Dir, Medical Safety - Bengaluru

The job holder will provide medical safety and monitoring support to pharmaceutical companies. They must have a medical degree from an accredited school with relevant experience in clinical medicine or equivalent combination of education and training. · ...

The Medical Director will be responsible for leading clinical research teams in Bengaluru. · Establish and meet priorities, deadlines, and objectives. · Provide consultation and advice on multiple assignments. · ...

The Director of Medical Safety will be responsible for providing consultation and advice on multiple assignments. They must have knowledge of applicable federal and local regulations and guidelines pertaining to clinical research. · ...

Project Role: Senior Medical Safety Advisor · Work Experience: 5+ Years. · Work location: Bengaluru. · Work Mode: Home Based · Must Have Skills: Pharmacovigilance, ICSR. · Job Overview · The objective of this position is to provide medical expertise in the evaluation of safety da ...

Provide medical expertise on pharmacovigilance services to divisions as requested. The Associate Medical Safety Director participates in all aspects of Medical Safety s involvement on assigned trials and stand alone safety projects with appropriate oversight from management or mo ...

The objective of this position is to provide medical expertise in the evaluation of safety data from a variety of sources as part of the overall pharmacovigilance process and determine the medical and scientific relevance of serious adverse event reports within the context of the ...

Provide medical expertise on pharmacovigilance services to divisions as requested. The Associate Medical Safety Director participates in all aspects of Medical Safety's involvement on assigned trials and stand alone safety projects with appropriate oversight from management or mo ...

The Senior Medical Safety Advisor will provide medical expertise in the evaluation of safety data from various sources, determining the medical and scientific relevance of serious adverse event reports within the context of product safety profiles. · ...

The objective of this position is to provide medical expertise in the evaluation of safety data from a variety of sources as part of the overall pharmacovigilance process. · Perform medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse ...

The objective of this position is to provide medical expertise in the evaluation of safety data from a variety of sources as part of the overall pharmacovigilance process and determine the medical and scientific relevance of serious adverse event reports within the context of the ...

Job Overview · The objective of this position is to provide medical expertise in the evaluation of safety data from a variety of sources as part of the overall pharmacovigilance process and determine the medical and scientific relevance of serious adverse event reports within the ...

+The objective of this position is to provide medical expertise in the evaluation of safety data from a variety of sources as part of the overall pharmacovigilance process and determine the medical and scientific relevance of serious adverse event reports within the context of th ...

The Associate Medical Safety Director participates in all aspects of Medical Safety's involvement on assigned trials and stand alone safety projects with appropriate oversight from management or more senior medical safety directors. · Essential Functions · • Perform medical revie ...

The Senior Medical Safety Advisor will provide medical expertise in the evaluation of safety data from a variety of sources as part of the overall pharmacovigilance process and determine the medical and scientific relevance of serious adverse event reports within the context of t ...

The Senior Medical Safety Advisor provides medical expertise in the evaluation of safety data from various sources as part of the overall pharmacovigilance process. · ...

+The objective of this position is to provide medical expertise in the evaluation of safety data from a variety of sources as part of the overall pharmacovigilance process. · ...

We are looking for an experienced Safety Medical Writer to join our team and lead high-complexity tasks related to safety reporting. · ...

We are looking for an experienced Safety Medical Writer to join our team and lead high-complexity tasks related to safety reporting. · Be responsible for the preparation of complex aggregate safety reports, Risk Management Plans (RMPs), and responses to Health Authority questions ...

We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations to be future ready. We offer accelerated, global growth opportunities for talent that's bold, industrious and nimble. With Indegene, you gain a unique career exp ...

As Medical Writer I, Patient Safety, you will be responsible for leading or contributing to the preparation and compilation of aggregate safety reports. You will also perform signal detection activities and manage signal tracking activities. · ...