Safety Associate

Conducting regular workplace inspections to identify potential hazards. - Evaluating the severity and likelihood of risks associated with identified hazards. - Developing and implementing safety procedures to control or eliminate identified hazards. - Creating and maintaining comprehensive safety policies and procedures. - Developing and delivering safety...

**Job Summary**: The Pharmacovigilance Associate plays a key role in monitoring and ensuring the safety of pharmaceutical products throughout their lifecycle. Working within a multidisciplinary team, the associate is responsible for the collection, assessment, and reporting of adverse events and safety information associated with medicinal products. This...

(India) **About Us** Kateric is a strategic partner for biopharmaceutical companies that consistently delivers superior quality regulatory documents through excellence, experience, and intelligent execution. Kateric’s resources are located across multiple time zones in the United States, as well as in India, the EU and Canada, and also have experience...

**Description** **Senior Safety & Pharmacovigilance Submissions Specialist** Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model...

As part of Parexel Consulting, you will create and maximize value for clients throughout the product lifecycle. You will be a strategic guide in getting products to market faster, smarter - and keeping them there -your scientific, technical, regulatory, and/or commercial expertise will put best practice standards to work for biopharmaceutical and medical...

The Medical Information Associate is responsible for providing technical and scientific information to healthcare professionals, consumers, and internal staff on a wide range of pharmaceutical medicines, OTCs, medical devices and therapeutic areas, including conducting complex literature searches and reviews using various medical database. Also responsible...

Collect and process adverse event (AE) reports from healthcare professionals, patients, and regulatory authorities. - Perform case intake and data entry into safety databases (e.g., Argus, ArisG). - Assist in triaging and prioritizing cases based on seriousness and timelines. - Perform quality checks to ensure accuracy and completeness of information. -...

Develop new opportunities by calling our existing customers to uncover new opportunities that we might help with. - Expand accounts by offering new products as well actively asking to be introduced to other people in their company - Educate our customers on what our latest products to keep their people safe and their operations running smoothly -...

**Responsibilities**: - To contribute to the production of client administrative documents and reports to be included in regulatory submissions - Compile, or supervise the compilation of regulatory dossiers in accordance with national requirements - LCM, Systems Management and Administration - Document and track regulatory submissions and regulatory...

(India) Looking for experienced regulatory writers **As we are expanding our team, we are thrilled to announce that we are looking for experienced Indian regulatory writers to join our dynamic, collaborative team to engage with biopharmaceutical clients and prepare clinical and safety regulatory documents. This is a full-time, remote, salaried...