Clinical Trial Assistant

Location: Aventura, FL, United States
Date Posted: 07-28-2016
Headquartered in Aventura, Florida, with regional offices and operations across North America and around the world, Biorasi is an award-winning fast growing, full-service, global CRO that delivers Clinical Research Optimized™ to the world's leading biotech and pharmaceutical companies.

Biorasi hires talent and personality, not position holders.  We’re a non-traditional work environment requiring only top performers.  Every team member is a stock-holding owner and our culture reflects it.

This is a remarkable opportunity to dedicate yourself to become a vital part of a growing company in a thriving industry and benefiting professionally and financially from your accomplishments. If you have a passion for achievement and are looking for a place to explore your potential, Biorasi wants to talk to you now.  This role is an exciting way to break into the clinical research industry with lots of growth paths available, one of these career paths is becoming a Clinical Research Associate. 
The Role
The Clinical Trial Assistant (CTA) provide support to the Clinical Trial Managers and Clinical Research Associates in multiple areas. The CTA perform administrative tasks to support team members with clinical trial execution as needed and acts as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
Duties include but not limited to:
  • Support Clinical Trial Manager (CTM) in preparing and/or reviewing study-related documents (e.g., Monitoring Plan, Laboratory Manual, Patient Diary, Clinical Site Procedures Manual, Pharmacy Manual, and CRF Completion Guidelines).
  • Support CTM preparing/reviewing site study documents (i.e., site-specific informed consent, study tools/worksheets).
  • Coordinates with the clinical project team the distribution, retrieval and review of regulatory documents required for initiation of a clinical trial.
  • Filing of required clinical trial documents maintained within Clinical Trial Master File (CTMF) throughout the clinical trial.
  • Prepares necessary study supplies for clinical trials and processes site requests for shipping supplies, as needed.
  • Assisting the study teams in meeting timelines.
Candidate Profile
  • Associates or Bachelor’s Degree
  • 1 year of clinical research experience preferred but not mandatory
  • Excellent verbal and written communication skills required.
  • Excellent organizational, multi-tasking and time management skills required.
  • Excellent verbal and written communications skills.
  • Fluency in written and spoken English.
Biorasi is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status. Biorasi is also committed to compliance with all fair employment practices regarding citizenship and immigration status.
this job portal is powered by CATS