Bucharest, Romania · On-site
Position Summary The Medical Safety Director, Clinical Scientist provides clinical science support to product activities, ensuring high-quality clinical input into routine maintenance documentation, safety and labeling d…
Skills: Clinical Science, Pharmacovigilance, Drug Safety, Risk Management, Regulatory Compliance
Birmingham, England, United Kingdom · On-site
Join Our Team as a Territory Business Manager! Are you passionate about wound care and eager to work for a renowned pharmaceutical company? We are looking for a dedicated Territory Business Manager to join our client’s s…
Skills: Medical sales, Wound care, Sales, Relationship management, Problem-solving
Phoenix, Arizona, United States · Remote OK
$23/hr–$26/hr
As the only global provider of commercial solutions, IQVIA understands what it takes to deliver nationally and internationally. Our teams help biopharma, medical device and diagnostic companies get their therapies to the…
Skills: Sales, Inside sales, Customer engagement, Pharmaceutical sales, Medical device support
Toronto, Ontario, Canada · On-site
$79k–$105k/yr
Aperçu du poste Effectuer les tâches au niveau national associées aux activités d’activation de sites (AS) conformément à la réglementation locale et/ou internationale applicable, aux procédures opérationnelles normalisé…
Skills: Clinical research, Site activation, Feasibility studies, Regulatory compliance, Project management
Parsippany, New Jersey, United States · Hybrid
$91k–$254k/yr
We are seeking an Associate Director, Business Systems to partner closely with Product Managers, Stakeholders and development teams on the Scion Delivery Platform portfolio. This Associate Director will translate stakeho…
Skills: Business analysis, Systems analysis, Product development, API documentation, Agile
Ciudad de México, Mexico · On-site
Job Overview Provide high level technical and general accounting services in accordance with IQVIA Finance Standard Operating Procedures (SOPs), US Generally Accepted Accounting Principles (US GAAP), Sarbanes-Oxley rules…
Skills: Accounting, US GAAP, Sarbanes-Oxley, Financial Reporting, Journal Entries
Carlsbad, California, United States · On-site
$40/hr–$42/hr
About the Role Our Women's Health Procedural Specialists experience a unique opportunity to leverage their clinical expertise while supporting healthcare providers through education and training on innovative women's hea…
Skills: Women's health, Clinical education, Procedural support, Medical device training, Breast imaging
São Paulo, São Paulo, Brazil · Remote Solely
Job Overview Review, assess, and process safety data and information across service lines, received from various sources. Distribute reports/data to both internal and external third parties following applicable regulatio…
Skills: Pharmacovigilance, Safety data processing, Adverse events collection, Database entry, Coding AEs
São Paulo, São Paulo, Brazil · Remote Solely
Job Overview Senior Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Senior Project Lead is an essenti…
Skills: Clinical Project Management, Clinical Trials, Strategic Planning, Risk Management, Stakeholder Management
Annapolis, Maryland, United States · On-site
$93k–$233k/yr
Overview Services rendered will adhere to applicable Sponsor SOPs, WIs, policies, codes of Good Clinical Practice (GCP), local regulatory requirements, etc., while serving as a subject matter expert and resource for qual…
Skills: Clinical trial management, ICH-GCP, Regulatory compliance, Site selection, Budget forecasting
Barcelona, Catalonia, Spain · On-site
As a Core Information Offering Specialist - MedTech, you will play a key role in driving the commercial success of IQVIA's MedTech information solutions across global markets outside the United States. You will support t…
Skills: MedTech, Business intelligence, Commercial excellence, Data analysis, Market insights
Chicago, Illinois, United States · Remote OK
$42k–$136k/yr
Job Overview: As a Recruiter you will play a crucial role in sourcing selecting and hiring qualified candidates to fill vacant positions within the organization. You will collaborate with management across various servic…
Skills: Talent acquisition, Sourcing, Interviewing, Candidate pipelining, Market intelligence
Durham, North Carolina, United States · Hybrid
$106k–$295k/yr
This role is based in the US and requires a hybrid work schedule going into the Wayne, PA or Durham, NC office. Job Overview The Director, Client Services directs a group of operations staff for a designated region to en…
Skills: Team leadership, Project management, Clinical trial payments, Strategic planning, Financial tracking
Mannheim, Baden-Württemberg, Germany · On-site
IQVIA™ – The Human Data Science Company™ – ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. IQVIA unterstützt Life Science Unternehmen, Verbände, …
Skills: Project management, Key account management, Sales strategy, Marketing strategy, Budget management
Durham, North Carolina, United States · On-site
$93k–$233k/yr
Job Overview Senior Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Senior Project Lead is an essenti…
Skills: Clinical Project Management, CNS Therapeutic Expertise, Bid Defense, Risk Management, Financial Forecasting
São Paulo, São Paulo, Brazil · Remote OK
Overview As a Contracts Manager within the IQVIA US Contracting Center (USCC), you will review, draft and/or redline contracts within the U.S. business unit with a focus on IQVIAs commercial services (data, analysis serv…
Skills: Contract drafting, Contract review, Redlining, Negotiation, Legal terminology
Taguig, Metro Manila, Philippines · Hybrid
Job Overview Under guidance, controls the report generation process and provides guidance and support to clients daily or as a specialist on specific products/services. Essential Functions Ensures the contract fulfillme…
Skills: Report generation, Data verification, Client inquiries, Problem solving, Analytical skills
Ciudad de México, Mexico · On-site
Support project development and execution to help clients grow in the pharmaceutical market, focusing on commercial, marketing, and financial aspects. Assist in market access research for new products, contribute to clie…
Skills: Market research, Consulting methodologies, Project development, Data analysis, Microsoft Excel
Reading, England, United Kingdom · Remote OK
Scheduler – Patient Engagement Services Fixed Term Contract (maternity cover) Remote (ideally located near to Reading, Berkshire but not essential) About the Role: We are seeking a dedicated Scheduler to join our team. T…
Skills: Organisational Skills, Time Management, Communication Skills, Customer Service Orientation, Empathy
Bogota, Capital District, RAP (Especial) Central, Colombia · Hybrid
Location: Colombia (Remote/Hybrid) Job Type: Full-time Department: Technology Product Development Support About the Role We are seeking a highly skilled Senior Support Engineer – Cloud & Data Engineering to join our prod…
Skills: Azure Databricks, Apache Spark, SQL, Apache Airflow, ETL/ELT Pipelines
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The Medical Safety Director provides clinical science support for product safety, labeling, and regulatory documentation. They collaborate with cross-functional teams to evaluate benefit-risk profiles and ensure scientific accuracy in safety reports.
Candidates must hold an MD, PharmD, PhD, or equivalent advanced life sciences degree with extensive experience in pharmacovigilance and regulatory deliverables. Strong expertise in drug safety processes and the ability to interpret complex clinical data are essential.
The Medical Safety Director, Clinical Scientist provides clinical science support to product activities, ensuring high-quality clinical input into routine maintenance documentation, safety and labeling deliverables, and issue resolution activities.
This role partners closely with cross-functional product teams, represents Clinical Science in key governance forums, and provides expert clinical review and recommendations to support product benefit-risk evaluation, regulatory compliance, and labeling consistency. The position works in close collaboration with the Global Clinical Science Lead, escalating critical issues and contributing to timely, scientifically robust decision-making.
Participate in relevant product-team meetings including Labelling Working Group (LWG)as the Clinical Science representative
Gather and provide necessary information under guidance from the GCL
Review draft documents (PBRER/PSUR, CCDS/CCSI, US Annual Report) from a Clinical Science perspective; share key points and any critical issues with the GCL
Participate in relevant Safety Management Team (SMT) meetings as the Clinical Science representative
Review Safety Validation and Evaluation Report draft documents; share key points and any critical issues with the GCL etc.
MD, PharmD, PhD, or equivalent advanced life sciences degree with strong clinical science expertise and the ability to interpret clinical, safety, and scientific literature within a benefit-risk framework.
Proven experience supporting regulatory and pharmacovigilance deliverables, including PBRER/PSUR, CCDS/CCSI, US Annual Reports, and Safety Evaluation Reports.
Hands-on experience reviewing and contributing to clinical sections of safety, regulatory, and labeling documents, ensuring scientific accuracy, consistency, and compliance.
Strong knowledge of drug safety, pharmacovigilance, risk management, and global labeling processes within the pharmaceutical industry.
Experience participating in cross-functional product teams, Safety Management Teams (SMTs), and Labeling Working Groups (LWGs) as a Clinical Science representative.
Demonstrated ability to evaluate clinical and safety data, identify risks, resolve issues, and provide clear, actionable recommendations and document wording.
Experience supporting CCDS updates, emerging safety topics, issue resolution activities, and responses to regulatory or local market queries.
Excellent scientific communication, stakeholder management, and collaboration skills within a global matrix environment.
Strong attention to detail, quality mindset, and ability to manage multiple priorities while delivering high-quality outputs within tight timelines.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA (NYSE:IQV) is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. IQVIA’s portfolio of solutions are powered by IQVIA Connected Intelligence™ to deliver actionable insights and services built on high-quality health data, Healthcare-grade AI™, advanced analytics, the latest technologies and extensive domain expertise. With approximately 88,000 employees in over 100 countries, including experts in healthcare, life sciences, data science, technology and operational excellence, IQVIA is dedicated to accelerating the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific progress, in an effort to advance healthcare. To learn more, visit www.iqvia.com.
Offices: 2400 Ellis Rd, Durham, North Carolina 27703, US
IQVIA (NYSE:IQV) is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. IQVIA’s portfolio of solutions are powered by IQVIA Connected Intelligence™ to deliver actionable insights and services built on high-quality health data, Healthcare-grade AI™, advanced analytics, the latest technologies and extensive domain expertise. With approximately 88,000 employees in over 100 countries, including experts in healthcare, life sciences, data science, technology and operational excellence, IQVIA is dedicated to accelerating the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific progress, in an effort to advance healthcare. To learn more, visit www.iqvia.com.
Offices: 2400 Ellis Rd, Durham, North Carolina 27703, US
