Merck & Co, Inc

Associate Director - Study Integration Manager, Data Integration and Automation - Hybrid

Merck & Co, Inc • $142K — $224K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree with 8+ years in relevant field, including 2 years in people management.
  • Advanced Degree (Masters or Doctorate) with 4+ years in relevant field, including 2 years in people management.
  • Deep subject matter expertise in clinical data management and related disciplines.
  • Proficiency in clinical data management lifecycle and multi-system data flows.
  • Experience with work tracking programs like Jira or Confluence.

Responsibilities

  • Lead the integrated program plan from design to close-out for all trials.
  • Ensure technical components are production-ready before first patient visit.
  • Directly manage complex trials as needed, acting as Study Integration Manager.
  • Synchronize release calendars and manage change control processes.
  • Maintain program RAID logs and lead risk mitigation efforts.
  • Partner with functional leads to align resources and manage service provider performance.
  • Identify and implement process improvements and contribute to SOP updates.

Benefits

  • Comprehensive medical, dental, and vision insurance for employees and families.
  • Retirement benefits including 401(k).
  • Paid holidays, vacation, and sick days.
  • Opportunities for career development and training.
  • Annual bonus and long-term incentive eligibility.
Full Job Description

Job Description

The Associate Director, Study Integration Manager (M-track) leads a team to deliver trial-level technical data-management components (eCRFs, integrations, edit checks, reports) with quality and compliance to GDMS/DI&A standards. This individual acts as a hands-on coach and technical reviewer by balancing workload, unblocking issues, and ensuring that documentation, validation, and change control are audit ready. The Associate Director, Study Integration Manager partners closely with Clinical, BARDS, DI&A/IT, service providers, and other stakeholders to drive on-time, inspection-ready delivery.


Responsibilities


Study technical planning & delivery:


  • Build and maintain the integrated program plan from design through close-out across all in-scope trials.
  • Drive program-level consistency in study-level technical deliverables.
  • Ensure all technical components are production-ready before first-patient-first-visit; monitor status/quality pre- and post-release; support end-of-study archival and decommissioning.
  • When needed, directly lead one or more complex trials as Study Integration Manager.

Cross-functional coordination, risk & governance:


  • Synchronize release calendars, dependencies, and change control; chair/participate in program change/governance meetings.
  • Plans across studies; runs risk/change control; aligns stakeholders; provides reliable status reporting and governance updates.
  • Maintain program RAID logs; lead risk mitigation and CAPA; ensure CSV/GxP validation evidence and inspection readiness; support/lead audits including appropriate documentation.
  • Partner with functional leads to secure/align resources; manage service provider SOWs/SLAs and performance; track delivery health and value.
  • Serve as the program point of contact for technical components; manage expectations; provide clear, decision-ready status to sponsors/steering.

Standards, quality & continuous improvement:


  • Identify and lead process/tool improvements (automation, test efficiency, templates); capture lessons learned; contribute to SOP/WI updates.
  • Guide and review SIM plans/specs; coach, mentor, and develop capability across the team.
  • Steward standards and change requests; arbitrate configuration vs. customization; ensure alignment with database/clinical standards.

People Management:


  • Align teams around a clear direction; set clear objectives aligned to organizational goals; assign work and set priorities accounting for work-life balance sustainability.
  • Conduct regular check-ins and annual reviews; coach for performance; provide recognition.
  • Develop career plans; create growth opportunities and promotion cases; ensure appropriate training and mentoring.
  • Lead recruiting and hiring and oversee performance management activities, including management of sensitive employee-relations matters in partnership with HR.
  • Coordinate on-shore/off-shore and contingent resources; ensure role clarity and effective handoffs.
  • Manage an operating budget and optimize spend against priorities.
  • Inspires and ensures that team leaders are effectively supporting and empowering their individual leaders.

Technical skills:


  • Ability to independently lead study-level design/build/test/release; author/peer-review specs (eCRF, edit checks, mappings).
  • Strong hands-on with clinical data management (CDM) lifecycle; working proficiency across multi-system data flows and API-based or file integrations.
  • Understanding of various clinical, data, and sponsor standards.
  • Experience with work tracking programs (e.g., Jira/Confluence/Smartsheet); exposure to automation (templated checks, reusable specs), and monitoring (listings/dashboards).

Non-technical skills:


  • Strong communication and negotiation skills, with ability to craft concise, decision-ready summaries and narratives for leadership and frames risks, options, and recommendations.
  • Aligns priorities with service providers and cross-functional leaders; manages escalations.
  • Able to operate effectively in ambiguity; drives consensus across functions; steers process/technology improvements.
  • Engages service provider, leadership, and industry forums; represents team professionally and credibly under pressure; maintains resilience and composure.
  • Strong ability to lead teams in a matrixed, global organization while ensuring delivery excellence.
  • Demonstrated success in coaching, developing, and performance-managing high-performing individuals.
  • Builds strong partnerships across technical, business, and quality functions to enhance collaboration and deliver integrated outcomes.
  • Balances business needs, resource capacity, and compliance requirements to make sound operational decisions.
  • Capable of leading teams through process and organizational transformation with empathy and clarity.
  • Guides and reviews work across teams/geographies; builds capability and consistency; fosters inclusive, high-trust culture.

Enterprise Leadership Skills:


  • Execution Excellence | Is results-focused per compliance standards; sets ambitious expectations for accomplishment and ensures others contribute to org strategies by focusing them on the most critical priorities; translates departmental goals into clear expectations.
  • Coaching & Development | Manages individual contributors and/or supervisors, provides technical guidance, and develops others through coaching, feedback, and guidance.
  • Entrepreneurship | Embraces patient customer focus, ensuring that internal or external customer perspective is the driving force behind strategic priorities, business decisions, org processes, and individual activities; crafts and implements service practices that meet customers' and own organization needs.

Qualifications & experience


  • Bachelors Degree with a minimum of 8 years experience working in relevant field for associated job description, including:
    • 2 years people management experience.
    • Demonstrated deep subject matter expertise in relevant discipline.

or

  • Advanced Degree (Masters or Doctorate) with a minimum of 4 years experience working in relevant field for associated job description, including:
    • 2 years people management experience.
    • Demonstrated deep subject matter expertise in relevant discipline.

clinicaltrialjobs  

EligibleforERP

#GDMS

Required Skills:

Clinical Data Management, Coaching, Collaborative Leadership, Decision Making, Enterprise Leadership, Operational Excellence, People Leadership, Strategic Thinking, Team Mentoring, Team Organization

Preferred Skills:

Current Employees apply

Current Contingent Workers apply

US and Puerto Rico Residents Only:

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 .

You can apply for this role through (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:

1st - Day

Valid Driving License:

No

Hazardous Material(s):

No

Job Posting End Date:

10/9/2026

*A job posting

About Merck & Co, Inc

Schering-Plough Corporation is a major U.S.-based manufacturer of pharmaceuticals. It operates in three segments: Prescription Pharmaceuticals, Animal Health, and Consumer Health Care. Schering-Plough develops products targeting on allergy, cancer, hepatitis, cardiovascular, central nervous system, respiratory system, and more.  It was founded in 1851 by Ernst Christian Friedrich Schering as Schering AG in Germany. Schering-Plough manufactured several pharmaceutical drugs, the most well-known of which were the allergy drugs Claritin and Clarinex, an anti-cholesterol drug Vytorin, and a brain tumor drug Temodar. It also developed drugs targeting on central nervous system and the respiratory system. Schering Plough also owned and operated the major foot care brand name Dr. Scholl's and the skin care line Coppertone. These also became a part of the new company. Schering-Plough was a full member of the European Federation of Pharmaceutical Industries and Associations (EFPIA), a membership which is also maintained by the new Merck.

Merck & Co, Inc Careers

Join the visionary team at Merck & Co, Inc, a global leader in healthcare dedicated to advancing the world of medicine. As part of our professional community, you'll find dynamic job opportunities that foster innovation and leadership across various fields. Merck & Co, Inc is not just a company; it's a place where you can make a difference.

Work You’ll Do

At Merck & Co, Inc, we are committed to improving global health through groundbreaking research and innovative healthcare solutions. Our team is at the forefront of developing new therapies and vaccines that significantly impact public health worldwide. By joining us, you will collaborate with some of the brightest minds in the industry, using your skills to contribute to projects that save and improve lives around the globe.

Explore Career Paths

Whether you're seeking an internship, a graduate opportunity, or a professional position, Merck & Co, Inc offers a range of career paths in environments that promote rapid professional growth and development. Explore job opportunities in research, digital transformation, manufacturing, and more, all while benefiting from a culture that supports diversity and inclusion.

Innovate and Lead

Merck & Co, Inc is an ideal environment for those who lead with curiosity and the drive to innovate. Our leadership is committed to fostering a culture where inventive thinking and collaboration are encouraged, making it a perfect place for professionals who seek to make an impact through their work.

Develop Your Skills

With Merck & Co, Inc, you are not just getting a job; you're gaining access to unparalleled career development opportunities. Enhance your skills through diverse training programs, workshops, and continuous learning courses designed to help you grow at every stage of your career.

Benefits and Culture

We understand that our employees are our greatest asset, which is why we offer competitive benefits designed to support the health and well-being of you and your family. From comprehensive health care coverage and retirement plans to flexible working conditions and wellness programs, our benefits package is designed to meet the diverse needs of our team members.

Join Our Team

Ready to advance your career at Merck & Co, Inc? Search open positions that match your skills and interests. We are continuously hiring and looking for passionate, creative, and solution-driven team players. Prepare your resume, sharpen your interview skills, and become part of a company that's dedicated to making a difference.

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Learn more about Merck & Co, Inc
Size
68,000 employees
Market Cap
$282.6 billion
Industry
Net Income
$7 billion
Founded
1668
5 Year Trend
+4.1%
Revenue
$47.9 billion
NASDAQ

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