Clinical Associate

Job Summary

Supporting the design and management of clinical trials, the full-time Clinical Associate will assist in planning, execution, and monitoring of studies while collaborating with cross-functional teams in a remote environment.

Key responsibilities

• Assist in the planning, execution, and monitoring of clinical trials, ensuring adherence to protocols and regulatory guidelines
• Coordinate study activities including site initiation, patient recruitment, and data collection to ensure timely and accurate documentation
• Maintain comprehensive study documentation and support study close-out activities, including data cleaning and analysis

Required qualifications

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