Clinical Systems Implementation Team Lead

Merck

Rahway (NJ)

On-site

USD 130,000 - 180,000

Full time

4 days ago
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Job summary

Merck in Rahway, NJ is seeking a Clinical Systems Implementation Team Lead to drive validation, deployment, and adoption of critical trial applications. You will lead a cross-functional team, ensure SDLC compliance, manage audits, and partner with IT, QA, and clinical operations to deliver reliable systems.

This role requires 2–5 years of people management, deep knowledge of CTMS/EDC/eTMF, and strong communication with senior stakeholders.

Qualifications

  • BS degree with or above; 10+ years' experience preferred.
  • MS/MBA/JD with 8+ years' experience; PhD with 5+ years in related fields.
  • Deep understanding of drug development processes and quality management tools.

Responsibilities

  • Lead validation, implementation, and adoption of clinical trial applications.
  • Ensure SDLC compliance and audit readiness.
  • Partner with IT, QA, and business stakeholders to deliver solutions at scale.
  • Develop and manage KPIs to measure outcomes and adoption.

Skills

Clinical Systems Implementation
People Leadership
Cross-Functional Teamwork
Project & Resource Management
Regulatory Compliance
Data Analysis
Communication Skills
GCP/ICH Understanding

Education

BS degree or higher
MS/MBA/JD or PhD with significant experience

Tools

CTMS
eTMF
EDC System
Clinical Portal
MS Office

Job description

Job Description

Clinical Systems Implementation Team Lead within BEO manages the full range of activities related to the successful validation, implementation, and adoption of applications that support our company’s clinical trials. These systems can be internally and/or externally facing, large or small, vendor or company developed and owned. The role also has people management responsibility for team members supporting similar activities.

The team lead should have needed experience and knowledge related to the systems and processes being supported by the team or prioritize gaining this experience once in the role.

Partner with various business areas within Global Clinical Development (GCD), with our Research & Development Division (https://go.msd.com/~vs4xix) -IT and vendors to understand business needs, identify solutions to support those needs and implement solutions with quality focus. The role ensures compliance to company policies, agency regulations and related guidance around technology and applies data stewardship and data governance principles in the management of the applications.

Accountable for supporting systems audits and inspections and follow-up of any findings and required CAPA management. Ensure systems quality lead is engaged early in process of upgrading or re-platforming of technology to ensure proper SDLC compliance. Ensure Clinical Systems Implementation team members are properly trained on SDLC requirements and maintain their training. As part of the BEO Leadership Team, identify topics and appropriate guest speakers for monthly department meeting agenda, propose projects/assignment for interns and support activities to identify appropriate candidates for internship, and schedule quarterly business review meetings to share team accomplishments and upcoming activities with other team leads.

Responsibilities
  • Partner with a cross-functional team of functional SMEs and end-users to independently assess emerging business needs and work with our Research & Development Division (https://go.msd.com/~vs4xix) -IT to identify innovative solutions to meet the need.

  • Monitor technology trends to match the business needs, profile partners and vendors and map capabilities to requirements to enable business processes in alignment with the GCTO strategy.

  • Partner with various business functional stakeholders and our Research & Development Division (https://go.msd.com/~vs4xix) -IT and create high-impact & high-value business cases for innovation opportunities and advance selected solutions from proof of concept to pilot and implementation at scale, ensuring required due diligence has been carried out, and the solution is audit/inspection ready, if applicable.

  • Collaborate with user experience experts and collect early and ongoing feedback from users to ensure solution being developed will provide optimum user experience once enabled.

  • Engage with business and IT sponsors to understand overall strategy for existing technology solutions to be able to develop and drive the technology and innovation roadmap.

  • Identify and manage the Key Performance Indicators (KPIs) to measure outcomes and success of technology solutions being implemented to improve clinical operations productivity and site and patient experiences.

  • As needed, provide workstream or sub-stream leadership or serve as a member for larger technology initiatives.

  • Create an effective change and communication plan for technology being enabled to support adoption of and to share best practices and lessons learned.

  • Provide system ownership of assigned system(s) and all activities associated with such ownership. Such activities may include system migrations and decommissioning.

Team Management
  • Manage team members that provide business system ownership of operational systems.

  • Ensure proper allocation of resources to maintain effective system support.

  • Identify need for and provide needed justification for additional headcount and if headcount is approved, work with HR recruiter to identify, interview and onboard the right candidate to fill the position.

  • Conduct regular 1:1s and ad-hoc meetings to ensure priorities are defined and delivered as planned, provide ongoing constructive feedback, conduct performance reviews, and manage any risks and escalations.

  • Obtain sufficient understanding of the applications being supported by team members to be able to proactively identify challenges, address any escalations, provide update to sponsors and serve as a back-up in case of staffing challenges.

  • Discuss opportunities for development, job satisfaction and career planning with team members.

  • Conduct check-in meetings with non-our Company (https://go.msd.com/~vs4xix) 's resources supporting the team about assignments and progress toward deliverables. Meet with partner line manager to discuss any relevant performance feedback.

  • Ensure compliance to required training for all team members.

Accountable for team members
  • Executing their role, with a focus on approving functional requirements, timely and quality completion of systems validation, implementation and operational activities; working with our Research & Development Division (https://go.msd.com/~vs4xix) -IT and/or Vendor to prioritize enhancements and drive future roadmap to meet business needs.

  • Working with our Research & Development Division (https://go.msd.com/~vs4xix) -IT and vendors to establish secure and timely data flow from/to upstream/downstream systems and have monitoring in place as needed.

  • Actively engaging in Platform and Information Governance teams as applicable.

  • Ensuring adequate helpdesk support, case tracking and trending is in place to support business users for all applications in scope of the team.

  • Performing business process impact assessments for new applications or enhancements to existing application and providing details to Business Process/Sub-process Owners to make necessary updates to the processes.

  • Ensuring Inspection Readiness status, having and maintaining systems story boards, current BCP and SOPs and ongoing tracking of planned/completed system releases and Account reviews for applicable systems.

  • Having ongoing collaboration with Regional Systems Business Leads and functional SMEs for optimum adoption and compliant use of applications.

Education
  • BS degree with or above10 years' experience;
OR
  • MS/MBA/JD degree with 8 years' experience; or PhD degree with 5 years' experience in Science, Clinical Research, Computer Science, or similar fields.
Experience and skills
  • Two to five years of people management experience is required.

  • Broad understanding of drug development -safety, clinical trials, trial design, data management, trial operations, regulatory, privacy, ICH, and GCP required.

  • Ability to quickly gain thorough understanding and become subject matter expert in a new business area as needed, e.g. Risk Based Monitoring, Structured Content Authoring, clinical content standards.

  • Strong verbal & written communication skills - able to present information confidentially and effectively to leadership, peers, and team.

  • Ability to proficiently interact with all levels of management, exert influence to achieve results without authority and successfully manage senior/Executive level stakeholders.

  • Project and Resource management experience.

  • Deep knowledge and understanding of Clinical Trial processes as well as quality management and control tools.
  • Experience with critical clinical systems such as CTMS, eTMF, Electronic Data Capture (EDC) system, clinical portal and basic reporting and MS Office tools.
  • Understanding metrics and being able to identify trends.
  • Experience in System Validation and Implementation, systems analysis and systems maintenance /support.
  • Fluency with the respective cross-functional interdependencies, roles and enabling tools/technologies.
  • Able to identify critical input and outputs that drive business processes and dependencies on process (workflow) vs. technology (dataflow).
  • Exposure to a global environment, with multi-cultural and organizational operating models; appreciation for country requirements/needs vs. US standards.
  • Management and leadership skills, analytical ability, good judgment, ability to multi-task, conflict resolution expertise and discretion.
  • Customer service orientation and the ability to work effectively with clients, third party vendors, quality and IT management/staff.
  • Experience in training user community.

#eligibleforERP

Required Skills

Adaptability, Benchmarking, Business Process Re-Engineering (BPR), Clinical Systems Implementation, Cross-Functional Teamwork, Data Analysis Tools, Decision Making, Good Manufacturing Practices (GMP), Innovation, IT Implementation, People Leadership, Professional Integrity, Quality Control Management, Risk Management, Strategic Planning

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