Clinical Research Associate

A Clinical Research Associate (CRA) is responsible for monitoring and managing clinical trials to ensure compliance with regulatory requirements, protocols, and Good Clinical Practice (GCP) standards. The CRA acts as a liaison between the sponsor, clinical sites, and regulatory bodies, ensuring high-quality data collection and patient safety throughout the trial process.

Key Responsibilities:

• Monitor clinical trial sites to ensure adherence to protocols, regulatory requirements, and SOPs.
• Verify that data reported by investigators is accurate, complete, and verifiable from source documents.
• Assist in site selection, initiation, and close-out visits.
• Maintain effective communication with investigators, site staff, and internal teams.
• Prepare and submit study-related reports, updates, and documentation to management and regulatory authorities.
• Ensure patient safety by monitoring adverse events and reporting them appropriately.
• Support the development and review of clinical trial protocols and informed consent forms.

• Strong knowledge of Good Clinical Practice (GCP) and clinical trial regulations.
• Excellent communication and interpersonal skills for interacting with investigators and internal teams.
• Attention to detail and strong organizational skills.
• Ability to analyze and interpret clinical data.
• Problem-solving and decision-making abilities.
• Proficiency in using clinical trial management systems (CTMS) and MS Office tools.

• Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Nursing, or related field.
• Previous experience in clinical research or monitoring is preferred.
• Certification in Clinical Research (e.g., ACRP, SOCRA) is a plus.

• Competitive salary and performance bonuses.
• Health insurance and wellness programs.
• Professional development and training opportunities.
• Paid time off and flexible work arrangements.
• Opportunities to work on cutting-edge research and collaborate with experts.