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Serves as Study Coordinator for pharmaceutical trials. Clinical Research Coordinator (CCRC) and/or Clinical Research Associate (CCRA) is preferred. Overview Clinical Research Nurse I, is an entry level support title in the Clinical Research Nurse Family.
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Preferred: Clinical Research Coordinator (CCRC) and/or Clinical Research Associate (CCRA) is preferred. Clinical Research Coordinator (CCRC) and/or Clinical Research Associate (CCRA) certification, along with a minimum of two years additional professional experience, will be considered in place of degree.
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Leading the cost planning, budget creation, machine specification, procurement, validation, installation, pre-productions trials and launch of machining or assembly battery production lines. 5+ years' experience in creating and implementing processes in a manufacturing environment (budget, schedule, trials, run off, etc.
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This role offers a flexible work-from-home arrangement, enabling you to engage in various activities such as online surveys, focus groups, clinical trials, product tests, and optional delivery services for food and groceries.
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Most trials don't require much effort and will be located near you. Potentially get paid to access the most cutting edge medicines combating your disease. Whether you are healthy, or have a specific illness, we'll connect you with the right trial.
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Other procedures include Nerve Blocks, Joint/Bursa, Spinal Cord Stimulation trials, Kyphoplasty, and PRP. Growing private practice in the highly desirable Triangle area is seeking an ACGME accredited fellowship trained Interventional Pain Physician for a full time position in our Greensboro, NC location, and willing to commute to our Winston-Salem office as well.
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This role will involve extensive travel outside NC and due to the training involved, candidates must have an interest in participating in multiple trials per year. Trials typically last three to five weeks.
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Designs pilot plant trials and full-scale manufacturing trials - writes operating procedures, trains operating team, provides technical supervision, documents the outcomes, and identifies next steps and shares best practices.
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Assists Litigation Attorney (s) with client cases, legal issues, and processes, including depositions, mediations, arbitrations, trials, motions, oral and written advocacy. May assist with conducting research and other details in preparation for trials, hearings, or other legal proceedings.
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Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials required. If you have previous experience as an Investigator for clinical research trials, we want to talk with you.
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