Study Start Up Associate I

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

📋 Description

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

• Execute site start-up and activation tasks at 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.

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

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

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

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

⛳️ Requirements

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

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

• Exceptional attention to detail and strong organizational abilities.

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

• Ability to work independently and juggle multiple tasks in a fast-paced environment.

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

🏝️ 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.