Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
Scoutfield Logo

See all jobs on Scoutfield

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Syneos Health

Project Manager, eCOA Manager

Syneos Health

. Provide customer-focused management of Clinical Surveillance & Training (CST) scoped services to support scientific integrity and data quality in clinical trials .

Posted 9/18/2026full-timeRemote • ArgentinaMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates expertise in Clinical Surveillance and Training management, ensuring scientific integrity and data quality in clinical trials. Proficient in project leadership, stakeholder communication, and compliance with Good Clinical Practice and regulatory guidelines.

Highest-signal resume keywords
Clinical Surveillance ManagementProject LeadershipGood Clinical Practice (GCP)Study CoordinationMS Office Proficiency

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Study CoordinationProject ManagementDocumentation ManagementMetric ReportingRisk IdentificationTraining DevelopmentTemplate DevelopmentLicense ProcurementScale Translation ManagementAudit Participation
Soft Skills
Communication SkillsInterpersonal SkillsOrganizational SkillsTime ManagementCustomer Service
Tools & Technologies
Study Training and Engagement PortalTrial Master FileMS Office Applications
Industry Keywords
Clinical TrialsContract Research Organization (CRO)PharmaceuticalBiotechnologyRater Training VendorInternational Conference on Harmonization (ICH)

About the role

Key responsibilities & impact
  • Provide customer-focused management of Clinical Surveillance & Training (CST) scoped services to support scientific integrity and data quality in clinical trials
  • Liaise with customers, vendors, and investigative sites from project start-up through final customer deliverables
  • Represent the CST team on small to large-sized studies or programs
  • Interact with functional groups, vendors, license holders, Key Opinion Leaders, and Sponsors
  • Serve as Project Lead in CST stand-alone projects and Functional Lead in full-scope or multiple-protocol projects
  • Manage CST deliverables for scoped-service vendors, scale license holders, and/or KOLs
  • Manage license procurement, scale translation requirements, and paper scale worksheet development
  • Manage CST service-related documentation and templates, including development and testing of the Study Training and Engagement Portal
  • Ensure quality, timely delivery, and implementation of CST services
  • Develop and maintain study-specific CST plans in accordance with SOPs and Work Instructions
  • Contribute to functional project plans
  • Provide status updates to internal and Sponsor project teams, including delivery risks and timeline delays
  • Serve as the central point of contact for CST-related project issues
  • Create and maintain CST metric reports for client delivery
  • Attend internal and Sponsor meetings as the lead CST representative
  • Maintain project documentation and ensure complete and accurate filing in the Trial Master File
  • Identify risks and develop mitigation plans
  • Participate in Sponsor, internal, or agency audits and inspections
  • Manage CST scope, out-of-scope activities, overburn, revenue recognition when delegated, invoice management, and/or KOL contracts and management
  • Plan, manage, and request CST resources and provide resource updates
  • Train and mentor internal team members

Requirements

What you’ll need
  • Bachelor’s Degree (or equivalent) level of qualification in Life Sciences, Medicine, Pharmacy, Nursing or related field equivalent preferred
  • Prior experience in study coordination, contract research organization (CRO), pharmaceutical, biotechnology or rater training vendor company preferred
  • Excellent written and spoken communication, presentation, and interpersonal skills
  • Good organizational, planning, customer service, and time management skills
  • Ability to multitask under tight deadlines while providing attention to detail
  • Ability to manage time and work independently
  • High level of competency in English language
  • Proficiency with MS Office Applications
  • Strong knowledge of Good Clinical Practice (GCP)/International Conference on Harmonization (ICH) guidelines and other applicable regulatory requirements
  • Ability to travel as necessary, up to 25%

Benefits

Comp & perks
  • Career development and progression
  • Supportive and engaged line management
  • Technical and therapeutic area training
  • Peer recognition
  • Total rewards program
  • Inclusive culture
  • Reasonable accommodations when appropriate