Project Manager II, Senior Project Manager – Early Phase Experience Required

Syneos Health

Project Manager overseeing interdisciplinary clinical research studies ensuring compliance and timely delivery at Syneos Health. Acts as a liaison between the Company and the Customer.

Posted 7/28/2026full-time🇨🇳 ChinaSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing interdisciplinary clinical research studies while ensuring compliance with Good Clinical Practice (GCP) and regulatory requirements. Proven ability to lead project teams, manage budgets, and develop strong client relationships to drive successful project outcomes.

Highest-signal resume keywords

Project ManagementGood Clinical Practice (GCP)Clinical Research Organization (CRO) ExperienceFinancial Performance AccountabilityExcellent Communication Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Project PlanningRegulatory ComplianceStudy ManagementRisk Mitigation StrategiesDatabase Management

Soft Skills

Organizational SkillsTime ManagementInterpersonal SkillsPresentation Skills

Industry Keywords

Clinical ResearchTherapeutic Area ExpertiseInspection ReadinessStandard Operating Procedures (SOPs)Interdisciplinary Collaboration

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Manages a project as a project manager overseeing interdisciplinary clinical research studies and ensures compliance with GCP, relevant SOP’s, and regulatory requirements.
Acts as a primary liaison between the Company and the Customer to ensure timely study launch, conduct, and closeout according to the Customer’s and the Company’s contractual agreement.
Lead project team to ensure quality, timelines and budget management.
Accountable for the financial performance of each project.
Coordinate activities and deliverables of all study conduct partners and proactively identify and manage issues.
Ensure studies are conducted in compliance with GCP, relevant SOP’s and regulatory requirements.
Accountable for all project deliverables for each project assigned.
Responsible for quality and completeness of TMF for assigned projects.
Accountable for maintenance of study information on a variety of databases and systems.
Responsible for study management components of inspection readiness for all aspects of the study conduct.
Oversight for development and implementation of project plans.
Plan, coordinate and present at internal and external meetings.
Prepare project management reports for clients and management.
Developing contingency planning and risk mitigation strategies to ensure successful delivery of study goals.
Develops strong relationships with current clients to generate new and/or add-on business for the future.

Requirements

What you’ll need

Bachelor’s Degree (or equivalent) level of qualification in life sciences, Medicine, Pharmacy, Nursing or equivalent combination of education and experience.
Clinical research organization (CRO) and relevant therapeutic experience preferred.
Strong knowledge of Good Clinical Practice/ICH guidelines and other applicable regulatory requirements.
Strong organizational skills.
Strong ability to manage time and work independently.
Direct therapeutic area expertise.
Ability to embrace new technologies.
Excellent communication, presentation, interpersonal skills, both written and spoken.
Ability to travel as necessary (approximately 25%).

Benefits

Comp & perks

We are passionate about developing our people, through career development and progression;
supportive and engaged line management;
technical and therapeutic area training;
peer recognition and total rewards program.
We are committed to building an inclusive culture – where you can authentically be yourself.