Job Description

Title: Senior Director, Clinical Science
Reports To: Senior Vice President, Clinical Development - Oncology
Location: Redwood City, California
Classification: Exempt

Overview:

The Senior Director, Clinical Science will drive the design, planning, implementation and execution of clinical development plans and programs in accordance with company processes, guidelines, study protocols and regulations. This role will work on cross functional programs to provide clinical development strategy, clinical program oversight and clinical interactions with regulatory agencies on program specific activities.

Principle Responsibilities and Duties:

• Partner with cross-functional program team members and key R&D stakeholders to contribute to the clinical strategy and creation of clinical development plans for one or more candidate clinical drug products.
• Provide clinical support for clinical study conduct, including operational feasibility, data management, communication plans, safety and medical monitoring, preparation of meeting materials and study updates.
• Perform medical and safety/efficacy data reviews. Prepare and communicate clear overviews of trial results.
• Identify issues related to study conduct and/or subject safety. Provide preliminary assessments and recommendations and collaborate with the clinical team to develop solutions ensure resolution.
• Provide organizational support for data review committees including operationalizing the charter, preparing updates and data reviews, development of meeting materials and data reports and execution of meetings.
• Author protocols and contribute to authoring of clinical study reports, IBs, ICFs, training documents, and other clinical and regulatory documents.
• Interact with internal and external stakeholders (study sites, vendors, KOLs, etc.) in support of program-level strategy as well as clinical trial objectives.
• Act as recognized clinical expert for assigned programs.
• Lead development of abstracts, posters, and content for scientific meetings, conferences and publications.

Experience and Education:

• PhD degree in health science field, PharmD, MD or non-US equivalent, or other relevant advanced degree in a health science field.
• 12+ years of experience as a Clinical Scientist or related roles at a pharmaceutical, CRO or biotechnology company. Minimum 8 years as Clinical Scientist in clinical oncology development is highly preferred.
• Experience in oncology or oncology immunotherapy clinical trials is required.
• Experience with data cleaning, analysis and interpretation.
• Thorough understanding of the drug development process, especially early vs late stage.
• Broad understanding of functional areas of drug development, including preclinical, regulatory, pharmacovigilance, drug supply, data sciences (data management, biostatistics, programming), and clinical operations (including site selection, study start-up, study conduct, and finalization).
• Demonstrated ability to communicate and write clearly, concisely, and effectively.
• Ability to understand, interpret and communicate clinical information including literature reviews, competitive intelligence, and changing treatment paradigms in order to apply knowledge to support a robust clinical development strategy.
• Understanding of trial design and statistics
• Ability to interpret, analyze, and present clinical data.
• Well-organized: ability to prioritize tasks with a successful track record of managing multiple projects in a fast-paced and deadline-driven environment.

The Base Salary Range for this position is $230,000 - $260,000. Coherus considers various factors, including professional background and work experience, when determining base pay. These considerations mean actual compensation will vary.

Coherus provides equal employment opportunities to all employees and applicants for employment and prohibits unlawful discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. We also prohibit discrimination based on the perception that anyone has any of these characteristics or is associated with a person who has or is perceived as having any of these characteristics.

** We are currently not accepting any unsolicited resumes from recruiters or employment agencies. **

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Full time, Contract work, For contractors, Work experience placement, For subcontractor, Work at office, Local area,

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