Clinical Research Associate

Leading company

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/Leader.

This candidate will also be responsible to coordinate all necessary activities required to set up a study, to participate 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 a candidates to become a team member for clinical studies which conduct in Ankara, Turkey.

A successful candidate should have:

• University degree in Medical Sciences (Pharmacy, Biology, Chemistry, Genetics, Medicine or a related field)
• Preferably 2-3 year experience in the related field (Good knowledge of ICH-GCP and local regulations for experienced candidates.)
• 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 detail,
• Ability to travel (Valid passport required in the case of international business travel),
• No military obligation (for male candidates).

This is a sponsor-dedicated position.