Pharmacovigilance Analyst (english-Spanish-Portuguese)

<h2>Job Overview:</h2><p style="margin: 0px;"><span style="font-size: 12pt;">Covance by Labcorp is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. </span><br /><br /><span style="font-size: 12pt;"><strong><u>We are recruiting for our Pharmacovigilance Team based in Sao Paulo, Brazil a team of Pharmacovigilance Analyst. This position will need to translate information from Portugues and Spanish into English.</u></strong></span></p><p style="margin: 0px;"><span style="font-size: 12pt;">Covance’s ongoing success offers team members unsurpassed growth and career development opportunities. </span><br /><span style="font-size: 12pt;">At Covance, we help make the miracles of medicine a reality. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career. This is your chance to become part of a team that helps to bring miracle of medicine to market sooner.</span></p><h2>Education/Qualifications:</h2><h2 style="margin: 0in 0in 0pt;"><span style="font-size: 12pt;">Required:</span></h2><ul><li style="color: #000000;"><span style="font-size: 12pt;">Non-degree + 3 yrs relevant experience** (or 1 yr safety experience) *</span></li><li style="color: #000000; font-family: 'Times New Roman',serif; font-size: 11pt;"><span style="font-size: 12pt;">Associates Degree + 2 yrs relevant experience** (or 1 yr safety experience) *</span></li><li style="color: #000000; font-family: 'Times New Roman',serif; font-size: 11pt;"><span style="font-size: 12pt;">Associate degree RN + 1 yr relevant experience**</span></li><li style="color: #000000; font-family: 'Times New Roman',serif; font-size: 11pt;"><span style="font-size: 12pt;">BS/BA + 0 yrs</span></li><li><span style="font-size: 12pt;"><strong><u>Fluency in English, Spanish and Portugues </u></strong></span></li></ul><p style="margin: 0px;"><span style="font-size: 12pt;">Degree preferred (but not necessary) to be in one or more of the following disciplines: Biological Sciences, Pharmacy, Nursing, Life Sciences, and Chemistry.</span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-size: 12pt;">*Safety experience includes actual experience processing AE/SAE reports, generating narratives, queries, working within safety databases, and experience with regulatory submissions.</span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-size: 12pt;">**Relevant experience includes experience in the pharmaceutical, biotechnology, or CRO industry, partly in related areas such as Medical Affairs, Clinical Data Entry and Clinical Data Management, Clinical Data Monitor, Regulatory Affairs, or Quality Assurance. </span></p><h2>Experience:</h2><h2 style="margin: 0in 0in 0pt;"><span style="font-size: 12pt;">Required:</span></h2><ul><li style="color: #000000;"><span style="font-size: 12pt;">High degree of accuracy with attention to detail.</span></li></ul><ul><li style="color: #000000;"><span style="font-size: 12pt;">Functions as a team player.</span></li></ul><ul><li style="color: #000000;"><span style="font-size: 12pt;">Good communication.</span></li></ul><ul><li style="color: #000000;"><span style="font-size: 12pt;">Good written and verbal communication skills <span style="font-family: Calibri, sans-serif;"><strong>(in English, and Portugues)</strong></span></span></li></ul><ul><li style="color: #000000;"><span style="font-size: 12pt;">Ability to work independently with moderate supervision.</span></li><li style="color: #000000;"><span style="font-size: 12pt; font-family: verdana, geneva;">Good keyboard skills with knowledge of MS Office and Windows application would be beneficial.</span></li></ul>