Clinical Trials Research Associate – Data Capture & Study Coordination

ViziRecruiter,LLC.; New York (NY); On-site; USD 55,000 - 75,000; Full time

Job summary

ViziRecruiter,LLC. is seeking a Clinical Research Coordinator I to assist in the conduct of clinical trials. This role involves collecting and managing patient clinical data, obtaining informed consent, and ensuring compliance with Good Clinical Practice.

The ideal candidate should have a Bachelor's degree, with a Master's degree preferred, along with relevant certifications. Responsibilities include data collection, subject screening, and coordination of study activities.

Qualifications

• Bachelor's Degree is required for this role.
• Master's Degree is preferred for better competency.
• ACRP (or SOCRA) certification is a plus.
• Medical Degree or equivalent is a valuable asset.

Responsibilities

• Collects and records study data. Inputs all information into database.
• Assists in clinical research activities like screening participants.
• Maintains source documents and subject files per hospital procedures.
• Ensures accurate compilation of subject data through reviews.
• Coordinates scheduling for multiple studies under supervision.
• Secures and ships clinical specimens as required by protocols.

Education

Bachelor's Degree

Master's Degree

ACRP (or SOCRA) certification

Medical Degree (or foreign equivalent)

Job description

ViziRecruiter,LLC. is seeking a Clinical Research Coordinator I to assist in the conduct of clinical trials. This role involves collecting and managing patient clinical data, obtaining informed consent, and ensuring compliance with Good Clinical Practice.

The ideal candidate should have a Bachelor's degree, with a Master's degree preferred, along with relevant certifications. Responsibilities include data collection, subject screening, and coordination of study activities.