Regional CRA - Nationwide - Ophthalmology

Regional CRA - Nationwide - Ophthalmology
  • Competitive
    HOUR
  • Temporary
  • Astoria NY, US Astoria QUEENS US 11106
Job Ref: JO000127348
Sector: Clinical
Sub-sector: Clinical
Date Added: 10 January 2022

Regional CRA - Nationwide - Ophthalmology

At SRG, we create meaningful connections that empower individuals and businesses to shape tomorrow’s world.

Working as part of the SRG team, you will work with our client which are Pharmaceutical or Bio-Pharmaceutical companies to ensure work quality and accuracy for our client in the Bio Pharmaceutical Industry. One of our clients is currently seeking to fill multiple Regional Clinical Research Associate (CRA) roles across the US! This position is a remote role based anywhere within close proximity to major airport in the United States. This is a long-term contract role (C2C, 1099 or W2) with a high potential to extend.
PURPOSE OF POSITION:

  • Performing independent on-site or remote Monitoring procedures, i.e., Site Qualification, Initiation, Interim Monitoring, Site Close-out and site management.
  • Overseeing study specific documentation such as Protocols, Monitoring Plans, CRFs, source documentation, CRF Completion Guidelines, Investigative Site training materials, maintenance of Trial Master File (TMF) format and studies, and QC of TMF.
  • Managing and training clinical study sites.
  • Providing Monitoring Visit Reports, Study Visits Communication Worksheets, Telephone Contacts and other reports as outlined in SOPs.
  • Reviewing case report forms for legibility, correctness, and adherence to protocol requirements.
  • Demonstrating a strong understanding of current GCP and ICH guidelines and regulations.
  • Bachelor’s Degree required – preferably within Life Sciences or other relevant technical area
  • 5+ years of industry experience required
  • 3+ years of monitoring experience for either CRO or sponsor is required
  • Experience working within Ophthalmology is highly desirable.
  • Candidates with experience in risk based monitoring will be considered first
  • Knowledge of FDA, ICH, GCP, etc. regulatory requirements
  • Professional certification through one or more relevant associations (e.g., ACRP, SOCRA, RAPS, etc.) desired
  • Strong interpersonal skills and ability to work within a team in a fast-paced environment
  • Experience working on multiple projects at one time
  • Strong written and verbal communication skills

SRG is an Equal Opportunity Employer - All qualified applicants will receive consideration without regard to race, color, religion, gender, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law.

SRGTalent
31/01/2022 12:00:00
USD 0.00 0.00 Hour
Contact Consultant:
Brian Houston

Submitting application, please wait..

Share location?

Do you want to share your location for better user experience ?