Regeneron Pharmaceuticals, Inc (USA) Posted October 9, 2026

Senior Manager, Global Site Start-Up Lead

Remote, United States Full time
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Regeneron Pharmaceuticals, Inc (USA) 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

Build Our Future Together

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Global Site Start-Up Lead to join our Global Development team, supporting complex, high-profile clinical trials across our global portfolio. In this role, you will lead the strategic execution of site and country start-up activities, driving efficient study activation and operational excellence while ensuring compliance with regulatory requirements and industry standards. Working closely with cross-functional partners, clinical operations teams, and CROs, you will play a critical role in accelerating study timelines, mitigating risks, and enabling the successful delivery of clinical development programs that bring innovative therapies to patients worldwide.

When & Where

Location: United States (Remote) or Regeneron office location

Work Model/Flexibility: Remote or Hybrid, based on business needs

Shift Requirements: Standard business hours with flexibility to support global teams across time zones

Travel Percentage: Up to 25%

Discover Your Role

Develop and execute global site and country start-up strategies for complex clinical trials, identifying risks, dependencies, and mitigation plans.

Lead site activation planning and forecasting activities to ensure study milestones and timelines are achieved.

Partner with Clinical Operations, Regulatory Affairs, CROs, and other stakeholders to drive efficient study start-up execution.

Monitor and evaluate start-up metrics, leveraging data and trends to improve performance and inform strategic decision-making.

Oversee site activation activities including regulatory document collection, submissions, site initiation readiness, and milestone tracking.

Provide leadership and direction to CRO partners and internal teams to ensure high-quality and compliant start-up delivery.

Serve as the primary escalation point for site start-up challenges, proactively resolving issues and driving cross-functional alignment.

Manage and develop a team of Site Start-Up professionals through coaching, performance management, mentoring, and career development initiatives.

This Role Requires

Must-Haves

Bachelor's degree and 8+ years of pharmaceutical, biotechnology, or clinical research industry experience.

Extensive experience leading global clinical trial start-up activities, including country and site activation strategies.

Strong knowledge of ICH-GCP guidelines, clinical trial regulations, and global study start-up processes.

Demonstrated ability to lead cross-functional teams and influence stakeholders across a global organization.

Proven experience managing vendors and CROs, including performance oversight and issue resolution.

Excellent project management, communication, negotiation, and risk management skills.

Preferred Qualifications

Previous direct line management experience with responsibility for staff development and performance management.

Experience supporting complex, high-profile, and global clinical development programs.

Strong analytical mindset with a data-driven approach to forecasting, metrics review, and operational decision-making.

Experience driving process improvements and operational excellence initiatives within Clinical Development.

Advanced understanding of country-specific regulatory and site activation requirements across multiple regions.

Physical Requirements

Ability to work primarily in a computer-based environment.

Ability to travel domestically and internationally up to 25% as required.

Ability to participate in meetings across multiple global time zones.

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all  qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Where necessary, we disclose salary ranges for roles in all countries in which we operate.  The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits.  Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/ . For other locations, additional information will be provided during the recruitment process.  If you have any questions, please speak with your recruiter.

Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.

As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.

For jobs in Canada: this posting is for an existing position.

Salary Range (annually)

$134,400.00 - $219,200.00

Job details

Seniority
Manager
Function
Clinical Development
Therapeutic area
Not listed
Location
Remote, United States
Employment type
Full time

How this role compares

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

We currently track 457 comparable Manager Clinical Development roles across 67 biopharma companies.

457Comparable roles tracked
408Currently active
67Companies hiring similar roles
43Countries represented

Salary context

147 of 457 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 $134,400/yr – $219,200/yr
Highest disclosed · Statistical Advisor · Gilead Sciences, Inc. $226,185/yr – $292,710/yr
Peer group range $95,500 – $259,448 (median $180,500)

Where these roles are based

Top locations among the 457 comparable roles

United States207
India49
United Kingdom31
Spain21
China15
Poland15

+ 37 more countries

Seniority mix

457 of 457 peers have a known seniority level

Manager287
Associate Director131
Associate39

Therapeutic area mix

39 of 457 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology20
Immunology8
Neuroscience3
Respiratory2
Ophthalmology2
Gastroenterology2
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.

60%similar
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60%similar
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Sanofi Vaccines US Inc. Swiftwater, United States Manager
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Amgen Inc. Remote, United States Manager
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60%similar
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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.

Or follow a whole field: get every new Clinical Development job in the United States, and choose locations and companies.

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.

60%
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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.