Senior Pharmacovigilance Associate.

<strong>Job Requirements </strong><br><p>job discription:</p><ul><li>To carry out duties in accordance with the International Committee on Harmonisation (ICH) Guidelines, Good Clinical Practises (GCPs), Good Pharmacovigilance Practises (GVP), Company Standard Operating Procedures (SOPs), and all relevant laws and regulations.</li></ul><p>Qualifications:</p><p>understanding of ICH GCP and other pertinent rules and regulations.</p><p>Having familiarity with industry-standard safety databases like Oracle Argus, ARISg, or AB Cube SafetyEasy.</p><p>Excellent interpersonal and organisational skills, attention to detail.</p><p>Ability to meet deadlines and provide prompt, effective feedback on any problems.</p><p>good written and verbal communication skills, and analytical abilities.</p><p>Effective Team Member.</p><p>Scientist performing clinical research</p><p>Industry Type: Hospitals and Medical Services</p><p>Office of Research and Development</p><p>Education Role Category: Pharmaceutical & Biotechnology Employment Type: Full-Time, Permanent</p><p>Any Graduate (UG)</p><p>PG: Any Postgraduate Core Competencies</p><p>CROCodingGCPPharmaproject administrationclinical development clinical trialsPharmacovigilanceprocessing casesOracle</p><br><br>