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Parexel

Global Study Associate – FSP

Parexel

. Support Phase 1, 2, 3, and 4 clinical studies with guidance .

Posted 11/11/2026full-timeRemote • Spain, Germany, Italy, Poland, United KingdomMid-Level💰 €42,000 - €45,000 per yearWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates expertise in managing clinical studies, including oversight of the Trial Master File, adherence to GCP regulations, and coordination of vendor activities. Proficient in study documentation, data review, and effective communication within cross-functional teams.

Highest-signal resume keywords
Clinical Study ManagementGood Clinical Practice (GCP)Trial Master File OversightVendor CoordinationMicrosoft Office Suite

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Clinical Study ManagementStudy Documentation PreparationData Review and Query ResolutionSite MonitoringStudy Tracking and MaintenanceKnowledge of GCP RegulationsUnderstanding of Study PhasesDatabase ManagementTrial Master File ManagementCTMS Knowledge
Soft Skills
Verbal CommunicationWritten CommunicationTeam CollaborationTask PrioritizationIndependent Work
Tools & Technologies
Veeva VaultSmartsheetSharePointCTMS
Industry Keywords
Clinical TrialsSOPsStudy FeasibilityStudy Close-Out ActivitiesRisk ManagementQuality AssuranceCross-Functional AlignmentClinical Development

Tech Stack

Tools & technologies
Vault

About the role

Key responsibilities & impact
  • Support Phase 1, 2, 3, and 4 clinical studies with guidance
  • Support study and site feasibility, start-up, maintenance, and close-out activities
  • Manage study and site essential document review, collection, and tracking
  • Support preparation and maintenance of study documents and manuals
  • Provide oversight of the Trial Master File
  • Ensure study documents are received, reviewed, and filed according to SOPs, GCP, and applicable regulations
  • Organize study-related meetings, prepare agendas, take minutes, and maintain risk, issue, and decision logs
  • Lead and present at study-related meetings as required
  • Perform site monitoring and co-monitoring visits
  • Address internal and site quality assurance findings from audits
  • Coordinate and oversee third-party vendor activities
  • Perform study tracking and maintenance, including status, enrollment, site queries, deviations, and study-level documents and plans
  • Participate in clinical trial team meetings and collaborative efforts
  • Support study site oversight and review site performance metrics and monitoring reports
  • Support study data activities, including data review, query creation and resolution, deviation reviews, and safety reviews
  • Provide cross-functional oversight of CRO and vendor activities
  • Review and verify contracted vendor activities and invoices
  • Support study reporting and tracking using applicable systems and technology
  • Support study leads in cross-functional alignment of study timelines
  • Complete required training, timesheets, expense reports, and CV updates
  • Comply with Parexel processes, ICH-GCPs, and applicable requirements

Requirements

What you’ll need
  • Strong verbal and written communication skills
  • Ability to work independently and as part of a team
  • Advanced knowledge of Microsoft Word, Excel, and PowerPoint
  • Ability to prioritize and manage multiple tasks simultaneously
  • A BA or BS degree, a nursing degree, or an equivalent qualification
  • At least 3 years of experience in clinical studies as a SCRA or Lead CRA
  • Working knowledge of Good Clinical Practice (GCP) regulations and Standard Operating Procedures
  • Understanding of study phases and their application to clinical development
  • Working knowledge of electronic systems, including the Trial Master File and CTMS (e.g., Veeva Vault, Smartsheet, SharePoint)
  • Knowledge of computer applications in database management
  • 10% to 20% travel may be required

Benefits

Comp & perks
  • Premium salary
  • Attractive benefits
  • Medical care plan: Health, Dental & Vision
  • Life Assurance
  • Excellent work environment
  • Culture of teamwork and collaboration
  • Innovative technology
  • Excellent training
  • Paid time off
  • Life insurance
  • Health insurance
  • Additional benefit offerings in accordance with applicable plans
  • Potential eligibility for additional incentives, bonuses, or other compensation programs