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Merck Associate Director Jobs (NOW HIRING)

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Merck Associate Director information

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$30.5K

$102.7K

$173K

How much do merck associate director jobs pay per year?

As of Jun 18, 2026, the average yearly pay for merck associate director in the United States is $102,728.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,000.00 and $141,000.00 per year, depending on experience, location, and employer.

What is the difference between Merck Associate Director vs Merck Senior Manager?

CriteriaMerck Associate DirectorMerck Senior Manager
Required credentialsAdvanced degree (MBA, PhD), relevant industry experienceBachelor's or Master's degree, significant industry experience
Work environmentStrategic leadership, cross-functional collaborationOperational management, team oversight
Employer and industry usageCommon in pharmaceutical and biotech sectorsWidely used in similar sectors for mid-to-senior roles
Search and comparison intentHigh overlap in responsibilities and qualificationsSimilar level, often compared for career progression

The Merck Associate Director typically holds a more strategic, leadership-focused role requiring advanced degrees and extensive industry experience. In contrast, the Merck Senior Manager is more operational, overseeing teams and projects. Both roles are integral in pharmaceutical companies, with the Associate Director often preparing for executive leadership, while the Senior Manager manages day-to-day functions.

What does a Merck Associate Director do?

A Merck Associate Director typically oversees teams or projects within a specific department, such as research, marketing, or regulatory affairs. They are responsible for developing strategies, ensuring compliance with company and regulatory standards, and achieving departmental goals. Associate Directors often manage budgets, mentor staff, and collaborate with other leaders to drive business objectives. Their role is critical in advancing Merck’s mission and maintaining high performance across their area of responsibility.

How much does an associate director at Merck make?

An associate director at Merck typically earns between $130,000 and $180,000 annually, depending on experience, location, and specific department. Compensation may also include bonuses, stock options, and benefits. This role often requires advanced degrees and leadership skills in the pharmaceutical or healthcare industry.

Who is the associate director of Merck?

The Associate Director at Merck is a senior leadership role responsible for overseeing specific departments or projects within the company. The individual in this position typically has extensive industry experience, advanced degrees, and leadership skills to manage teams and drive strategic initiatives.

What are some common challenges faced by an Associate Director at Merck, and how can candidates prepare to address them?

As an Associate Director at Merck, one common challenge is balancing strategic leadership with hands-on project management, especially in a fast-paced, highly regulated environment. You'll often need to coordinate cross-functional teams and align diverse stakeholders, so strong communication and organizational skills are key. Candidates should be prepared to navigate shifting priorities, regulatory changes, and tight deadlines while ensuring alignment with Merck’s mission and compliance standards. Proactively building knowledge in pharmaceutical regulations and stakeholder management can help you succeed in this role.

What are the key skills and qualifications needed to thrive as a Merck Associate Director, and why are they important?

To thrive as a Merck Associate Director, you typically need a relevant advanced degree (such as in life sciences, business, or a related field), substantial industry experience, and strong leadership capabilities. Familiarity with regulatory compliance systems, data analysis tools, and project management software is often required, along with any specialized certifications pertinent to the business area. Strategic thinking, effective communication, and the ability to lead cross-functional teams are crucial soft skills in this role. These competencies are vital for driving business objectives, ensuring regulatory adherence, and fostering effective team collaboration within a complex corporate environment.

Is it hard to get a job at Merck?

Securing a position as a Merck Associate Director can be competitive due to the company's reputation and rigorous hiring process. Candidates typically need relevant experience, advanced degrees, and strong leadership skills, along with a thorough interview process. Preparation and a solid understanding of the pharmaceutical industry can improve chances of success.

Is an associate director a high level position?

An Associate Director is considered a senior-level position within organizations like Merck, often responsible for managing teams and overseeing projects. It typically requires significant experience, leadership skills, and industry knowledge, making it a high-level role in the corporate hierarchy.
More about Merck Associate Director jobs
What cities are hiring for Merck Associate Director jobs? Cities with the most Merck Associate Director job openings:
What states have the most Merck Associate Director jobs? States with the most job openings for Merck Associate Director jobs include:
Infographic showing various Merck Associate Director job openings in the United States as of June 2026, with employment types broken down into 1% Internship, 10% As Needed, 2% Full Time, 83% Part Time, and 4% Nights. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $102,728 per year, or $49.4 per hour.
Associate Principal Scientist (Associate Director) -Outcomes Research

Associate Principal Scientist (Associate Director) -Outcomes Research

Merck & Co., Inc.

Rahway, NJ • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 16 days ago


Merck rating

7.8

Company rating: 7.8 out of 10

Based on 50 frontline employees who took The Breakroom Quiz

42nd of 71 rated pharmaceutical


Job description

Job Description
Title:
Associate Principal Scientist/Associate Director, Outcomes Research
Division / Area:
Value and Implementation
Workday Job Profile:
Consult with Global Human Resources
Band / Pathway / Level:
Consult with Global Human Resources
Workday Job Family ID:
Consult with Global Human Resources
Role Summary
  • Under the guidance of a senior leader, an Associate Principal Scientist/Associate Director, has primary responsibility for planning/managing real world and economic evidence activities for in-line and pipeline products to meet the value evidence needs of clinicians, payers, policymakers, HTA/reimbursement agencies, and health systems globally.
  • Types of studies executed include prospective and retrospective observational studies to characterize disease burden and epidemiology, treatment patterns, healthcare resource utilization and costs, physician and patient satisfaction surveys, clinical and patient reported outcomes assessments, systematic reviews and meta-analyses, and economic modelling. Key responsibilities also include development of American Managed Care Pharmacy (AMCP) dossiers for US payers, and Global Value Dossiers for use by local subsidiaries in their HTA submissions. The incumbent is expected to work cross-functionally with clinical development, medical affairs, biostatistics, market access, commercial and country affiliates. The incumbent may supervise external vendors or partners to execute these activities. The incumbent may have direct interactions with health technology assessment (HTA) agencies, reimbursement decision makers, or national immunization technical advisory groups.

Responsibilities and Primary Activities
  • Participates in value evidence teams and serves as outcomes research representative on cross-functional regional and global teams
  • Critically assesses drivers and barriers to reimbursement and market access, and provide input into clinical, regulatory, payer/access, marketing and evidence generation strategy and programs
  • In collaboration with internal teams and external partners, designs studies, authors study protocols, develops measurement questionnaires, case report forms, data analysis plans, final study reports, scientific presentations, and publications
  • Responsible for study-related contracting, budgets, and vendor/partner management, and to ensure study conduct is aligned with company Policies and SOPs and world-wide regulations and standards, including Good Pharmacoepidemiology Practice (GPP) for applicable work.
  • Develops American Managed Care Pharmacy (AMCP) dossiers for US payers, and Global Value Dossiers
  • Develops supplementary clinical data package in close partnership with markets and HTA statistics group for submission to HTA agencies
  • Supports country affiliates to understand local evidence generation needs, adapts health economic evaluations, customizes outcomes research documents, such as protocols and reimbursement dossiers, according to local requirements
  • Works closely with cross-functional teams to effectively communicate outcomes research and health economic modelling data internally and to external customers
  • Maintains awareness of new scientific and methodological developments within therapeutic area
  • Builds relationships with scientific experts worldwide
  • Presents outcomes research data at national and international congresses and publishes articles in scientific journals

Required Qualifications, Skills, & Experience
Minimum
Masters degree (MSc, MPH) in relevant discipline (health services research, outcomes research, epidemiology, public health, health economics, pharmacoeconomics, pharmacy administration)
1-3 years post degree
Preferred
Doctoral degree (PhD, DrPH, ScD, PharmD) in relevant discipline (health services research, outcomes research, epidemiology, public health, health economics, pharmacoeconomics, pharmacy administration)
Required Skills:
Data Management, Researching, Stakeholder Relationship Management, Strategic Planning
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
$156,900.00 - $247,000.00
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:
Yes
Travel Requirements:
10%
Flexible Work Arrangements:
Hybrid
Shift:
Not Indicated
Valid Driving License:
No
Hazardous Material(s):
n/a
Job Posting End Date:
06/17/2026
*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.

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