Site Care Partner – 1 Year 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.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

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 sites using global site and study operations 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 enrollment targets • Maintain communications with investigative sites to track status and study-goal delivery • Act as the operational point of contact for site questions and escalate issues to appropriate teams • Assure quality and consistency in monitoring delivery and drive monitoring efficiencies • Coordinate with Study Monitor, Investigator Contracts Lead, Site Activation Partner, and Clinician to improve communication and site-level quality

🎯 Requirements

• Experience in project management • Solid audit experience • Strengths in site management, relationship building, and cross-functional collaboration • Experience working in clinical research site start-up, conduct, and closeout in a regulated environment • Ability to communicate clearly and effectively with internal and external stakeholders • Patient-focused mindset, strong attention to detail, and proactive approach to 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) • Demonstrated experience in site management with prior experience as a site monitor • Demonstrated experience in study start-up activities through site activation, and in conduct and closeout activities • Knowledge of quality and regulatory requirements, including country-level GCP requirements that may differ from client procedures • Strong verbal and written communication skills in English • Ability to travel across Türkiye

🏖️ Benefits

• Diverse teams and continuous learning opportunities • Career paths and opportunities to expand skills across clinical research