Senior Clinical Research Associate, Contractor – Turkey – Home based
- Türkiye
- Kontrat
- Tam zamanlı
- Conduct all types of visits - site qualifications, initiation, interim monitoring, site management and study close-out visits
- Review study subject safety information and informed consent and conduct source document verification for compliance, patient safety, and veracity of data
- Actively participate in study team and investigator meetings
- Compile and ensure completeness of regulatory documents and ethical submission documentation and review study subject safety information and informed consent and study material (e.g. CRFs, manuals)
- Excellent interpersonal, oral, and written communication skills in English and local language
- Superior organizational skills with attention to details, and the ability to work independently
- Broad understanding of clinical research principles and process
- Proficiency in Microsoft Office, CTMS and EDC Systems
- At least two years independent on-site clinical monitoring experience
- Demonstrable experience of handling multiple protocols across a range of therapeutic indications
- Four-year college curriculum in life sciences, OR Two-year college curriculum or equivalent education / training (nursing degree or equivalent life science degree)
- Ability to meet the travel requirements of the job
Vacancies in Turkey