Senior Project Specialist – Sponsor Dedicated

Syneos Health

Responsible for planning and coordinating clinical trial activities according to ICH-GCP at Syneos Health. Collaborate with trial teams to ensure timely and efficient trial conduct.

Posted 7/28/2026full-timeRemote • Maine, Montana, North Carolina, Ohio, Rhode Island • 🇺🇸 United StatesSenior💰 $47,000 - $79,900 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in project management for clinical trials, ensuring compliance with ICH-GCP guidelines and local regulatory demands. Proficient in managing trial correspondence, planning clinical trial supplies, and compiling data for reporting.

Highest-signal resume keywords

Project Management in Clinical TrialsFamiliarity with ICH-GCP GuidelinesClinical Trial Supplies PlanningStrong Communication SkillsKnowledge of Local Regulatory Demands

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Project ManagementClinical Trial PlanningData CompilationRegulatory ComplianceBudget Management

Soft Skills

Strong CommunicationProblem Solving

Tools & Technologies

Trial Management SystemsReporting Tools

Industry Keywords

ICH-GCPClinical TrialsRegulatory DemandsEthics/Authorities

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Responsible for planning, coordination and conduct of trial activities according to ICH-GCP
Assures seamless conduct of trials within defined timelines
Collaborate with trial team members and interface functions
Independently manage correspondence and budget overviews
Address and answer complex questions from trial teams and sites
Support planning of clinical trial supplies
Keep overview of records and update to address regulatory demands
Organize and supervise trial related wrap-up activities
Ensure appropriate set-up and maintenance of systems and tools
Compile data for internal and external reporting purposes

Requirements

What you’ll need

Experience in project management in clinical trials
Familiarity with ICH-GCP guidelines
Strong communication skills
Ability to manage correspondence and complex reports
Experience with clinical trial supplies planning
Knowledge of local regulatory demands from Ethics/Authorities

Benefits

Comp & perks

Health benefits to include Medical, Dental and Vision
Company match 401k
Eligibility to participate in Employee Stock Purchase Plan
Eligibility to earn commissions/bonus based on company and individual performance
Flexible paid time off (PTO) and sick time