Contractor Senior Clinical Research Associate - 1 FTE - Turkey - Remote

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Requirements:

• At least two years of independent clinical monitoring experience
• Demonstrable experience in 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

Responsibilities:

• 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)