Research Assistant

About Care Access

Care Access is working to make the future of health better for all. With hundreds of research locations, mobile clinics, and clinicians across the globe, we bring world-class research and health services directly to communities that often face barriers to care. We are dedicated to ensuring that every person has the opportunity to understand their health, access the care they need, and contribute to the medical breakthroughs of tomorrow.

With programs like Future of Medicine , which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers , which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Through partnerships, technology, and perseverance, we are reimagining how clinical research and health services reach the world. Together, we are building a future of health that is better and more accessible for all.

To learn more about Care Access, visit www.CareAccess.com .

How This Role Makes a Difference

Central Clinical Services enables decentralized and hybrid clinical trials by providing staff who virtually support patients and sites. The Research Assistant (RA) position delivers a strong customer experience for both sites and patients by providing virtual study support under the delegation of a PI. The RA is accountable for study delivery at the patient level and is expected to support the patient experience, data management, and other study administrative tasks with a quality-first approach. This is an early-to-mid experience position with the expectation that the RA has working knowledge of and experience in the clinical research industry. Candidates will be hired at the RA I or RA II level depending on experience.

How You'll Make An Impact

Patient Engagement

Identify, recruit, educate, and pre-screen potential patients for a study

Analyze, understand, and be knowledgeable of the study protocol and the associated disease(s) in combination to be able to educate patients and their families on what participating in the study means for the patient

Speak about studies with patients in a manner they can understand

Interpret patient reported medical history and medication use to determine pre-screening qualification for a study

Assess if a patient is ready to be scheduled for a screening visit for a study or if more time is needed for them to become informed about the study, including a potential discussion with the study doctor

Review next required study visits for patients and the timeline in the protocol to ensure they are scheduled within protocol window

Work closely with the Central Study Coordinator to understand all aspects of the study to which each patient consented, and ensure they are being scheduled for all applicable protocol mandated activities

Proactively contact patients to collect information, remind them of upcoming appointments, and engage in other patient retention activities

Verify completion of study visits through systems checks and then process patient stipend payments accordingly

Communicate PI decisions on study eligibility to patients

Communicate via various mediums such as phone, email, and video conference

Document all patient interaction appropriately and in accordance with GCP and ALCOA-C

Help troubleshoot technology issues for patients as they arise

Systems Maintenance and Data Management

Maintain up-to-date information across multiple study portals

Review data backlog and use good judgement prioritize data entry, clean-up work, and addressing queries according to study needs and requirements