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Director/Senior Director, CMC Regulatory Affairs


Title:                        Director/Senior Director, CMC Regulatory Affairs
Reports To:          Vice President, CMC Regulatory AffairsLocation:               Redwood City, CA  Classification:     Exempt As the Director/Senior Director, you will develop and implement robust regulatory CMC strategy that align with Clinical, Technical Operations, and Quality functions. You will be responsible for high quality submission packages within target timelines. Job Responsibilities: 

  • Leads the development and implementation of CMC regulatory strategy for programs in early-/mid- development stage, in preparation of licensure.
  • Actively seeks out regulatory knowledge and incorporates this knowledge into submission planning and execution. Stays current with regulatory requirements.
  • Proactively identifies regulatory risks and regulatory opportunities.
  • Contributes to the appropriate execution of CMC regulatory strategy, including authoring regulatory documents (e.g. IND/BLA sections and meeting packages).
  • Operates with effectiveness across functions.
  • Builds and manages relationships through active partnering with key internal and external stakeholders.
  • Ensures CMC dossiers meet format and content requirements, as well as specific local requirements of individual countries.
  • Analyzes and exercises judgment on complex issues, guided by a thorough understanding of CMC. 

Skills and Requirements: 

  • Bachelor's Degree in a relevant scientific discipline, advanced degree preferred.
  • Minimum 8 years of relevant experience in CMC Regulatory Affairs.
  • Experience in biologics drug development and license applications.
  • Demonstrated track record of successful submissions to FDA and/or other health authorities  
  • Ability to apply scientific principles to assess regulatory issues, request and collect relevant information, analyze data, establish facts, and draw valid conclusions.
  • Excellent interpersonal, verbal, and written communication skills as well as the ability to effectively lead and influence others are essential in this collaborative work environment.
  • Comfortable in a fast-paced small company environment with minimal direction and able to adjust workload based upon changing priorities.

The Base Salary Range for this position is $185,000 to $250,000. 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. **

Life at Coherus BioSciences

Thrive Here & What We ValueCollaborative effort with communication and rapport across all internal stakeholders | Adhere to corporate SOPs and ensure vigilant compliance with relevant legal and regulatory guidelines governing scientific interactions with physicians and healthcare professionals across all activities, including those related to clinical trials, scientific interactions with internal and external groups, and responses to unsolicited request for medical/ scientific information. | Participate in/support the training of Coherus field and home office employees | Facilitate research collaborations (including REMS programs, Real World Data [RWD] generation and investigator initiated trials [IITs) with key investigators including helping identify, establish and maintain such collaborations. | Represent the company at medical meetings through Medical Affairs’ Scientific Booth coverage and other related activities. | Engage in speaker identification, training and evaluation and provide support for advisory board meetings as requested. | Collaborate with Market Access and Commercial colleagues for thought leader and institutional engagement where appropriate.</s> | 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. | Coherus considers various factors, including professional background and work experience, when determining base pay. These considerations mean actual compensation will vary.</s> | Coherus BioSciences is a fully integrated, commercial stage innovative oncology company whose main focus is developing promising immuno-oncology products that improve the lives of patients. | The Oncology Account Manager role requires building sustained relationships with physicians, pharmacists, nurses, administrators, billing, finance, office practice managers mid-levels and other pertinent staff. | Equal employment opportunities for all employees and applicants for employment | 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.</s>
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