Research Assistant ensuring compliance with clinical trial protocols at Evolution Research Group. Preparing documents and performing clinical tasks under FDA regulations and Good Clinical Practices.
Responsibilities
Ensure compliance with protocol and overall clinical objectives
Prepare source documents for study visits
Perform vitals, ECGs, and phlebotomy
Data Entry from patient visit
Manage lab kit inventory
Ship and process specimens
Undertake protocol trainings as assigned
General office tasks such as filing, copying, and scanning
Requirements
1 year of clinical experience is preferred
High School Diploma or its equivalent; College degree preferred
Understand regulatory requirements, as well as Good Clinical Practices (GCP) and International Conference of Harmonization (ICH) guidelines
Knowledgeable in medical terminology
Organization skills required
Good organizational and interpersonal skills
Attention to detail
Excellent communication skills (interpersonal, written, verbal)
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