Senior Director, Program Lead - Cardiovascular

MSD; Rahway (NJ); Presencial; USD 180.000 - 240.000; Jornada completa

Descripción de la vacante

Merck & Co., Inc. in Rahway, NJ seeks an experienced Senior Program Lead to provide strategic and operational leadership across complex clinical development programs, spanning multiple disease areas.

You will direct global cross-functional teams, manage program plans and timelines, and drive risk mitigation and operational excellence across portfolios. The role emphasizes staff development, inspection readiness, regulatory submissions, and collaboration with stakeholders to deliver trials on

Formación

• Clinical Trials Monitoring, Cross-Functional Teamwork, Data Management, Ethical Standards, Exercises Judgment, Global Clinical Studies, Patient Safety, Regulatory Submissions, Scientific Writing, Therapeutic Knowledge

Responsabilidades

• Lead global cross-functional teams in end-to-end clinical development.
• Develop and maintain the Clinical Operations Project Schedule with timelines for key milestones.
• Provide operational input on protocol design and program-level development planning documents.
• Provide program-level oversight to inform trial enrollment, site feasibility and engagement strategies.
• Conduct resource planning and staffing across a program or asset; manage Trial Managers.
• Oversee inspection readiness and collaboration with CQRM/CST to ensure quality and compliance.

Conocimientos

Clinical Trials Monitoring

Cross-Functional Teamwork

Data Management

Ethical Standards

Exercises Judgment

Global Clinical Studies

Patient Safety

Regulatory Submissions

Scientific Writing

Therapeutic Knowledge

Educación

Bachelor’s degree + 15 years

Master’s + 12 years

PhD/PharmD + 8 years Pharmaceutical and/or clinical drug development experience

Descripción del empleo

Job Description

This position provides expert strategic and operational leadership in the planning and execution of highly complex program(s) (e.g., spanning multiple disease areas/indications, involving large outcome trials). In this position, you will have the opportunity to lead and direct global, cross-functional teams in end-to-end clinical development activities (strategic planning through post-marketing approval). You will apply project management and organizational leadership expertise in our fast paced, industry-leading, dynamic bio-pharmaceutical company. You will have both direct & indirect reports, managing team(s) across programs/within a disease area.

Your responsibility in this role will include:

• Leading and directing teams within a program/disease area/asset on key program planning and execution elements (e.g., program-level overviews; senior management and governance meetings).
• Providing operational input at the CST level during protocol design (e.g., feasibility, execution risk, operational implications of design choices) and on program-level development planning documents (e.g., Clinical Development Plan, Protocol Concept Sheet, Protocol), ensuring program-level consistency and delivery of program objectives.
• Developing and maintaining the Clinical Operations Project Schedule, defining timelines for key trial milestones (e.g., DBL), and providing ongoing operational oversight of trial plan deliverables (e.g., Central Lab plan, Specimen Management Plan).
• Providing program-, disease-area, or asset-level oversight & context to inform trial-level enrollment, site feasibility & selection, and leading patient and site engagement strategies with Patient Advocacy Groups and Key Opinion Leaders across trials.
• Conducting resource planning and staffing across a program, disease area, or asset (hiring and/or project onboarding; management of Trial Managers; may include management of other Program Leads).
• Holding overarching responsibility and oversight of program, disease-area, or asset-level execution, providing innovative ideas to achieve organizational objectives, tracking key trial milestones and metrics across the program, proactively managing delays, and surfacing execution risks.
• Leading efforts and applying expertise to maximize operational feasibility and efficiency, and ensuring consistency and quality across the assigned portfolio.
• Serving as the primary escalation point for trial teams on operational issues, fielding and resolving cross-functional issues, promoting cross-functional solutions, and escalating to management as needed.
• Partnering with Portfolio Sourcing & Relationship Management (PSRM) on program-level service provider strategy (e.g., selection, qualification, contracting, oversight), resolving escalated issues and promoting consistent standards across studies.
• Reviewing and providing expert operational input on trial-level regulatory submissions (e.g., IND, CTA, Article 46), Health Authority responses and meeting material, Risk Language, and the Clinical Study Report.
• Reviewing trial-level ADI/RAID logs, Quality Plans, and readouts from quality metric dashboards (e.g., protocol deviations, temperature excursions), and proactively identifying and minimizing operational risks across the program/disease area/asset (e.g., clinical supply disruptions, service provider performance issues), escalating issues to CST and PDT as needed.
• Collaborating with CQRM, CQOM, and CST to develop, maintain, and review the program-level RACT (including program-specific metrics and thresholds, e.g., KRIs, QTLs), and reviewing and approving the Program Quality Plan.
• Reviewing protocol-level CTQ factors and key trial plans to ensure program-/disease-area/asset-level consistency as appropriate and quality control (e.g., reduction of manual data tracking/review efforts, appropriate balance between site & central monitoring).
• Owning proactive inspection readiness across the trial/program lifecycle, including supporting the authoring of post-inspection observation responses and CAPA/SQI management, in close collaboration with Clinical Quality Operations.
• Serving as the operational representative on the Product Development’s Clinical Subteam to elevate trial-/program-/disease-area-/asset-level risks, quality issues, and timeline/cost challenges, integrating solutions into program-level planning.
• Collaborating and facilitating interactions with key internal and external stakeholders (e.g., KOLs, vendors) in support of clinical program/disease-area/asset objectives.
• Leading and implementing process improvement and strategic initiatives (e.g., digital transformation).
• Potentially leading operational components of mergers and acquisitions (e.g., due diligence activities, portfolio integrations).
• Training, upskilling, and supervising direct and indirect reports, and managing the professional development and performance of direct reports, which may include Trial Managers and other Program Leaders.
• Supporting CTT onboarding and developing Trial Manager role-specific training.
• Championing and driving initiatives for digital proficiency/AI fluency to enhance efficiency and data-driven decision-making in clinical operations.

Qualifications, Skills & Experience Core Skills:

• Expert knowledge of GCP and ICH regulations.
• Expert understanding of end-to-end clinical research process, TA, and competitive landscape.
• Drives strategic adoption of scalable digital and AI-enabled approaches; experience in reviewing AI output, understanding limitations and constraints.
• Advanced knowledge of clinical database platforms, central monitoring/RBQM platforms & data review tools.
• Demonstrate advanced delegation, project-management, and program-wide decision-making skills to meet business needs and drive changes that shape the support, resourcing, and implementation of projects, programs, and/or technologies according to a budget/project plan.
• Ability to interact collaboratively and navigate high-stake conflicts with key internal/external stakeholders, leading through deep expertise and strategic influence.
• Demonstrate advanced problem solving, critical thinking, and scenario-planning skills (i.e. resolving complex technical, operational, and financial problems by weighing resource availability against department objectives), keeping an enterprise vision/view.
• Demonstrate advanced verbal and written communication skills.
• Demonstrate strong leadership by influencing internal & external stakeholders, and building talent through oversight, coaching, and mentoring.

Education/Experience:

• Bachelor’s degree + 15 years

OR

• Master’s + 12 years

OR

• PhD/PharmD + 8 years Pharmaceutical and/or clinical drug development experience.

Preferred:

• Degree in life sciences, preferred.
• Project Management Professional (PMP) certification preferred.

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Required Skills:

Clinical Trials Monitoring, Cross-Functional Teamwork, Data Management, Ethical Standards, Exercises Judgment, Global Clinical Studies, Patient Safety, Regulatory Submissions, Scientific Writing, Therapeutic Knowledge

Preferred Skills:

Adaptability, Innovation, Strategic Thinking

Employee Status:

Regular

Relocation:

No relocation

VISA Sponsorship:

No

Travel Requirements:

10%

Flexible Work Arrangements:

Not Applicable

Shift:

1st - Day

Valid Driving License:

No

Hazardous Material(s):

No

Job Posting End Date:

11/18/2026

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

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.

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