BA Pharmacovigilance
Omni Inclusive
Pharmacovigilance Case Processing And Business Analyst Bachelor's degree in Life Sciences, Pharmacy, or related field. 10-15 years of experience in pharmacovigilance case processing and business analysis. Strong business analysis skills with the ability to understand and document business process and requirements. Experience in working with ARGUS processing system is a must. Excellent communication skills, both written and verbal. Proven ability to bridge the gap between business requirements and tec Omni Inclusive
$239.9k - $399.8k
...conduct, and analysis within Hematology. The medical director works closely with other functions such as regulatory affairs, pharmacovigilance, biostatistics, and medical affairs to ensure that the clinical development program meets the scientific, ethical, and regulatory...SuggestedPermanent employmentFull timeInternshipH1bLocal areaVisa sponsorshipWork visaRelocation package2 days per week- ...manage non-Ph.D. scientistsQualificationsBachelor’s degree (BS/ BA) in the life sciences (molecular/ cellular biology,... ...Pharmacodynamics, Pharmacokinetics, Pharmacology, Pharmacometrics, Pharmacovigilance, Process Improvements, Product Improvements, Relationship Building...SuggestedFull timeLocal areaAfternoon shift
$106.2k - $167.2k
...labeling experience or other relevant pharmaceutical industry experience (e.g., Medical Affairs, Regulatory Affairs, Clinical, or Pharmacovigilance). An advanced degree with relevant labeling or pharmaceutical industry experience gained during graduate studies may be...SuggestedFull timeFor contractorsLocal areaFlexible hours$166.5k - $203.5k
...workforce strategy to ensure we have the right talent, at the right time, in the right way.Reporting to the Senior Director, Global Pharmacovigilance Compliance, Standards and Training, this role will focus on the collaboration with business process owners (BPOs) develop and/...SuggestedMinimum wageFull timeWork at officeLocal areaFlexible hours- MSD Malaysia is offering a Future Talent Program internship in Pharmacovigilance - Operations & Global Process Enablement for 10-12 weeks. You will collaborate with cross-functional global teams to enhance PV policies, contribute to AI-driven process improvements, and support...SuggestedInternship
- ...Pharmacovigilance Safety Specialist Education: Bachelor's degree or Master's degree or Advance level degree in a life science/healthcare/pharmaceutical related field. Required: Candidate is required to have at least 2 years of pharmacovigilance safety experience...For contractorsFlexible hours2 days per week
- ...Trial Designs, Coaching, Critical Thinking, Drug Discovery Development, Emerging Technologies, Molecular Diagnostics, Organizing, Pharmacovigilance, Presentation Design, Process Improvements, Productivity Planning, Scientific ResearchSummaryLocation: Malvern, Pennsylvania,...Full timeLocal area
$39.11k - $111.11k
...passionate about healthcare, innovation, and regulatory excellence? We are seeking a motivated and detail-oriented intern to join our Pharmacovigilance - Operations & Global Process Enablement team for a 10-12 week paid internship. If you thrive in a dynamic environment, love...Fixed term contractInternshipWorldwideRelocationVisa sponsorshipFlexible hoursShift work- Responsibilities: Manages and directs functions to comply with standard operating procedures, regulatory safety and pharmacovigilance and business technology quality standards in compliance with national and international regulations, such as relevant GxP guidelines and...Local area
- CSL Behring is seeking a Senior Pharmacovigilance professional in the United States to lead global PV activities, ensuring compliance with GxP and regulatory requirements. You will oversee signal detection, safety data analysis, and the preparation for regulatory inspections...
$143.01k - $168.47k
...are completed within established timelines.Collaborate with Data Management, Clinical Supply, Biometrics, Regulatory Affairs, Pharmacovigilance, Medical Writing, and other cross-functional teams to support successful study execution.Monitor study enrollment, subject tracking...Minimum wageFull timeWork at officeLocal areaFlexible hours- CSL is seeking a GVP Auditor in King of Prussia, PA, to ensure compliance with global audit plans and safety data accuracy. The successful candidate will conduct extensive audits of both external partners and internal safety functions, requiring strong regulatory knowledge...
- ...Coaching, Consulting, Critical Thinking, Drug Discovery Development, Emerging Technologies, Molecular Diagnostics, Pharmacogenetics, Pharmacovigilance, Process Improvements, Quality Assurance (QA), Relationship Building, Research Documents, Scientific Research, Technologically...Full timeLocal area
- CSL Plasma seeks a Senior Pharmacovigilance Leader to direct functions ensuring compliance with GxP, safety reporting, and regulatory standards across global operations. You will lead PV strategy, oversee inspections, manage CAPA/SOP development, and provide advanced safety...
- ...Trial Designs, Coaching, Critical Thinking, Drug Discovery Development, Emerging Technologies, Molecular Diagnostics, Organizing, Pharmacovigilance, Presentation Design, Process Improvements, Productivity Planning, Scientific ResearchSummaryLocation: Malvern, Pennsylvania,...Full timeLocal area
$117k - $201.25k
...delivering enterprise-scale scientific data products.Experience supporting drug discovery, development, clinical research, or pharmacovigilance organizations.Experience developing predictive models in drug discovery, development, clinical research, or pharmacovigilance...Full timeLocal areaImmediate start- ...Coaching, Consulting, Critical Thinking, Drug Discovery Development, Emerging Technologies, Molecular Diagnostics, Pharmacogenetics, Pharmacovigilance, Process Improvements, Quality Assurance (QA), Relationship Building, Research Documents, Scientific Research, Technologically...Full timeLocal area
$117k - $201.25k
...execute a scientific data product strategy across discovery, translational science, preclinical safety, clinical development, pharmacovigilance, and real-world evidence. Design data integration frameworks and harmonization strategies (SEND, SDTM, ADaM, MedDRA, Imaging,...Immediate start- ...requires close collaboration with Clinical Operations, Regulatory Affairs, Biostatistics and Data Management, Drug Safety and Pharmacovigilance, Translational Medicine, Medical Affairs, and other key partner functions, as well as contribution to governance discussions and...
$117k - $201.25k
...Trial Designs, Coaching, Critical Thinking, Drug Discovery Development, Emerging Technologies, Molecular Diagnostics, Organizing, Pharmacovigilance, Presentation Design, Process Improvements, Productivity Planning, Scientific ResearchThe anticipated base pay range for this...Full timeContract workLocal areaImmediate start$231.9k - $365k
Job DescriptionWe aspire to be the premier research-intensive biopharmaceutical company with over 130-year history. We’re at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. Our...Full timeFor contractorsLocal area- ...partners and internal safety functions, you identify the findings and non-compliance trends that could impact the reliability of our pharmacovigilance system. We are looking for an experienced auditor who can navigate complex safety environments and work collaboratively with...Full timeLocal area
$142.4k - $224.1k
Job DescriptionJob Description: The Nonclinical Drug Safety department is seeking a motivated and talented toxicologist to conduct and/or monitor toxicity studies (GLP and non-GLP) as a Study Director or Study Monitor. Toxicologists at our Company are integral members ...Full timeFor contractorsLocal area$24 - $25 per hour
A leading pharmaceutical company is seeking a Process Operator in Phoenixville, PA, to micronize and mill active pharmaceutical ingredients. This role requires adherence to rigorous safety and cGMP standards, with opportunities for overtime. Candidates should possess a ...- We’re a company of agile, customer-oriented individuals with a shared commitment to integrity, servant leadership, and teamwork. Our associates take pride and ownership in their work, and innovate to provide the highest quality, life-enhancing medical technology in the ...Flexible hoursShift work
- A prominent Pharmaceuticals Company seeks a Project Manager - Technical I to oversee artwork request management for biopharmaceutical products. The role involves coordinating with stakeholders, ensuring compliance with regulatory timelines, and supporting large-scale projects...Contract work
- ...Coaching, Consulting, Critical Thinking, Drug Discovery Development, Emerging Technologies, Molecular Diagnostics, Pharmacogenetics, Pharmacovigilance, Process Improvements, Quality Assurance (QA), Relationship Building, Research Documents, Scientific Research, Technologically...Local area
$190.8k - $300.3k
Job DescriptionThe Nonclinical Drug Safety (NDS) Therapeutic Area Leader (TAL) is a senior scientific leader responsible for advancing the vision and goals of NDS and our company as an industry leader in drug development, product registration, and post-marketing support...Full timeFor contractorsSecond jobLocal areaFlexible hours$141.08k - $235.13k
...Drug Research, Drug Target Identification, Metabolism, PBPK Modeling, Pharmaceutical Products, Pharmacokinetics, Pharmacology, Pharmacovigilance, Target Research* If you are based in Cambridge, MA; Waltham, MA; Rockville, MD; or San Francisco, CA, the annual base salary...Relocation package- JOB TITLE: Project Manager - Technical I CLIENT: A prominent Pharmaceuticals Company CONTRACT: 12 months initial contract (5/22/2017 )- there is a possibility of extension LOCATION: Collegeville - PA 19426 Pay Rate: To be discussed over the phone POSITION SUMMARY Responsible...Contract workWork experience placementLocal area
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