Clinical Research Associate (I-III)

This is an incredible CRA opportunity allowing all CRAs to monitor an average of 6 visits per month, allowing 𝐘𝐎𝐔 to decide what sites can be monitored remotely and which will need an in-person visit.

If you’re looking for an excellent work-life balance withr minimal red tape, flat hierarchy, and great flexibility to allow you and other CRAs to work on a maximum of 3 protocols and giving 𝐘𝐎𝐔 the option to work with multi-sponsors or on their FSP model.

With most sites regionalised specifically to the allocated CRA, we have developed an incredibly low staff turnover rate of 16% in the Turkey CRA team. If you're sick and tired of being limited in your work, being allocated protocols to fulfil a ludicrous amount of monitoring visits and would like to value quality over quantity, then this is certainly an opportunity worth exploring.

Responsibilities :

• Creates and implements subject enrolment strategies for assigned investigative sites.
• Conducts study site visits (pre-study, initiation, monitoring, and close-out) and completes site visit deliverables within given timelines in the Monitoring Plan.
• Ensures proper storage, dispensation, and accountability of all investigational product(s) and trial-related material.
• Participate and act as Lead CRA on studies where you can add assistance
• Maintains tracking records for assigned sites including tracking of subject status, subject case report form (CRF) retrieval / source document review (SCV), regulatory documents, and investigational product.

Experience / Qualifications