Pharmacovigilance Associate

**Key Accountabilities**: - Responsible for review of investigational new drug safety reports (INDSR) and submission to FDA (as applicable) - Responsible for negotiation and implementation of pharmacovigilance agreements (PVA) with business partners - Supports PV Clinical Specialists in tasks and projects as needed - Responsible for identifying and...

Clinical trials is a crucial field in the pharmaceutical industry focused on drug safety. Professionals in this area monitor, assess, and prevent adverse drug reactions to protect public health.Qualification & Specifications :MBBS,BDS,BHMS,BAMS,BSMS,PHARMACYB.Sc/M.Sc (Life Sciences / Biology / Bio Chemistry / Micro Biology / Nursing / Bio Technology), B.P.T,...

**Job Location**: New Delhi, India **Requirements**: - At least 2 years of experience in quality assurance in GCP, preferably pharmacovigilance, in the CRO or pharmaceutical industry - Awareness of global regulatory and pharmacovigilance environment - Strong written and verbal communication skills - Willingness to work from job...

The main role of a Drug Safety Associate is to monitor the safety of drugs and medical devices once they are on the market and ensure that they are being used safely. - Reviewing and evaluating adverse event reports (AERs) to determine if they meet regulatory reporting requirements. - Entering and maintaining adverse event information in safety databases -...

At Turacoz, we are a leading global provider of innovative healthcare communication solutions. We work with pharmaceutical companies, medical device manufacturers, research institutes, and healthcare organizations to deliver high-quality scientific writing, medical communications, regulatory writing, and digital marketing services. Our goal is to connect...

Company Description We are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs...

Role & responsibilities• Provide timely support for medical assessment of initial case triage and also assist in reviewing medical information queries pertaining to ICSRs. • Able to properly rank event based on seriousness criteria, labeling and causality assessment • Causality assessment for all events based on WHO algorithm and ICH guidelines also...

We are seeking life science graduates interested in building a long-term career in the Clinical Research domain. This opportunity is part of our industry-integrated Clinical Research Training Program designed to prepare candidates for roles such as CRA, CRC, and Drug Safety Associate .Role Responsibilities (Post-Training Readiness)Understand and support...

**Job Purpose**: - Provide scientific and technical expertise of the highest standards for local medical information, including interactions with Key External Experts (KEEs) and Key Opinion Leaders (KOLs) - Provide medical and scientific input and information for business strategy for the region. **Key Responsibilities**: - Develop and sustain credible...

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals...