Site Care Partner – 1 Year Contract

This is a fully remote position, open to applicants in Turkey.

📋 Description

• Contribute insights towards the country strategy, site planning, and site recommendations utilizing regional site expertise and performance metrics.

• Assist with local requirements for the importation and exportation of investigational medical products and related supplies.

• Qualify and activate designated sites employing global site and study operations strategies.

• Provide country and regional insights to outreach surveys, protocol feasibility, standards of care, and local medical practices.

• Execute site start-up tasks, which include PTA, coordination of the activation checklist, finalization of ICD, and management of SIV.

• Drive site recruitment planning and ensure delivery aligns with enrollment targets.

• Maintain communication with investigative sites to monitor status and achieve study goals.

• Serve as the operational primary contact for site inquiries and escalate issues to the appropriate teams.

• Ensure quality and consistency in monitoring delivery while enhancing monitoring efficiencies.

• Collaborate with the Study Monitor, Investigator Contracts Lead, Site Activation Partner, and Clinician to enhance communication and site-level quality.

⛳️ Requirements

• Experience in project management.

• Strong audit background.

• Proficient in site management, relationship development, and cross-functional collaboration.

• Experience in clinical research site start-up, execution, and closeout within a regulated setting.

• Ability to communicate clearly and effectively with both internal and external stakeholders.

• Patient-centered mindset, keen attention to detail, and a proactive approach to risk identification.

• Bachelor's degree or Registered Nurse qualification in a related field, or equivalent combination of education, training, and experience (minimum of 7 years of experience).

• Proven experience in site management with prior site monitor experience.

• Demonstrated experience in study start-up activities through site activation, as well as conduct and closeout activities.

• Understanding of quality and regulatory standards, including country-specific GCP requirements that may differ from client procedures.

• Excellent verbal and written communication skills in English.

• Willingness to travel throughout Türkiye.

🏝️ Benefits

• Diverse teams and ongoing learning opportunities.

• Career advancement pathways and chances to enhance skills across clinical research.