Clinical Lead – Site Activation Lead

Premier Research

. Coordinate and collaborate with functional leads to deliver site activation .

Posted 10/23/2026full-timeRemote • United States, France, Italy, Spain, GermanySenior💰 $116,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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

Demonstrates expertise in site activation coordination and project management, with a strong focus on client objectives, timelines, and adherence to ICH/GCP regulations. Proven ability to lead teams, analyze project status, and communicate effectively with stakeholders.

Highest-signal resume keywords

Site Activation CoordinationProject ManagementLeadership in Study Start-UpUnderstanding of ICH/GCP RegulationsData Analysis for Decision Making

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Project Financial ManagementCTMS Data EntryStudy Budget ReviewSite Selection StrategyRisk Mitigation Strategies

Soft Skills

Interpersonal SkillsTeam CollaborationOrganizational SkillsTime ManagementPresentation Skills

Tools & Technologies

Premier PredictCTMS

Certifications & Qualifications

Licensed Health-Care Professional

Industry Keywords

Clinical ResearchStudy Start-UpSite ActivationProject TimelinesClient Objectives

About the role

Key responsibilities & impact

Coordinate and collaborate with functional leads to deliver site activation
Organize and oversee strategic efforts for quality and efficient site activation delivery according to contractual obligations
Lead Site ID Kick Off Meetings and attend internal and external kick-off meetings
Understand client objectives, timelines, and study start-up strategy; review study budget and start-up scope
Oversee SSU and clinical activation deliveries in alignment with project timelines and strategy
Update Premier Predict/study projections through site activation
Collaborate with Project Strategist, Medical Informatics, Medical Affairs, PM, RSMs, CLs, and SSU Country Leads to finalize country mix and site selection
Escalate and track risks to PM and Sponsor and identify mitigation strategies
Use data to drive decisions, next steps, and team communication
Propose proactive solutions for risks or issues affecting site activation delivery
Oversee and support CTMS data entry through site activation to ensure data quality
Provide rationale for delays and contingency plans when forecasted timelines are not achieved
Monitor and analyze project/program site activation status and provide metrics
Provide progress updates to internal teams, clients, and upper management during weekly teleconferences and as needed

Requirements

What you’ll need

Undergraduate degree or its international equivalent in clinical, science, or a health-related field from an accredited institution is preferred
Licensed health-care professional is preferred
5 years professional experience as a CL, RSM, PM, SSUA, or equivalent
Demonstrated ability in leadership of a team of individuals in study start-up and across other functions
Understanding of project financial aspects and adherence to project timelines and study budget
Excellent interpersonal skills and ability to collaborate and build an effective team
Comfortable in customer-facing meetings such as Bid Defense Meetings
Excellent organizational, time-management, presentation, technical, and written/verbal communication skills
Strong knowledge of ICH/GCP regulations

Benefits

Comp & perks

Comprehensive benefits package, which may include health insurance, retirement plans, and paid time off
Flexibility and balance to support your life requirements
Skills and opportunities to excel at work