Manager, Regulatory Affairs

Location
94080, South San Francisco
Posted
Jul 16, 2018
Hotbed
Biotech Bay
Required Education
Bachelors Degree
Position Type
Full time

MANAGER, REGULATORY AFFAIRS

Position Summary:

The Manager, Regulatory Affairs will provide regulatory guidance on global Chemistry, Manufacturing and Controls (CMC) regulatory activities for Global Blood Therapeutics (GBT) compounds for the treatment of sickle cell disease (SCD) and other disorders.  Responsibility will focus mainly on CMC regulatory filings, and providing strategic as well as operational management of the project teams in this area.  In addition, responsibilities may include support to on-going clinical activities.  The candidate will develop regulatory strategies and manage US/ex-US clinical applications and regulatory responses to requests for information for the product candidates. This position will report to the Associate Director, Regulatory Affairs CMC.

Essential Duties and Responsibilities:

  • Manage internal review/approval process for CMC related submissions and regulatory questions; manage internal stakeholder meetings, adjudications meetings, and maintain internal trackers and databases, as appropriate
  • Provide interpretation of regulatory authorities’ feedback, policies and guidelines to GBT personnel.  Support GBT during regulatory authority inspections on designated programs
  • Develop regulatory strategic plans in conjunction with project teams and assist in the preparation of CMC submissions required for regulatory approval
  • Evaluate proposed CMC changes for global regulatory impact to ongoing and existing filings, and provide a regulatory assessment and a submission strategy for optimal implementation of changes
  • Work with project teams to resolve complex project issues.  Utilize regulatory expertise and knowledge of regulatory requirements and regulations to strategically interpret, plan, and communicate requirements to ensure regulatory agency approvals are obtained
  • Responsible for supporting the filing of IND/CTA/NDA/MAA submissions.  Support strategy developed for submissions of product registration documents to health authorities worldwide.  Interact with other functions and external vendors, as necessary, in the preparation, review, and completion of documents for regulatory submissions
  • Support the planning and preparation of formal meetings with regulatory agencies.   Assure compliance with project team timelines and milestones
  • Provide organizational support as company grows its product development pipeline

Qualifications:

  • Bachelor degree in a life sciences, chemistry, or related discipline, advanced degree preferred
  • 3 to 5 years of biopharmaceutical experience, of which at least 3 years including hands-on Regulatory Affairs and successful IND and NDA/MAA submission experience
  • Experience and knowledge in analytical chemistry is preferred but not required
  • Experience in eCTD format and structure
  • Balance strategic thinking and strong analytical skills with ability to execute.  Detail oriented with strong written, verbal communication and presentation skills
  • Experience with international and particularly EU regulatory submissions and an understanding of worldwide small molecule guidelines and regulations a plus
  • Demonstrated excellence in regulatory liaison/strategy
  • Strategic thinking, leadership skills, assertiveness, strong technical background, and excellent negotiation and project management skills as evidenced by past performance on drug development project teams

Fit with GBT culture:

  • Ability to build strong relationships with co-workers of various backgrounds and expertise
  • Ability to function at a high level in a team setting whether leading the group or acting as an individual contributor
  • Values-based leadership consistent with GBT's Core Values
  • Excitement about the vision and mission of GBT
  • Flexibility
  • Integrity

NOTE:  This position summary is not intended to be all-inclusive. Employee may perform other related duties as negotiated to meet the ongoing needs of the organization.

Global Blood Therapeutics is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color,