Clinical Research Associate – Manager

MSD

Clinical Research Associate Manager leading Merck’s clinical trial monitoring teams. Developing CRAs, managing performance and ensuring compliant study and site execution.

Posted 8/4/2026full-timeRemote • New Jersey • 🇺🇸 United StatesJuniorMid-Level💰 $142,400 - $224,100 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in Clinical Research Management, including team leadership, compliance with ICH GCP regulations, and effective project management. Proven ability to mentor and develop Clinical Research Associates while ensuring high-quality study performance and operational efficiency.

Highest-signal resume keywords

Clinical Research ManagementICH GCP ComplianceTeam LeadershipProject ManagementCore Trial Management Systems

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical ResearchCRA MonitoringTrial Management SystemsGood Documentation PracticesCapacity PlanningPerformance ReviewsResource AllocationConflict ResolutionManpower ReportingSite Performance Management

Soft Skills

Excellent Interpersonal SkillsStrong Decision-MakingHigh Emotional IntelligenceInfluencing SkillsOrganizational Skills

Industry Keywords

Clinical TrialsLocal RegulationsSOPsInvestigator MeetingsStudy CRMPeople ManagementTeam DevelopmentLocal Language ProficiencyBusiness English ProficiencyConflict Management

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Manage a team of 6–14 Clinical Research Associates (CRAs)
Ensure excellent study and site performance while adhering to local regulations, company SOPs and ICH GCP
Provide training, support and mentoring to CRAs
Manage CRA work allocation, career development, performance reviews and performance issues
Contribute to capacity and resource planning, including manpower reporting and CRA capacity forecasting
Coordinate with CRAs, PLMs and other functions to ensure consistent processes and protocol implementation across the country
Interact with sites to resolve site or CRA operational issues in coordination with the study CRM
Attend local Investigator Meetings when requested
Interface with GCTO partners on clinical trial execution
Escalate site performance issues to the CRM and Clinical Research Director
Support and resolve escalated issues from CRAs
Liaise with local HR and finance functions as required
Manage local conflicts between resources and work
Ensure CRA compliance with corporate policies, procedures and quality standards

Requirements

What you’ll need

Minimum of 5 years’ experience within Clinical Research
Minimum of 3 years’ experience as a CRA monitoring clinical trials
Bachelor’s degree in Science
Line management experience preferred or, at minimum, team leader experience
Ability to work independently and in a team environment
Excellent people, time, project management and organizational skills
History of strong performance
Strong decision-making and stewardship skills
Fluent in the local language
Business proficient in English, verbal and written
Excellent working knowledge of applicable ICH/GCP regulations and Good Documentation Practices
Expertise in core trial management systems and tools
High emotional intelligence
Strong leadership skills with proven success in people management
Excellent interpersonal, communication and conflict management skills
Ability to build relationships and communicate effectively with external customers, sites and investigators
Influencing skills
Valid driving license

Benefits

Comp & perks

Annual bonus eligibility
Long-term incentive eligibility, if applicable
Medical healthcare
Dental healthcare
Vision healthcare
Other insurance benefits for employee and family
Retirement benefits
401(k)
Paid holidays
Vacation
Compassionate days
Sick days
Remote work arrangement