Site Activation Partner

🕒 July 6

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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

• Lead or support operational activities from study start-up to close-out for assigned studies and investigator sites • Initiate and coordinate activities and essential document management for high-quality Investigator Initiation Packages leading to site initiation approval • Support issue resolution and escalate site issues when applicable • Manage and coordinate supporting roles to ensure timely site activation and operational activities • Collaborate with in-country regulatory groups and provide applicable site documents for regulatory and ethics submissions • Update and maintain clinical trial systems tracking site compliance and performance within project timelines • Identify and resolve investigator site issues

🎯 Requirements

• School diploma/certificate with equivalent combination of education, training and experience • BS/BA or bachelor’s degree in life sciences preferred • Minimum 2 years relevant experience in a clinical trials environment and clinical site activation • Experience working in the pharmaceutical industry or CRO is an asset • Knowledge of clinical trial methodologies, ICH/GCP, FDA, and global and local country regulations • Must be fluent in the local language and English • Multi-language capability is an asset