In House CRA I - Estonia

<p>A formula for clinical innovation: Labcorp Drug Development. With comprehensive drug development services and de-identified data from 70 million patients worldwide, our 60,000 employees advance life-changing medicines across a wide range of therapeutic areas.</p><p>In this role, you will work with our renowned key sponsors and advance the development of innovative, life-changing medications for a variety of therapies. If you are looking to jump-start your career in clinical research and drug development, to learn and gain exposure within a world-class pharmaceutical working environment, this is a fantastic opportunity!</p><p></p><p><i>This is an entry level position designed to thoroughly train you to become a commercial Clinical Research Associate. </i></p><p></p><p><b>What we have to offer:</b></p><ul><li>flexible working hours, capped overtime and compensatory time off in lieu</li><li>a permanent employment contract</li><li>travel time = work time</li><li>highly competitive compensation packages, including Christmas and vacation allowances</li><li>regular, merit-based salary adjustments</li><li>significant employer contribution to an attractive pension scheme</li><li>excellent training and career development opportunities as well as support with furthering your education</li><li>strong support from Line Management and more than 20'000 colleagues worldwide</li><li>the world's most renowned pharmaceutical companies as our satisfied, repeat customers for many years</li></ul><p></p><p><b>Your responsibilities:</b></p><ul><li>Perform remote study site visits as required by the monitoring plan for your assigned studies, nurture and document site contacts as required per the study guidelines, and create contact reports for each telephone session (outbound or inbound) with your study sites</li><li>Serve as a point of contact for project teams and investigative sites and coordinate activities, escalations, meetings etc. with internal and external stakeholders as needed</li><li>Monitor the sites’ performance and implement action plans for sites not meeting expectations</li><li>Collaborate closely with traveling CRAs to ensure all agreed-upon quality standards and regulatory requirements are being met and all submissions and reports are delivered in time</li><li>Support traveling CRAs in their preparation for site visits (i.e. run reports, ensure all required documents are available, follow up on action items from previous visits)</li><li>Perform Case Report Form reviews, generate queries where applicable and resolve any issues according to established data review guidelines on our or client data management systems</li><li>Assist with the coordination of study visits and the shipment of drug and ancillary supplies as well as any laboratory kits and samples that are needed at the study sites</li><li>Assist in submissions and notifications to German ethics committees and regulatory authorities</li></ul><p></p><p><b>Education:</b></p><ul><li>Degree in a relevant field such as life sciences, pharmacology, biology, chemistry, health care, health management, (veterinary) medicine, nursing, etc</li><li>In lieu of the above, a completed vocational education or professional experience (e.g. as study nurse, study coordinator) in a relevant field</li></ul><p></p><p><b>Experience:</b></p><ul><li>First professional experience in a related field (e.g. medical, clinical, pharmaceutical or laboratory research, data analysis, data management, technical writing…)</li><li>Previous experience in clinical research / drug development a definite plus</li><li>Basic understanding of biology and biological processes</li><li>Experience following protocol guidelines and/or SOPs</li><li>Familiarity with and/or practical application of ICH guidelines and GCP</li><li>Good organizational and time management skills</li><li><b>Excellent communication skills in business fluent English - both written and verbal – are a must</b></li></ul><p></p><p>#LI-AR1</p><p></p><p><b>Labcorp is proud to be an Equal Opportunity Employer:</b></p><p></p><p>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.</p><p></p><p>For <span>more information about how we collect and store your personal data, please see our </span><span><a href="https://www.labcorp.com/hipaa-privacy/web-privacy-policy" target="_blank">Privacy Statement</a></span><a href="https://www.labcorp.com/hipaa-privacy/web-privacy-policy" target="_blank"><span>.</span></a><span> </span></p>