Research Nurse (On-Call) / Madison, WI (On-Site)

As one of the largest Clinical Research Organizations in the world, we have four Early Phase Clinical Research Units in the UK and US.We are currently seeking a Clinical Research Nurse I (On-Call), to interact directly with our healthy volunteer participants while learning to read clinical research protocols and enjoy working in a fast-paced team-oriented environment. Each day is different, you will be exposed to a wide variety of Therapeutic Indications and study types (ascending dose, first-in-human, food effect, drug to drug interactions, etc.)This is a full-time, office/clinic-based job in Madison, WIIf you join us, you will work with some of the world´s leading pharmaceutical, biotechnology, and medical device companies in a vital stage of clinical development: establishing the safety, tolerability and pharmacokinetics of a new drug.Many Nurses are drawn to this profession because of its direct impact on patient care. If this is your case, you will not miss that working in Phase 1 trials. Whilst allowing you to have a close face-to-face relationship with participants, and as you continue to practice your clinical skills and knowledge, you´ll be involved with the latest medical technologies and treatments, witnessing their development firsthand. When the drug you worked with gets approved, you know you´ll touch many patient´s lives around the world.WHAT YOU WILL DO:You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care clinical research.Other key responsibilities :Ensure that the dignity, health, safety, and welfare of participants is given the highest priority at all timesBe current with appropriate emergency certifications and company emergency policy and proceduresRespond to emergency situations based upon nursing standardsUtilize skills, knowledge, nursing diagnosis, and clinical judgement in order to provide a high standard of care for participants in clinical trialsUtilize nursing assessment skills to observe participant general well-being and potential adverse events. Document adverse events and takes appropriate action as neededObtain Informed Consent and continue the ICF process by educating, explaining and informing participants of study proceduresAdminister investigational compounds (inclusive of parenteral) to participants according to the protocol and applicable regulationsPerform study related activities such as cannulation, telemetry, holters, vital signs, ECGs, venipunctureUndertake any other duties as requiredEducation / Experience:Associates Degree or BS degree in nursing with current licensure in applicable state.CPR/AED certifiedACLS-certified preferred upon entry to role. ACLS certification maybe be gained in role if not yet certifiedAdditional experience may be substituted for education requirementsYOU NEED TO BRING…0-1 year of related experienceAdditional experience may be substituted for education requirementsThe important thing for us is you are comfortable working in an environment that is:Fast paced : where no deviations from the study protocol are allowed, and not meeting a timeline for even few minutes will create a quality issue.Changing priorities constantly asking you to prioritize and adapt on the spot.Teamwork and people skills are essential for the study to run smoothly.Technology based . We collect our data directly into an electronic environment.Physical Requirements:Ability to work in an upright and /or stationary position for 6-8 hours per day.Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment.Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.Ability to access and use a variety of computer software developed both in-house and off-the-shelf.Learn more about our EEO & Accommodations request here . #J-18808-Ljbffr