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MSD

Associate Specialist, Clinical Research

MSD

Clinical Research Associate overseeing clinical trials in Portugal. Ensuring compliance and managing site relationships through the trial phases.

Posted 5/26/2026full-timeRemote • 🇵🇹 PortugalJuniorMid-LevelWebsite

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
clinical researchclinical trialsdata analysissite managementmonitoring activitiessite selectionsite qualificationreport preparationGCPICH
Soft Skills
communicationrelationship buildingproblem solvingorganizational skillsverbal communicationwritten communicationability to manage complex issues
Tools & Technologies
CTMSeTMFMS Officeclinical IT applications
Industry Keywords
clinical research lawsclinical research guidelinesphases of clinical trials

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Ensures the implementation of clinical trials in compliance with standards
  • Acts as primary site contact and manager throughout clinical research phases
  • Develops strong site relationships
  • Performs site management and monitoring activities
  • Participates in site selection and qualification activities
  • Conducts site visits and prepares reports in a timely manner
  • Communicates with investigators and site staff
  • Manages documentation in CTMS, eTMF, and other systems

Requirements

What you’ll need
  • Fluent in Portuguese and English (verbal and written)
  • Excellent communication skills
  • Solid understanding and practical knowledge of clinical research and the phases of clinical trials
  • Up-to-date knowledge of GCP/ICH and local clinical research laws and guidelines
  • IT skills (MS Office, clinical IT applications)
  • Ability to understand and analyze data and metrics
  • Capable of managing complex issues

Benefits

Comp & perks
  • Flexible work arrangements: Remote
  • Commitment to keeping the patient at the center of everything we do
  • Diverse and inclusive work environment