Research Assistant

About the Role

The Research Assistant supports the conduct of clinical trials by performing protocol-required procedures, coordinating study activities, and engaging directly with study participants. This role is responsible for collecting and documenting clinical data, obtaining informed consent, managing investigational product accountability, processing biological samples, and maintaining regulatory documentation. The Research Assistant ensures compliance with study protocols, regulatory requirements, and company policies while meeting timelines and delivering high-quality support to patients, investigators, and internal teams.

Duties and Responsibilities

• Communicate effectively and courteously with study participants.
• Collect patient medical histories and obtain informed consent.
• Dispense and manage study drug accountability per protocol.
• Perform protocol-specific procedures including EKGs, vital signs, and phlebotomy.
• Collect, process, and ship biological samples (blood, urine, tissue).
• Verify accuracy of collected clinical data and ensure timely documentation.
• Support temperature monitoring and investigational product (IP) storage.
• Interact directly with COVID-19 positive patients when required.
• Manage study startup documentation, training, and adherence to timelines.
• Ensure all protocol requirements and deadlines are met consistently.
• Adhere to all company policies, procedures, and compliance standards.
• Maintain strict patient confidentiality and regulatory compliance.

Qualifications

• Bachelor’s degree in Biology or a related field, or equivalent clinical experience is preferred.
• Completed a Medical Assistant education program approved by the Arizona Medical Board is required.
• Certified Phlebotomy Technician (CPT) is preferred.
• Proficiency in Microsoft Office and electronic data systems is required.
• Ability to travel between clinical sites as needed.
• Strong knowledge of medical terminology.
• Ability to work independently with minimal supervision.