Precision Medicine Group

Senior Clinical Research Associate

Precision Medicine Group

full-time

Posted on:

Location Type: Remote

Location: Turkey

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Job Level

About the role

  • Monitor and own the progress of clinical studies at investigative sites.
  • Ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards.
  • Coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.).
  • Handle appropriately sized clinical trials and support Project Managers with trials that are larger in scope.
  • Train and mentor junior staff members.
  • Directly interact with clients, initiate payments, and participate in proposal activities, including development and client presentations.

Requirements

  • University degree in life science/pharmacy/other health related discipline or equivalent experience in a scientific or healthcare discipline or be a licensed health care professional.
  • 3.5 years or more as a CRA in either a CRO or pharmaceutical/biotech industry or equivalent, relevant experience and/or demonstrated competencies.
  • Significant site management experience or equivalent experience in clinical research.
  • Oncology monitoring experience.
  • Excellent communication and organizational skills are essential.
  • Evidence of a client focused approach.
  • Experience using computerized information systems, electronic spreadsheets, word processing and electronic mail required.
  • Ability to travel overnight. Up to 60% travel on average, based on regional requirements. International travel as needed.
  • Fluency in English and Turkish.
Benefits
  • Great company culture
  • High CRA retention rates
  • Flexibility in work/life balance
  • Influence in decision making
  • Support from direct line management
Applicant Tracking System Keywords

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

Hard Skills & Tools
clinical research associate (CRA)site managementoncology monitoringregulatory submissionsclinical trial managementprotocol adherenceSOPsICH-GCPdata reportingclient presentations
Soft Skills
communication skillsorganizational skillsclient focused approachmentoringtraininginterpersonal skillsproblem-solvingteam collaborationleadershipadaptability
Certifications
university degree in life sciencelicensed health care professional