Senior Director, Regulatory Affairs

BioSpace; Radnor (Delaware County); Sur place; USD 250 000 - 270 000; Plein temps

Résumé du poste

Immunocore is seeking a Senior Director of Regulatory Affairs to lead regulatory strategy for late-stage biologics, drive IND/CTA submissions, and manage global health authority interactions.

Based in Gaithersburg, MD, Radnor, PA, and Oxford, UK, the role requires strong leadership, cross-functional collaboration, and a track record of successful BLA/MAA filings to support commercialization.

Qualifications

• Experience leading regulatory strategy for late-stage biologics.
• Proven ability to manage IND/CTA/BLAs and MAAs.
• Strong leadership and cross-functional collaboration skills.
• Extensive experience with US FDA and global health authorities.

Responsabilités

• Provide regulatory leadership for IND/CTA submissions and BLA/MAA filings.
• Lead health authority interactions (FDA, EMA, MHRA) and governance reviews.
• Develop and target regulatory strategies to support product development and commercialization.
• Mentor and guide regulatory leads and ensure global consistency.

Connaissances

Leadership

Regulatory strategy

FDA liaison

Global regulatory

Cross-functional leadership

Formation

Advanced degree in science or medicine (MS/PhD/MD/PharmD) or BS with extensive experience

Description du poste

Vacancy Name

Senior Director, Regulatory Affairs

Vacancy No

VN870

Employment Type

Full Time

Location of role

Gaithersburg, MD, Radnor, PA, Oxford, UK

Department

Regulatory Affairs

Key Responsibilities

The Senior Director of Regulatory Affairs will be responsible for assigned projects and all of the regulatory affairs activities by providing expertise to Immunocore’s development programs to include regulatory scientific and tactical strategy development, IND development/submission/maintenance, BLA/sBLA development/submission/maintenance, agency liaison and regulatory intelligence. The role will also involve interacting with our global sites, both in-house and outsourced. Establishing a successful relationship with the FDA, along with being responsible for overseeing submissions to the EMA, and MHRA providing a fantastic and unique opportunity to develop worldwide regulatory experience.

The ideal candidate will have experience gained in biologics and the preparation of late-stage regulatory fillings supported by excellent leadership skills. This role will also require someone who can work within a highly innovative, agile and entrepreneurial environment and is able to lead the regulatory strategy through effective collaboration and be able to deliver and work well under pressure as this will be a high-profile role.

This role will be responsible for presentations of proposed scientific and tactical regulatory strategies at Immunocore governance meetings, with an ability to make appropriate changes based on feedback leading to full alignment. This role will also be responsible for providing regulatory leadership for implementation of plans within a project team, including leadership for all health authority interactions globally. As the organization grows this role will be responsible for overseeing, guiding and mentoring direct reports for their assigned projects, either as support for the same assigned project and/or for another assigned project. The role will also provide review/guidance and approval for direct reports and dotted line reports regulatory tactical and administrative plans to ensure consistency across the organization. This role will also provide preliminary review of direct reports regulatory scientific strategies and discuss with Head of Regulatory Sciences to gain alignment prior to governance meeting review(s).

• To provide regulatory leadership and support to cross functional development project teams to jointly achieve strategic objectives.
• To be responsible for the US regulatory activities associated with the project teams.
• Develop regulatory scientific and tactical strategies and target labelling to support development of products.
• Provide leadership for the development and writing of regulatory submission documents, ex. Briefing documents, IND/CTA supporting documents, labelling, and CTD/BLA/MAA documentation for eCTD compliant submissions.
• You will manage, prepare, co-ordinate and be responsible for the submission of the documentation supporting regulatory submissions to the US and wider international regulatory authorities, in support of CTA/INDs, BLAs/MMAs, CTA safety reports and updates, along with all other regulatory submissions.
• To be the center of excellence (point of contact) of all regulatory requirements and guidelines globally, in particular within the US, and monitoring the regulatory environment for oncology, anti-infectives, autoimmune diseases, and biologics.
• Contribute to the establishment and development of procedures and working practices commensurate with the requirements of a company in late-stage development and commercialization.
• Overseeing regulatory review of clinical trial labelling and CMC submissions for regulatory compliance, in junctions with the Director of Regulatory CMC.
• Will need to demonstrate a high level of professionalism, efficiency and leaderships within the team whilst demonstrating critical thinking, effective problem solving and a strong knowledge of regulatory strategies and alignment with all necessary compliance.
• To be responsible for reviewing and ensuring the quality of detailed scientific and technical information are presented clearly and supporting conclusions are adequately evidenced by the data.
• To review and provide input/guidance and approval for tactical and administrative plans for more junior level global regulatory leads and ensure consistency of implementation across the organization. This will be for both direct reports and others with a dotted line reporting for such reviews.
• Provide input/guidance for scientific regulatory strategies for direct reports and discuss with the Head of Regulatory Sciences prior to governance meetings to ensure alignment.

SUPERVISORY RESPONSIBILITY

This position may include line manager responsibilities for direct reports and dotted line reporting

• Leads a review and approval of tactical and administrative regulatory plans to ensure global consistency of both direct reports and dotted line reports for these regulatory aspects.
• Provides guidance to direct reports for scientific regulatory strategies and gains alignment with Head of Regulatory Sciences.
• Promotes communication and cooperation among functions to create a spirit of unity in the organization

Essential

EXPERIENCE & KNOWELEDGE

• Solid track record in drug development and leadership within a dynamic project team(s)
• Solid scientific background with evidence of ability to develop regulatory scientific strategies.
• Strong understanding of global regulatory requirements to be able to form tactical regulatory strategies.
• Excellent knowledge of US regulatory requirements and extensive experience with submissions gained within drug development. Global experience desirable. Experience in working cross functionally and globally within Regulatory Affairs.
• Experience in supporting global clinical studies
• Experience in managing, preparing, submitting INDs/CTAs, BLAs/NDAs, and MAAs. Submission of at least 1 NME BLA/NDA is highly desirable.
• Experience in preparing and conducting Health Authority Meetings (FDA required). Ability to develop and maintain an ongoing liaison relationship with FDA and other global Health Authorities.
• Demonstrate ability to be agile to accommodate changing priorities
• Must have proven leadership, excellent communication and interpersonal skills.

Preferred Experience & Knowledge

• Experience in preparing and conducting Health Authority Meetings (FDA required). Ability to develop and maintain an ongoing liaison relationship with FDA and other global Health

Education & Qualifications

Advanced degree preferred – M.S., PharmD, Ph.D., or M.D. with 8-12 years’ experience or BS with 10-15 years’ experience.

US Salary Range

$250,000- $270,000

About The Company

Immunocore (NASDAQ: IMCR) is a pioneering, commercial-stage T cell receptor biotechnology company whose purpose is to develop and commercialize a new generation of transformative medicines which address unmet patient needs in oncology, infectious diseases and autoimmune disease. Our leaders in R&D are internationally recognised as some of the biotech industry’s most successful drug developers. We are creating not just an environment where great minds can interact but an innovation powerhouse answering the big questions.

Focused on delivering first-in-class biological therapies to patients, we have developed a highly innovative soluble TCR platform. Our ImmTAX molecules underpin a new generation of precision engineered drugs that harness the immune system to treat a broad spectrum of diseases with high unmet medical need, including oncology, infectious diseases and autoimmune diseases.

At Immunocore, we recognize that our employees are our greatest asset. We value the unique contributions each person brings to our team. By embracing Science, Trust, Respect, Integrity, Diversity, and Entrepreneurship (STRIDE), we create an environment where collaboration thrives, ideas flourish, and transformative changes happen. STRIDE represents more than just letters; it embodies our shared identity and drives our mission. We are dedicated to developing breakthrough therapies that transform patients’ lives, advancing medicine, and supporting one another in these pursuits.

Immunocore is proud to be an equal opportunity employer. As such, we are committed to fostering an inclusive workplace where everyone feels valued, respected, and empowered. We encourage applications from individuals of all backgrounds, regardless of race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, or any other characteristic protected by law.