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CLINICAL RESEARCH ASSOCIATES, LISBON, PORTO

Laboratory Corporation of America Holdings (Covance)

Lisbon, Portugal

<h2>Job Overview:</h2><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;">New job: </span><strong><span style="font-size: 11.0pt; color: windowtext;">home based CRAs </span></strong><span style="font-size: 11.0pt; color: windowtext;">based in</span><span style="font-size: 11.0pt; color: windowtext;"><strong> Lisbon</strong> OR <strong>Porto</strong>.  </span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;"> Limited visits per month</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;"><strong><span style="font-size: 12pt; color: windowtext;">LABCORP</span></strong></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;"> </span></p><p style="margin-right: 1.7pt;"><strong><span style="font-size: 11.0pt; font-family: 'Arial',sans-serif; color: windowtext;">Covance is now Labcorp, and we are much more than a typical CRO</span></strong><span style="font-size: 11.0pt; font-family: 'Arial',sans-serif; color: windowtext;">:</span></p><p style="margin-right: 1.7pt;"><span style="font-size: 11.0pt; font-family: 'Arial',sans-serif; color: windowtext;"> </span></p><ul style="margin-top: 0cm;"><li style="color: windowtext; margin-right: 1.7pt;"><span style="font-size: 11.0pt; font-family: 'Arial',sans-serif;">We were named to <strong>Fast Company magazine’s list of 2021 Most Innovative Companies</strong> for ourleadership in scientific innovation in the fight against COVID-19. </span></li></ul><p style="margin: 0cm 1.7pt .0001pt -18.0pt;"><span style="font-family: 'Arial',sans-serif; color: windowtext;"> </span></p><ul style="margin-top: 0cm;"><li style="color: windowtext; margin-right: 1.7pt;"><span style="font-size: 11.0pt; font-family: 'Arial',sans-serif;">We were also recognized with the <strong>2020 Global CRO Company of the Year Award</strong> by Frost & Sullivan for our capacity to integrate digital technologies, remote monitoring, and telemedicine services to ensure continuity of and decentralizing clinical trials.</span></li></ul><p style="margin-right: 1.7pt;"><span style="font-size: 11.0pt; font-family: 'Arial',sans-serif; color: windowtext;"> </span></p><p style="margin-right: 1.7pt;"><span style="font-size: 11.0pt; font-family: 'Arial',sans-serif; color: windowtext;">We believe in harnessing science for human good. And in our pursuit for answers, our Clinical Reasearch Associate Team is expanding in Portugal.</span></p><p style="margin-right: 1.7pt;"><span style="font-size: 11.0pt; font-family: 'Arial',sans-serif; color: windowtext;"> </span></p><p style="margin-right: 1.7pt;"><span style="font-size: 11.0pt; font-family: 'Arial',sans-serif; color: windowtext;"> </span></p><p style="margin: 0px;"><strong><span style="font-family: verdana, geneva; font-size: 12pt;"><span style="color: windowtext;">THE SPONSOR-DEDICATED CRA JOB:</span></span></strong></p><p style="margin-right: 1.7pt;"><span style="font-family: 'Arial',sans-serif; 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 fully dedicated to </span><span style="font-size: 11.0pt; color: windowtext;">one sponsor</span><span style="font-size: 11.0pt; color: windowtext;">, a Global Top Pharmaceutical company. </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;">Labcorp has a strong presence in Portugal: as one of the biggest CROs in the country we can offer you not only a job, but a estable, long-term international career. Some benefits of this job:</span></p><p style="margin: 0px;"><strong><span style="font-family: 'Arial',sans-serif; color: windowtext;"> </span></strong></p><ul><li><span style="font-size: 11.0pt; color: windowtext;">You will have a flexible visit schedule with up to 6 visits per month (including both on site & remote)</span></li><li><span style="font-size: 11.0pt; color: windowtext;">We have Clinical Operations Managers based Portugal not in distant lands, which ensures strong day-to-day support to CRAs</span></li><li><span style="font-size: 11.0pt; color: windowtext;">Unlike other CROs and sponsor CRA jobs, our CRAs do not perform Submissions, as we have our own Start-up and Regulatory Portuguese teams.</span></li><li><span style="font-size: 11.0pt; color: windowtext;">Likewise, eTMF work and payments are tasks removed from our CRAs</span></li><li><span style="font-size: 11.0pt; color: windowtext;">We offer great opportunity to progress in Portugal into a variety of areas such as Project Manager, CTL, Line Manager, Start-up or Quality. If you want to explore our Global Clinical Development team, there are no barriers!</span></li><li><span style="font-size: 11.0pt; color: windowtext;">You will be joining a large and very collaborative team and will be able to engage with a broader Iberic Structure.  </span></li></ul><p style="margin: 0px;"><strong><span style="font-size: 11.0pt; color: windowtext;"> </span></strong></p><p style="margin: 0px;"><span style="font-size: 12pt;"><strong><span style="font-family: 'Arial',sans-serif; color: windowtext;">Responsibilities include:</span></strong></span></p><ul><li style="color: windowtext;"><span style="font-size: 11.0pt; font-family: 'Arial',sans-serif;">Responsible for all aspects of study site monitoring including routine monitoring (both onsite and remote) and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; etc</span></li></ul><p style="margin: 0px;"><span style="color: windowtext;"> </span></p><p style="margin: 0px;"><span style="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><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;">University degree, life science.</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;">Extensive knowledge of:</span></p><ul><li style="margin: 0cm 1.7pt .0001pt 36.0pt;"><span style="font-size: 11.0pt; color: windowtext;">Drug development process and client needs.</span></li><li style="margin: 0cm 1.7pt .0001pt 36.0pt;"><span style="font-size: 11.0pt; color: windowtext;">ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs.</span></li></ul><p style="margin: 0cm 1.7pt .0001pt 36.0pt;"><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;">Native Portuguese speaker – fluent English required. Good knowledge of Spanish would be considered also a nice extra… - not mandatory</span></p><h2>Experience:</h2><p style="margin: 0px;"><strong><span style="font-size: 12pt;">Is this you?</span></strong></p><p style="margin: 0px;"> </p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt;">Minimum 1 years of clinical monitoring experience </span><span style="font-size: 11.0pt; color: windowtext;">(pre-study/initiation/ routine monitoring and closeout visits) </span><span style="font-size: 11.0pt;">of international, multicenter ph I-IV clinical trials in Portugal</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;">Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines</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;">Have a full understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs</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;">Ability to resolve project-related problems and prioritize workload for self and team</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;">Strong computer skills</span></p>

Job posted: 2021-12-28

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