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Regeneron via Workday

Senior Manager, Global Site Start Up Lead

United States $134.4k–219.2k/yr Travel up to 25% manager
still open verified 1d ago posted 2d ago seen 1h ago
Apply at regeneron.wd1.myworkdayjobs.com

This is the employer's own posting, not a copy on a job board.

What we know

Is it still open?

Confirmed still open

Last checked 1d ago — checked against the employer's own applicant tracking system, which is the company answering directly.

We re-read the employer's own applicant tracking system and the posting was still there. That is the company answering directly.

Check this listing's status as JSON

How old is it?

Posted 2d ago

The date the source published, not the day we noticed it (2026-10-09). Last seen at its source 1h ago.

We have tracked this listing since 10 Oct 2026 (1 days). The employer's own board has carried it every time we have read it, most recently 1 hour ago.

Is it remote?

The listing says yes

The location field doesn't say remote, so our assessment is based on the title or the description. Read the listing before applying.

Who may apply?

United States

The description agrees: it names United States.

What the ad says
…Location: United States (Remote) or Regeneron office location Work Mod…

Pay

$134.4k–219.2k/yr

Read out of the job description by us, not from a structured field. Shown in the posting's own currency and period; we never convert.

Skills named in the ad

MentoringNegotiationPerformance ManagementProject ManagementRisk Management

Recognised terms only, from a fixed vocabulary — this is what CV matching compares against.

Carried by 1 source

The listing

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
  • 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
Apply at regeneron.wd1.myworkdayjobs.com