Senior Director / Vice President, Regulatory Affairs - Obesity and Associated Metabolic Diseases

Rivus Pharmaceuticals, Inc.

Senior Director / Vice President, Regulatory Affairs – Obesity and Associated Metabolic Diseases

Location: San Francisco Bay Area, CA

 

Rivus Pharmaceuticals is searching for a Senior Director / Vice President, Regulatory Affairs to set and lead the regulatory strategy to advance a new class of investigational medicines called controlled metabolic accelerators (CMAs) that have the potential to improve metabolic health for people with obesity and associated metabolic diseases. This role will report to the CMO. The individual will develop and implement regulatory strategies for all phases of product development, from early product pipeline to post-approval commercial production. They will be responsible for the planning and execution of regulatory filings with in a rapid timeline. They will also provide guidance to cross-functional and matrix team members on regulatory strategy and tactics.

Key Responsibilities

Develop and implement the short term and long term regulatory strategies for all development programs, working with the CMO, from pre-IND meetings to pivotal Clinical Trials and through marketing authorization and post-approval submissions.

Represent Regulatory Affairs on Development Leadership Team providing regulatory guidance and assessing the accuracy and appropriateness of submissions to regulatory authorities

Serve as primary author and oversee the development, preparation of documents and management of submissions and interactions with regulatory authorities regarding IND/NDA submissions, scientific advice/briefing materials, CTAs, and responses to regulatory agency questions to support clinical and non-clinical development.

Coordinate with external publishing resources for on-time delivery of high-quality regulatory submissions to regulatory agencies

Participate in regulatory intelligence gathering activities and maintain knowledge of US, EU and ROW regulatory requirements

Experience working with FDA, EMA, PDMA and other international regulatory agencies

Perform as a key member on internal and external project teams and serve as the regulatory point of contact to facilitate CMC regulatory development as it relates to global clinical trials, global health authority interactions and global product submissions and approvals

Ensure compliance with all GCP/ ICH and regulatory guidelines

Demonstrates ability to anticipate risks and responsible for developing solutions to identified risks and discussing with direct reports and management; understands probabilities of technical success for the solutions.

Provide regulatory strategy support to diligence for potential collaborations as appropriate

Identify and assess regulatory risks associated with product development and define strategies to mitigate risks

Recruits, interviews, and trains new staff as well as manages performance of direct reports and internal contractors , external CROs, and other vendors, as necessary..

Establish relevant processes and procedures to support the Regulatory Affairs function

Provide mentorship and guidance to direct reports in carrying out responsibilities and will be responsible for coordinating activities and career development of direct reports

Develop and maintain departmental procedures, identify opportunities for process improvement,SOP development and propose implementation plans

 

Experience and Qualifications

BS 17+ years, MS 15+ years. PhD 12+ years 10+ years of pharmaceutical industry regulatory affairs experience will include 10 years regulatory experience working on Small Molecule Therapeutics with in Metabolic or Obesity indications.

Previous hands-on experience in interfacing with regulatory authorities and leading regulatory submissions including IND, NDA/sNDA submissions, briefing documents, etc.

Preparation of supportive amendments and supplements (non-clinical, clinical and CMC)

Demonstrated ability to manage multiple assignments, appropriately identify and resolve regulatory issues, and communicate upwards, as needed, to management

Proven successful record of positive FDA interactions required; international global registrations

Experience interacting with external and internal strategic partner on complex regulatory issues.

Ability to work independently and within project teams, etc. to attain group goals

Knowledge of the Code of Federal Regulations and FDA, EMA and ICH guidelines

Experience and knowledge in the preparation of electronic submissions (CTD)

Experience in the oversite of regulatory CMC is a plus

Interested candidates may forward a CV and Cover letter to Careers@rivuspharma.com

Sector

Therapeutics

Job Type

Full-time

Upload your resume to apply for this role through CvilleBioHub. If the company accepts applications through email, they will also receive your resume.

  • Hidden
  • Your resume must be .pdf file format.
    Accepted file types: pdf, Max. file size: 100 MB.
  • Your cover letter must be .pdf file format.
    Accepted file types: pdf, Max. file size: 100 MB.
  • This field is for validation purposes and should be left unchanged.