Gbu Icsr Medical Oversight

**Major duties and responsibilities as per SMP**: Oversees the Medical Review (MR) of ICSRs as per predefined activity and job-role in PV safety database, with special focus on case medical accuracy and documentation, - Maintains overall accountability for the timeliness and quality of medical case management activities outsourced to service providers, -...

Oversees the Medical Review (MR) of ICSRs as per predefined activity and job-role in PV safety database, with special focus on case medical accuracy and documentation, - maintains overall accountability for the timeliness and quality of medical case management activities outsourced to service providers, - leads or participates in cross-functional projects or...

Major duties and responsibilities: - oversees the Medical Review (MR) of ICSRs as per predefined activity and job-role in PV safety database, with special focus on case medical accuracy and documentation, - maintains overall accountability for the timeliness and quality of medical case management activities outsourced to service providers, - leads or...

**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...

ProductLife Group is looking for a Medical Writing Officer to join our dynamic team to contribute to the activities performed in the Hub: **Responsibilities**:Signal Management and Regulatory Intelligence**: Perform Signal Management Activities for clients Preparation of Signal Schedule Maintenance of Signal trackers Sharing of recommendation with...

**Description**: We are looking for a **Data Officer** to have responsibility for allocated tasks within the pharmacovigilance activities delivered by the platform. - Data entry of vigilance cases in the relevant databases - Submission of cases to the competent authorities - Carrying out specific queries in the databases in order to draft reports -...

Description:We are looking for a Data Officer to have responsibility for allocated tasks within the pharmacovigilance activities delivered by the platform. Data entry of vigilance cases in the relevant databases Submission of cases to the competent authorities Carrying out specific queries in the databases in order to draft reports Monitoring and downloading...

We are looking for experienced candidates for the position of Senior Drug Safety Physician with minimum 2 Years of ICSR experience.Location - Chandigarh/Mohali/Hyderabad/ Homebased Job Purpose:Provide medical review, analysis and guidance during the case handling and reporting cycle of Adverse Event and Adverse Reaction reports received for investigational...

We are looking for experienced candidates for the position of Senior Drug Safety Physician with minimum 2 Years of ICSR experience.Location - Chandigarh/Mohali/Hyderabad/ Homebased Job Purpose:Provide medical review, analysis and guidance during the case handling and reporting cycle of Adverse Event and Adverse Reaction reports received for investigational...

We are looking for experienced candidates for the position of Senior Drug Safety Physician with minimum 2 Years of ICSR experience.Location - Chandigarh/Mohali/Hyderabad/ Homebased Job Purpose:Provide medical review, analysis and guidance during the case handling and reporting cycle of Adverse Event and Adverse Reaction reports received for investigational...

Provide oversight and support to vendors to ensure productivity and quality of all activities - Maintain technical and global regulatory expertise - Ensure adequacy of training on different topics: Database, SOP, and knowledge in pharmacovigilance field, library and clinical development in order to improve flexibility, professionalism of all resources -...

Provide oversight and support to vendors to ensure productivity and quality of all activities Maintain technical and global regulatory expertise Ensure adequacy of training on different topics: Database, SOP, and knowledge in pharmacovigilance field, library and clinical development in order to improve flexibility, professionalism of all resources Ensure...

**Writer, Medical Information - Evidera** 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...

**Writer, Medical Information - Evidera** 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...

Writer, Medical Information - EvideraAt 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...

**Description** **Central Monitor I** 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 brings the customer and the patient to the...

Job DescriptionDescription Performs review of clinical monitoring visit reports for allocated projects ensuring consistency across protocols and/or regions and escalates any protocol, site, and/or CRA issues or trends noted during the report review process to CTM. Liaises with clinical monitoring staff for prompt trip report review submission and approval...

Job DescriptionDescription Performs review of clinical monitoring visit reports for allocated projects ensuring consistency across protocols and/or regions and escalates any protocol, site, and/or CRA issues or trends noted during the report review process to CTM. Liaises with clinical monitoring staff for prompt trip report review submission and approval...

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...

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...