000 - 150,000; Full time

Job summary

A leading biopharmaceutical company is seeking a Director, Clinical Scientist to lead study design and execution in hematology/oncology. The ideal candidate will have a minimum of 5 years of experience, strong communication skills, and expertise in oncology studies. This role is fully remote in the UK and offers a full-time position with a focus on strategic planning and execution of clinical data.

Qualifications

• Minimum of 5+ years overall related experience with PhD or like degree.
• Minimum of 2+ years’ experience in conducting/supporting oncology/hematology clinical studies.
• Excellent written and verbal communication.

Responsibilities

• Leads/contributes to study design and amendments.
• Collaborates on authoring and submission of regulatory documentation.
• Develops input for clinical presentation slides and materials.
• Prepare clinical presentations and materials for meetings and site trainings.
• Develop start-up documents/resources (ICF, Lab Manual, EDC, safety plan).
• Lead safety reviews and communicate study results to stakeholders.
• Support communications strategies for publications and major meetings.

Skills

Excellent written and verbal communication skills

Expertise in interpreting immunology/immuno-oncology translational data

Education

MS or equivalent required; PhD, PharmD, or MD preferred

PhD/MD/PharmD preferred

Job description

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Location: Remote UK

Overview of Role

The Director, Clinical Scientist is responsible for leading/contributing to study design and execution of clinical studies in hematology/oncology. As a leader within the clinical organization, this individual will partner with clinical operations, translational, and other matrix team members to design and refine clinical plans, author key clinical/regulatory documents, and ensure exceptional delivery and interpretation of clinical data. The Director, Clinical Scientist will strive to drive study enrollment, build and maintain collaborative relationships with investigators and clinical site staff, CROs, and Summit colleagues. The role fosters a proactive and thoughtful approach to clinical study execution where obstacles are anticipated and effectively mitigated/resolved.

Role and Responsibilities

• Leads/Contributes to study design and amendments in collaboration with internal and external scientific stakeholders
• Collaborates with MD, regulatory and other internal partners/stakeholders on authoring and submission of protocols, protocol amendments, regulatory filings, and other regulatory documentation
• Collaborates with clinical operations, data management and CRO to develop and implement the overall data quality plan and leads internal medical data review and safety trend analysis on one or more studies/programs
• Point‑of‑contact for clinical inquiries from CRO medical monitor and other stakeholders
• Develops and provides input for clinical presentation slides and other materials for internal/external meetings and/or ongoing communications (e.g., investigator meetings, pre‑study site selection visits, study coordinator or clinical research administrator training, study newsletters, communications to study sites, etc.)
• Partners with clinical operations and CRO in developing and maintaining study start‑up documents/resources (e.g., ICF, Lab Manual, EDC, Safety monitoring Plan, etc.)
• Participates in safety meetings and tracks, analyzes, and reviews documentation for any potential safety events
• Leads/Contributes to the development and implementation of communications strategies to support existing and concluded studies. Includes KOL interactions, advisory boards, major medical meetings, congresses and other events, publications and other materials
• Writes and/or reviews abstracts, posters, content for scientific meetings, conferences, other events and presentations, and other publicly distributed materials and coordinates further reviews with internal partners and stakeholders
• Coordinates submissions to scientific meetings and/or other appropriate venues or groups
• Writes clinical science sections of meeting packages and assists in the development and review of other clinical documentation required for regulatory submissions and other regulatory processes
• All other duties as assigned

Experience, Education and Specialized Knowledge & Skills

• MS (or equivalent) required; PhD, PharmD, or MD preferred
• Minimum of 5+ years overall related experience with PhD or like degree; Minimum of 2+ years’ experience in conducting/supporting oncology/hematology clinical studies
• Excellent written and verbal communication skills
• Expertise in interpreting immunology/immuno‑oncology translational data in addition to clinical data

Summit does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact Summit’s Talent Acquisition team at [e-mail] to obtain prior written authorization before referring any candidates to Summit.

Seniority Level

• Director

Employment Type

• Full‑time

Job Function

• Strategy/Planning and Information Technology

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