Study Coordinator - Safety Pharmacology

<h2>Job Overview:</h2><p style="margin-bottom: 7.5pt; text-align: justify;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><strong>Do you have a BSc and want to work in a team where you can develop and grow to your full potential?</strong></span></p><p style="margin-bottom: 7.5pt; text-align: justify;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><strong>Are you interested in Cardiovascular Safety Pharmacology?</strong></span></p><p style="margin-bottom: 7.5pt; text-align: justify;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><strong>Do you want the opportunity to make a difference and work on a variety of studies within a global organization?</strong></span></p><p style="margin-bottom: 7.5pt; text-align: justify;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Covance by Labcorp is a global, world-leading Life Sciences Contract Research Organisation that provides dedicated and fully comprehensive laboratory testing and drug development services to the pharmaceutical industry. We strive to make a difference to people’s everyday lives by bringing essential medicines to the market. At our site in <strong>Huntingdon, Alconbury</strong> we are looking to recruit a <strong>Study Coordinator</strong> to join our team.</span></p><p style="margin-bottom: 0.0001pt; text-align: justify;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">The <strong>Study Coordinator</strong> is responsible for coordinating the activities of routine and non-routine Safety Pharmacology studies, in compliance with the appropriate company standards and regulatory guidelines. General assistance to the Study Directors is an essential part of the role and additional non study specific support may also be given to key clients. This is a brand new, office based role within the Cardiovascular Safety Pharmacology team so you will really have the opportunity to make it your own!</span></p><p style="margin-bottom: 0.0001pt; text-align: justify;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;"> </span></p><p style="margin-bottom: 0.0001pt; text-align: justify;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><strong>The Study Coordinator:</strong></span></p><ul style="text-align: justify;"><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Provides scientific and administrative support to the Study Director for assigned Cardiovascular Safety Pharmacology studies. This involves multiple study set up tasks including protocol development, scheduling and initiation meetings</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Liaises with clients, study monitors, Principal Investigators and internal departments to ensure accurate and timely protocol and amendment development and distribution</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Assists with client visits and internal study meetings, including preparation and logistical planning to ensure smooth progress of the agenda</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Understands the importance of study design and meeting relevant regulatory requirements in servicing our customers</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Learns/maintains full awareness of Good Laboratory Practice (GLP) through organized refresher courses and by reference to published GLP guidelines</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Learns to follow and understand all department specific Standard Operating Procedures (SOPs), processes and best practices relevant to role</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Learns to interpret data for some study types. May interpret data and provide input on protocols/reports for some study types</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Learns about critical phases of studies. May monitor critical phases of studies and reports problems to the study management team</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Learns how pre-clinical safety studies/discovery pharmacology/in vitro studies fit into drug development process</span></li></ul><p style="margin-bottom: 0.0001pt; text-align: justify;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><strong>What Covance by Labcorp can offer you:</strong></span></p><ul><li style="text-align: justify;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Exposure to a variety of studies and the opportunity to interact with departments involved in safety pharmacology studies</span></li><li style="text-align: justify;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">The opportunity to work with global clients</span></li><li style="text-align: justify;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Competitive salaries and a comprehensive benefits package including health cover and contributory pension</span></li><li style="text-align: justify;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Unrivalled opportunities to develop a successful career in the scientific industry</span></li><li style="text-align: justify;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Unsurpassed career development opportunities where you can learn as you develop in a supported team environment</span></li></ul><h2>Education/Qualifications:</h2><ul><li style="text-align: justify;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif; color: black;">Bachelor degree (BSc) in related science field. Experience may be substituted for education</span></li></ul><h2>Experience:</h2><ul><li><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif; color: black;">Related scientific experience in Cardiovascular Safety Pharmacology either from higher education or from previous role/employment</span></li><li><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif; color: black;">Demonstrates excellent communication, time management, team work and organisational skills with the ability to manage multiple tasks/projects</span></li><li><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif; color: black;">Proficient with computers and software programs</span></li><li><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif; color: black;">Excellent attention to detail and consistent accuracy whilst managing multiple changing priorities</span></li><li><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Basic knowledge of GLPs and regulatory agency guidelines desirable</span></li></ul>