ICON Pharmacovigilance Specialist Jobs

<h2>ICON Hiring Pharmacovigilance Specialist – High-Paying Drug Safety Jobs in Chennai & Trivandrum</h2> <p>ICON plc is hiring experienced professionals for Pharmacovigilance Specialist roles in Chennai and Trivandrum with flexible remote or office work options. This is a full-time opportunity in the Pharmacovigilance & Patient Safety department for candidates with strong experience in drug safety, adverse event reporting, and regulatory compliance.</p> <p>Multiple openings are expected for this role, targeting experienced professionals with 6+ years of experience in pharmacovigilance and clinical safety. If you are looking to move into a high-growth, high-paying clinical research career with a global CRO, this role offers strong long-term potential.</p> <hr /> <h2>Company Overview</h2> <p>ICON plc is a globally recognized clinical research organization (CRO) and healthcare intelligence provider. The company partners with leading pharmaceutical, <a class="wpil_keyword_link" title="Biotechnology" href="https://pharmastuff.org/jobs/biotechnology" data-wpil-keyword-link="linked" data-wpil-monitor-id="15823">biotechnology</a>, and medical device organizations to accelerate drug development and improve patient outcomes.</p> <p>With operations across more than 100 countries, ICON plays a critical role in clinical trials, regulatory consulting, and drug safety monitoring. The organization is known for its strong compliance framework, advanced data analytics, and commitment to patient-centric innovation.</p> <hr /> <h2>Job Role & Responsibilities</h2> <h3>Pharmacovigilance Specialist (Drug Safety)</h3> <ul> <li>Review, collect, and analyze adverse event reports to ensure compliance with global pharmacovigilance regulations</li> <li>Perform signal detection and risk assessment to identify potential safety concerns</li> <li>Prepare and submit safety reports to regulatory authorities within defined timelines</li> <li>Collaborate with clinical, regulatory, and medical teams for safety evaluations</li> <li>Support audits, inspections, and pharmacovigilance system compliance activities</li> <li>Stay updated with global drug safety regulations, including ICH guidelines and local requirements</li> </ul> <hr /> <h2>Eligibility / Qualifications</h2> <ul> <li>Educational Qualification: B.Pharm, M.Pharm, Pharm.D, BSc, MSc (Life Sciences, Biotechnology, Microbiology, <a class="wpil_keyword_link" title="Biochemistry" href="https://pharmastuff.org/jobs/biochemistry" data-wpil-keyword-link="linked" data-wpil-monitor-id="15824">Biochemistry</a>)</li> <li>Experience: Minimum 6+ years in pharmacovigilance or drug safety roles</li> <li>Strong knowledge of adverse event reporting, signal detection, and regulatory submissions</li> <li>Experience in clinical research or pharmaceutical industry preferred</li> <li>Excellent analytical, communication, and documentation skills</li> </ul> <p>Relevant Courses: B.Pharm, M.Pharm, Pharm.D, BSc Life Sciences, MSc Biotechnology, MSc Microbiology, MSc Biochemistry</p> <hr /> <h2>Location & Salary</h2> <ul> <li>Job Location: Chennai, Tamil Nadu & Trivandrum, Kerala</li> <li>Work Mode: Remote / Hybrid / Office</li> <li>Salary Range: ₹10 LPA – ₹22 LPA (approximate based on pharmacovigilance experience and CRO standards)</li> </ul> <p>This salary reflects strong demand for experienced drug safety professionals in global clinical research organizations.</p> <hr /> <h2>Application Process</h2> <p>Apply directly through the official ICON careers portal:</p> <p>Apply Here: <a href="https://careers.iconplc.com/job/pharmacovigilance-specialist-in-india-chennai-jid-50335">https://careers.iconplc.com/job/pharmacovigilance-specialist-in-india-chennai-jid-50335</a></p> <hr /> <h2>Frequently Asked Questions (FAQs)</h2> <h3>Is this role suitable for freshers?</h3> <p>No, this role requires a minimum of 6 years of pharmacovigilance experience.</p> <h3>What is pharmacovigilance?</h3> <p>Pharmacovigilance involves monitoring the safety of medicines by detecting, assessing, and preventing adverse effects.</p> <h3>What career growth can I expect?</h3> <p>You can grow into Senior Drug Safety Specialist, Pharmacovigilance Manager, or Global Safety Lead roles.</p> <h3>Is this a remote job?</h3> <p>Yes, this role offers flexible remote or hybrid working options.</p> <hr /> <h2>Summary</h2> <table> <thead> <tr> <th>Category</th> <th>Details</th> </tr> </thead> <tbody> <tr> <td>Company</td> <td>ICON plc</td> </tr> <tr> <td>Vacancies</td> <td>Pharmacovigilance Specialist</td> </tr> <tr> <td>Required Education</td> <td>B.Pharm, M.Pharm, Pharm.D, BSc, MSc (Life Sciences, Biotechnology, Microbiology, Biochemistry)</td> </tr> <tr> <td>Experience</td> <td>6+ years in pharmacovigilance / drug safety</td> </tr> </tbody> </table>

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