Clinical Research Nurse (M-F day shift)

<h2>Job Overview:</h2><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif;"><span style="font-size: 12pt;">Join our screening team as a Research Nurse to help improve lives. The shift is M-F (6/7am-3/4pm)</span></span></p><ul><li><span style="font-family: arial, helvetica, sans-serif;"><span style="font-size: 12pt;">Ensure that the dignity, health, safety, and welfare of participants is given the highest priority at all times</span></span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Be current with appropriate emergency certifications and company emergency policy and procedures</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Respond to emergency situations based upon nursing standards</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Utilize skills, knowledge, nursing diagnosis, and clinical judgement in order to provide a high standard of care for participants in clinical trials</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Utilize nursing assessment skills to observe participant general well-being and potential adverse events. Document adverse events and takes appropriate action as needed</span></li><li><span style="font-family: arial, helvetica, sans-serif;"><span style="font-size: 12pt;">Obtain Informed Consent and continue the ICF process by educating, explaining and informing participants of study procedures, </span><span style="font-size: 12pt;">obtain medical history</span></span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Administer investigational compounds (inclusive of parenteral) to participants according to the protocol and applicable regulations</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Perform study related activities such as cannulation, telemetry, holters, vital signs, ECGs, venipuncture</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Collect and process biological samples according to the protocol and Standard Operating Procedures</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Record data obtained in a timely, error free manner according to the protocol and Standard Operating Procedures.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Maintain an understanding of current regulatory requirements</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Transcribe source data onto the Case Report Form</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Take responsibility for quality control of study data</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Attend all required meetings, as appropriate</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Maintain accurate records of all work undertaken</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Maintain skills to perform all study tasks, as required</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Maintain constant awareness of participant safety and dignity at all times</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Handle participant complaints efficiently and effectively in order that their satisfaction is maintained</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Ensure that client and participant confidentiality is maintained</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Respond to client and team queries in a timely manner</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Take ownership for the quality and standard of own work.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Record Adverse Events (AEs) as required</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Be competent in all aspects of dosing as required by study</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Contribute to clinic projects as required</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Assist lead nurse in medical programs (such as Hep B and TB) within the clinic, as required</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Undertake any other duties as assigned</span></li></ul><h2>Education/Qualifications:</h2><ul><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Associates Degree or BS degree in nursing with current licensure in applicable state.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">CPR/AED certified</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">ACLS-certified preferred upon entry to role. ACLS certification maybe be gained in role if not</span><br /><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">yet certified</span><br /><br /></li></ul><h2>Experience:</h2><ul><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">1+ years of related experience;clinical research experience is highly preferred</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Additional experience may be substituted for education requirements</span></li></ul><p style="margin: 0px;"><span style="font-family: 'times new roman', times; font-size: 12pt;">#LI-ML1</span></p>