Study Delivery Specialist

This is a fully remote position, open to applicants in Poland, +3 more countries.

📋 Description

• Assist in overseeing clinical trial sites, ensuring compliance with study protocols, regulatory standards, and Good Clinical Practice (GCP) guidelines.

• Aid in site management tasks, encompassing documentation preparation, data entry, and monitoring site performance metrics.

• Work collaboratively with cross-functional teams to enhance communication and resolve site-related challenges.

• Keep precise records of site activities and assist in the creation of monitoring reports.

• Engage in training and development programs to improve knowledge and skills in clinical trial management.

⛳️ Requirements

• A Bachelor's degree in a relevant discipline such as life sciences, healthcare administration, or clinical research.

• Prior experience in clinical research, site management, or similar administrative roles is desirable but not essential.

• Strong organizational abilities and meticulous attention to detail, with a capacity to effectively manage multiple tasks.

• Basic understanding of clinical trial processes and regulatory standards is advantageous.

• Exceptional communication and interpersonal skills, with the capability to work collaboratively in a team setting.

• Legal authorization to work in the country where the position is located.

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

• Health and wellness programs that may include medical, dental, and vision coverage where applicable.

• Retirement and pension plans.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

• Opportunities for learning and development through structured training and career pathways.