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Job Detail
- AUTO-TRANSLATED TO RUSSIAN: Yes
Job Description
Company/Name: Bespoke Recruitment.
Location: Sutton.
Job Type: Full Time.
Specialism: Healthcare.
Clinical Trial Associate’s Responsibilities:
Initiate investigator site activities, including collection and submission of regulatory documents, customization, and negotiation of informed consent documents, serve as the point of contact for a sites ERB and Competent Authority (CA)(where applicable), communicate and negotiate budgets with site personnel and internal teams, negotiate and obtain a fully-executed contract, track and ensure site compliance to required training, and effectively drive timelines aligned with company priorities
Communicate directly with sites to enable start-up and maintain an active collaboration with sites during maintenance and close-out
Ensure country-specific regulatory and data privacy requirements are incorporated into submission documents and any other documents/systems
Populate internal systems to ensure accuracy of trial/site performance
Populate Trial Master Files and libraries for future reference
Qualification Requirements:
Bachelors degree preferably in a scientific or health-related field, two years clinical research / clinical trial experience or relevant experience preferred
Understanding of the overall clinical development paradigm and the importance of efficient site initiation
Fluency in Ukrainian or Russian is essential
*EU/UK Passport or Irish Stamp 4 visa essential*
Reference ID: A.M
Job Types: Full-time, Permanent
Salary: Up to ?49,000.00 per year
Schedule:
8 hour shift