Senior Clinical Project Manager, Associate Director – Global Role, Multisponsor

Syneos Health

Clinical Sr Project Manager managing clinical research projects ensuring compliance with regulatory requirements. Leading cross-functional teams to achieve project goals, timelines, and budgets.

Posted 5/30/2026full-timeRemote • Arizona, Maine, North Carolina, Ohio, Rhode Island • 🇺🇸 United StatesSenior💰 $114,000 - $210,900 per yearWebsite

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

project managementclinical researchGood Clinical Practices (GCP)Standard Operating Procedures (SOP)regulatory requirementsfinancial performance managementTrial Master Filesclinical monitoring proceduresdrug development processinspection readiness

Soft Skills

communication skillspresentation skillsinterpersonal skillstime managementindependent workflexibilitymentoringmulti-taskingdeadline managementquality work

Tools & Technologies

tracking toolsanalysis tools

Industry Keywords

clinical research organization (CRO)therapeutic experienceICH guidelineslife sciencesMedicinePharmacyNursing

About the role

Key responsibilities & impact

Manages a project as Project Manager overseeing interdisciplinary clinical research programs ensuring compliance with Good Clinical Practices (GCPs), relevant Standard Operating Procedures (SOPs) and regulatory requirements
Acts as primary liaison between the Company and the Customer to ensure project launch, conduct, and closeout according to the Customer’s and the Company's contractual agreement
Leads clinical team to ensure quality, timelines and budget management
Accountable for the financial performance of assigned projects
Accountable for all project deliverables for assigned projects and/or project regions
Coordinates activities and deliverables of all project conduct partners and proactively identifies and manages issues
Maintains and evaluates project progress by maintaining timelines and other tracking/analysis tools
Responsible for project management components of inspection readiness for all aspects of the project conduct, including Trial Master Files
Prepares project management reports for clients and management

Requirements

What you’ll need

Bachelor’s Degree (or equivalent) level of qualification in life sciences, Medicine, Pharmacy, Nursing or related field or equivalent combination of education and experience
Strong knowledge of Good Clinical Practice/ICH guidelines, regulatory requirements, drug development process and clinical monitoring procedures
Clinical research organization (CRO) and relevant therapeutic experience preferred
Strong ability to manage time and work independently
Ability to embrace new technologies
Excellent communication, presentation, interpersonal skills, both written and spoken
Flexibility and the ability to mentor and manage new staff and to handle multiple tasks to meet deadlines delivering high quality work in a dynamic environment
Ability to travel as necessary (approximately 25%)

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