Associate Clinical Research Manager

Assisting with various aspects of clinical trials, the full-time Associate Clinical Research Manager will manage project documentation, support study conduct, and liaise with project teams and study subjects in an office environment. Key responsibilities Actively participate with project team members to meet project needs, projections, and deadlines Oversee organization and accuracy of project documents and support study conduct Liaise with sites to track enrollment projections against actuals, reviewing quality and timelines Required qualifications Bachelor's degree or equivalent relevant qualification 0 to 2 years of experience in clinical research or related field Basic knowledge of Phase I processes and clinical study operations Fundamental understanding of FDA and EMEA regulations and ICH GCP guidelines Proficiency in Microsoft Office applications