Site Activation Partner, I

This is a fully remote position, open to applicants in Poland.

📋 Description

• Execute site start-up and activation tasks to an exceptional standard

• Aid in the preparation and submission of regulatory documents, such as clinical trial applications and ethics committee submissions

• Collaborate with both internal and external stakeholders to secure the necessary approvals and authorizations for study commencement

• Ensure accurate and current records of regulatory submissions and approvals are maintained

• Assist study teams in the creation of study documents, including protocols, informed consent forms, and investigator brochures

• Engage in study start-up meetings and contribute insights regarding regulatory requirements and timelines

⛳️ Requirements

• Bachelor's degree in life sciences or a related discipline

• Previous experience in clinical research or regulatory affairs is preferred, though not mandatory

• Exceptional attention to detail and strong organizational abilities

• Outstanding communication and interpersonal skills, with the capability to collaborate effectively across diverse teams

• Capacity to work independently while managing multiple tasks concurrently in a dynamic environment

• Willingness to travel as necessary (approximately 5%)

• 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 including medical, dental, and vision coverage where applicable

• Retirement and pension plans

• Life assurance and disability coverage

• Employee assistance programs and wellness resources

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