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CLINICAL & ANCILLARY SUPPLIES SPECIALIST, EMEA

Laboratory Corporation of America Holdings (Covance)

Kiev, Ukraine

<h2>Job Overview:</h2><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;">IMPs don´t fall from heaven … IMP on site on time is the result of substantial coordination and planning.</span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;"> </span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;">This is what our Clinical and Ancillary Supplies Specialists live for: orchestrating the activities that will allow the entire clinical supplies lifecycle happen smoothly, no mistakes, no delays.</span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;"> </span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;">We have an opened a </span><span style="font-size: 11.0pt; color: windowtext;">Global Clinical and Ancillary Supplies Specialists</span><span style="font-size: 11.0pt; color: windowtext;"> job in Europe:</span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;"> </span></p><ul><li style="margin: 0cm 1.7pt .0001pt 36.0pt;"><span style="font-size: 11.0pt; color: windowtext;">Our ideal locations are: Hungary, Ukraine or Bulgaria, although we will accept applications from any EMEA country with Covance offices.</span></li><li style="margin: 0cm 1.7pt .0001pt 36.0pt;"><span style="font-size: 11.0pt; color: windowtext;">This is an office-based job, but you will also have the possibility to work home-based a few days a week (depending on your seniority and the country policy) </span></li></ul><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;"> </span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;">Covance by Labcorp</span><span style="font-size: 11.0pt; color: windowtext;"> has supported the pharmaceutical industry develop more medicines worldwide than any other company, including the top 50 best-selling drugs on the market today. Frost & Sullivan has recognized us with the </span><span style="font-size: 11.0pt; color: windowtext;">2020 Global CRO Company of the Year Award</span><span style="font-size: 11.0pt; color: windowtext;">. </span><span style="font-size: 11.0pt; color: #0a0a0a;">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 .0001pt 0cm;"><span style="font-size: 11.0pt; color: #0a0a0a;"> </span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: #0a0a0a;">We can offer you not only a job, but a stable, long-term international career.</span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;"> </span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;"> </span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;">THE JOB</span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;"> </span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;">You will be accountable for the set-up and maintenance of all logistical activities around IMP/NIMP and Ancillary Supplies (implementing and monitoring the whole supply strategy, ensure IMP are labelled, packaged, released and distributed in the best way to support the start and the quality of the whole Clinical Trial) from the issue of the protocol until the final reconciliation at study end for your assigned projects.</span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;"> </span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;"> </span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;">To thrive in this job you will:</span></p><ul><li style="margin: 0cm 1.7pt .0001pt 36.0pt;"><span style="font-size: 11.0pt; color: windowtext;">translate study protocols into operational demand </span></li><li style="margin: 0cm 1.7pt .0001pt 36.0pt;"><span style="font-size: 11.0pt; color: windowtext;">have to take ownership and drive </span><span style="font-size: 11.0pt; color: windowtext;">IMP label development</span><span style="font-size: 11.0pt; color: windowtext;">. The design and customization of core and country labels (at a global level) will be essential for your success, and the bread and butter of a normal day for you here. </span></li><li style="margin: 0cm 1.7pt .0001pt 36.0pt;"><span style="font-size: 11.0pt; color: windowtext;">be engaged with primary and secondary </span><span style="font-size: 11.0pt; color: windowtext;">packaging</span><span style="font-size: 11.0pt; color: windowtext;"> design and provide input to Drug & Ancillary Supply </span><span style="font-size: 11.0pt; color: windowtext;">Forecasting</span><span style="font-size: 11.0pt; color: windowtext;"> projections, and </span><span style="font-size: 11.0pt; color: windowtext;">IMP Distribution Plans, </span><span style="font-size: 11.0pt; color: windowtext;">contracting and managing with Covance´s </span><span style="font-size: 11.0pt; color: windowtext;">drug distribution </span><span style="font-size: 11.0pt; color: windowtext;">external</span><span style="font-size: 11.0pt; color: windowtext;"> partners</span><span style="font-size: 11.0pt; color: windowtext;"> to make them happen. </span></li><li style="margin: 0cm 1.7pt .0001pt 36.0pt;"><span style="font-size: 11.0pt; color: windowtext;">coordinate the regulatory and logistics aspects of </span><span style="font-size: 11.0pt; color: windowtext;">importation</span></li><li style="margin-left: 36.0pt;"><span style="font-size: 11.0pt; font-family: 'Arial',sans-serif; color: windowtext;">ensure connection and alignment of the various stakeholders to ensure the delivery of IMP/NIMP and ancillaries on time at the right quality and within budget</span></li><li style="margin-left: 36.0pt;"> </li></ul><p style="margin: 0px;"><span style="font-size: 11.0pt; font-family: 'Arial',sans-serif; color: windowtext;">You will enjoy having a consultative role advising globally (EU, Americas, AsiaPac) on site storage, resupply, returns, drug inventory and expire date tracking processes. </span></p><p style="margin: 0px;"><span style="font-size: 11.0pt; font-family: 'Arial',sans-serif; color: windowtext;"> </span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt;">EMEA AND THE SAME JOB REF</span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt;">#LI-NC1 EMEA  Remote</span></p><h2>Education/Qualifications:</h2><h2 style="margin: 0in 0in 0pt;">Required:</h2><ul><li style="color: #000000;"><span style="font-size: 11pt;">University/College Degree (preferably postgraduate degree) AND 4 years relevant clinical research/GMP experience</span></li></ul><ul><li style="color: #000000;"><span style="font-size: 11pt;">Thorough understanding of global drug development and the clinical trial project management process, with a special emphasis on investigator sites, patient recruitment and retention</span></li></ul><ul><li style="color: #000000;"><span style="font-size: 11pt;">Thorough and practical working knowledge of ICH-GCP Guidelines, Clinical GMP, including relevant international requirements/guidelines for the conduct of global clinical development programs</span></li></ul><p style="margin: 0in 0in 6pt 40.5pt;"><em><span style="font-size: 10pt;">In lieu of the above requirements, candidates with <u>></u> six (6) years clinical research experience including monitoring in the pharmaceutical or CRO industries will be considered</span></em></p><p style="margin: 0in 0in 0pt;"><strong><span style="font-size: 11pt;">Preferred:</span></strong></p><ul><li style="color: #000000;"><span style="font-size: 11pt;">3 years Experience in Clinical Supply distribution/ GMP environment</span></li></ul><h2>Experience:</h2><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;">IS THIS YOU?</span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;"> </span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;">In this job, you will be doing much more than managing drug inventories… from </span><span style="font-size: 11.0pt; color: #0a0a0a;">pre-study activities to Drug Ready, through maintenance until destruction;</span><span style="font-size: 11.0pt; color: windowtext;"> providing global advice as internal expert, and working in collaboration with a wide range of teams needing your input for them to deliver (Clinical Trial Design & Strategy, Vendor Management, Quality Assurance, Business Development and Operations) – that´s you. </span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;"> </span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;">For that reason, we need you to be able to independently interpret complex clinical protocols and create your action plans out of that understanding, so you are familiar with: </span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;"> </span></p><ul><li style="margin: 0cm 1.7pt .0001pt 36.0pt;"><span style="font-size: 11.0pt; color: windowtext;">The different study and protocol designs </span></li><li style="margin: 0cm 1.7pt .0001pt 36.0pt;"><span style="font-size: 11.0pt; color: windowtext;">Drug formulation</span></li><li style="margin: 0cm 1.7pt .0001pt 36.0pt;"><span style="font-size: 11.0pt; color: windowtext;">Stability</span></li><li style="margin: 0cm 1.7pt .0001pt 36.0pt;"><span style="font-size: 11.0pt; color: windowtext;">Packaging/Labeling design and operations</span></li><li style="margin: 0cm 1.7pt .0001pt 36.0pt;"><span style="font-size: 11.0pt; color: windowtext;">Drug Supply Logistics</span></li><li style="margin: 0cm 1.7pt .0001pt 36.0pt;"><span style="font-size: 11.0pt; color: windowtext;">GMP – Annex 13</span></li></ul><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;"> </span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;">This is why we are particularly interested in candidates who have developed that clinical research knowledge working in an international CRO, ideally with end to end (full service) clinical and ancillary supplies management, directly liaising with third party clinical supplies packaging and labeling projects. At least 3 years background in Clinical Supply distribution/GMP environment</span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;"> </span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;">Also important for this job is your experience in roles where you have had to inspire effective teamwork and motivate staff within a matrix system, so you excel at networking abilities. </span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;"> </span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;">You are an expert developing specifications for IxRS systems.</span></p>

Job posted: 2021-12-20

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