Site Activation Partner

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

📋 Description

• Oversee the initiation of clinical trials while ensuring adherence to regulatory standards.

• Execute site start-up and activation tasks to a high level of quality, collaborating closely with your team and stakeholders.

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

• Liaise with both internal and external stakeholders to secure necessary approvals and authorizations for the commencement of studies.

• Keep precise and current records of regulatory submissions and approvals.

• Provide support to study teams in the creation of study documents such as protocols, informed consent forms, and investigator brochures.

• Engage in study start-up meetings and offer insights on regulatory requirements and timelines.

⛳️ Requirements

• A Bachelor’s degree in life sciences or a related discipline.

• Previous experience in clinical research or regulatory affairs is preferred but not mandatory.

• Strong attention to detail along with excellent organizational abilities.

• Outstanding communication and interpersonal skills, capable of effective collaboration with cross-functional teams.

• Ability to work independently and manage multiple tasks in a dynamic environment.

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

🏝️ Benefits

• Competitive base salary along with performance-based incentives.

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

• Retirement and pension plans available.

• Life insurance and disability coverage offered.

• Employee assistance programs and wellness resources provided.

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