Safety Nurse - Pharmacovigilance Case Handler

<h2>Job Overview:</h2><p style="margin: 0cm 0cm 12pt 54pt; text-align: left;"><span style="font-family: verdana, geneva; font-size: 10pt;">Are you ready to redefine what’s possible, and discover your extraordinary potential at Labcorp Drug Development? A career here provides the unique chance to create a lasting impact and difference in our patient’s lives. Joining our team will offer you a rewarding career, an opportunity to work in a high-energy & collaborative workplace. Your work will be meaningful, the patient outcomes are real, and the results are lasting. With the support of exceptional people from across the globe and an energized purpose, you’ll be empowered to own your career journey with mentoring, training and personalized development planning.<br /><br />Our mission is to help our clients bring the miracles of medicine to market sooner by <span style="border: none windowtext 1.0pt; padding: 0cm;">performing drug safety data management </span>-- join us for your next career move.<span style="border: 1pt none windowtext; padding: 0cm;"> </span></span></p><p style="margin-bottom: 0cm; padding-left: 40px;"><span style="font-size: 10pt;"><span style="font-family: Verdana, sans-serif;"><strong>As a Safety Nurse you will: </strong></span></span></p><ul><li style="margin-left: 39.75pt;"><span style="font-size: 9.0pt; font-family: 'Verdana',sans-serif; color: black;">Implement and promote use of consistent, efficient and quality processes to meet timelines and deliverables according to requirements and standard operating procedures</span></li><li style="margin-left: 39.75pt;"><span style="font-size: 9.0pt; font-family: 'Verdana',sans-serif; color: black;">Ensure compliance of operations with governing regulatory requirements</span></li><li style="margin-left: 39.75pt;"><span style="font-size: 9.0pt; font-family: 'Verdana',sans-serif; color: black;">Create, maintain and assume accountability for a culture of high customer service</span></li><li style="margin-left: 39.75pt;"><span style="font-size: 9.0pt; font-family: 'Verdana',sans-serif; color: black;">Undertake primary medical review of cases, including medical assessment of the case for seriousness, listedness/labeling, causality, adverse event coding and narrative review.</span></li><li style="margin-left: 39.75pt;"><span style="font-size: 9.0pt; font-family: 'Verdana',sans-serif; color: black;">Update and document daily case data, case-feedback in appropriate trackers/tools to facilitate tracking and workflow management</span></li><li style="margin-left: 39.75pt;"><span style="font-size: 9.0pt; font-family: 'Verdana',sans-serif; color: black;">Assume complete responsibility for all assigned deliverables in line with expected quality, compliance and productivity SLAs and KPIs.</span></li><li style="margin-left: 39.75pt;"><span style="font-size: 9.0pt; font-family: 'Verdana',sans-serif; color: black;">Undertake and complete additional tasks/activities, assigned by supervisor, as required</span></li><li style="margin-left: 39.75pt;"><span style="font-size: 9.0pt; font-family: 'Verdana',sans-serif; color: black;">Provide training</span></li></ul><p style="padding-left: 40px;"><strong style="font-family: verdana, geneva; font-size: 10pt;"><span style="border: 1pt none windowtext; padding: 0cm;">Covance is proud to be an Equal Opportunity Employer:</span></strong></p><p style="margin: 0px;"> </p><p style="padding-left: 40px;"><span style="font-family: verdana, geneva; font-size: 10pt;"><span style="border: 1pt none windowtext; padding: 0cm;">As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.</span></span></p><h2>Education/Qualifications:</h2><ul><li style="margin-left: 39.75pt;"><span style="font-size: 9.0pt; font-family: 'Verdana',sans-serif; color: black;">Bachelor’s degree in Medical Science or equivalent degree (Nursing)</span></li></ul><p style="margin-bottom: 0cm;"><span style="font-size: 10pt;"><strong><span style="font-family: Verdana, sans-serif; color: black;">Special Skills & Knowledge </span></strong></span></p><ul><li style="margin-left: 39.75pt;"><span style="font-size: 9.0pt; font-family: 'Verdana',sans-serif; color: black;">Clinical Research</span></li><li style="margin-left: 39.75pt;"><span style="font-size: 9.0pt; font-family: 'Verdana',sans-serif; color: black;">Good understanding of regulatory requirements and ICH-GCP guidelines</span></li><li style="margin-left: 39.75pt;"><span style="font-size: 9.0pt; font-family: 'Verdana',sans-serif; color: black;">Technical proficiency with Microsoft Office suite of applications</span></li></ul><p style="margin-bottom: 0cm;"><span style="font-size: 10pt;"><strong><span style="font-family: Verdana, sans-serif; color: black;">Key Competencies </span></strong></span></p><ul><li style="margin-left: 39.75pt;"><span style="font-size: 9.0pt; font-family: 'Verdana',sans-serif; color: black;">Strong working knowledge of medical sciences, diagnosis and therapeutics including drug treatments and procedures</span></li><li style="margin-left: 39.75pt;"><span style="font-size: 9.0pt; font-family: 'Verdana',sans-serif; color: black;">Good verbal and written communication skills</span></li><li style="margin-left: 39.75pt;"><span style="font-size: 9.0pt; font-family: 'Verdana',sans-serif; color: black;">Focus on quality and attention to detail</span></li><li style="margin-left: 39.75pt;"><span style="font-size: 9.0pt; font-family: 'Verdana',sans-serif; color: black;">Ability to review, analyze & synthesize medical information</span></li><li style="margin-left: 39.75pt;"><span style="font-size: 9.0pt; font-family: 'Verdana',sans-serif; color: black;">Good understanding of customer needs and expectations</span></li></ul><p style="margin: 0px;"><span style="font-size: 9.0pt; font-family: 'Verdana',sans-serif; color: black;">Highly focused on quality and timelines for medical deliverables<br /></span></p><h2>Experience:</h2><ul><li style="margin-left: 39.75pt;"><span style="font-size: 9.0pt; font-family: 'Verdana',sans-serif; color: black;">2+ years of clinical practice experience</span></li><li style="margin-left: 39.75pt;"><span style="font-size: 9.0pt; font-family: 'Verdana',sans-serif; color: black;">Typically up to 2 years of pharmaceutical industry experience, including pharmacovigilance (case processing, medical review) and / clinical research preferred</span></li></ul>