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The Clinical Research Assistant is an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while learning the skills necessary to be a Clinical Research Coordinator.
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Due to enhanced experience in Care Access’ decentralized clinical research process, the Travel Clinical Research Coordinator will be able to assume a greater study workload, overall study responsibility, and more detailed, Site, Sponsor and CRO interactions, while conveying a positive image of Care Access Research to the community, Sponsors, CROs, and study participants and their family members.
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Care Access does not engage in any unfair or forced labor practice and does not tolerate, under any circumstances, the use of any form of forced or involuntary labor, child labor, or human trafficking.
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Obtain informed consent per Care Access Research SOP and document process when revised ICF discussed with patient during course of the trial. Care Access has a revolutionary model that breaks down traditional barriers to clinical trials that limit participation among physicians and patients to 3.
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Communicate sponsor updates, patient specific concerns/progress, unforeseen issues, and overall trial management with appropriate members of Care Access Research team in an ongoing fashion.
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Interact in a positive, professional manner with patients, sponsor representatives, investigators and Care Access Research personnel and management. Maintain effective relationships with study participants and other Care Access Research personnel.
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Obtain informed consent per Care Access Research SOP, under the direction of the Clinical Research Coordinator (CRC). The Travel Clinical Research Assistant is an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while learning the skills necessary to be a Clinical Research Coordinator.
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Care Access is a unique, multi-specialty network of research sites which operates as one connected team of physician investigators, nurse coordinators, and operations managers. Interact in a positive, professional manner with patients/participants, sponsor representatives, Investigators and Care Access Research personnel and management.
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This position has potential growth and advancement within the Care Access Research organization. Care Access complies with all employment laws and regulations with respect to its employment practices, terms and conditions of employment, and pay equity and wages.
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Prefer1 year of experience as a Care Access Research Clinical Research Coordinator. The Site Manager is responsible for the most pivotal and complex protocols and study designs being conducted at Care Access Research sites.
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Care Access is unable to sponsor work visas at this time. By removing this bottleneck, Care Access is helping accelerate the approval and delivery of critical and life-saving therapies.
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We embrace and support a culture providing equitable opportunities which empowers health care access and information serving diverse CA populations. In the Department of Health Care Access and Information (HCAI) work environment, staff handle confidential patient data.
$8,093 a monthFull-timeExpandUpdated 28 days ago - UpvoteDownvoteShare Job
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Obtain informed consent per Care Access Research SOP, under the direction of the CRC. Care Access is currently unable to sponsor work visas. Care Access is delivering the future of medicine today.
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This extends to suppliers, partners, or other third parties with whom Care Access does business. At Care Access, every day, we are advancing medical breakthroughs. Obtain informed consent per Care Access Research SOP.
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Care Access values and promotes the protection of human rights everywhere. A minimum of 1-year recent working experience as a Medical Assistant, EMT, LPN, Clinical Research Assistant or Phlebotomist.
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Company: Care Access
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