Clinical Trial Associate

Job Summary

Supporting the design, implementation, and management of clinical trials, the full-time Clinical Trial Associate will assist in planning, coordinating study activities, and maintaining comprehensive documentation while working remotely.

Key responsibilities

• Assist in the planning, execution, and monitoring of clinical trials to ensure adherence to protocols and regulatory guidelines
• Coordinate study activities including site initiation, patient recruitment, and data collection to ensure timely and accurate documentation
• Collaborate with cross-functional teams to support the successful execution of clinical trials and maintain compliance with regulations

Required qualifications

• Bachelor's or advanced degree in Life Sciences, Health Sciences, or a related field
• Previous experience in clinical research or healthcare, preferably within the pharmaceutical, biotechnology, or CRO industry
• Strong organizational and time management skills with the ability to prioritize tasks effectively
• Excellent attention to detail and problem-solving abilities to ensure data accuracy and compliance
• Effective communication and interpersonal skills for collaboration with study teams and clinical sites