Job Title. Clinical Research Spec. Job Location Type. In person. Location –. Mounds View, Minnesota 55112. Job type –. 24 months. Shift Schedule –. 1st shift. Job Description. We are seeking a Clinical Research Specialist to support the design, execution, and oversight of clinical studies for medical devices. This role partners with cross-functional teams, manages site activities, and ensures clinical operations align with Good Clinical Practice ...
Dermico is seeking a reliable, detail-oriented Clinical Research Specialist to support our clinical studies, with a primary focus on participant consenting. This role is essential to ensuring that every participant clearly understands study goals, procedures, risks, and rights, and that all consent activities meet ethical and regulatory standards. Beyond consenting, the Clinical Research Specialist will provide key administrative and operational ...
Job Title. Sr. Clinical Research Specialist. Pay Rate. $60 to $66/HR. Duration. 12 months. Location. Irvine, CA (Hybrid - Mon & Tue working onsite). We are looking for. a Sr. Clinical Research Specialist. to. perform clinical site management. activities, including. reviewing informed consent forms (ICFs). to ensure compliance with regulatory requirements, maintaining site essential documents in alignment with ALCOA standards, performing database ...
At Stanford University School of Medicine the work we do touches lives today and tomorrow. Through education, research , and healthcare, the School of Medicine improves health through leadership, diversity , collaborative discoveries, and innovation. Whether working in departments with faculty, or in units that support the school, our staff are a part of teams that propel us on our journey toward the future of medicine and Precision Health. The d...
Position is 100% onsite in Hagerstown, MD. Make a meaningful impact in advancing clinical research at Meritus Health. Meritus Health is seeking a highly skilled and motivated. Clinical Research Specialist. to support the planning, coordination, and daily operations of clinical research trials across our health system. In this vital role, you’ll work directly with the Associate Dean of Research, Principal Investigators, sponsors, and regulatory ag...
Make a meaningful impact in advancing clinical research at Meritus Health. Meritus Health is seeking a highly skilled and motivated. Clinical Research Specialist. to support the planning, coordination, and daily operations of clinical research trials across our health system. In this vital role, you’ll work directly with the Associate Dean of Research, Principal Investigators, sponsors, and regulatory agencies to ensure that every study is conduc...
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, ...
Overview. Virginia Oncology Associates, the largest group of medical professionals in Hampton Roads and Northeast North Carolina devoted exclusively to cancer care and blood disorders, has an exciting opportunity for a Clinical Research Specialist support our office in Norfolk. Please take this quick survey once you've submitted your resume to complete the application process. Clinical Research PI Link. If you have completed the survey before, ev...
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Job Description. Reg or CII Exempt Staff. Qualifications. Reg or CII Exempt Staff. Job. Reg or CII Exempt Staff. Shift. Day Job. Organization. School of Medicine - Institute of Human Virology. Job Posting. Dec 11, 2025. Unposting Date. Jan 11, 2026, 4:59:00 AM.
CLINICAL RESEARCH SPECIALIST. Study Start-Up & Regulatory Compliance. Facilitate study initiation, including regulatory document collection and IRB submissions. Maintain investigator site files and manage ongoing regulatory affairs. Ensure compliance with GCP, study protocols, and investigational product handling. Communicate with sponsors and regulatory authorities, including during audits and inspections. Participant Recruitment & Study Conduct...