Clinical Research Associate I/II
Precision For Medicine
full-time
Posted on:
Location Type: Remote
Location: Turkey
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Tech Stack
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.).
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.
- At least 6 months of experience as a CRA in either a CRO or pharmaceutical/biotech industry or equivalent, relevant experience and/or demonstrated competencies.
- Site management experience or equivalent experience in clinical research.
- Oncology monitoring experience.
- Excellent communication and organizational skills are essential. A team player.
- 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
- Health insurance
- Flexible work arrangements
- Professional development opportunities
- Paid time off
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)oncology monitoringregulatory submissionssite managementICH-GCPSOPsclinical study monitoringdata recordingprotocol adherencehealthcare discipline
Soft Skills
communication skillsorganizational skillsteam playerclient focused approach
Certifications
university degree in life sciencelicensed health care professional