Icon Job Opening for Multiple Positions Apply Now

Icon, a global leader in clinical research, is excited to announce job openings across various positions. Whether you’re an experienced professional or looking to advance your career in the clinical research field, Icon offers numerous opportunities to join a dynamic and innovative team. Apply now to be a part of a company dedicated to improving healthcare through rigorous scientific research.

Clinical Research Associate I/II/Sr.

Icon is seeking Clinical Research Associates at multiple levels (I, II, Sr.) to join their team. These roles involve monitoring clinical trials, ensuring compliance with regulatory requirements, and maintaining accurate documentation. Candidates should have a background in clinical research, strong attention to detail, and excellent communication skills. If you are passionate about clinical research and looking for an opportunity to grow, apply now to become part of Icon’s dedicated team.

Pharmacovigilance Reporting Associate

The Pharmacovigilance Reporting Associate position at Icon focuses on ensuring the safety of pharmaceutical products. This role involves monitoring and reporting adverse events, conducting safety assessments, and maintaining compliance with regulatory standards. Ideal candidates will have experience in pharmacovigilance, a keen eye for detail, and strong analytical skills. Join Icon and contribute to the critical task of ensuring drug safety for patients worldwide.

CRA I

Icon is hiring CRA I professionals to support clinical trials from start to finish. This role involves site monitoring, data collection, and ensuring that trials adhere to protocol and regulatory requirements. Candidates should have a degree in life sciences, excellent organizational skills, and a commitment to high-quality research. If you’re looking to start or advance your career in clinical research, apply now for the CRA I position at Icon.

Group Lead – TMF Operations

The Group Lead – TMF Operations role at Icon involves managing the Trial Master File (TMF) process for clinical trials. This position requires overseeing document management, ensuring compliance with regulatory standards, and leading a team of TMF specialists. Candidates should have extensive experience in clinical trial documentation, strong leadership skills, and a detail-oriented mindset. Apply now to lead TMF operations at Icon and ensure the integrity of critical trial documents.

Senior Pharmacovigilance Reporting Associate

Icon is looking for a Senior Pharmacovigilance Reporting Associate to join their pharmacovigilance team. This role involves advanced monitoring and reporting of adverse events, conducting in-depth safety analyses, and mentoring junior associates. Candidates should have significant experience in pharmacovigilance, strong analytical abilities, and excellent communication skills. Join Icon in this senior role and play a key part in safeguarding patient safety.

CRA II

The CRA II position at Icon involves more advanced responsibilities in clinical trial monitoring. This role includes overseeing multiple trial sites, ensuring data accuracy, and providing guidance to junior CRAs. Candidates should have experience as a CRA, strong project management skills, and a thorough understanding of clinical trial processes. Apply now for the CRA II role at Icon and take your career in clinical research to the next level.

Scientific Affairs Specialist I

As a Scientific Affairs Specialist I at Icon, you will support scientific research and regulatory activities. This role involves preparing scientific reports, coordinating with regulatory agencies, and assisting with product development documentation. Candidates should have a background in scientific research, excellent writing skills, and experience in regulatory affairs. Join Icon and contribute to the advancement of scientific knowledge and regulatory excellence.

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Clinical Research Associate I/II/Sr.

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Pharmacovigilance Reporting Associate

Group Lead – TMF Operations

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