Drug Safety Associate

**Job Purpose**: Principal Safety Physician is responsible for performing medical & safety monitoring tasks in the assigned projects and contribute to medical review, analysis and guidance in all required safety reports. Principal project teams, business development and pre-award activities. - Provide medical review, analysis and guidance during the case...

**Responsibilities**: - Monitor patient safety during clinical trials by reviewing adverse events, SAEs, and providing medical assessments. - Ensure timely and accurate reporting of SAEs and safety signals to regulatory authorities. - Provide medical expertise to clinical study teams, investigators, and safety personnel for safety - related queries and...

Team: Professional ServicesCountry: IndiaRemote Work Available: YesVeeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $2B in revenue in our last fiscal year with extensive growth potential...

Job Overview - Maintain a repository of, and communicate on, international, regional and national legislations, recommendations and guidelines related to vigilances for all ranges of products such as medicinal products, medical devices, cosmetics, nutraceuticals. - Appropriately identify and address potential regulatory issue that may have an impact on the...

We are looking for a Team lead/ Manager/ senior medical advisor/reviewer proficient in all aspects of clinical and post-marketing drug safety. **Responsibilities**: Clinical Phase: - Lead as a medical monitor/Medical expert - Medical Monitoring experience is a must and the ability to effectively communicate with the clients, attend investigator meetings as...

As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. **Responsibilities**: The Clinical Research Associate is ultimately responsible for the successful management of investigator sites throughout the trial lifecycle. Key responsibilities include: - Full ownership of...

As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.**Responsibilities**: - The Clinical Research Associate is ultimately responsible for the successful management of investigator sites - throughout the trial lifecycle. Key responsibilities include: - Full ownership of...

We are looking for a Team lead/ Manager/ senior medical advisor/reviewer proficient in all aspects of clinical and post-marketing drug safety.Responsibilities:Clinical Phase:Lead as a medical monitor/Medical expertMedical Monitoring experience is a must and the ability to effectively communicate with the clients, attend investigator meetings as required and...

Primary point of contact between site staff and NN. Acts as ambassador for the company and contributes to making NN the preferred partner. Responsible for managing the site to meet patient recruitment rate and target. Delivers results that have direct impact on the successful completion of the clinical program. Coordinates with PM and communicates to them...

Our leading herb territory is currently in need of a Regulatory Scientist to join our fast-growing team. The ideal candidate will be intricately involved in filing and getting Licences and other supporting documents for herb marketing and will regularly look for other supporting certificates and updates via theoretical approaches for the smooth establishment...