Research Assistant

About the Role

The Research Assistant will ensure compliance with protocol and overall clinical objectives. In executing these position responsibilities, the Research Assistant is guided by FDA regulations, Good Clinical Practice (GCP), and company standard operating procedures and policies.

Responsibilities

• Prepare source documents for study visits.
• Perform vitals, ECGs, and phlebotomy.
• Data entry from patient visits.
• Manage lab kit inventory.
• Ship and process specimens.
• Undertake protocol trainings as assigned.
• General office tasks such as filing, copying, and scanning.
• Additionally, this role may encompass responsibilities beyond those outlined above, as required by the evolving needs of the organization. This job description is intended as a foundation and may be subject to expansion or modification to best suit ERG's objectives.

Skills and Qualifications

• 1 year of clinical experience is preferred.
• High School Diploma or its equivalent; College degree preferred.

Requirements

• 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).
• Must be willing to work a NIGHT SHIFT.