Clinical Project Manager İş İlanı

QUALIFICATIONS AND JOB DESCRIPTION

• University degree in life sciences (Pharmacy, Biology, Chemistry, Genetics, Medicine or a related field),
• Minimum 5 years of on-site monitoring experience in clinical studies,
• Excellent command of written and spoken English,
• Good knowledge of MS Office applications,
• Strong project management skills together with a solution oriented teamwork attitude,
• Self-motivated personality,
• Good communication skills at all levels,
• Good time management, presentation, planning and organizational skills,
• Exceptional attention to detail,
• Ability to travel (Valid passport required in the case of international business travel)
• No military obligation. (for male candidates)

İŞ TANIMI

We are looking for a Clinical Project Manager to become a team member for local and international clinical studies.

Brief Job Description:

The candidate will be responsible for conducting clinical studies, managing & monitoring study sites in accordance with Study Protocols, SOPs, ICH-GCP (International Clinical Harmonization-Good Clinical Practice) and local regulations. She/he will manage multiple projects, support Project Teams.

She/he will also be responsible for coordinating all necessary activities required to set up a study, participating in the start-up processes including reviewing protocols, reviewing Case Report Forms (CRFs), preparing Informed Consent Forms (ICFs), developing study documents, organizing investigator and study specific training meetings, presenting study related material and ensuring that the study meets planned timelines and high quality data is generated.

This is a sponsor-dedicated position.