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- JR135319 Pharmacovigilance Associate ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future...Remote job
- ...program and company issues. Collaborating with other employees in problem solving and systems improvement. • Review regulatory/pharmacovigilance publications and information sources to keep updated on current regulations, practices, procedures and proposals. • Maintain...Remote job
- Work Schedule Standard (Mon-Fri) Environmental Conditions Office Join Us as a Safety Admin – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 ...Remote job
- ..., accurate, and compliant submission of individual case safety reports (ICSRs) related to clinical trials. This role supports pharmacovigilance and clinical operations teams by managing safety documentation, coordinating with stakeholders, and maintaining regulatory compliance...
- ...Executive Search Firm Monroe Consulting Group is recruiting a Pharmacovigilance Associate on behalf of a multinational company who specializes in patient-centric drug development and commercialization services, aiming to provide reliable clinical research solutions to...
- ...and Regional Operations. Collaborates internally with HQ functions, regional and local operations, EU Clinical Development, Pharmacovigilance, Global Medical Affairs to align on key issues/decisions across the trials. Consult with GHH as needed. What You Must have...
- ...Executive Search Firm Monroe Consulting Group Philippines is recruiting a Pharmacovigilance - Quality Assurance Assistant on behalf of a multinational CRO company. The role will report to the Regional Head with mainly remote working setup with night shift work schedule...
- ...~ Support Operational Management and Oversight Your profile: ~ Medical degree (MD) or equivalent. ~ Experience in pharmacovigilance and drug safety within the pharmaceutical or CRO industry. ~ Strong understanding of Good Clinical Practice (GCP) and pharmacovigilance...Remote job
- ...healthcare! As a Regulatory Affairs Officer at B. Braun you plays a vital role in ensuring compliance with regulatory and pharmacovigilance (PV) requirements. This position is responsible for supporting regulatory submissions, maintaining regulatory documentation,...
- ...Medicine, Nursing and Life Sciences) Must have at least 3 months of relevant experience Knowledge with clinical terms and pharmacovigilance is a plus Excellent communication skills in both spoken and written English Amenable to work on a full onsite work set-...
- ...health authorities of any safety issues including SSI/ESI and Signals. Maintain up-to-date knowledge of local requirements for pharmacovigilance, cosmetic and device vigilances including reporting requirements (for all applicable product classes in the territory) and...
- ...Quality Control: Monitor fieldwork performance, conduct back-checks, and ensure compliance with data collection standards and pharmacovigilance procedures. Data Support: Code open-ended responses, assist in data cleaning, and coordinate with data processing teams to...
- ..., Data Quality, Data Visualization, Digital Strategy, Drafting Agreements, Operational Metrics, Ownership and Accountability, Pharmacovigilance, Process Improvements, Project Management, Regional Management, Regulatory Affairs Compliance, Regulatory Affairs Management {...
- ...and tracking of patient support programs, market research programs to ensure compliance to ethical guidance and monitor for any pharmacovigilance issues. ~ New Product Introductions Assist the Senior Medical Manager in providing the business development unit,...
- ...complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that...
ProPharma Group
Makati4 days ago - ...enquiries on company products and works collaboratively with other enablers to address any issues that may arise Member of the Pharmacovigilance Risk Assessment Committee (PRAC) Develops and implements procedural documents in compliance with applicable regulations and...
Unilab, Inc.
Mandaluyong1 day ago - ...Required: A minimum of 5 or more years with contact center experiencePreferred: Prior experience in Medical/Drug Information, Pharmacovigilance, and/or Product Complaints within the pharmaceutical industry.Preferred: Prior experience in contact center in highly regulated...
ProPharma Group
Makati4 days ago - ...Pharma Chief Medical Officer (CMO).* Vigilance & Integrity: Safeguard the company’s reputation by overseeing strict adherence to Pharmacovigilance (GVP), Clinical Practice (GCP), and local ethical codes.**Who you are:**You are:* **Credentialed Expert:** You hold a Medical...
F. Hoffmann-La Roche AG
Taguig1 day ago - ...SOPs, ICH GCP and country regulations This may include data management, study start up, patient recruitment, medical monitoring, pharmacovigilance and Quality Assurance (QA). Supports Inspection Readiness for clinical trial management scope. Oversees CRAs and Central...
- ...care innovators in the world. Established in 1995, we provide expertise in clinical operations, biometrics, regulatory affairs, pharmacovigilance, medical affairs, and toxicology to help our partners advance healthcare by accelerating clinical trials with data‑driven...
ClinChoice Inc.
Pasig1 day ago - ...regulatory agency guidelines -Experience in product registration, LTO renewals, and labeling compliance -Familiar with GMP, GDP, and pharmacovigilance processes -Strong analytical, organizational, and documentation skills -Proficient in Microsoft Office applications (Word,...
Asia Cosmos Cosmetics Manufacturing
Quezon Citya month ago - ...Qualification: - Bachelor’s Degree in Health Care Studies (Pharmacy, Medicine/Alternative Medicine, Nursing and Life Sciences) - Minimum of 3 months relevant experience - Knowledge with clinical terms and pharmacovigilance is a plus - Strong communication skills
RSD Human Resource Management Consultancy
Taguiga month ago
