Site Care Partner – Temporary Contract

🔥 0 minutes ago

🇹🇷 Turkey – Remote

⏰ Full Time

🟠 Senior

🔴 Lead

🪙 Affiliate Manager

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Parexel

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1983

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 Venture Round on 1990-01

Consulting • Healthcare • Logistics

Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.

📋 Description

• Provide input into country strategy, site planning, and site recommendations using regional site knowledge and performance metrics • Support local requirements for importation and exportation of investigational medical products and ancillary supplies • Qualify and activate assigned investigative sites according to global site and study strategies • Provide country and regional input to outreach surveys, protocol feasibility, standard of care, and local medical practices • Conduct site start-up activities, including PTA, activation checklist coordination, ICD finalization, and SIV management • Drive site recruitment planning and delivery against global, country, and local enrollment targets • Maintain regular communication with investigative sites regarding recruitment and data-entry timelines • Act as the operational point of contact for site questions and escalate issues to appropriate teams • Assure quality and consistency in monitoring delivery and promote monitoring efficiencies and best practices • Coordinate with Study Monitors, Investigator Contracts Leads, Site Activation Partners, and Clinicians to improve communications and site-level quality • Serve as the primary client contact for investigative sites throughout the study lifecycle

🎯 Requirements

• Experience in project management • Solid audit experience • Strengths in site management, relationship building, and cross-functional collaboration • Experience in clinical research site start-up, conduct, and closeout in a regulated environment • Clear and effective communication with internal and external stakeholders • Patient-focused mindset, strong attention to detail, and proactive risk identification • Bachelor's degree or Registered Nurse designation in a related field, or equivalent combination of education, training, and experience • At least 7 years of experience when qualifying through the equivalent combination pathway • Demonstrated site management experience with prior experience as a site monitor • Demonstrated experience in study start-up through site activation, and conduct and closeout activities • Knowledge of quality and regulatory requirements, including country-level GCP requirements • Strong verbal and written communication skills in English • Ability to travel across Türkiye

🏖️ Benefits

• Continuous learning opportunities • Career path exploration and skill expansion • Diverse teams and growth-oriented environment • Full-time employment