Drug Safety Associate

We are looking for an Associate Content Editor to join our team in Hyderabad. This is an amazing opportunity to work on OFF-X, a translational drug safety intelligence portal. The team consists of 20 people located in Spain and India and is reporting to the Regulatory and drug safety manager line. We have a great skill set in the analysis of drug safety and...

(Associate) Content Editor - Drugs team As an Associate Content Editor in Drugs team, you will be responsible for the thorough, timely, and accurate interpretation of data relevant to drugs in the form of research, analysis and delivery of weekly database filling milestones. We are looking for an Associate Content Analyst/Content Editor to join our Drugs...

(Associate) Content Editor - Drugs team As a Content Editor in Drugs team, you will be responsible for the thorough, timely, and accurate interpretation of data relevant to drugs in the form of research, analysis and delivery of weekly database filling milestones. - We are looking for an Associate Content Analyst/Content Editor to join our Drugs team in...

Job Desciption Responsibilities Receiving and answering calls from people requiring medical services or clarifications regarding a Medical Entity or Medical Device or Vaccines or Cosmetics.Understanding the requirements of the callers and provide precise information during Inbound/Outbound calls.Working quickly by multi-tasking and demonstrating the ability...

**Responsibilities**: 3. Complete case entry including case narrative writing, coding from the MedDRA dictionary and WHO drug dictionary as per applicable SOPs and Client requirements. Perform Call handler/QC Reviewer activity as needed. Send the reviewed and signed TCFs/ CDRs to the Client’s point of contact (POC). 4. Responsible for adding/ updating new...

Centella AI Therapeutics, a pioneering AI-powered drug discovery company, is seeking a passionate and inquisitive AI Drug Discovery intern to join our mission of revolutionizing healthcare through AI application. In this pivotal role, you'll delve into the world of AI and contribute to building AI models for their use in our cutting-edge drug development...

2600+ Aggregate Reports annually! Dynamic teams at Novartis are committed to scientifically evaluate benefit-risk profile of the marketed products and collaborate with Health Authorities towards the ultimate goal of Patient Safety. Your skills & experience will help us on our journey of re-imagining patient safety. - Your responsibilities include, but are...

**Summary**: The Preclinical Safety (PCS) department within the Novartis Biomedical Research - Translational Medicine Unit provides non-clinical safety strategy of products in -discovery, -development and -market, globally, with state-of-the-art regulatory compliance. As a Principal Scientist-2, you will join our PCS team in India to discuss strategies and...

Your responsibilities include, but are not limited to: - Assess seriousness, causality and labeling of serious adverse events and quality check ICSRs to ensure accurate and consistent Argus data entry from source documents and product and event coding, narrative writing and follow-up for missing or other medical important information. Including daily...

Responsible for the drug surveillance program including the necessary follow-up, risk assessment, and relatedness to product on adverse reaction reports, oversight of safety in clinical trials and post marketing programs. Participates in the resolution of any legal liability and complying with governmental regulations. Provides and contributes trending and...

Location: HyderabadRole: Associate Director, GDD Data TeamFunction & Responsibilities: Development Data Team is responsible to design and execute data management strategy across Drug Development line functions i.e. Clinical Operations, Clinical Data Standards, Technical Research & Development, Regulatory Affairs and Patient Safety. Function also collaborates...

Job Title: Safety AssociateDepartment: QuestLocation: [Delhi/LKR/NUP/EUP]Job Summary:The Safety Associate will play a crucial role in promoting and maintaining a safe and compliant work environment within the organization. This position involves actively participating in safety initiatives, conducting audits, and supporting the development and implementation...

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...

**Summary**: About the role The Preclinical Safety (PCS) department within the Novartis Biomedical Research Translational Medicine Unit provides world class preclinical safety profiling and assessment for optimal drug discovery, development and commercialization, with state-of-the-art regulatory compliance. As a Preclinical Safety Profiling Expert, you will...

As an Associate/Content Editor on the Clinical Trials team, you will analyse, cross-reference, and update all new or previously updated information in the clinical trial records from a variety of sources, including company websites, presentations, conferences, press releases, clinical trial repositories, and other potential internet sources. We are looking...

Work Experience: 7-12 yearsLocation: HyderabadConduct safety analysis activities collaborating with the onsite Principal FSM & global team as needed.Collaborate closely with the senior leaders across the other COE functions in Hyderabad.Create documents and/or evidence packages to support certification of roadmap or custom software projects.Partner with...

Work Experience: 7-12 yearsLocation: HyderabadConduct safety analysis activities collaborating with the onsite Principal FSM & global team as needed.Collaborate closely with the senior leaders across the other COE functions in Hyderabad.Create documents and/or evidence packages to support certification of roadmap or custom software projects.Partner with...

We are looking for an Associate Content Analyst/Content Analyst to join our Deals team in Hyderabad/Chennai. This is an amazing opportunity to work on Cortellis Deal Intelligence and Cortellis Digital Health Intelligence. The team consists of 11 people and is reporting to Rosary L - Team manager. We have a great skill set in Deals, Drugs and Clinical trials...

When our values align, there's no limit to what we can achieve.   Job Purpose:   Responsible for management of scheduled and unscheduled aggregate reports including but not limited to Periodic Safety Reports (PSRs) including Periodic Safety Update Reports (PSURs), Periodic Benefit-Risk Evaluation Reports (PBRERs), Addendum to Clinical Overviews...