Research Assistant ensuring compliance with clinical objectives and protocols at a leading neuroscience clinical development company. Engaging in various clinical tasks to support trial execution.
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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