Clinical Trial Associate

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