Full-Time Senior Clinical Research Associate I

Preparation, conduct, and reporting of selection, initiation, routine and closeout monitoring visits

Site management, general administration of clinical research studies in Turkey

Contact for clinical investigators, vendors and support services in regard to study progress

Monitoring trial progress and ensuring that the project timelines are met

Facilitation of site budgets and contract negotiations

Effective and open communication within the project team

Delivering training of investigators, site staff and project teams

Preparation and delivering of presentations at Investigator’s Meetings

Preparation for and attendance at company’s audits; resolution of audit findings

Support to Regulatory Affairs in procurement of site regulatory documents

Maintenance of appropriate documentation regarding clinical site management

Participation in query resolution

University degree in Life Sciences, Pharmacy, or an equivalent combination of education, training and experience

Significant hands-on industry experience at a similar position, with full scope of monitoring responsibilities within Phase II/III Clinical Trials

Independent monitoring experience in Turkey and knowledge of the local clinical research environment

Experience in regulatory submissions, contract negotiations, site management and feasibility assessment

Fluent Turkish and English, both spoken and written

Team oriented with excellent communication and interpersonal skills including a positive and professional attitude to tasks and projects

Attention to detail, organizational and time-management skills

Valid driver’s license and ability to travel

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