Position Summary

We are seeking a meticulous and dedicated Clinical Research Associate (CRA) to join our team. In this position, you will be responsible for managing and supporting clinical trials while ensuring compliance with regulatory requirements and ethical standards, such as Good Clinical Practice (GCP). You will collaborate closely with medical teams, study participants, and research personnel to facilitate the smooth execution of clinical studies.

Primary Responsibilities

• Conduct thorough evaluations of study documentation to verify accuracy and adherence to protocols.
• Monitor participant activities to ensure compliance with trial procedures and safety protocols.
• Work alongside healthcare professionals to gather key data and assist with patient assessments.
• Safeguard the confidentiality of data while adhering to regulatory guidelines, including HIPAA.
• Oversee data collection, entry, and validation processes to maintain accuracy throughout the trial.
• Contribute to the preparation of regulatory documentation, aligning with requirements such as those from the FDA.
• Provide training to site staff on study-related protocols, procedures, and compliance expectations.
• Stay up-to-date with industry developments, regulatory updates, and best practices in clinical research.

Qualifications and Skills

• A degree in life sciences, nursing, or a related field is preferred.
• Previous experience in clinical research or a similar domain is beneficial.
• Strong understanding of GCP guidelines and regulatory frameworks, including FDA standards.
• Proficiency in data management, documentation review, and related processes.
• Excellent organizational skills and attention to detail.
• Ability to monitor participant interactions and ensure their well-being during trials.
• Exceptional verbal and written communication skills to collaborate effectively with diverse teams.