GlaxoSmithKline LLC Posted August 28, 2026

Manager, Global Regulatory Strategy - Oncology

Durham Blackwell Street, United States Full time
Regulatory Affairs Oncology Manager
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GlaxoSmithKline LLC is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Business Introduction

At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success. We’re uniting science, technology, and talent to get ahead of disease together.

Find out more:

Our approach to R&D

Responsibilities include:

This role will provide YOU the opportunity to lead key activities to progress YOUR career.  These responsibilities include some of the following:

Regulatory Strategy:  Proactively develop or implement regulatory strategies to ensure the submission and approval of clinical trial applications and other deliverables within agreed timescales.

Cross-functional Collaboration:  Ensure effective interaction with cross-functional teams, global/regional counterparts, and local operating companies.

Compliance:   Maintain compliance with global and regional regulatory requirements throughout the product lifecycle.

Regulatory Intelligence:  Assess precedent , regulatory intelligence, and the competitive environment to inform and refine regulatory strategies.

Why You?

Basic Qualifications

We are looking for professionals with these required skills to achieve our goals:

Bachelor’s degree in life sciences, pharmacy, medicine or a related field.

1+ year s of experience in the drug development process within regulatory affairs.

Experience with oncology drug development, including clinical trial applications and regulatory submissions.

Experience working in matrix teams across functions and regions.

Preferred Experience

If you have the following characteristics, it would be a plus:

Advanced Scientific Degree (PhD, MD, PharmD).

Strong matrix working skills, with the ability to facilitate dialogue and idea contribution among team members.

Proactive problem-solving skills to identify and resolve project or team issues in advance.

Creative regulatory problem-solving capabilities, balancing agency expectations and compliance.

A focus on continuous improvement and excellence, with the ability to challenge current processes and recommend strategic changes.

Ability to develop networks within GSK to secure support and achieve project outcomes.

#GSK-LI

Skills

Business Resilience, Communication, Digital Fluency, Matrix Leadership, Pharmaceutical Regulatory Compliance, Regulatory Strategies, Resource Management, Stakeholder Management

• If you are based in Cambridge, MA; Waltham, MA; Rockville, MD; or San Francisco, CA, the annual base salary for new hires in this position ranges $138,750 to $231,250. The US salary ranges take into account a number of factors including work location within the US market, the candidate’s skills, experience, education level and the market rate for the role. In addition, this position offers an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. Available benefits include health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave. If salary ranges are not displayed in the job posting for a specific country, the relevant compensation will be discussed during the recruitment process.

Please visit  GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.

Why GSK?

Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at -  usrecruitment.adjustments@gsk.com

GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.

Important notice to Employment businesses/ Agencies

GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

Job details

Seniority
Manager
Function
Regulatory Affairs
Therapeutic area
Oncology
Location
Durham Blackwell Street, United States
Employment type
Full time

How this role compares

Computed from every other active Regulatory Affairs role in our database, not just this employer's listings.

We currently track 184 comparable Manager Regulatory Affairs roles across 63 biopharma companies.

184Comparable roles tracked
165Currently active
63Companies hiring similar roles
29Countries represented

Salary context

58 of 184 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject $138,750/yr – $231,250/yr
Lowest disclosed · Associate, Quality Records · Pfizer $64,600/yr – $107,600/yr
Peer group range $86,100 – $245,000 (median $180,500)

Where these roles are based

Top locations among the 184 comparable roles

United States81
India14
Japan13
United Kingdom13
Poland9
China9

+ 23 more countries

Seniority mix

184 of 184 peers have a known seniority level

Manager135
Associate Director41
Associate8

Therapeutic area mix

20 of 184 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology10
Neuroscience5
Immunology3
Dermatology & Aesthetics2

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

100%similar
Gilead Sciences, Inc. Foster City, United States Manager
Same function Same therapeutic area Same seniority Same country
100%similar
Regeneron Pharmaceuticals, Inc (USA) Tarrytown, United States Manager
Same function Same therapeutic area Same seniority Same country
100%similar
Regeneron Pharmaceuticals, Inc (USA) Manager
Same function Same therapeutic area Same seniority Same country

Open in 2 locations

Warren, United StatesTarrytown, United States
100%similar
Amgen Inc. Remote, United States Manager
Same function Same therapeutic area Same seniority Same country
90%similar
E.R. Squibb & Sons,L.L.C. Princeton, United States Associate Director
Same function Same therapeutic area Adjacent seniority Same country
90%similar
E.R. Squibb & Sons,L.L.C. Princeton, United States Associate Director
Same function Same therapeutic area Adjacent seniority Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

100%
Manager, Content Strategy and Development (Medical Writing)- Oncology
Gilead Sciences, Inc. · Foster City, United States · Manager
Function Therapeutic area Seniority Country
100%
Manager, Regulatory Affairs Strategy - Oncology
Regeneron Pharmaceuticals, Inc (USA) · Tarrytown, United States · Manager
Function Therapeutic area Seniority Country
90%
Associate Director, Regulatory Excellence & Hematology/Oncology Operations
E.R. Squibb & Sons,L.L.C. · Princeton, United States · Associate Director
Function Therapeutic area Adjacent seniority Country
85%
Regulatory Affairs Manager, Oncology Therapeutic Group, Global Regulatory Affairs
GlaxoSmithKline Services Unlimited · UK – London – New Oxford Street, United Kingdom · Manager
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.