Executive Director, Head, Global Trial Optimization

MSD; Rahway (NJ); Híbrido; USD 256 000 - 403 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Health insurance

401(k) plan

Paid holidays

Vacation and sick days

Hybrid work

Resumo da oferta

MSD in Rahway, NJ is seeking a Head of Global Trial Optimization (GTO) to lead senior GTO staff, optimize processes, and manage resources and budget. You will drive data-driven feasibility, recruitment strategies and cross-functional collaboration with PDTs and legal, ensuring high-quality deliverables.

You will mentor senior leaders, shape portfolio risk plans, and advance end-to-end trial execution with global programs. Requires 15+ years in clinical research and strong leadership.

Qualificações

• Minimum 15 years clinical research experience in pharmaceutical industry (US and international).
• Strong leadership, collaboration and disciplined decision-making aligned with leadership principles.
• Excellent written and spoken English; ability to influence at senior regional and global levels.

Responsabilidades

• Provide vision, leadership and mentorship to the GTO team, driving high-quality deliverables.
• Optimize organizational design, processes and resource allocation across GTO.
• Manage budget, risk, and portfolio-level strategies for trial optimization and site engagement.
• Collaborate with cross-functional teams (CSSM, GPAM, Legal, Country Operations) to ensure compliance and strategic alignment.
• Lead and implement continuous improvement initiatives and data-driven trial execution enhancements.

Conhecimentos

Leadership

Strategic thinking

Communication

GCP/ICH knowledge

Data-driven decision making

Formação académica

Bachelor of Science/Arts; advanced degree preferred

Ferramentas

Microsoft Word

Excel

Data analytics tools

Descrição da oferta de emprego

Job Summary

The Head of Global Trial Optimization (GTO) provides vision, leadership, oversight, mentoring and coaching of senior GTO staff in producing GTO deliverables. This includes continual optimization of the organizational design and resources, ownership and optimization of key processes, talent and succession management, overall operating budget management and oversight of all high priority programs and studies.

Primary Activities/Responsibilities

Accountable for ensuring that assigned deliverables meet regulatory, business, patient-centricity standards (as appropriate) that all functional contributions drive towards strategic approaches versus transactional tasks. Responsible for implementing forward-thinking philosophies to improve quality and increase ease of compliance. Subject matter expert for the GTO. Provide vision, leadership and oversight of the GTO group in implementing data driven approaches to feasibility and development of recruitment and retention strategies. The Head, GTO is accountable for the communication of progress, status updates, mitigation plans and escalation of issues for trial or program level deliverables to Sr. Management. Provide strategic leadership, coaching and people management for the GTO leadership team, with accountability for quality deliverable generation (i.e., Program Review, Program/Trial Feasibility, Allocation, and Recruitment strategies, plans, and tactics) and issue resolution across the portfolio. Ensure staff are trained to apply Real World Data as inputs into trial execution simulations based on protocol/patient knowledge and collaborations with PDT members. Accountable for identifying portfolio-level risks and ensuring appropriate risk mitigation strategies are developed and implemented across programs. Provide trial execution support by implementing streamlined enterprise level vendors where needed and standardizing the digital presence while retaining flexibility to customize tactics as needed. They will drive compliance with the GCTO Country footprint strategy and respond to internal/external challenges by evolving and adapting the process as the business landscape evolves. Provide strategic and operational oversight of the Trial Engagement and Site Partnership organization, ensuring integrated, fit-for-purpose strategies that strengthen investigator and site relationships, improve the site experience, and support trial screening, enrollment, retention and execution. Partner with GCTO team members to develop strategies, processes to enable key GCTO innovations in end-to-end clinical trial execution. Have an established network both internal and external to our company and will be expected to work in close collaboration with CSSM, CQM, Country Operations, GPAM, Clinical Directors, Legal and other key stakeholders to ensure all are equipped with the ability to anticipate the needs of upcoming studies and expeditiously address study needs. Determination of resource needs through the review of authorized and anticipated clinical development activities and close collaboration with CSSM and GPAM leaders. Keeping abreast of pharmaceutical industry best practices, regulatory requirements and corporate strategies that impact the organization. Responsible for driving continuous improvement within GTO to optimize predictability and accuracy of deliverables. Collaborates to establish performance metrics and monitors these metrics to continually enhance capabilities and improve overall quality. May lead operational components of mergers and acquisitions (e.g., due diligence activities, portfolio integrations). May lead and/or implement process improvement and strategic initiatives.

Required

Bachelor of Science/Arts; advanced degree preferred

Required Experience and Skills

A minimum of 15 years clinical research experience in pharmaceutical industry (US and exUS) Strong understanding and dedication to our company's Leadership principles, with an emphasis on fostering collaboration, rapid/disciplined decision-making and integrity/ethics. Strong communication skills requiring proficiency in written and spoken English. The incumbent must be competent and effective in written and verbal communication, including the ability to influence and represent the organization at senior regional and global levels.

Digital Proficiency

Sponsors enterprise-level digital, analytics, automation-enabled and approved AI-enabled capabilities and uses data-driven insights to shape portfolio, organizational and resource strategy.

Risk-Based Decision-Making & Leadership

Establishes and governs risk-informed decision frameworks across the portfolio, balancing quality, compliance, business objectives, resources and strategic priorities.

Critical Thinking

Applies enterprise-level judgment to complex and ambiguous situations, anticipates future organizational needs and guides strategic decisions impacting long-term clinical operations performance.

Flexible / Agile Mindset

Builds a culture of agility, innovation and continuous improvement, enabling proactive response to evolving business, regulatory, technology and portfolio demands.

Accountability & Decision Rights

Owns governance frameworks, escalation pathways and outcomes within delegated authority and enterprise expectations.

Entrepreneurship

Creates and champions opportunities for the organization by applying deep knowledge of the pipeline, patient and investigator landscape, health system and external environment; aligns pipeline, platforms, policy and people, embeds end-to-end ownership and directs innovation and operating-model choices that strengthen competitiveness and patient access to trials.

Strategic Planning & Execution Excellence

Sets strategy and execution direction, defining portfolio and capability priorities, investment and resource choices, scenarios, “what must be true” conditions, trade-offs and governance; translates direction into execution standards and measurable outcomes and reallocates resources to protect pipeline delivery, quality and long-term organizational capability.

Enterprise Relationship Management & Partnerships

Influences senior internal and external stakeholders and champions the global trial optimization network required for clinical operations success across our company's research division, GCD, GCTO, countries, institutions, investigators, and vendors; builds high-value partnerships, represents the organization in strategic discussions and governance forums, and shapes accountabilities that reduce silos and advance capability, pipeline delivery and clinical research outcomes.

Project Management or Site Ready support knowledge and experience

Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines Superior presentation skills Training and curriculum development Computer skills including proficiency in aspects of data analysis and presentation software, Microsoft Word and Excel.

Preferred Experience

Proficiency with data modelling software where applicable.

Process Management International collaboration Sigma training

Required Skills: Clinical Research Organizations (CRO) Management, Clinical Trials Operations, Cross-Cultural Awareness, Flexibility (Inactive), Influence, People Leadership, Resource Allocation, Results-Oriented, Strategic Thinking

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.

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.

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 - New Jersey - Rahway

Where required by law, the compensation range for this role is provided below. The salary range for the primary location of this role is: $255,800.00 - $402,700.00

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.

• medical, dental, vision healthcare and other insurance benefits (for employee and family)
• retirement benefits, including 401(k)
• paid holidays
• vacation
• 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: Domestic/International

VISA Sponsorship: Yes

Travel Requirements: 25%

Flexible Work Arrangements: Hybrid

Shift: 1st - Day

Valid Driving License: No

Hazardous Material(s): N/A

Job Posting End Date: 11/6/2026

*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.

Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.