Associate Director, CSSM Systems Lead, Hybrid
MSD
Rahway, New Jersey
Full-Time
$6,687
HybridDirector
Job Description
Our Clinical Research and Pharmacovigilance teams advance global healthcare through clinical research and innovation. In support of Global Clinical Trial Operations (GCTO), this role ensures effective execution of trial-level processes supported by technology by representing Clinical Sciences & Study Management (CSSM) user needs and driving adoption of business systems.
Position Description:
Education:
Experience:
While this role is part of Business Enablement Organization, under Regional Systems Team, the role will partner closely with the CSSM Center of Excellence (CoE) and CSSM Sr leadership team, to translate operational pain points, training needs, and process gaps into system and adoption priorities. This role is also responsible for ensuring alignment between business needs and enabling technologies. A key focus of the role is driving training, change management, data compliance, and user support to ensure consistent and compliant execution of trial-level activities across CSSM users.
CORE Accountabilities and Duties:
Trial-Level Business Representation
Represent CSSM and trial-level user needs in system enhancements, implementations, and ongoing optimization efforts.
Act as a key liaison between CSSM Center of Excellence team, CSSM users, BSOs, systems SMEs and IT to ensure technology solutions align with trial execution requirements.
Partner with Global Clinical Development process owners , CSSM CoE and CSSM leadership to ensure systems support end-to-end trial processes.
User Support & Issue Management
Build and sustain a high-performing CSSM Systems SME network, enabling scalable user support, knowledge sharing, and consistent system utilization. Set clear expectations for type of support to be provided by these SMEs, define escalation pathway for users to follow for issues and how-to questions.
Serve as a point of contact for CSSM Systems SMEs for system-related inquiries, issues, and escalations.
Collaborate with IT product teams, Technology Operations & Services (TOPS) team, and BSOs to troubleshoot system issues and identify root causes.
Identify recurring challenges and drive improvements through system enhancements and /or process updates.
Training & Change Management
Work with CSSM CoE, Regional Systems Leads (RSLs) and CSSM Systems SMEs to design and deliver training programs to support CSSM users across clinical systems and trial processes.
Work with BSOs for applicable systems and tools to develop targeted training materials and communications to support new system implementations, enhancements, and process updates.
Partner with Change Management teams to drive adoption and ensure effective transition to new ways of working and drive better system use.
Process Improvement & Innovation
Analyze trial-level workflows to identify inefficiencies and opportunities for technology-enabled improvements.
Support continuous improvement initiatives aligned to CSSM and trial execution needs.
Support innovation pilots and contribute to the implementation of new digital or system capabilities.
Data Quality & Compliance Support
Promote and support high-quality, timely, and compliant data entry within clinical systems (e.g., CTMS, eTMF).
Partner with RSLs, CSSM Systems SMEs, Data Integration & Automation (DIA) team to address data quality issues and ensure adherence to Global Clinical Development procedures.
Support activities related to data monitoring, issue resolution, and compliance readiness.
Stakeholder Engagement & Communication
Engage regularly with CSSM CoE, other CSSM stakeholders and trial teams to gather feedback and communicate updates.
Analyze system usage, data quality, and user behavior trends to proactively identify risks, inefficiencies, and improvement opportunities.
Partner with CSSM CoE communications teams to ensure clear, effective messaging to CSSM users.
#eligibleforERP
#clinicaltrialjobs
Required Skills:
Change Management, Clinical Project Management, Clinical Trial Management Systems (CTMS), Clinical Trials Operations, Communication, Cross-Functional Collaboration, Influencing Skills, Process Improvements, Root Cause Analysis (RCA), Stakeholder Management, Training and DevelopmentPreferred Skills:
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The salary range for this role is
$142,400.00 - $224,100.00This 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
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Employee Status:
RegularRelocation:
No relocationVISA Sponsorship:
NoTravel Requirements:
10%Flexible Work Arrangements:
HybridShift:
1st - DayValid Driving License:
NoHazardous Material(s):
n/aJob Posting End Date:
07/14/2026*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.