Similar Jobs at Pfizer
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
Authors, reviews, and maintains clinical trial Basic Results disclosures for ClinicalTrials.gov, CTIS, and EudraCT. Translates clinical data and statistical outputs into compliant results records, coordinates with clinical, statistical, legal, medical writing, and study teams, addresses quality and regulator comments, maintains audit-ready documentation, and supports disclosure process improvements, training, and best practices.
Top Skills:
42 Cfr Part 11Clinicaltrials.GovCtisEu Ctd 536/2014Eu Ctr 536/2014EudractFdaaa 801Xogene Prime
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
Manage and improve Pfizer’s enterprise PKI and certificate lifecycle services. Responsibilities include designing, deploying, integrating, testing, upgrading, and supporting Microsoft Certificate Authority environments, certificate automation, HSMs, and related security services. The role provides technical leadership, operational oversight, incident and problem management, stakeholder coordination, mentoring, and 24x7 support for critical PKI services.
Top Skills:
C++Certificate Lifecycle Management (Clm)Digital SignaturesHardware Security Modules (Hsm)Identity And Access Management (Iam)ItilJavaMicrosoft Certificate AuthorityPublic Key Infrastructure (Pki)PythonRegistration AuthorityRemote Key ManagementSecurity Worlds
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
Manages Pfizer’s clinical trial data sharing and disclosure operations, including study registration, results posting, external data requests, compliance, quality reviews, metrics, and policy support. Partners with clinical, medical, legal, statistics, data management, communications, and external stakeholders to deliver disclosure commitments across ClinicalTrials.gov, EudraCT, and Pfizer.com. Leads project tracking, vendor coordination, performance analysis, risk resolution, and cross-functional execution in a global pharmaceutical environment.
Top Skills:
CdiscClinicaltrials.GovElectronic Medical Record SystemsEudractFhirHl7ExcelMS OfficeMicrosoft Powerpoint
In this pharmacovigilance role, you will carry out processing activities of Individual Case Safety Reports (both clinical trials and post-marketing sources) in the ARGUS Safety database.
Processing activities include assessing case validity, undertaking duplicate checks, creating cases in the database, prioritizing cases as per company guidance, updating cases with information provided in XML source documents, identifying adverse events, confirming their seriousness, coding products, undertaking causality and listedness assessments, drafting narratives, determining appropriate case follow-up, reviewing processed cases to verify technical judgment, accuracy, and compliance with company requirements, etc.
Here Is What You Need (Minimum Requirements):
Education = B. Pharm, M. Pharm, or Pharm. D only.
Experience = FRESHERS ONLY!
Keen attention to detail.
Solid analytical skills.
Good written and oral communication skills.
Collaborative skills.
Continuous Learning.
Bonus Points If You Have (Preferred Requirements):
Course completion and/or certification in Pharmacovigilance or good knowledge of medical terminology and global regulatory requirements for drug safety.
Publications in peer reviewed journals.
Work Location Assignment: Hybrid .
Work Location Assignment: Hybrid
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Medical
Processing activities include assessing case validity, undertaking duplicate checks, creating cases in the database, prioritizing cases as per company guidance, updating cases with information provided in XML source documents, identifying adverse events, confirming their seriousness, coding products, undertaking causality and listedness assessments, drafting narratives, determining appropriate case follow-up, reviewing processed cases to verify technical judgment, accuracy, and compliance with company requirements, etc.
Here Is What You Need (Minimum Requirements):
Education = B. Pharm, M. Pharm, or Pharm. D only.
Experience = FRESHERS ONLY!
Keen attention to detail.
Solid analytical skills.
Good written and oral communication skills.
Collaborative skills.
Continuous Learning.
Bonus Points If You Have (Preferred Requirements):
Course completion and/or certification in Pharmacovigilance or good knowledge of medical terminology and global regulatory requirements for drug safety.
Publications in peer reviewed journals.
Work Location Assignment: Hybrid .
Work Location Assignment: Hybrid
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Medical
Pfizer Chennai, Tamil Nadu, IND Office
Chennai, India
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