A company is looking for a Clinical Associate to support the design, implementation, and management of clinical trials.
Key Responsibilities
Assist in planning, execution, and monitoring of clinical trials, ensuring compliance with protocols and regulations
Coordinate study activities including site initiation, patient recruitment, and data collection
Maintain study documentation and support close-out activities including data cleaning and report preparation
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
Commitment to data accuracy and compliance
Effective interpersonal skills for cross-functional collaboration
Clinical Associate • Houston, Texas, United States