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

📋 Description

• Support the planning, execution, and oversight of clinical trials, ensuring compliance with protocol specifications, regulatory requirements, and industry standards.

• Organize study activities such as site initiation, patient enrollment, data collection, and monitoring visits.

• Work collaboratively with the Clinical Operations, Data Management, and Biometrics teams.

• Keep thorough study documentation and records in alignment with regulations and standard operating procedures.

• Assist in study close-out tasks, including data cleaning, analysis, and the preparation of clinical study reports.

⛳️ Requirements

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

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

• Strong organizational and time management capabilities, with the ability to prioritize tasks and effectively manage competing priorities.

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

• Proficient communication and interpersonal abilities, enabling collaboration across functions and the establishment of strong relationships with study teams and clinical sites.

• Willingness to travel as necessary.

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