For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and
Company: Novo Nordisk Global Business Services (GBS) Shape the safety profile of medicines that reach millions of patients worldwide – from first-in-human trials through to marketed products across diabetes, obesity, and rare diseases. Your new role
Job Title: Lead - Aggregate Reporting Employment Type: Full-time Work Type: Remote About ClinChoice: ClinChoice is a partner to the largest pharmaceutical, medical device, and consumer care innovators in the world. Established in 1995, we provide
Some careers open more doors than others. If you’re looking for a career that will unlock new opportunities, join HSBC and experience the possibilities. Whether you want a career that could take you to the top,
Welcome to Haleon. We’re a purpose-driven, world-class consumer company putting everyday health in the hands of millions. In just three years since our launch, we’ve grown, evolved and are now entering an exciting new chapter –
Overview As a Risk Analyst (Project Controls) at Linesight, you will work with highly experienced, culturally diverse, and passionate teams nurturing a strong social dynamic and a shared sense of achievement. You will gain vast industry
Career CategorySafety Job Description The Global Safety Therapeutic Areas serve as the safety experts for all Amgen products globally and are accountable for the safety strategy and major safety deliverables for each Amgen product. Leaders in
The Risk Evidence Writer collaborates with relevant teams and functions and conducts standard scientific literature searches to produce evidence-based reports/position statements. These documents will be used by the business for product benefit-risk analyses and risk management
At Demo SA, one of EU’s largest pharmaceutical manufacturers for injectable products, we are looking for a talented Regulatory Affairs Senior Associate - Labeling to join our team. The job responsibilities for this position include post-marketing
THE POSITION: The Medical Review Lead (MRL) is responsible for supporting the timely and compliant execution of product surveillance activities for client projects. The role involves oversight and contribution to aggregate reports (PADERs, PBRERs), Risk Management
PV Physician: Lead medical oversight of pharmacovigilance activities, including benefit-risk assessment, signal detection, aggregate report review, risk management plans, regulatory responses, and safety documentation. Collaborate across functions to ensure patient safety, regulatory compliance, and accurate safety
Job Description Drug Safety Physician We are seeking a drug physician in Biocon Biologics Pharmacovigilance who independently or in association with senior physicians will be responsible for continuous evaluation of the safety profile of company products
This job is with Reckitt, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ business community. Please do not contact the recruiter directly. We are Reckitt Home to the
The Risk Evidence Writer collaborates with relevant teams and functions and conducts standard scientific literature searches to produce evidence-based reports/position statements. These documents will be used by the business for product benefit-risk analyses and risk management