Research Assistant

ALLIANCE CLINICAL LLC•Phoenix, AZ

18h•Onsite

About The Position

We’re people with a purpose, dedicated to advancing medical innovation and healing technology through groundbreaking research, diligent patient care and strong executive management. Our hands-on management team and medical staff are committed to rapid, efficient trials that bring life-changing drugs to market faster; our research staff brings years and years of “in the trenches” experience conducting Phase 1-4 clinical studies. And each one is dedicated to curing disease and improving individual quality of life. Mission Statement: At Alliance Clinical Network, our mission is to advance medical research by enrolling diverse populations in high-quality clinical trials. We are committed to maintaining the highest standards of integrity and excellence, and to ensuring that every participant receives respectful and compassionate care. We strive to build a tightly knit, supportive and collaborative environment where our team members can thrive and make meaningful contributions to human health.

Requirements

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.
Excellent verbal, written, and interpersonal communication skills.
Strong problem-solving skills and the ability to adapt quickly in a dynamic environment.
Outstanding customer service skills with both internal teams and external stakeholders.

Nice To Haves

Certified Phlebotomy Technician (CPT) is preferred.
Bachelor’s degree in Biology or a related field, or equivalent clinical experience is preferred.

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.