Merck Posted August 13, 2026

Associate Director, Global Data Management and Standards, Talent & Capability Development (Hybrid)

Rahway, New Jersey, United States of America FULL_TIME
Clinical Development Associate Director

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

The Associate Director, Global Data Management & Standards (GDMS) Academy reports to the Head of Global Data Management & Standards (GDMS) Business Operations and leads the strategy and execution for GDMS onboarding and the global skill and knowledge development framework. In collaboration with GDMS functional area leaders, translates capability needs into learning pathways, appropriately leveled knowledge content, and role-based curricula. The role defines standards for curriculum design, evaluation, and learning operations, and builds scalable mechanisms for training delivery and consumption. Partnering with enterprise learning and development, leverages curated training and learning sources, ensures alignment on learning technologies, aligns to training record keeping requirements and recommendation, and employs learning analytics to guide continuous improvement.

Responsibilities

Strategic Alignment & Stakeholder Partnership

In collaboration with Global Data Management & Standards (GDMS) leadership, defines and maintains GDMS onboarding material and associated processes; ensures alignment with broader organizational onboarding activities

In partnership with GDMS leadership and subject matter experts, defines skill and knowledge requirements that align with business needs and organizational priorities

Working with representatives from the GDMS global data management centers, defines and implements a skill and knowledge development strategy inclusive of role-based competency frameworks, role-based curricula, and delivery mechanisms

Engages with Human Resources, enterprise learning and development, Global Clinical Trial Operations ( GCTO), and external partnerships to source curated training and learning material that aligns with organizational priorities

Own and drive the GDMS Academy learning and development strategy, proactively identifying capability gaps and building the business case for learning priorities

Learning Operations, Curriculum Development, & Delivery Enablement

Leads delivery and coordination of the GDMS learning portfolio, ensuring quality, consistency, and on-time execution

Establishes standards for content design, facilitation, and evaluation; coach subject matter experts and facilitators to those standards

Defines annual skill and knowledge development plan, success criteria, and measurement model; publishes dashboards and drives follow-through on actions to continuously improve

Coordinates with Human Resources, enterprise learning and development and Global Clinical Trial Operations ( GCTO) on tools, LMS (Learning Management System) integrations, and enterprise talent initiatives that relate to GDMS learning

Lead continuous improvement of the GDMS Academy curriculum using learning analytics, stakeholder feedback, and benchmarking insights to regularly assess and evolve design, delivery mechanisms, and measurement frameworks

Engagement, Knowledge Sharing, & Talent Development

Manages onboarding, rotation, shadow, and intern programs end-to-end, including selection, matching, objectives, and outcomes tracking

Builds external engagement plan (industry forums, benchmarking, associations) and evaluates insights for internal learning opportunities and curriculum refinement

Develops and coordinates recognition and learning campaigns that motivate skill and knowledge uptake

Qualifications, Skills & Experience 

Technical Skills:

In depth knowledge of clinical trial operations and clinical data management

Proficiency in designing curriculum architecture and learning pathways aligned to role-based competency and skills frameworks

Experience developing assessment strategy and evaluation methods including competency-based validation

Experience building and sustaining communities of practice and peer-learning mechanisms (facilitation, mentoring, knowledge sharing)

Working knowledge of learning analytics and dashboarding (coverage, completion, proficiency, impact/behavior change, ROI/benefits).

Experience integrating curricula and reporting with enterprise learning technologies (e.g., LMS/LXP) while applying data privacy and access controls.

Ability to translate internal/external insights and lessons learned into learning assets

Non-technical Skills:

Demonstrated strategic leadership and ability to influence senior-level leaders and stakeholders across functions, geographies, and levels

Exceptional communication, collaboration, and interpersonal skills across global and matrixed environments

Strong conceptual and analytical thinking; able to translate strategy into actionable execution

Demonstrated success in mentoring, coaching, and developing talent in a global organization

Demonstrated success driving change and alignment across complex, cross-functional structures

High resilience, adaptability, and professional maturity in evolving business environment

Enterprise Leadership Skills:

Business Savviness | Uses organizational and industry insights to identify trends, assesses Data Management operating practices and performance, evaluates process or operating model changes, and anticipates impacts on delivery, resourcing, and stakeholders

Strategic Planning | Triages activities and assignments by business criticality, and reprioritizes work as timelines, risks, and stakeholder needs shift

Execution Excellence | Proactively takes initiative beyond assigned responsibilities to unblock delivery, close gaps, and achieve program and operational results

Qualifications & experience: 

Bachelor's Degree with a minimum of 8 years of experience working in the pharmaceutical or biotech industry, data management, or clinical trial operations and a minimum of 3 years in learning and development.

OR

Advanced Degree (Masters or Doctorate) with a minimum of 4 years of experience working in the pharmaceutical or biotech industry, data management, or clinical trial operations and a minimum of 3 years in learning and development.

eligibleforERP

clinicaltrialjobs

GDMS

Required Skills:

Biopharmaceutical Industry, Business Acumen, Competency Framework Design, Curriculum Development, Detail-Oriented, Good Clinical Data Management Practice (GCDMP), Good Clinical Practice (GCP), Interpersonal Relationships, Learning Analytics, Learning and Development (L&D), Strategic Planning, Strategic Thinking

Preferred Skills:

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 salary range for this role is

$142,400.00 - $224,100.00

This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this 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 .

You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.

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

VISA Sponsorship:

No

Travel Requirements:

10%

Flexible Work Arrangements:

Hybrid

Shift:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

N/A

Job Posting End Date:

08/6/2026 *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.

Requisition ID:R404318

Job details

Seniority
Associate Director
Function
Clinical Development
Therapeutic area
Not listed
Location
Rahway, New Jersey, 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 309 comparable Associate Director Clinical Development roles across 48 biopharma companies.

309Comparable roles tracked
273Currently active
48Companies hiring similar roles
28Countries represented

Salary context

65 of 309 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 $142,400/yr – $224,100/yr
Peer group range $90,199 – $315,000 (median $180,000)

Where these roles are based

Top locations among the 309 comparable roles

United States106
India87
China13
Poland11
United Kingdom11
Spain9

+ 22 more countries

Seniority mix

309 of 309 peers have a known seniority level

Manager146
Senior91
Associate Director72

Therapeutic area mix

24 of 309 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology9
Immunology6
Cardiovascular / CVRM4
Neuroscience3
Dermatology & Aesthetics1
Ophthalmology1

Similar opportunities

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.

60%similar
AbbVie Irvine, CA Associate Director
Same function Same seniority Same country
60%similar
AbbVie Associate Director
Same function Same seniority Same country

Open in 2 locations

Irvine, United StatesNorth Chicago, United States
60%similar
GlaxoSmithKline LLC Upper Providence, United States Associate Director
Same function Same seniority Same country
60%similar
Corixa Corporation Home Worker, United States Associate Director
Same function Same seniority Same country
60%similar
Regeneron Pharmaceuticals, Inc (USA) Tarrytown, United States Associate Director
Same function Same seniority Same country
60%similar
E.R. Squibb & Sons,L.L.C. Cambridge Crossing, United States Associate Director
Same function Same seniority Same country

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.

60%
Associate Director, Aesthetics Clinical Development
AbbVie · Irvine, CA · Associate Director
Function Therapeutic area Seniority Country
60%
Associate Director of Clinical Sciences
GlaxoSmithKline LLC · Upper Providence, United States · Associate Director
Function Therapeutic area Seniority Country
60%
Associate Director, Global Clinical Physician (Neuropsychiatry)
E.R. Squibb & Sons,L.L.C. · Cambridge Crossing, United States · Associate Director
Function Therapeutic area Seniority Country
60%
Clinical Scientist Associate Director – Early Development Inflammation
Amgen Inc. · Remote, United States · Associate Director
Function Therapeutic area Seniority Country
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.