Parexel

Senior Clinical Research Associate – Oncology

Parexel

contract

Posted on:

Location Type: Remote

Location: France

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Job Level

Senior

Tech Stack

AEMGoogle Cloud Platform

About the role

  • Oversight of Monitoring Responsibilities and Study Conduct
  • Ensuring regulatory, ICH-GCP and protocol compliance.
  • Verifies the process of obtaining informed consent has been adequately performed and documented for each subject as required.
  • Manages reporting of protocol deviations and appropriate follow up.
  • Documents activities via follow up letters, monitoring reports, communication logs, and other required project documents as per SOPs and CMP and SMP.

Requirements

  • Bachelor’s degree or Registered Nurse (RN) in a related field or equivalent combination of education, training, and experience.
  • Networking and relationship building skills.
  • Ability to communicate effectively and appropriately with internal and external stakeholders.
  • Ability to adapt to changing technologies and processes.
  • Proficiency in local language is required.
  • Advanced level or fluency in English is required.
Benefits
  • Health insurance
  • Professional development opportunities
Applicant Tracking System Keywords

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

Hard Skills & Tools
regulatory complianceICH-GCPprotocol complianceinformed consentprotocol deviationsSOPsCMPSMP
Soft Skills
networkingrelationship buildingeffective communicationadaptability
Certifications
Bachelor's degreeRegistered Nurse (RN)