As the world's largest FSP organization, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. As a Clinical Research Coordinator at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
Facilitating the coordination and execution of clinical research studies, including participant recruitment, enrollment, and follow-up activities. Collaborating with principal investigators, study sponsors, and regulatory authorities to ensure compliance with study protocols, regulatory requirements, and ethical standards. Collecting and maintaining accurate and complete clinical trial data, including documentation of adverse events, protocol deviations, and study outcomes. Managing study-related documentation, including informed consent forms, case report forms, and regulatory submissions. Providing support and guidance to study participants, including education, counseling, and assistance with study-related procedures.
Bachelor's degree in a relevant scientific discipline or healthcare-related field. Previous experience working in clinical research or healthcare settings preferred. Knowledge of clinical research regulations, including FDA/EMA regulations, ICH-GCP guidelines, and HIPAA requirements. Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Competitive base salary and performance related incentives Health and wellbeing programs including medical, dental, and vision coverage where applicable Retirement and pension plans Life assurance and disability coverage Employee assistance programs and wellbeing resources Learning and development opportunities through structured training and career pathways
Inclusion and Accessibility We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
Project Specialist, Full Time, Day Shift in olive branch at Unknown Company
This position is listed as full time and onsite.