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Full-Time

Director/Senior Director

Clinical Science

Confirmed live in the last 24 hours

Coherus BioSciences

Coherus BioSciences

201-500 employees

Develops next-generation immuno-oncology therapies

Biotechnology

Compensation Overview

$190k - $260kAnnually

Senior, Expert

San Carlos, CA, USA

Category
Physicians & Surgeons
Medical, Clinical & Veterinary
Required Skills
Communications
Data Analysis
Requirements
  • PhD degree in health science field, PharmD, MD or non-US equivalent, or other relevant advanced degree in a health science field
  • Minimum 7+ years of experience for Director, 12+ years of experience for Senior Director at a pharmaceutical, CRO or biotechnology company as a clinical scientist or related role
  • Experience in oncology or oncology immunotherapy clinical trials preferred
  • Early stage drug development experience required
  • Experience with data analysis and interpretation
  • Thorough understanding of the drug development process
  • 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
  • Impeccable attention to detail
Responsibilities
  • 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

Coherus BioSciences is dedicated to developing a diversified portfolio of next-generation immuno-oncology therapies, including the FDA-approved toripalimab-tpzi, to transform cancer treatment and improve patient outcomes. The company's focus on immuno-oncology technologies and differentiated PD-1 inhibitor demonstrates its commitment to advancing innovative cancer treatments.

Company Stage

IPO

Total Funding

$1.2B

Headquarters

Redwood City, California

Founded

2010

Growth & Insights
Headcount

6 month growth

-5%

1 year growth

-5%

2 year growth

-9%

Benefits

Competitive base salary

Target bonus based on performance

stock options

Medical, dental, & vision coverage

PTO

401(k) plan

FSA