Pharmacovigilance Associate

**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...

**Company Description** Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because **Good Health Can’t Wait**. We started in 1984 with a modest...

**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...

Assist in the management of key initiatives within PV management - Assist Program Manager for the Hosted Only Programs - Plan, attend and participate in client meetings - In conjunction with PV Management, define, track and execute implementation timelines and strategies - Track action items from client team and PV Staff meetings. - Participate in SOP review...

**Company Description** Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because **Good Health Can’t Wait**. We started in 1984 with a modest...

CTD Dossier Drafting (Modules 2, 3, 4) - Regulatory writing - Clinical Regulatory & Pharmacovigilance Regulatory - Regulatory commitment & compliance - Any other Regulatory activities on need basis - Support Line manager & Matrix manager in Regulatory projects - Coordination and interaction with cross-functional teams Mandatory Skills Effective...

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...

The purpose of this role is to manage the regulatory information management (RIM) system for all Consumer Healthcare products worldwide to support key regulatory processes and enable the company to meet its regulatory, legal and pharmacovigilance obligations. This role is responsible for the operation of the regulatory systems and processes used to prepare...

**SPVG Scientific Spec II - Literature Review** **-** **(** **22007651** **)** **Description** **SPVG Scientific Specialist II** Come discover what our 25,000+ employees already know: work here matters everywhere. We’re a growing and evolving biopharmaceutical industry leader, which means you’ll have endless opportunities to work with experts around...

**Functional Lead** **Qualification**: Masters in Business Administration ** Responsibility**: **Requirement Gathering and Gap Analysis**: - Understand business requirements through business workshops, one on one interviews. - Analyze business requirement document. - Analyze gaps in order to meet business requirements. **Solution Engineering**: -...

Job Purpose: The purpose of this role is to manage the regulatory information management (RIM) system for all Consumer Healthcare products worldwide to support key regulatory processes and enable the company to meet its regulatory, legal and pharmacovigilance obligations. This role is responsible for the operation of the regulatory systems and processes used...

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through...

**Summary**: - Contributes, with appropriate oversight, to all relevant aspects of global clinical trial(s) activities to deliver study outcomes within schedule, budget, quality/compliance and performance standards. May lead specific aspects of global clinical trial(s). Core member of the Clinical Trial Team. -Applicable to Clinical Scientific Expert IThe...

**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...

About the Job">We are seeking a highly skilled Regulatory Writer Expert to join our team at Sanofi Global Hub in Hyderabad, India.">As a key member of our medical writing team, you will be responsible for creating high-quality safety and clinical documents, including Periodic Benefit-Risk Evaluation Reports, Clinical Study Reports, and product alerts.">Your...

Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. We connect talented professionals with opportunities in pharma, biotech, health sciences, healthtech and IT domains.About ProPharma GroupFor the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device,...