Postdoctoral Research Fellow-Ironwood Pharmaceuticals, Regulatory Affairs

About the Opportunity

About the Opportunity:

Northeastern 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, Ironwood Pharmaceuticals is offering a two-year Regulatory Affairs PharmD fellowship based in Boston.

About Ironwood Pharmaceuticals:

Ironwood Pharmaceuticals is a biotechnology company developing and commercializing life-changing therapies for people living with gastrointestinal (GI) and rare diseases. Ironwood is advancing apraglutide, a next-generation, long-acting synthetic GLP-2 analog being developed for short bowel syndrome patients who are dependent on parenteral support. In addition, Ironwood has been a pioneer in the development of LINZESS (linaclotide), the U.S. branded prescription market leader for adults with irritable bowel syndrome with constipation (IBS-C) or chronic idiopathic constipation (CIC). LINZESS is also approved for the treatment of functional constipation in pediatric patients ages 6-17 years old. Building upon our history of innovation, we keep patients at the heart of our R&D and commercialization efforts to reduce the burden of diseases and address significant unmet needs.

Founded in 1998, Ironwood Pharmaceuticals is headquartered in Boston, Massachusetts, with a site in Basel, Switzerland.

Responsibilities:

The purpose of the Regulatory Affairs (RA) Fellowship is to provide the fellow with training in the functional area and to prepare them to enter an industry role as an individual contributor in Global Regulatory Affairs after the end of their 2-year fellowship. By gaining experience in Global Regulatory Affairs, the fellow will be able to pursue a successful career in the Regulatory Affairs and will have a practical understanding of the other function's responsibilities to enable them to be an optimal collaborator and colleague.

During the fellowship, the fellow will work within Regulatory Affairs to gain experience in maintenance of IND/CTAs and/or NDAs/MAAs, regulatory strategy, regulatory intelligence, Agency meeting management and correspondence, global/regional labeling, and regulatory operations.

The fellow will have the opportunity to work collaboratively with other functional areas within Ironwood, including global patient safety, clinical development, medical scientific affairs, program management, data sciences, quality and compliance, nonclinical, medical writing and publications, and chemistry, manufacturing, and controls, as well as experience partner interactions and engage in vendor oversight. The fellowship training will enable them to collaborate effectively with colleagues across various disciplines which is essential to both the development of a therapeutic product and management of that product throughout its lifecycle.

Additionally, the fellow will have the opportunity to attend meetings and conferences, present guidance reviews, and other opportunities as they arise.

Additional Responsibilities:

Assist in the planning and coordinating all aspects of regulatory submissions necessary to support clinical trials, product registrations, and post marketing requirements and commitments

Assist in the development of regulatory strategies for assigned projects or product(s) across all phases of product development aimed at achieving marketing authorization and appropriate product labeling

Assist in planning, authoring, reviewing and preparing investigational new drugs (INDs) / clinical trial applications (CTAs), new drug applications (NDAs), Marketing Authorization Applications (MAAs), and related annual reports, amendments, supplements, and other activities required for life-cycle management of approved products

Support the preparation for regulatory agency meetings for assigned products, including meeting plan, development of briefing books, and ensuring submitted documents are compliant and of the highest quality

Work with Regulatory Operations team members to establish and meet timelines for regulatory submissions

Keep abreast of and communicate changes and meaningful trends in the regulatory environment in the US and pertinent international jurisdictions

Support and participate in the development of Regulatory Department systems and processes

Assist with performance and compliance metrics for internal and external responsibilities

Collaborate with internal teams and vendors to prepare for inspections and audits

Present and assist in coordinating guidance reviews and other presentations

Interact with partners and engage in vendor oversight as required

Participate in fellowship recruitment activities and interviews

Additional responsibilities to be assigned based on individual interests or as business needs require.

The successful candidate will provide:

Doctor of Pharmacy (PharmD) from an accredited college or university before the start of the fellowship term

Motivation to learn new skills and gain experience within Global Regulatory Affairs

Ability to interpret and discuss regulations and guidelines related to drug development

Ability to interpret and discuss medical, epidemiological, and clinical data and publications

Ability to perform the assigned activities in full compliance with applicable regulations and internal procedures.

Ability to leverage a deep understanding of oneself through knowing one's strengths and weaknesses, proactively asking for feedback to balance self-perception, and being resilient in order to increase one's effectiveness

Ability to work cooperatively with colleagues and take initiative to build relationships despite differences in interest, offering support and help to peers without being asked, and proactively seeking input from others to solve problems

Excellent interpersonal skills in order to effectively manage expectations and facilitate collaborative working relationships.

Ability to recognize opportunities and/or issues and apply analytical and creative thinking to maximize performance.

Excellent written and verbal communication skills as well as organizational and project management skills, ability to function in an extremely fast-paced environment with changing priorities.

Proficiency and experience with Microsoft Office Suite, especially Excel, Outlook, PowerPoint, and Word.

Ironwood Pharmaceuticals is an equal opportunity employer, welcoming diversity in our workforce

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 Information

Applicants should submit the following application materials:

• Curriculum vitae (CV), uploaded
  
• Unofficial PharmD transcripts, uploaded
  
• Cover letter, uploaded
  
• Letter of intent describing why the candidate would like to join Ironwood's Fellowship program
  

Three formal letters of recommendation (LORs) should be sent directly from the letter writer to PharmDFellowships@northeastern.edu by July 1, 2026. LOR writers must include the candidate's name and the fellowship program(s) in the subject line (e.g., Smith, John - Ironwood Pharmaceuticals).

Address the cover letter, letter of intent, and letters of recommendation to:

J. Andrew Orr-Skirvin, PharmD, BCOP
Clinical Professor, Department of Pharmacy & Health Systems Sciences

Pharmaceutical Industry Fellowship Program Director

360 Huntington Ave, 140 The Fenway R218
Boston, MA 02115

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:
$60,315.00 - $85,192.50

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.


To apply, visit https://northeastern.wd1.myworkdayjobs.com/en-US/careers/job/Boston-MA-Main-Campus/Postdoctoral-Research-Fellow-Ironwood-Pharmaceuticals--Regulatory-Affairs_R140067







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About Northeastern University

Founded in 1898, Northeastern University is a private research university located in the heart of Boston. Northeastern is a leader in worldwide experiential learning, urban engagement, and interdisciplinary research that meets global and societal needs. Our broad mix of experience-based education programs?our signature cooperative education program, as well as student research, service learning, and global learning?build the connections that enable students to transform their lives. The University offers a comprehensive range of undergraduate and graduate programs leading to degrees through the doctorate in nine colleges and schools.

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