Drug Safety Associate

(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...

**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...

About the RoleWe are seeking a highly skilled Pharmaceutical Safety Professional to join our team. This fresher-level position is ideal for individuals with 0 to 1 year of work experience.The role is available in multiple locations, including Hyderabad, Pune, Bangalore Urban, Chennai, and Vijayawada, and offers options for full-time, remote, internship, or...

Research Associate in a pharmaceutical company with 1 to 2 years of experience and a background in both MSc and BSc education, your role focuses on supporting research and development activities to advance drug discovery, development, and optimization processes. Here's a brief job description: **Key responsibilities**: - Conducting literature reviews and...

**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...

**Job Type**: Full-Time, Entry-Level **Job Summary**: We are seeking a highly motivated Pharmacovigilance Associate to join our team. As a fresher in pharmacovigilance, you will be responsible for supporting drug safety efforts by assisting with adverse event reporting, case processing, and safety data analysis. **Key Responsibilities**: - Assist in...

About the Role:We are seeking an experienced Pharmaceutical Safety Expert to join our team in Hyderabad, India.Job Overview:This role is a key member of our Preclinical Safety (PCS) department and will be responsible for providing non-clinical safety strategy for products globally. The ideal candidate will have a strong background in toxicology and...

**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...

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...

Responsible for performing the qualification and calibration of analytical instruments like HPLC, UV-Vis spectrophotometer, IR and other standalone instruments (like water content, pH meter, Balances etc.,). - Responsible for execution of Analytical Method Transfer / Analytical Method Validation / Analytical Method verification / Analytical method...

**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...

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...

**Job Summary**: **Laboratory position which involves development and validation of analytical methodology in support of the research projects involving testing of pharmaceutical components and/or drug products. Under general supervision, the position may require proficiency in support formulation, development method improvement and validation, testing per...

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...

**NITZ Consulting private Limited Inc. (“NItz”) **is committed to providing quality service in the field of pharmacovigilance to clients. Our clients range from mid-size to small pharmaceutical companies located worldwide who are engaged in developing a proprietary pipeline of novel therapies for the treatment of solid tumors and hematological...

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...

**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...