Site Activation Partner I – Temporary Contract

🕒 Yesterday

🇹🇷 Turkey – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🪙 Affiliate Manager

🚫👨‍🎓 No degree required

👻 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

• Initiate and coordinate clinical trial site activation activities and essential document management • Compile high-quality Investigator Initiation Packages leading to site initiation approval • Prepare, validate, and submit regulatory documents including IIP, IRB approval forms, and FDA 1572/Attestation Forms • Coordinate supporting roles and activities to ensure timely site activation • Support central and local ethics committee packages, submissions, approvals, and communications • Support investigators with local IRB workflows from preparation through approval • Prepare, handle, and distribute clinical documentation and reports • Support and implement activities in the Shared Investigator Platform • Coordinate essential documents and updates throughout study conduct, including protocol amendments, FDA 1572/Attestation revisions, and annual ethics approvals • Maintain IRB/Ethics and other committee activities • File documents to the Trial Master File and assist with periodic quality reviews • Update and maintain clinical trial systems tracking site compliance and performance • Support investigator sites and study teams with audit and inspection responses • Maintain communication with study teams and investigator sites; provide country/site updates • Disseminate ethics approvals and communicate site approvals to stakeholders • Conduct site personnel awareness sessions as needed • Identify and resolve investigator site issues and support corrective and preventive actions • Act as a subject matter expert or point of contact for site activation, systems, processes, and global initiatives • Support mentoring of new hires • Complete required training, timesheets, expense reports, and CV updates • Maintain compliance with Parexel processes, ICH-GCP, and applicable requirements

🎯 Requirements

• School diploma or certificate with equivalent combination of education, training and experience, or Bachelor of Science/Bachelor of Arts or equivalent • Minimum 2 years relevant experience in clinical site management • Experience working in the pharmaceutical industry or CRO in study site activation preferred • Knowledge of clinical trial methodologies, ICH/GCP, FDA, and global and local country regulations • Must be fluent in Turkish and English • Effective verbal and written communication skills • Good technical skills and ability to learn and use multiple systems • Knowledge of clinical research and development processes and clinical trial operational elements • Understanding of quality expectations and right-first-time principles • Understanding of basic medical terminology and GCP requirements • Proficiency in computer operations, Microsoft Suite, CTMS, eTMF, eISF, document exchange portals, Shared Investigator Platform, and ethics/regulatory portals • Ability to work independently and as a team member • Ability to organize tasks, manage time and priorities, and multitask • Ability to work flexible/off-hours in a global environment when applicable • Able to travel as needed, including possible international travel

🏖️ Benefits

• Temporary contract • Full-time employment