pharmacovigilance scientist

Accenture

Skill required: Pharmacovigilance Services - Pharmacovigilance &amp; Drug Safety Surveillance 
Designation: Pharmacovigilance Services Analyst 
Qualifications:Any Graduation/Bachelor of Pharmacy/Master of Pharmacy
 
Years of Experience:2 to 5 years
 
Language - Ability:Japanese - Elementary
 
About Accenture 
Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song&mdash; all powered by the world&rsquo;s largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We embrace the power of change to create value and shared success for our clients, people, shareholders, partners and communities.Visit us at www.accenture.com
 
What would you do? You will be aligned with our Life Sciences R&amp;D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance &amp; Regulatory, helping the world&acirc;&euro;&trade;s leading biopharma companies bring their vision to life &acirc;&euro;&ldquo; enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience. Pharmacovigilance Services involve the detection, assessment, and prevention of adverse effects related to pharmaceutical products. These services ensure the safety and efficacy of medications by monitoring and analyzing data from clinical trials, healthcare providers, and patients. The goal is to identify potential risks and take appropriate actions to protect patient health. They also help pharmaceutical companies comply with regulatory requirements. Effective pharmacovigilance services are essential for maintaining public trust in medications. Create and manage case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database as per client guidelines and applicable global regulatory requirements. 
What are we looking for? &bull;Ability to work well in a team &bull;Adaptable and flexible &bull;Agility for quick learning &bull;JLPT (N3 to N5)
 
Roles and Responsibilities: &bull;In this role you are required to do analysis and solving of lower-complexity problems &bull; Your day to day interaction is with peers within Accenture before updating supervisors &bull; In this role you may have limited exposure with clients and/or Accenture management &bull; You will be given moderate level instruction on daily work tasks and detailed instructions on new assignments &bull; The decisions you make impact your own work and may impact the work of others &bull; You will be an individual contributor as a part of a team, with a focused scope of work &bull; Please note that this role may require you to work in rotational shifts
 
Any Graduation,Bachelor of Pharmacy,Master of Pharmacy

Pharmacovigilance Services Analyst

Abbott

<div>Pharmacovigilance Specialist
Working at Abbott 
At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You&rsquo;ll also have access to:
Career development with an international company where you can grow the career you dream of.
A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.
A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.
The Opportunity 
This position works out of our Dubai location.
Divisional Information
Established Pharmaceuticals
We are committed to bringing the benefits of our trusted medicines to more people in the world&rsquo;s fastest-growing countries. Our broad portfolio of high-quality and differentiated branded generic medicines reaches across multiple therapeutic areas including gastroenterology, women's health, cardiometabolic, pain management/central nervous system, and respiratory.
Primary Job Function:
The Affiliate Safety Representative Back Up (ASR BU) in GEM and Egypt ensures that all activities related to pharmacovigilance (PV) for both Abbott EPD investigational and registered medicinal products are performed at cluster level in accordance with internal Abbott policies and procedures as well as with local regulatory requirements. The ASR further is the primary pharmacovigilance interface of Abbott EPD with local health authorities and represents pharmacovigilance internally within the Affiliate organization.
Core Job Responsibilities:<ul><li>
Acts as a local contact point on a 24/7/365 basis in UAE.</li><li>
Support of Sr. PV Specialist - GEM with maintenance of the Affiliate PV System Country Chapter and additional local PV procedures, forms, and templates</li><li>
PV business continuity planning and notification of any business interruptions that pose a threat locally or globally to pharmacovigilance processes or endanger regulatory compliance</li><li>
Receipt, recording, and reconciliation of safety information</li><li>
Safety surveillance including literature and health authority website screening and preparation of local periodic safety reports and Risk Management Plans</li><li>
Regulatory submission of safety information</li><li>
Basic PV training of local EPD staff</li><li>
PV record retention and archiving</li><li>
Implementation of out-of-office coverage for receiving and recording safety-relevant information</li><li>
Maintenance of local PV product list</li><li>
Ensure PV matters in local interventional studies and local non-interventional organized data collection schemes.</li><li>
Negotiation and implementation of local commercial pharmacovigilance agreements and local pharmacovigilance service agreements</li><li>
Due Diligence for product acquisition or in-licensing negotiated by an Affiliate organization.</li><li>
Provision of local PV Compliance metrics and management of non-compliances</li><li>
Coordination/management of PV audits and inspections at the Affiliate level</li><li>
Ensure vigilance compliant to local legislation for Abbott EPD products beyond medicinal products such as medical devices and food supplements.</li></ul>
Position Accountability/Scope:
The role takes responsibility for implementation and maintenance of a functional and compliant local PV system:<ul><li>
Implementation of local legislative and Abbott internal requirements in GEM affiliate (UAE, Kuwait, Bahrain, Qatar, Oman, Iran, Iraq, Yemen, Lebanon, Jordan, Syria) and Egypt during the absence of the ASRs.</li><li>
Local PV interface to Health Authorities</li><li>
PV point of contact for Affiliate non-PV functions and GPV headquarter.</li><li>
Works in collaboration with local non-PV stakeholders to maintain a timely and complete exchange of PV-relevant information.</li><li>
Supports the Sr. PV Specialist &ndash; GEM, Manager PV Regional or GPV headquarter for specific global projects, as assigned.</li></ul>
Minimum Education:
Ideally graduate with a Life Sciences or Pharmacy degree or equivalent qualification.
Minimum Experience/Training Required:<ul><li>
PV experience in pharmaceutical company is preferred.</li><li>
Understanding of local PV regulation.</li><li>
Ability to give attention to the detail.</li><li>
Computer literacy (Windows, MS Office).</li><li>
Good English language skills.</li><li>
Good communication skills with internal and external stakeholders.</li></ul>
Apply Now
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at abbott.com, on LinkedIn at https://www.linkedin.com/company/abbott-/, and on Facebook at https://www.facebook.com/AbbottCareers.</div>

Pharmacovigilance Specialist

Ypske

Job DescriptionWe are seeking an experienced Senior Pharmacovigilance Data Analyst (AI-Enabled) to support a U.S.-based life sciences client in a fully remote, contract role. This position is ideal for professionals based in Lahore with strong pharmacovigilance and drug safety experience who are comfortable working with global teams and AI-assisted workflows.Key Responsibilities<ul><li>Analyze pharmacovigilance data, including ICSRs, to support safety monitoring</li><li>Assist with signal detection, trend analysis, and safety data review</li><li>Perform MedDRA coding review and ensure data quality and compliance</li><li>Support reconciliation activities and regulatory reporting readiness</li><li>Collaborate with AI-assisted tools and automation workflows to improve PV efficiency</li><li>Work closely with U.S.-based stakeholders across time zones</li></ul>Required Qualifications<ul><li>Bachelor&rsquo;s or Master&rsquo;s degree in Pharmacy, Pharmacology, Life Sciences, or related field</li><li>4+ years of experience in Pharmacovigilance / Drug Safety</li><li>Strong hands-on experience with ICSR case processing</li><li>Solid knowledge of MedDRA coding and PV compliance requirements</li><li>Experience with safety databases such as Argus Safety or ArisG</li><li>Excellent written and verbal English communication skills</li></ul>Preferred Qualifications<ul><li>Exposure to AI, automation, or analytics tools in PV or clinical data</li><li>Experience supporting U.S. or EU regulatory environments</li><li>Familiarity with signal detection methodologies</li></ul>Work Arrangement<ul><li>Location: Remote (Lahore-based candidates preferred)</li><li>Contract Type: Contract / Hourly</li><li>Time Zone: Ability to overlap with U.S. working hours as needed</li></ul>Why Join<ul><li>Work with a U.S. life sciences client on high-impact safety projects</li><li>Fully remote role with long-term contract potential</li><li>Opportunity to gain exposure to AI-enabled pharmacovigilance workflows</li></ul>Job Types: Full-time, ContractWork Location: Remote

Senior Pharmacovigilance Data Analyst (AI-Enabled) – Remote (Lahore)

White Mastery Systems

<ul><li>Data &amp; Tech: Data Scientist, AI/Machine Learning Specialist, Software Developer, Data Analyst, Python Developer.</li><li>Research &amp; Development: Research Scientist, Biochemist, Junior Research Fellow, Lab Technician, Biotech Researcher, Pharmacovigilance Associate.</li><li>Healthcare: Assistant Dietician, Radiographer, Clinical Research Associate, roles in Pharmacy.</li><li>Education &amp; Academia: University Lecturer, Professor, PGT Teacher (with B.Ed.).</li><li>Engineering: Electrical Engineer, Automation Tester, roles in Water Quality.</li><li>Government &amp; Other Sectors: Roles in ISRO, Ministry of Defense, Finance, Environmental Agencies, and</li></ul>Job Types: Full-time, Permanent, FresherPay: ₹18,086.00 - ₹52,273.64 per monthBenefits:<ul><li>Health insurance</li><li>Paid sick time</li><li>Paid time off</li><li>Provident Fund</li></ul>Work Location: In person

M.Sc freshers

EVA Pharma

<div>Join EVA Pharma, a leading pharmaceutical company dedicated to empowering the fight for Health and well-being as a fundamental human right. Recognized and certified as a best place to work, we are committed to fostering a supportive and innovative environment for our team members.
Job Summary 
We are looking for a dedicated QPPV Specialist to join our dynamic Pharmacovigilance team. The ideal candidate will be responsible for ensuring the safety and efficacy of our products, as well as maintaining compliance with regulatory requirements.
Key Responsibilities:<ul>
<li><ul><li>
Ensure the PSMF &amp;PSSF are accurate, up-to-date, and aligned with SFDA requirements.</li></ul></li>
<li><ul><li>Manages timely collection, assessment, and submission of ICSRs to the SFDA within legal timelines.</li></ul></li>
<li><ul><li>Ensure continuous monitoring of safety signals and management of emerging safety issues.</li></ul></li>
<li><ul><li>Act as the single PV contact point for the SFDA and PV inspections (24/7 availability).</li></ul></li>
<li><ul><li>Ensure compliance with all national pharmacovigilance requirements, risk minimization measures, and safety communication obligations.</li></ul></li>
<li><ul><li>Ensure timely SFDA submission of PSUR/PBRER, RMP, DHPC, and any safety-related regulatory requests.</li></ul></li>
<li><ul><li>Create and maintain local PV SOPs covering all SFDA-required PV activities.</li></ul></li>
<li><ul><li>Participate in audits, CAPA planning, and implementation of corrective/preventive measures.</li></ul></li>
</ul>
Requirements<ul><li><ul>
<li>
Bachelor&rsquo;s degree or higher in Pharmacy or Medicine
</li><li>Licensed by the Saudi Commission for Health Specialties
</li><li>Full-time resident in Saudi Arabia (KSA)
</li><li>Pharmacovigilance experience preferred
</li><li>PV training in ICSR processing and MedDRA coding preferred
</li><li>PV training in signal detection preferred
</li><li>Knowledge/training in PSUR/PBRER, RMP, PSMF, and KSA PV regulations preferred</li></ul></li></ul></div>

QPPV Specialist

Unilever

<div>
 
 Job Title:
 
 Manager (Medical Doctor), Global Market Vigilance (GMV)
 
 
 
 Location:
 
 Unilever Bangalore R&amp;D
 
 
 
 Function:
 
 Global Regulatory Affairs (GRA), Wellbeing Collective (WBC)
 
 
 
 Job Summary
 
 
 
 The ideal candidate is a medical doctor who can leverage their healthcare professional background and hands-on experience in Pharmacovigilance to ensure the highest standards of safety assessment and regulatory compliance. The role applying clinical judgment, conducting in depth adverse event reviews, and contributing proactively to ensure the safety of our products and consumers.
 
 
 
 Key Responsibilities
 
 
 
 <ul>
 <li>
 Case Assessment and Medical/ Clinical Review:
 </li>
 <ul>
 <li>
 Conduct comprehensive and in-depth review of health-related complaints (i.e. adverse events or AEs) regarding our products received from various sources (consumers, healthcare professionals, clinical studies, etc.)
 </li>
 <li>
 Evaluate case seriousness, expectedness, and identify any missing or incomplete information while ensuring data integrity and accuracy.
 </li>
 <li>
 Ensure all AEs are documented and coded accurately using industry-standard medical terminologies like MedDRA (Medical Dictionary for Regulatory Activities).
 </li>
 <li>
 Actively participate in the analysis of aggregate safety data to identify potential safety signals or trends.
 </li>
 </ul>
 <li>
 Global Regulatory Compliance and Quality Assurance:
 </li>
 <ul>
 <li>
 Ensure all medical review and case processing activities are executed in strict adherence to a complex web of global and local regulatory requirements (e.g., FDA 21 CFR 312, EMA Good Pharmacovigilance Practices (GVP), etc.) and internal Standard Operating Procedures (SOPs).
 </li>
 <li>
 Contribute to internal and external audits and inspections, acting as a subject matter expert on adverse event case management.
 </li>
 </ul>
 <li>
 Strategic Cross-Functional Collaboration:
 </li>
 <ul>
 <li>
 Serve as a key liaison for safety-related inquiries from internal partners, including Legal, Marketing, R&amp;D, and Quality Assurance.
 </li>
 </ul>
 <li>
 Mentorship and Continuous Improvement:
 </li>
 <ul>
 <li>
 Serve as a mentor to team members working in AE management process and provide training as well as guidance on case assessment approaches.
 </li>
 <li>
 Identify and propose improvements to existing workflows and tools to enhance efficiency, accuracy, and compliance within the GMV team.
 
 </li>
 </ul>
 </ul>
 
 Required Skills, Qualifications, And Experience
 
 
 
 <ul>
 <li>
 Education: Medical degree (MBBS or MD) from an accredited institution is required.
 </li>
 <li>
 Experience:
 </li>
 <ul>
 <li>
 Minimum of 3+ years of strong expertise in pharmacovigilance and patient/ consumer safety working in the Pharmaceutical, Medical Device or Consumer Healthcare industries.
 </li>
 <li>
 Extensive firsthand experience using global pharmacovigilance databases. Experience with Veeva Vault Safety is highly desired.
 </li>
 <li>
 Ability to perform robust medical reviews and assessments of adverse event and serious adverse cases.
 </li>
 <li>
 Well versed in safety &amp; causality assessments, medical narrative writing, using MedDRA coding and reviewing MedWatch and CIOMS reports.
 </li>
 </ul>
 <li>
 Technical and Professional Skills:
 </li>
 <ul>
 <li>
 Medical and Scientific Knowledge: Strong foundational understanding of human physiology, clinical pharmacology as well as side effects associated with use of pharmaceuticals, medical devices, consumer products etc. Ability to apply this knowledge to interpret consumer complaint information, clinical data, lab results, and medical reports.
 </li>
 <li>
 Regulatory Acumen: In-depth knowledge of global pharmacovigilance regulations, guidelines, and industry best practices (especially US FDA, Health Canada).
 </li>
 <li>
 Communication &amp; Collaboration: Exceptional ability to communicate complex medical concepts clearly and concisely, both verbally and in writing, to both scientific and non-scientific audiences.
 </li>
 <li>
 Analytical Rigor: Excellent critical thinking and critical thinking skills with a meticulous diligence and a high degree of accuracy.
 
 </li>
 </ul>
 </ul>
 
 Our commitment to Equality, Diversity &amp; Inclusion
 
 
 
 Unilever embraces diversity and encourages applicants from all walks of life! This means giving full and fair consideration to all applicants and continuing development of all employees regardless of age, disability, gender reassignment, race, religion or belief, sex, sexual orientation, marriage and civil partnership, and pregnancy and maternity.
 
 
 
 "All official offers from Unilever are issued only via our Applicant Tracking System (ATS). Offers from individuals or unofficial sources may be fraudulent&mdash;please verify before proceeding."
 
</div>

Manager (Medical Doctor), Global Market Vigilance (GMV)

<div>Job Title: Manager (Medical Doctor), Global Market Vigilance (GMV)
Location: Unilever Bangalore R&amp;D
Function: Global Regulatory Affairs (GRA), Wellbeing Collective (WBC)
Job Summary
The ideal candidate is a medical doctor who can leverage their healthcare professional background and hands-on experience in Pharmacovigilance to ensure the highest standards of safety assessment and regulatory compliance. The role applying clinical judgment, conducting in depth adverse event reviews, and contributing proactively to ensure the safety of our products and consumers.
Key Responsibilities:<ul><li>
Case Assessment and Medical/ Clinical Review:<ul><li>
Conduct comprehensive and in-depth review of health-related complaints (i.e. adverse events or AEs) regarding our products received from various sources (consumers, healthcare professionals, clinical studies, etc.)</li><li>
Evaluate case seriousness, expectedness, and identify any missing or incomplete information while ensuring data integrity and accuracy.</li><li>
Ensure all AEs are documented and coded accurately using industry-standard medical terminologies like MedDRA (Medical Dictionary for Regulatory Activities).</li><li>
Actively participate in the analysis of aggregate safety data to identify potential safety signals or trends.</li></ul></li><li>
Global Regulatory Compliance and Quality Assurance:<ul><li>
Ensure all medical review and case processing activities are executed in strict adherence to a complex web of global and local regulatory requirements (e.g., FDA 21 CFR 312, EMA Good Pharmacovigilance Practices (GVP), etc.) and internal Standard Operating Procedures (SOPs).</li><li>
Contribute to internal and external audits and inspections, acting as a subject matter expert on adverse event case management.</li></ul></li><li>
Strategic Cross-Functional Collaboration:<ul><li>
Serve as a key liaison for safety-related inquiries from internal partners, including Legal, Marketing, R&amp;D, and Quality Assurance.</li></ul></li><li>
Mentorship and Continuous Improvement:<ul><li>
Serve as a mentor to team members working in AE management process and provide training as well as guidance on case assessment approaches.</li><li>
Identify and propose improvements to existing workflows and tools to enhance efficiency, accuracy, and compliance within the GMV team.</li></ul></li></ul>
Required Skills, Qualifications, and Experience<ul><li>
Education: Medical degree (MBBS or MD) from an accredited institution is required.</li><li>
Experience:<ul><li>
Minimum of 3+ years of strong expertise in pharmacovigilance and patient/ consumer safety working in the Pharmaceutical, Medical Device or Consumer Healthcare industries.</li><li>
Extensive firsthand experience using global pharmacovigilance databases. Experience with Veeva Vault Safety is highly desired.</li><li>
Ability to perform robust medical reviews and assessments of adverse event and serious adverse cases.</li><li>
Well versed in safety &amp; causality assessments, medical narrative writing, using MedDRA coding and reviewing MedWatch and CIOMS reports.</li></ul></li><li>
Technical and Professional Skills:<ul><li>
Medical and Scientific Knowledge: Strong foundational understanding of human physiology, clinical pharmacology as well as side effects associated with use of pharmaceuticals, medical devices, consumer products etc. Ability to apply this knowledge to interpret consumer complaint information, clinical data, lab results, and medical reports.</li><li>
Regulatory Acumen: In-depth knowledge of global pharmacovigilance regulations, guidelines, and industry best practices (especially US FDA, Health Canada).</li><li>
Communication &amp; Collaboration: Exceptional ability to communicate complex medical concepts clearly and concisely, both verbally and in writing, to both scientific and non-scientific audiences.</li><li>
Analytical Rigor: Excellent critical thinking and critical thinking skills with a meticulous diligence and a high degree of accuracy.</li></ul></li></ul>
Our commitment to Equality, Diversity &amp; Inclusion
Unilever embraces diversity and encourages applicants from all walks of life! This means giving full and fair consideration to all applicants and continuing development of all employees regardless of age, disability, gender reassignment, race, religion or belief, sex, sexual orientation, marriage and civil partnership, and pregnancy and maternity. 
 
&quot;All official offers from Unilever are issued only via our Applicant Tracking System (ATS). Offers from individuals or unofficial sources may be fraudulent&mdash;please verify before proceeding.&quot;</div>

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524 pharmacovigilance scientist jobs NEAR_ME

Pharmacovigilance Services Analyst

Pharmacovigilance Specialist

Senior Pharmacovigilance Data Analyst (AI-Enabled) – Remote (Lahore)

M.Sc freshers

QPPV Specialist

Manager (Medical Doctor), Global Market Vigilance (GMV)

Manager (Medical Doctor), Global Market Vigilance (GMV)