The main function of a clinical trials associate is to help organise and monitor different phases of clinical drug trials.
A typical clinical trials associate is responsible for writing drug trial methodologies, support trial study centres, provide clinicians with instructions, and monitor trial progress.
Job Responsibilities:
Support the set up, operation and disbanding of trial study centres.
Design trial materials and provide support and instructions to clinicians on how to conduct trials.
Good working knowledge of regulations and industry best practices.
Writing reports and monitoring progress throughout the course of the trials.
Collecting and authenticating case report forms Conducts on-site monitoring visits and document audits
Skills:
Verbal and written communication skills, problem solving skills, customer service and interpersonal skills.
Basic ability to work independently and manage one’s time.
Good commercial awareness
Basic knowledge of medical terminology and controlled clinical trials principles and methodologies
Basic ability to develop and implement clinical research monitoring plans and operating practices
Education/Experience:
Bachelor's degree required.
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At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws.This position's pay range is $20.00/hr - $23.96/hr.
