Senior Clinical Research Associate
New
P
Precision Medicine GroupClinical Research
Remote, TurkeyFull-TimeSenior
Salary not disclosed
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Job Details
- Languages
- English and Turkish
- Experience
- 3.5 years or more as a CRA
Requirements
- University degree in life science, pharmacy, or health-related discipline.
- 3.5 years or more experience as a CRA in CRO, pharmaceutical, or biotech industry.
- Significant site management experience.
- Oncology monitoring experience.
- Excellent communication and organizational skills.
- Evidence of a client-focused approach.
- Experience using computerized information systems, electronic spreadsheets, word processing, and email.
- Ability to travel overnight up to 60%.
- Fluency in English and Turkish.
Responsibilities
- Monitor and own the progress of clinical studies at investigative sites.
- Ensure clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations.
- Coordinate study setup activities including investigator identification and regulatory submissions.
- Conduct pre-study and initiation visits.
- Handle appropriately sized clinical trials and support Project Managers with larger scope trials.
- Train and mentor junior staff members.
- Interact directly with clients and initiate payments.
- Participate in proposal activities including development and client presentations.
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