Clinical Research Associate

MONITOR MEDİKAL ARAŞTIRMA VE DANIŞMANLIK TİC. LTD

Job Description:

Clinical Research Associate (CRA) will be responsible for conducting clinical studies, managing & monitoring of study sites in accordance with SOPs, ICH-GCP (International Clinical Harmonization-Good Clinical Practice) and local regulations. CRA will manage multiple projects, support Project Team and report directly to Clinical Project Manager.

This candidate will also be responsible to coordinate all necessary activities required to set up a study,toparticipate in the start-up process including reviewing protocols, reviewing CRFs, preparing Informed Consent forms, developing study documents, organizing and presenting at investigator meetings and study specific training meetings, to meet the planned study timelines and to generate high quality data.

Qualifications,

We are looking for preferably experienced candidates to become a team member for clinical studies.

A successful candidate should have:

• University degree in Medical Sciences (Pharmacy, Biology, Chemistry, Genetics, Medicine or a related field)
• Minimum 1 year experience in on-site monitoring of clinical studies,
• Excellent command of written and spoken English,
• Good knowledge of MS Office applications,
• Strong project management skills together with teamwork,
• Organised, creative and confident with good communication skills,
• Good time management,
• Excellent presentation, planning and organization skills,
• Exceptional attention to details,
• Ability to travel,
• No military obligation (for male candidates).