Site Activation Partner

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

📋 Description

• Executing site start-up and activation tasks to a high standard.

• Aiding in the preparation and submission of regulatory documents, including clinical trial applications and ethics committee submissions.

• Collaborating with internal and external stakeholders to secure necessary approvals and authorizations for study initiation.

• Keeping accurate and current records of regulatory submissions and approvals.

• Assisting study teams in developing study documents such as protocols, informed consent forms, and investigator brochures.

• Engaging in study start-up meetings and providing insights on regulatory requirements and timelines.

⛳️ Requirements

• A Bachelor's degree in life sciences or a related field.

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

• Strong attention to detail along with excellent organizational skills.

• Exceptional communication and interpersonal abilities, allowing for effective collaboration with cross-functional teams.

• Capability to work independently and manage multiple tasks concurrently in a fast-paced environment.

• Openness to travel as necessary (approximately 5%).

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

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

• Retirement and pension plans.

• Life assurance and disability coverage.

• Employee assistance programs and wellbeing resources.

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