Clinical Research Assistant

Key Responsibilities

• Assist with data collection for clinical trials
• Support documentation and record-keeping for study activities
• Help maintain organized trial files and regulatory documents
• Perform administrative tasks to support clinical research operations
• Collaborate with study teams under supervision
• Contribute to the execution of clinical studies for pharmaceutical clients

Requirements

• Basic understanding of clinical research processes
• Strong attention to detail for data accuracy
• Proficiency in standard office software (e.g., MS Office)
• Ability to follow protocols and standard operating procedures
• Good organizational and time management skills
• Effective communication for team collaboration

Keywords