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Associate Director Biostatistics Jobs in Basking Ridge, NJ

Associate, Medical Economics

New York, NY ยท Hybrid

$123K - $161K/yr

You will report to the Associate Director of Medical Economics, and is part of a team that serves ... Economics, Actuarial Science, Health Economics, Biostatistics, Health Informatics, Health Services ...

Associate, Medical Economics

New York, NY ยท On-site

$123K - $161K/yr

You will report to the Associate Director of Medical Economics, and is part of a team that serves ... Economics, Actuarial Science, Health Economics, Biostatistics, Health Informatics, Health Services ...

Showing results 41-60

Associate Director Biostatistics information

See Basking Ridge, NJ salary details

$31.4K

$105.9K

$178.3K

How much do associate director biostatistics jobs pay per year?

As of Aug 7, 2026, the average yearly pay for associate director biostatistics in Basking Ridge, NJ is $105,867.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,100.00 and $145,300.00 per year, depending on experience, location, and employer.

What are some common challenges an associate director biostatistics faces when leading cross-functional project teams?

As an Associate Director of Biostatistics, one common challenge is balancing statistical rigor with project timelines, especially when collaborating with clinical, regulatory, and data management teams. You often need to translate complex statistical concepts for non-statistical colleagues while ensuring data integrity and compliance with regulatory standards. Managing multiple projects simultaneously and mentoring junior statisticians also requires strong organizational and leadership skills. Effective communication and adaptability are key to navigating the dynamic environment typical in pharmaceutical and biotech organizations.

What does an associate director biostatistics do?

An Associate Director of Biostatistics is responsible for leading biostatistical support for clinical trials and research studies, often within pharmaceutical, biotechnology, or medical research organizations. They manage teams of biostatisticians, oversee statistical analysis plans, ensure compliance with regulatory requirements, and collaborate with cross-functional teams. Their role also involves reviewing and interpreting data, contributing to study design, and providing strategic input for data-driven decision-making. This position typically requires advanced knowledge of statistical methods and experience in clinical research.

What is the difference between Associate Director Biostatistics vs Senior Biostatistician?

AspectAssociate Director BiostatisticsSenior Biostatistician
CredentialsMaster's or PhD in Biostatistics or related fieldMaster's or PhD in Biostatistics or related field
Work EnvironmentLeadership role in clinical trials, overseeing teamsHands-on statistical analysis, supporting projects
Employer & Industry UsagePharmaceuticals, biotech companies, CROsPharmaceuticals, biotech, research institutions

The main difference between Associate Director Biostatistics and Senior Biostatistician lies in their responsibilities and seniority. The Associate Director typically has leadership duties, overseeing teams and strategic planning, while the Senior Biostatistician focuses on conducting complex analyses and supporting project execution. Both roles require similar educational backgrounds and are common in the pharmaceutical and biotech industries.

What are the key skills and qualifications needed to thrive as an associate director biostatistics, and why are they important?

To thrive as an Associate Director Biostatistics, you need advanced expertise in statistical methodologies, clinical trial design, and a graduate degree (often PhD or MS) in biostatistics or a related field. Proficiency with statistical software such as SAS, R, and experience with regulatory submission requirements are typically necessary, along with knowledge of CDISC standards. Strong leadership, communication, and project management skills enable effective collaboration with cross-functional teams and mentoring of junior statisticians. These competencies are vital to ensure rigorous data analysis, regulatory compliance, and the successful delivery of clinical research projects.
What cities near Basking Ridge, NJ are hiring for Associate Director Biostatistics jobs? Cities near Basking Ridge, NJ with the most Associate Director Biostatistics job openings:
Infographic showing various Associate Director Biostatistics job openings in Basking Ridge, NJ as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 26% Part Time, 1% Temporary, and 3% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $105,867 per year, or $50.9 per hour.

Health Equity Research Associate Director

MSD

Rahway, NJ โ€ข Hybrid

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 7 days ago


Job description

Job Description

Job Description:

In BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our company's renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health.

The Health Research (HER) Associate Director will join a hybrid scientific working team that generates centric realworld data (RWD) and realworld evidence (RWE) to inform clinical program design, access strategies, and policy for highpriority therapeutic areas. Reporting into the HER leadership within the RWE Capabilities & Analytics organization, this role leads design and execution of mixedmethods and RWD/RWE studies, integrates social determinants of health (SDoH) and patientreported measures, develops partnerships with MinorityServing Institutions (MSIs), Federally Qualified Health Centers (FQHCs), safetynet providers and community organizations, and translates findings into actionable protocol, site, and policy recommendations that embed bydesign across the development lifecycle.


Primary responsibilities (but are not limited to):

  • Lead design and execution of centered RWD/RWE projects by therapeutic area that quantify disease burden, access, testing, treatment patterns, and outcomes across underrepresented populations.
  • Develop mixedmethods studies (EHR/claims analyses, registry data, SDoH integration, patient surveys, and qualitative interviews) and ensure outputs are timed to inform clinical programs, as well as relevant policy and commercial colleagues.
  • Work cross-functionally to develop study protocols, statistical analysis plans, and methodological approaches that address selection bias, missingness in race/ethnicity/SDOH variables, causal inference, and subgroup inference.
  • Integrate policy analysis into evidence generation: identify policy levers (e.g., Medicaid policy, payer coverage, reimbursement pathways) and translate study findings into policy recommendations.
  • Manage strategic external collaborations and vendor relationships: identify and evaluate data partners, MSIs, FQHCs, safetynet hospitals, communitybased organizations.
  • Colead codevelopment of primary research with external partners (MSIs, FQHCs, community organizations) to ensure nonextractive, trustbased engagement and sustainable relationships that support recruitment and retention and poststudy continuity of care.
  • Work closely with embedded/internal cross-functional partners to translate evidence into protocol design recommendations, site selection guidance, eligibility optimization, and outreach strategies.
  • Produce actionable deliverables: TAspecific, -centric RWD/RWE publications and plain language summaries and dissemination materials for both scientific and nontechnical audiences.
  • Present findings to internal forums and to external stakeholders; publish in peerreviewed journals and present at scientific conferences.
  • Mentor and build capacity across the HER Champion community; contribute to HER learning materials, SharePoint resources, and training modules.
  • Ensure research adheres to ethical standards, privacy/regulatory requirements (HIPAA/GDPR where applicable), and community engagement best practices.

Education

  • Master's degree in epidemiology, public health, health services research, biostatistics, health policy, social science, nursing, social work, or a related quantitative discipline required.
  • Doctoral degree (PhD, DrPH, or MD with research training) preferred.

Required experience and skills

  • 3+ years with PhD, or 5+ years with Master's degree, hands-on experience in the design and implementation of quantitative and/or qualitative science methods in healthcare industry.
  • Demonstrated experience designing and executing RWD/RWE and/or primary mixedmethods studies (EHR/claims/registry analyses, patient surveys, qualitative methods).
  • Experience designing, conducting, and managing research in international settings, including ex-US observational, real-world data/evidence, and/or primary research studies, with knowledge of country-specific data sources, healthcare systems, regulatory requirements, and cultural considerations.
  • Strong applied quantitative skills and familiarity with geospatial and smallarea estimation techniques and handling missingness in race/ethnicity/SDOH data.
  • Experience integrating SDoH, PROs, and other relevant measures into research and evaluating representativeness of datasets.
  • Experience working with external partners (MSIs, FQHCs, community organizations, data vendors, health systems) and managing data governance and compliant collaborations.
  • Familiarity with regulatory, payer and policy environments and how evidence informs access, reimbursement, and policy decisions.
  • Demonstrated excellence in interpersonal communications (written and oral) and consistent ability to execute on objectives
  • Outstanding organizational and time-management skills to manage multiple and competing priorities
  • Proven ability to operate in a matrixed, crossfunctional environment and to manage multiple stakeholders and project timelines.
  • Commitment to communityengaged, culturally competent research and ethical practices.

Competencies and attributes

  • centered scientific mindset, cultural humility, and strong community engagement orientation.
  • Strategic thinker who links evidence generation to policy and access outcomes.
  • Collaborative: excels at building internal and external partnerships and translating science into operational change.
  • Results oriented with strong project management, prioritization, and organizational skills.


Team model and working relationships

  • Member of the HER Hybrid Scientific Working Team, working closely with HER Champions embedded across the organization to operationalize bydesign in scientific process platforms.
  • Hybrid work model: typically three days on site per week (per enterprise policy) unless designated remote or business needs require otherwise.

BARDS2020

#eligibleforERP

Required Skills:

Bioethics, Biostatistics, Clinical Programs, Data Governance, Data Management, Health Equity, Qualitative Research, Researching, 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:

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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:

No relocation

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:

08/4/2026

*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.