Sub-Investigator (Remote/Travel) at Care Access


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At Care Access, we are advancing medical breakthroughs through our revolutionary Decentralized Clinical Research process. The work that we do brings life-changing therapies to those who are in need and paves the way for newer and greater treatments to reach the world. We’re proud to advance these breakthroughs and to work with our Pharmaceutical partners utilizing our clinical network, mobile sites, and pop-up clinics in the pursuit of revolutionizing the Clinical Trial process. Through innovation and a unique technology-enabled service model, our team of experts is paving the way to take this vision forward.

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 Physician Assistants to support clinical trial related activities in states throughout the USA.

DUTIES INCLUDE, BUT NOT LIMITED TO (as applicable per project):

    • 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 Pl
    • 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

    • *Perform other duties as trained for and assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.


    • 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


    • Nurse Practitioner or Physician Assistant with 5+ years of clinical experience
    • Currently licensed in good standing in one or more states listed above
    • A minimum of 1 year of relevant work experience as Sub-Investigator (preferred) in a Clinical Research setting
About us
We care. Our values are rooted in being genuine, finding new ideas, and building something meaningful. Influenced by our values, we have built a culture valuing communication and dialogue: we care about what everyone has to say and we spend energy on being equal and inclusive. Along the way, we are caring for each other, accelerating medicine, and seeding a long-term impact for generations to come.

We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.

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Applications are now closed

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