Regional Clinical Trial Lead DACH - sponsor-dedicated

<h2>Job Overview:</h2><p style="margin: 0cm 0cm 3.0pt 18.0pt;"><span style="font-family: 'times new roman', times;"><strong><span style="font-size: 12.0pt;">Regional Clinical Trial Lead DACH - sponsor-dedicated </span></strong></span></p><p style="margin: 0cm 0cm 3.0pt 18.0pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;">Location: Munich, Germany / Home Office, Germany</span></p><p style="margin-bottom: 3.0pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;"> </span></p><p style="margin: 0cm 1.7pt 3.0pt 18.0pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;">If you are an experienced clinical research professional looking for an opportunity to take on more responsibility, hone your leadership skills and significantly raise your profile within the pharmaceutical industry, while leverage your know-how in clinical trials as well as your project and relationship management talents, this role is a great opportunity!</span></p><p style="margin: 0cm 1.7pt 3.0pt 18.0pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;">As Regional Clinical Trial Lead DACH, you are central to the successful delivery of complex clinical trials (phases I-III) in the region. Not only will this position allow you to stay up to date with the latest scientific breakthroughs across a wide variety of therapeutic areas, collaborating exclusively with one of our most important, international clients - your work has a genuine impact on improving the health and lives of thousands of patients every day.</span></p><p style="margin: 0cm 1.7pt 3.0pt 18.0pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;">Join us and see why more than 90% of the top 20 global pharmaceutical companies are repeat customers!</span></p><p style="margin: 0cm 1.7pt 3.0pt 18.0pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;"> </span></p><p style="margin: 0cm 1.7pt 3.0pt 18.0pt;"><span style="font-family: 'times new roman', times;"><strong><span style="font-size: 10.0pt;">What you can expect from us:</span></strong></span></p><ul><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Rewarding work in a stable, diverse and respected company</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">A thorough onboarding with support from your personal mentor</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">flexible working hours, capped overtime and compensatory time off in lieu</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">100% home-based, permanent employment contract with Labcorp Drug Development</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">travel time = work time</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">highly competitive compensation packages, including Christmas and vacation allowances</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">regular, merit-based salary adjustments</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">significant employer contribution to an attractive pension scheme</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">excellent training and career development opportunities as well as support with advancing your education</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">strong support from Line Management and more than 20'000 colleagues worldwide</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">the world's most renowned pharmaceutical companies as our satisfied, repeat customers for many years</span></li></ul><p style="margin-bottom: .0001pt;"><span style="font-size: 10pt; font-family: 'times new roman', times;"> </span></p><p style="margin: 0cm 0cm 3.0pt 18.0pt;"><span style="font-family: 'times new roman', times;"><strong><span style="font-size: 10.0pt;">Your responsibilities:</span></strong></span></p><ul><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Oversee the local clinical trial activities for your assigned protocols in compliance with international guidelines like ICH / GCP as well as all applicable local regulations, client policies, SOPs, agreed quality standards and adverse event reporting requirements </span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Act as the primary point of contact for clinical activities, team members / issues and escalations for both internal and external stakeholders</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Support your team members in ensuring adequate patient recruitment, maximum patient safety and other aspects of professional site management, including timely completion of all necessary trainings</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Oversee payments, collect approvals, reconcile payments at study close-out and ensure accurate data in our financial systems</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Detect, assess, mitigate or escalate any risks to the success of your assigned protocols as appropriate and ensure audit-readiness at any given time</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Prepare and oversee country submissions, collaborating with Institutional Review Boards (IRBs), Independent Ethics Committees (IECs) and other local regulatory authorities as well as our sponsor</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Collaborate closely with other internal and sponsor departments to ensure all regional deliverables are met in alignment with global project timelines</span></li></ul><h2>Education/Qualifications:</h2><ul><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Degree in a relevant field such as pharmacology, life sciences, clinical trial management, health care, nursing, chemistry, biology,, etc.</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">In lieu of the above, a completed vocational education in a related field or equivalent professional experience</span></li></ul><h2>Experience:</h2><ul><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Solid professional experience in clinical trials within a CRO or a biotech / pharmaceutical company, supporting a number of studies in the DACH region</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">In-depth familiarity with submissions to the regulatory authorities in Germany, Austria and / or Switzerland - observing all local regulations and guidelines as well as international standards such as ICH and GCP</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">The leadership skills needed to guide, inspire and lead heterogeneous clinical teams to successful  project delivery</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Autonomous work style with excellent time and project management skills and a high sense of  accountability</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Capable of building trustful, sustainable relationships with diverse internal and external audiences</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Excellent listening and communication skills</span></li><li><strong><span style="font-family: calibri, sans-serif;"><span style="font-size: 10pt;">Business fluency in German and English – both spoken and written – is a must</span></span></strong></li></ul><p style="margin-bottom: 3.0pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;"> </span></p><p style="margin-bottom: 3.0pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;">Remote</span></p><p style="margin-bottom: 3.0pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;">#LI-AR1</span></p>