Research Assistant

Topography Health • Albuquerque, NM

1d

About The Position

This role will assist with the coordination of research in an exciting new environment, with the full backing of a new type of research architecture and a top-tier technology team, challenging the paper-heavy, old-school way that studies are run. This role will require the desire to learn and grow rapidly, and include the opportunity to work closely with Topography’s partner healthcare groups. This role will be evaluated on patient experience, protocol management and adherence, and data quality. You will need to be able to thrive with multiple balls in the air, and where independent problem solving is a daily need. You will need to lead with empathy for patients, and care deeply about creating new access to clinical research in communities across the country.

Requirements

• High School Diploma or Equivalent
• Knowledge of FDA regulations and ICH/GCP guidelines
• Ability to draw blood, run labs, take vitals
• Strong communication skills, teamwork, cooperation, self-awareness, and flexibility

Responsibilities

• Act as research assistant to clinical trials conducted within physician practices, including but not limited to:
• Visit preparation activities
• Visit follow-up activities
• Supply and inventory coordination
• Third party vendor coordination
• Patient recruitment and identification
• Assist with patient study visits
• Assist with clinical and lab procedures such as ECG, phlebotomy, vitals signs and body measurements, laboratory processing, etc.
• Assist with the informed consent process with care and quality
• Adhere to study protocol and GCP
• Provide high quality source data capture and documentation
• Supporting the IP distribution and accountability process
• Adverse Event tracking and follow-up
• Data entry to CRF/EDC and query resolution
• Protocol deviation tracking, reporting, and reconciliation
• Attending sponsor visits including SIVs, IMVs, and COVs, as needed
• Use and help improve Topography’s proprietary tool set
• Understand and comply with all regulations, policies, and guidelines applicable to clinical research, including our SOPs
• Follow the study protocols
• Maintain meticulous accuracy in completing all documentation
• Any other duties assigned by manager

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: High school or GED