Justin Busby Email & Phone Number

United States

Serving as a field-based expert, supporting the conduct and patient recruitment of argenx global clinical trials at investigative sites, through local and relational support.

Greater Tampa Bay Area

Owner of Clinexus Solutions, LLC, Licensed Practical Nurse with over 8 years of clinical research experience in phase I-IV trials, PK/first-in-human protocols and novel drugs/indications. Experienced in multiple therapeutic areas from pre-study visits through close-out visits. Highly proficient with multiple EDC, EMR, CTMS programs, Microsoft Office Suite, Adobe, Windows operating system and Macintosh operating system.

United States

As a Clinical Research Associate at Medpace, Inc., I participated in the CRF and protocol review process for multiple clinical trials in areas of unmet medical needs. In my role, I worked on multi-center phase II-III clinical research studies, conducting pre-study, site initiation, interim and closeout visits as both the primary CRA and clinical mentor. I have been assigned to multiple protocols and indications concurrently and ensured investigative sites' adherence to GCP, ICH guidelines, and local regulations. I served as the liaison between Medpace and assigned sites, building relationships to ensure timelines were met and maintaining effective and positive relationships with Principal Investigators. Additionally, I have conducted source document verification of CRFs against medical records, performed safety reviews/SAE reconciliations, created trip reports, and evaluated data query trends for improvement of data quality. I have identified site issues, ensured proper escalation and resolution, responded to audit findings, attended and participated in study team meetings, identified and evaluated potential investigators for future studies, and maintained annual training records. My role has required attention to detail, timely submission of expense reports, and adherence to company travel policy. I consistently and effectively monitored 20+ sites over multiple protocols and pharmaceutical companies during my time at Medpace.

United States

Integra Research, located in Nashville, TN, provides a rewarding and fulfilling experience for Contract Clinical Research Associates. I have had the opportunity to contract work for Integra Research. As a current CRA, I have been mentored by the Principal CRA, gaining invaluable knowledge in all aspects of clinical research. I have had the opportunity to work on multi-center clinical trials in areas of unmet medical needs, ensuring the investigative sites' adherence to GCP, ICH guidelines, and local regulations. My daily activities include conducting source document verification, reviewing case report forms, performing drug accountability, and ensuring the prompt reporting of adverse events. With the opportunity to work on multiple protocols as a contract CRA, Integra Research has provided me with a dynamic and fulfilling experience in the field of clinical research.

Tampa, Florida, United States

• Conduct research studies with efficiency and accuracy based on individual study protocols and requirements, while managing clinical data and maintaining GCP and accurate documentation throughout. • Complied with all regulations for adverse events and severe adverse events as mandated by study resources, medical advice, and training.• Processed, inspected, recorded, and controlled investigational medications, including mixing, dispensing, administering the drug orally, topically, and intravenously, as well as provide medication/device education to patients while providing a distinct research-minded environment.• Organized and initiated new studies through generating study sources, compiling resources and personnel for the initiation of studies, as well as consenting, recruiting and enrolling, and scheduling patients for each active study as delegated by the PI, meeting randomization goals for studies, and maximizing number of patient visits with good time management.• Facilitated communication between patients, medical providers and facilities, primary investigators, and monitors in order to maintain proper documentation, adhere to each protocol, and solve queries as necessary.• Promoted to Senior Clinical Research Coordinator, oversaw the training of entry level clinical staff, and directed priorities for clinical team, and led the team through identifying and resolving problems effectively and efficiently.

• Carries out designated nursing procedures, including administration of medications without error, assisting in the planning and formulation of nursing care plans; observes, records and reports symptoms, reactions and changes in the conditions of all inmates. Provides care based upon inmate need/condition.• Provides for emotional and physical comfort and safety of inmates; assist with activities of daily living with special attention to therapeutic significance; triage inmates for sick call; refer inmates to an RN or upper-level provider as indicated; render care and treatment according to Protocol. • In addition, provides new employees with the proper initial training necessary to carry out the designated nursing procedures according to protocol at Pinellas County Jail.

St Petersburg, Florida, United States

Assists the physician with patient care and minor surgery in office. Provides wound care, dressing changes, wound vac care and application, staple and Jackson Pratt removal, and suture removal, while maintaining a safe environment for employees and clients.

Bachelor Of Applied Science - Basc

Activities and Societies: Magna Cum Laude

Licensed Practical/Vocational Nurse Training

Bachelor Of Science - Bs, Bible/Biblical Studies, High Honors