Site Activation Partner I

🔥 4 minutes ago

🌐 Argentina, Brazil – Remote

🇦🇷 Argentina – Remote 🇧🇷 Brazil – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🪙 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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ICON plc

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1990

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • Logistics

ICON plc is a global provider of clinical, consulting, and commercial services across various sectors in the healthcare and pharmaceutical industries. They offer a wide range of clinical solutions, including decentralised clinical trials, cardiac safety solutions, early clinical laboratories, and medical imaging. ICON also provides technology solutions that support drug development from early phases to post-marketing. Their therapeutic expertise spans cardiovascular, oncology, internal medicine, and more, with a strong focus on transformative therapies like cell and gene therapies and biosimilars. ICON is recognized as a leading Contract Research Organisation (CRO), regularly providing thought leadership and contributing to industry publications and events. Their services are tailored to optimize clinical trials, offer regulatory intelligence, and deliver real-world evidence through robust data analysis and patient-centric solutions.

📋 Description

• Facilitate the initiation of clinical trials, ensuring compliance with regulatory requirements • Deliver site start-up and activation work to a high standard • Prepare and submit regulatory documents, such as clinical trial applications and ethics committee submissions • Coordinate with internal and external stakeholders to obtain approvals and authorizations for study initiation • Maintain accurate and up-to-date records of regulatory submissions and approvals • Support study teams in developing study documents, including protocols, informed consent forms, and investigator brochures • Participate in study start-up meetings and provide input on regulatory requirements and timelines

🎯 Requirements

• Bachelor's degree in life sciences or a related field • Previous experience in clinical research or regulatory affairs preferred but not required • Required experience with local Ethics Committee requirements and submission processes • Strong attention to detail and organizational skills • Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams • Ability to work independently and manage multiple tasks simultaneously in a fast-paced environment • Legal right to work in the country where the role is based

🏖️ Benefits

• Competitive base salary and performance related incentives • Health and wellbeing programmes including medical, dental, and vision coverage where applicable • Retirement and pension plans • Life assurance and disability coverage • Employee assistance programmes and wellbeing resources • Learning and development opportunities through structured training and career pathways