Site Activation Partner

🕒 August 27

🇨🇦 Canada – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🪙 Affiliate Manager

🚫👨‍🎓 No degree required

👻 Ghost score 24%

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

• Lead or support operational activities from study start-up to close-out for assigned studies and investigator sites • Ensure compliance with study timelines, prevailing laws, Good Clinical Practices, and sponsor standards • Initiate and coordinate activities and essential document management for high-quality Investigator Initiation Packages leading to site initiation approval • Support issue resolution and timely escalation of site issues • Manage and coordinate with supporting roles to ensure timely site activation and operational activities • Collaborate with in-country regulatory groups and provide applicable site documents, including for parallel regulatory authority and ethics submissions • Accurately 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 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 • Fluency in the local language and English • Multi-language capability is an asset