Title: Clinical Research Associate
Location: Buffalo, NY
Duration: 6 months (Contract)
Roles & Responsibilities:
The Clinical Research Associate supports the clinical research mission of the Institute and Clinical Research Services (CRS) through the creation, submission and maintenance of research regulatory documents.
The employee adheres to the Code of Federal Regulations (Title 21) and guidelines set up by the GCP/ICH and the FDA.
Associate's degree in a health or science related field.
The preferred candidate will have Bachelor’s Degree in a Health Related Field, ACRP or SOCRA Certification, One year current Regulatory job role experience, and proficiency in Microsoft Office Software (Outlook, Word, Excel).
The candidate will possess professional verbal and/or written communication skills, ability to multi-task effectively in a busy working environment, and the ability to verbalize knowledge of applicable Regulatory guidelines.