Site Management Associate
Location
Romania
Posted
1 day ago
Salary
0
Seniority
Mid Level
Job Description
Site Management Associate
ICON plc
• Support the management of clinical trial sites by assisting with site monitoring activities • Ensure compliance with study protocols and maintain high standards of operational efficiency • Assist in the monitoring of clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines • Support site management activities, including documentation preparation, data entry, and tracking site performance metrics • Collaborate with cross-functional teams to facilitate communication and address site-related issues effectively • Maintain accurate records of site activities and contribute to the preparation of monitoring reports • Participate in training and development initiatives to enhance knowledge and skills in clinical trial management
Job Requirements
- Bachelor's degree in a relevant field such as life sciences, healthcare administration, or clinical research
- Global study operational level experience in clinical research, site management
- Strong organizational skills and attention to detail, with the ability to manage multiple tasks effectively
- Strong knowledge of clinical trial processes and regulatory requirements
- Excellent communication and interpersonal skills, with the ability to work collaboratively within a team environment
- Excellent English language skills
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
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