Site Activation Partner

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

📋 Description

• Oversee the commencement of clinical trials, ensuring adherence to regulatory standards.

• Execute site start-up and activation tasks to a high-quality benchmark.

• Prepare and file regulatory documents, including clinical trial applications and submissions to ethics committees.

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

• Ensure precise and current documentation of regulatory submissions and approvals is maintained.

• Assist study teams in the creation of study materials, such as protocols, informed consent documents, 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 comparable field.

• Prior experience in clinical research or regulatory affairs is preferred.

• Exceptional attention to detail and strong organizational capabilities.

• Outstanding communication and interpersonal skills, with the ability to effectively collaborate with cross-functional teams.

• Capacity to work independently and juggle multiple tasks simultaneously in a dynamic environment.

• Proficient in both German and English.

• Willingness to travel as needed (approximately 5%).

• Employment with ICON is contingent upon possessing the legal right to work in the location of the role.

🏝️ Benefits

• Competitive base salary complemented by performance-related incentives.

• Health and wellness programs, including medical, dental, and vision coverage where applicable.

• Retirement and pension schemes.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

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