RapidTrials® improves medical research site performance and accelerates the completion of phase II-IV clinical trials. Founded in 1996, RapidTrials® is the industry’s only company focused exclusively on driving clinical trial performance at the site level, offering assistance and advocacy to research centers — directly and through sponsors and CROs.

RapidTrials, secures opportunities for health care providers (HCPs) to work with biopharmaceutical, medical device and diagnostic companies on a part-time, full- time and/or project basis. Rapidtrials matches industry project requirements with the skills and interests of clinicians. HCPs can participate in projects based on interest, experience and availability. Prior industry experience is not necessarily required.

Examples of typical projects include:

1- Interventional clinical trials for device, diagnostic, drug, biologic and gene therapy studies

2- Serum and/or tissue screening studies for antibodies, liquid biopsy, and/or genetic testing protocols

3- Observational studies and clinical registries

Project involvement may include: chart reviews, patient, family and/or caregiver education, performing clinical assessments, obtaining initial informed consent, consulting with and providing researchers with patients' medical history, test results and medication history, reporting adverse events, completing patient screening visit procedures (i.e., blood draws, assessments and imaging) conducting study visits, administering study drug/biologics and/or providing on-call coverage for the study PIs.

RapidTrials helps physicians (MD, DO), Physician Assistants (PA), Nurse Practitioners NP, ACNP, MSN, DSN), Genetic Counselors, Pharmacists Phlebotomists, Physical and Respiratory Therapists (PT/RT) tap into the research community and collaborate with industry to find cures for patients with progressive and debilitating diseases.