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

📋 Description

• Assist in the planning, execution, and oversight of clinical trials, ensuring compliance with protocol requirements, regulatory standards, and industry best practices.

• Coordinate study activities, which include site initiation, patient recruitment, data collection, and monitoring visits.

• Collaborate with teams from Clinical Operations, Data Management, and Biometrics.

• Maintain thorough study documentation and records in accordance with regulations and standard operating procedures.

• Support study close-out activities, including data cleaning, analysis, and the preparation of clinical study reports.

⛳️ Requirements

• Bachelor’s degree in a relevant scientific discipline or a healthcare-related field.

• Prior experience in clinical research or healthcare, ideally within the pharmaceutical, biotechnology, or CRO industries.

• Strong organizational and time management abilities, with a talent for prioritizing tasks and managing competing demands effectively.

• Exceptional attention to detail and problem-solving skills, with a dedication to ensuring data accuracy, integrity, and compliance.

• Strong communication and interpersonal skills, capable of collaborating cross-functionally and fostering robust relationships with study teams and clinical sites.

• Willingness to travel as necessary.

• Legal authorization to work in the country where the position is based.