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Syneos Health

Project Manager II – Alzheimer’s

Syneos Health

Project Manager overseeing interdisciplinary clinical research studies ensuring compliance with GCP at Syneos Health. Collaborating with project teams to deliver quality results on time and within budget.

Posted 4/15/2026full-timeRemote • New Jersey • 🇺🇸 United StatesMid-LevelSeniorWebsite

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
  • May participate in bid defense meetings where presented as potential project manager

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
  • 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

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools
project managementclinical researchGCPSOPregulatory compliancefinancial performance managementrisk mitigationstudy managementdatabase managementinspection readiness
Soft Skills
organizational skillstime managementindependent workcommunication skillspresentation skillsinterpersonal skillsrelationship buildingproblem-solvingteam leadershipcontingency planning
Certifications
Bachelor’s Degree in life sciencesBachelor’s Degree in MedicineBachelor’s Degree in PharmacyBachelor’s Degree in Nursing