Sub Investigator
Listed on 2026-01-12
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Healthcare
Clinical Research
1 day ago Be among the first 25 applicants
About Care AccessCare 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 into 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
The Sub-Investigator will be responsible for regional travel mixed with remote tele-medicine work to support our clinical research. Care Access is looking for Nurse Practitioners or Physicians Assistants to support clinical trial related activities in states throughout the USA.
How You ll Make An Impact- Work closely with the Principal Investigator to oversee the execution of study protocols, delegating study related duties to site staff, as appropriate, and ensuring site compliance with study protocols, study-specific laboratory procedures, standards of Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), quality (QA/QC) procedures, OSHA guidelines, and other state and local regulations as applicable
- Attends and participates in meetings with the director, other managers, and staff as necessary
- Complies with regulatory requirements, policies, procedures, and standards of practice
- Read and understand the informed consent form, protocol, and investigator s brochure
- Be available to see subjects virtually or in-person as dictated by project design, answer their questions, and resolve medical issues during the study visit
- Sign and ensure that the study documentation for each study visit is completed
- Perform all study responsibilities in compliance with the IRB approved protocol
- Review screening documentation and approves subjects for admission to study
- Review admission documentation and approves subject for randomization
- Provide ongoing assessment of the study subject/patient to identify Adverse Events
- Ensure that serious and unexpected adverse events are reported promptly to the PI
- Review and evaluates all study data and comments to the clinical significance of any out of range results
- Perform physical examinations as part of screening evaluation and active study conduct
- Provide medical management of adverse events as appropriate
- Excellent working knowledge of medical and research terminology
- Excellent working knowledge of federal regulations, good clinical practices (GCP)
- Ability to communicate and work effectively with a diverse team of professionals
- Strong organizational skills:
Able to prioritize, support, and follow through on assignments - Communication Skills:
Strong verbal and written communication skills as evidenced by positive interactions with coworkers, management, clients and vendors - Team Collaboration Skills:
Work effectively and collaboratively with other team members to accomplish mutual goals. Bring positive and supportive attitude to achieving these goals - Strong computer skills with demonstrated abilities using clinical trials database, IVR systems, electronic data capture, MS word and excel
- Ability to balance tasks with competing priorities
- Critical thinker and problem solver
- Curiosity and passion to learn, innovate, able to take thoughtful risks and get things done
- Friendly, outgoing personality; maintain a positive attitude under pressure
- High level of self-motivation and energy
- Ability to work independently in a fast-paced environment with minimal supervision
- Must have a client service mentality
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