Merck Posted October 20, 2026

Director, Site Budgets

North Wales, Pennsylvania, United States of America FULL_TIME
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Merck 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

Job Description

Our Company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us. Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.

The Head, Site Budgets serves as the global capability leader for clinical trial site budgeting within Regional Operations. The role is accountable for the performance, quality, consistency, competitiveness, and strategic advancement of our company's site budget capability worldwide. Through leadership of the Trial Initiation Specialist (TIS) organization and partnership with Regional Operations, Clinical Operations, Compliance, Finance, and Site Budgets and Payments Operational Excellence, the position ensures that site budget expertise, negotiation practices, decision frameworks, and organizational capabilities evolve to meet changing portfolio, market, and business needs while enabling timely and compliant trial execution.

Primary Responsibilities:

Own the global Site Budgets capability, defining its strategic direction and ensuring budget expertise, methodologies, negotiation practices, and organizational capabilities evolve to meet changing portfolio, market, and business needs.

Lead the Trial Initiation Specialist (TIS) organization, with accountability for workforce capability, organizational performance, service delivery, budget quality, and stakeholder outcomes.

Serve as the senior business authority for clinical trial site budgeting, providing leadership on budget strategy, competitiveness, negotiation approaches, Fair Market Value application, and emerging industry trends.

Establish and maintain a globally consistent site budget operating model that incorporates regional and country perspectives while promoting clear decision rights, escalation pathways, and appropriate local ownership.

Builds strategic relationships across country, regional, global and external stakeholders to strengthen delivery.

Promote risk-based decision-making and governance frameworks that empower country and regional teams while ensuring appropriate oversight of complex, novel, or higher-risk scenarios.

Use operational data, market intelligence, and stakeholder insights to guide strategic priorities, workforce planning, performance improvement, and business decisions.

Partner with Site Budgets and Payments Operational Excellence to define business requirements, priorities, and future capability needs, ensuring enabling processes, systems, analytics, training, governance, and change solutions effectively support business outcomes.

Represent Regional Operations in governance forums and cross-functional partnerships as the accountable leader for the Site Budgets capability.

Ensure site budget strategies and decisions are aligned with applicable regulations, Fair Market Value principles, standard of care requirements, and compliant business practices.

Foster a culture of accountability, sound judgment, negotiation excellence, continuous improvement, innovation, collaboration, and empowered decision-making.

Required Education:

A minimum of a bachelor's degree is required (scientific, business, or related discipline preferred); advanced degree a plus.

Required Experience and Skills:

10+ years of clinical research experience in the pharmaceutical/biotech industry, including experience leading operational teams and driving business outcomes in complex environments.

Strong business acumen and understanding of clinical trial financial operations, including site budgets, investigator grants, payments, Fair Market Value principles, and related operational processes.

Experience managing directly or indirectly teams of professional employees.

Proven success leading teams, developing talent, and driving operational performance in a matrixed environment.

Ability to leverage data and insights to support decision-making, continuous improvement, and achievement of business objectives.

Demonstrated ability to communicate complex issues and influence decision-making at senior leadership levels.

Strong collaboration, stakeholder management, and relationship-building skills, with the ability to develop effective partnerships across functions and geographies.

Demonstrates initiative, innovative thinking, and a continuous improvement mindset, with the ability to challenge traditional approaches and identify opportunities to simplify, modernize, and transform how work is performed.

Strong communication, presentation, and change leadership skills.

Knowledge of and ability to apply Good Clinical Practice (GCP)/ International Council for Harmonisation (ICH) and applicable regulatory requirements

Strong organizational, prioritization, and execution management skills.

Sponsors responsible digital, data-driven and AI-enabled ways of working.

clinicaltrialjobs

Required Skills:

Business Decisions, Clinical Trial Management, Clinical Trials Operations, Ethical Standards, Executive Presence, ICH GCP Guidelines, Motivating People, Multiple Therapeutic Areas, Organizational Leadership, People Leadership, Process Improvements, Relationship Management, Stakeholder Analysis, Strategic Analysis, Strategic Thinking, Strategy Development

Preferred Skills:

Clinical Research, Global Experience

Current Employees apply HERE

Current Contingent Workers apply HERE

US and Puerto Rico Residents Only:

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.  As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.  For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:

EEOC Know Your Rights

EEOC GINA Supplement​

We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.

Learn more about your rights, including under California, Colorado and other US State Acts

The primary location for this posting is:

USA - Pennsylvania - North Wales (Upper Gwynedd)

Where required by law, the compensation range for this role is provided below.

The salary range for the primary location of this role is:

$173,200.00 - $272,600.00

This range reflects the Company's reasonable expectation of the base salary applicable to this role at the time of posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits .

Additional location(s): Please note the salary range above applies to the Primary Location of the position. Where a role has other listed locations, different compensation guidelines may apply. You may find the salary ranges for additional locations below. If the salary range is not listed for the location you are applying to, our Talent Acquisition team will provide further information to you relevant to your location.

Additional location(s) Compensation Information:

San Francisco Residents Only:  We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

Los Angeles Residents Only:  We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance

Search Firm Representatives Please Read Carefully 

Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company.  No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status:

Regular

Relocation:

No relocation

VISA Sponsorship:

No

Travel Requirements:

25%

Flexible Work Arrangements:

Not Applicable

Shift:

1st - Day

Valid Driving License:

No

Hazardous Material(s):

N/A

Job Posting End Date:

10/22/2026 *A job posting is effective until 11:59:59PM on the day BEFORE  the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Requisition ID:R422281

Job details

Seniority
Director
Function
Clinical Development
Therapeutic area
Not listed
Location
North Wales, Pennsylvania, United States of America
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 339 comparable Director Clinical Development roles across 57 biopharma companies.

339Comparable roles tracked
318Currently active
57Companies hiring similar roles
18Countries represented

Salary context

173 of 339 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 Not listed on this posting
Lowest disclosed · Patient Safety, Medical Director · Vertex Pharmaceuticals Inc (US) $0/hr – $0/hr (≈ $0–$0/yr)
Peer group range $0 – $392,100 (median $264,000)

Where these roles are based

Top locations among the 339 comparable roles

United States270
United Kingdom22
Switzerland9
India8
Spain6
China4

+ 12 more countries

Seniority mix

339 of 339 peers have a known seniority level

Director241
Senior Director54
Principal44

Therapeutic area mix

100 of 339 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology59
Neuroscience9
Immunology8
Cardiovascular / CVRM8
Respiratory6
Ophthalmology3
Dermatology & Aesthetics3
Vaccines & Infectious Disease3
Rare Disease1

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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.

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Open in 2 locations

Waltham, United StatesSouth San Francisco, United States

Notify me about similar jobs

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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.

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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.