Education: Bachelor's degree or related field
- Assisting in the monitoring of clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. - Supporting site management activities, including documentation preparation, data entry, and tracking site performance metrics. - Collaborating with cross-functional teams to facilitate communication and address site-related issues effectively. - Maintaining accurate records of site activities and contributing to the preparation of monitoring reports. - Participating in training and development initiatives to enhance knowledge and skills in clinical trial management.
You will bring relevant clinical research experience, along with the following qualifications and skills.
- Bachelor's degree in a relevant field such as life sciences, healthcare administration, or clinical research. - Some experience in clinical research, site management, or related administrative roles is preferred but not mandatory. - Strong organizational skills and attention to detail, with the ability to manage multiple tasks effectively. - Basic knowledge of clinical trial processes and regulatory requirements is a plus. - Excellent communication and interpersonal skills, with the ability to work collaboratively within a team environment. - Willingness to travel as required (approximately 25%)
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 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
Benefits may vary depending on role and location.
Visit our careers site to about the benefits ICON offers.
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here .
Are you a current ICON Employee? Please click here to apply
Search Study Delivery Specialist jobs near Poland, Warsaw → Browse all live jobs
This posting was published by ICON plc on their own careers system and is shown here with a direct link to apply there. Employers: for corrections or removal, contact jobs@veritahire.com.