Site Care Partner – Temporary Contract

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

📋 Description

• Contribute to the country strategy, site planning, and site recommendations by leveraging regional site insights and performance metrics.

• Assist with local requirements for the import and export of investigational medical products and ancillary supplies.

• Qualify and activate designated investigative sites in line with global site and study strategies.

• Provide regional and country-specific input for outreach surveys, protocol feasibility, standard of care, and local medical practices.

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

• Lead site recruitment planning and achieve targets for global, country, and local enrollment.

• Ensure regular communication with investigative sites concerning recruitment and data-entry timelines.

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

• Ensure quality and consistency in monitoring delivery while promoting efficiencies and best practices in monitoring.

• Collaborate with Study Monitors, Investigator Contracts Leads, Site Activation Partners, and Clinicians to enhance communication and improve site-level quality.

• Act as the main client liaison for investigative sites throughout the study lifecycle.

⛳️ Requirements

• Proven experience in project management.

• Strong audit background.

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

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

• Proficient and effective communication skills with both internal and external stakeholders.

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

• Bachelor's degree or Registered Nurse designation in a relevant field, or equivalent education, training, and experience.

• Minimum of 7 years of experience when qualifying through the equivalent combination pathway.

• Proven site management experience with prior roles as a site monitor.

• Demonstrated experience in study start-up, from site activation to conduct and closeout activities.

• Familiarity with quality and regulatory requirements, including country-specific GCP standards.

• Strong verbal and written English communication skills.

• Willingness to travel throughout Türkiye.

🏝️ Benefits

• Opportunities for continuous learning.

• Pathways for career exploration and skill development.

• Diverse teams within a growth-oriented environment.

• Full-time employment.