BridgeBio-- Regulatory Affairs Postdoctoral Research Fellow

Northeastern University; San Francisco (CA); On-site; USD 66,000 - 94,000; Full time

Job summary

Northeastern University, in partnership with Eidos (BridgeBio), offers a two-year Regulatory Affairs fellowship based in San Francisco. The program focuses on regulatory strategy, labeling, and interactions with health authorities, with opportunities across clinical development, pharmacovigilance, and related areas.

The fellow will work with cross-functional teams and gain experience in preparing regulatory submissions and labeling documentation while pursuing continued professional development

Qualifications

• Doctor of Pharmacy degree from ACPE-accredited institution.
• Eligible for pharmacist licensure in Massachusetts.
• Excellent oral and written communication skills.
• Strong time management and leadership abilities.
• Ability to work independently and take initiative on projects at both the industry site and Northeastern.

Responsibilities

• Develop and implement regulatory strategy to support Eidos development programs.
• Build proficiency in the Veeva regulatory management system for submissions (CTA/IND/NDA/MAA).
• Maintain knowledge of ICH, GCP, GMP and global guidelines for compliance.
• Collaborate with Clinical, Statistics, Medical Affairs, Commercial, and Nonclinical teams.
• Support regulatory interactions with health authorities, including meeting requests and briefing documents.
• Prepare responses to labeling-related queries and manage labeling strategy.

Skills

Pharmacist licensure

Communication skills

Time management

Leadership

Independent work

Education

Doctor of Pharmacy degree

Job description

## BridgeBio-- Regulatory Affairs Postdoctoral Research FellowApply: San Jose, CA: Full time: Posted Today: R142328**About the Opportunity**## About the OpportunityNortheastern University Pharmaceutical Industry Fellowships Program is a two-year experiential program designed to advance lifelong learning and the education and training of Pharm.D. graduates. A key element of the program’s success is preparing Fellows to meet evolving workforce needs across various sectors of the pharmaceutical industry. Fellows have the opportunity to work closely with our innovative biopharmaceutical industry partners, while engaging with Northeastern University faculty in professional and career development, teaching, service, and scholarly activities. In partnership with Northeastern University, Eidos, a BridgeBio Pharma, Inc. Affiliate is offering a two-year Regulatory Affairs fellowship, based in San Francisco, California.## About About Eidos and BridgeBio Pharma Inc.BridgeBio Pharma, Inc. (BridgeBio/BBIO) is a biopharmaceutical company founded to discover, create, test and deliver transformative medicines to treat patients who suffer from genetic diseases. BridgeBio’s pipeline of development programs ranges from early science to advanced clinical trials. BridgeBio was founded in 2015 and its team of experienced drug discoverers, developers, and innovators are committed to applying advances in genetic medicine to help patients as quickly as possible.BridgeBio exists to bring meaningful medicines to patients as quickly and as safely as possible. We’re passionate about fostering open and transparent relationships with patients and their families by staying connected, listening to their experiences, and applying their insights into our work. We hope that by developing these relationships with patients, families, and patient advocacy organizations early in the development phase of our therapies that we can also craft our clinical trial protocols with the patient experience at the forefront.Eidos is an affiliate that operates under the BridgeBio umbrella. We are focused on the treatment of ATTR-CM, and our product, Acoramidis (marketed as Attruby), which recently received FDA approval in November 2024. While the fellowship position will be focused on Regulatory Affairs deliverables for Eidos, there may be opportunities to contribute to projects within other functional areas, e.g., clinical development, pharmacovigilance, etc. and/or other projects that are being led by other BBIO affiliates.## ResponsibilitiesRegulatory Strategy* Manage, develop, and implement regulatory strategy in support of Eidos development programs.* Develop proficiency within the Veeva regulatory management system where you will support the planning, preparation and execution of high-quality regulatory submissions (e.g. Clinical Trial Application (CTA)/Investigational New Drug (IND) application and amendments, annual reports, initial license applications (New Drug Application (NDA)/Marketing Authorization Application (MAA), etc.) and supplements/variations).* Develop and maintain knowledge of International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH), Good Clinical Practice (GCP), Good Manufacturing Practice (GMP), and other relevant global guidelines to ensure compliance of regulatory strategies and submissions.* Work in cross-functional teams with members from Clinical, Statistics, Medical Affairs, Commercial, and Nonclinical groups to help operationalize regulatory strategy.* Support regulatory interactions with regulatory bodies including preparation of meeting requests and briefing documents.Global Labeling* Gain in-depth knowledge of labeling regulations regarding Company Core Data Sheet (CCDS), US Package Insert (USPI), Summary of Product Characteristics (SmPC), and Structured Product Labeling (SPL).* Support development of regulatory labeling strategy and the negotiation and maintenance of competitive labeling with global health authorities.* Maintain core labeling documents.* Provide strategic guidance on labeling regulations, competitor labeling, and labeling trends and work with cross-functional team to ensure that the regulatory labeling strategy is aligned with the global regulatory strategy.* Assist in preparation of responses to labeling-related queries from health authorities.Advertising and Promotion (Medical, Legal, and Regulatory (MLR))* Support regulatory review of promotional and non-promotional materials in accordance with business goals and objectives, health authority regulations, ICH guidelines, Pharmaceutical Research & Manufacturers of Americans (PhRMA) guidelines, company policies and established precedents and recommend revisions/actions that achieve fair balance.* Support the review and approval of promotional and non-promotional materials in a cross-functional promotional review committee that includes Commercial, Medical Affairs, and Legal.* Coordinate timely and accurate review of materials for submission to the United States Food and Drug Administration (FDA).## Qualifications• Doctor of Pharmacy degree from an ACPE-accredited institution • Eligible for pharmacist licensure in the State of Massachusetts • Excellent oral and written communication skills • Strong time management and leadership abilities • Ability to work independently and take initiative on a variety of projects at both the industry site and Northeastern## Additional InformationApplicants should submit the following application materials by the priority deadline of October 31, 2026:1. Curriculum vitae (CV), uploaded 2. Unofficial PharmD transcripts, uploaded 3. Cover letter, uploaded**Letters of Recommendation**Three formal Letters of Recommendation (LORs) must be submitted directly by the letter writers no later than **November 23, 2026**.Each letter writer must include:* The candidate's full name* The fellowship program(s) to which the candidate is applying (e.g., **Smith, John – Alnylam, GSK**)Please ask your letter writers to complete and submit the **Letter of Recommendation Form** along with their recommendation. **Click here** to access the form and share it with your letter writers.Recommendations must be submitted directly by the recommender and cannot be submitted by the applicant.Address cover letter and letters of recommendation to:J. Andrew Orr-Skirvin, PharmD, BCOP Clinical Professor, Department of Pharmacy & Health Systems SciencesPharmaceutical Industry Fellowship Program Director360 Huntington Ave, 140 The Fenway R218 Boston, MA 02115*Northeastern University will not provide H-1B, TN, O-1, E-3, or any other type of employment visa sponsorship for the successful applicant to this position, now or in the future. STEM OPT is not compatible for this position. The successful applicant must be able to maintain valid work authorization in the United States throughout the entire appointment without Northeastern University's sponsorship for a visa.***Position Type**Research**Additional Information**Northeastern University considers factors such as candidate work experience, education and skills when extending an offer.Northeastern has a comprehensive benefits package for benefit eligible employees. This includes medical, vision, dental, paid time off, tuition assistance, wellness & life, retirement- as well as commuting & transportation. Visit https://hr.northeastern.edu/benefits/ for more information.All qualified applicants are encouraged to apply and will receive consideration for employment without regard to race, religion, color, national origin, age, sex, sexual orientation, disability status, or any other characteristic protected by applicable law.**Compensation Grade/Pay Type:**108S**Expected Hiring Range:**$66,345.00 - $93,712.50*With the pay range(s) shown above, the starting salary will depend on several factors, which may include your education, experience, location, knowledge and expertise, and skills as well as a pay comparison to similarly-situated employees already in the role. Salary ranges are reviewed regularly and are subject to change.*