Clinical Research Associate

New

Precision Medicine GroupClinical Trial Services

Remote, TurkeyFull-TimeMiddle

Salary not disclosed

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Job Details

Languages: English and Turkish
Experience: At least 6 months of experience as a CRA

Requirements

University degree in life science, pharmacy, or health-related discipline.
At least 6 months of CRA experience in CRO, pharmaceutical, or biotech industry.
Oncology monitoring experience.
Site management experience.
Experience with computerized information systems.
Excellent communication and organizational skills.
Fluency in English and Turkish.
Ability to travel overnight (up to 60%).

Responsibilities

Monitor clinical study progress at investigative sites.
Ensure compliance with protocol, SOPs, ICH-GCP, and regulations.
Identify investigators.
Prepare regulatory submissions.
Conduct pre-study visits.
Conduct initiation visits.
Manage study documentation and reporting.

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