About The Position

The Associate Director, Portfolio Resourcing actively manages the relationship with the functional areas regarding the project study costs and resource forecasting data both ad hoc and on set frequencies. In this role the individual will collaborate across multiple functional stakeholders in identifying, establishing, validating and managing the resource demand to complement our portfolio demand.

Requirements

  • Bachelor's degree required
  • 7+ years of related business experience.
  • Deep understanding of Clinical Development, Operations, and Resourcing
  • Proven project and/or resource management experience
  • Familiarity with resource planning tools & processes, Planisware specific experience required.
  • Effective communication skills both orally and written
  • Strong Analytical skills including advanced MS Excel capabilities including formula writing and model development.
  • Ability to influence and negotiate with functional leadership.
  • Strong understanding of customer and ability to focus on customer needs.
  • Ability to drive strategic partnerships with Functional Areas and support teams
  • Strategic thinker
  • Detail-oriented
  • Flexible and adaptable
  • Process oriented
  • Budget Development
  • Clinical Development
  • Clinical Trial Management
  • Decision Making
  • Performance Monitoring
  • Planisware
  • Project Management
  • Resource Management
  • Risk Management
  • Status Reporting
  • Team Communication
  • Teamwork

Nice To Haves

  • Current Employees apply HERE
  • Current Contingent Workers apply HERE
  • US and Puerto Rico Residents Only:
  • 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 place, introductions are position specific. Please, no phone calls or emails.
  • Employee Status: Regular
  • Relocation: No relocation
  • VISA Sponsorship: No
  • Travel Requirements: 10%
  • Flexible Work Arrangements: Remote
  • Shift: 1st - Day
  • Valid Driving License: No
  • Hazardous Material(s): No
  • Job Posting End Date: 05/13/2026
  • 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.

Responsibilities

  • Manage Global Clinical Development (GCD), and as requested, Global Clinical Supply (GCS), and Early Development, global headcount, capacity, and resource planning in support of clinical trial execution, based on our Company's authorized and projected Book of Business (BoB).
  • Ensure logic checks are applied to the project cost estimates and/or resource forecast demand prior to issuance to the functional areas for review and approval.
  • Support Late Development Review Committee (LDRC) and other governance meetings by providing baseline and incremental resource demand estimates.
  • Post-meeting, communicate the approvals to appropriate functional management.
  • Support functional areas in the following manner: Review and cascade time reporting compliance reports and analyze time data as a source to validate algorithms/single equation templates e.g., project target vs. project actual %.
  • Develop, manage, and maintain function-level, role specific resource algorithms within Planisware and other supporting tools in order to perform monthly resource forecast analyses, develop assumptive scenarios and identify resource mitigation recommendations.
  • Work with functional leadership to understand global headcount, capacity, and resource planning in support of clinical trial execution, based on forecast system outputs and analytics reports.
  • Maintain and track approved full-time equivalent headcount (fixed & flex), for assigned functions.
  • Continuously assess existing resource planning and headcount/capacity processes and tools to identify areas for improvement/increased efficiencies.
  • Ensure consistency, simplification and standardization across functions to ensure global alignment and execution on the resourcing and headcount/capacity strategies and processes.
  • Implement, monitor and continually improve trending and analytics outputs to optimize resource demand to fit financials and BoB.
  • Support integration and quality control efforts with other tools as needed to improve the data accuracy of derived resource forecasts.
  • Ensure adherence to GDP's, SOP's, internal processes, and all corporate policies and procedures

Benefits

  • 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.

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What This Job Offers

Job Type

Full-time

Career Level

Director

Number of Employees

5,001-10,000 employees

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