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Job Overview Review, assess and process Safety data and information, across service lines, received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations SOPs and internal guidelines under guidance and support of senior operation team members. Essential Functions • To Prioritize and complete the assigned trainings on time • Process Safety data according to applicable regulations, guidelines, Standard Operating procedures (SOPs) and project requirements. • To perform Pharmacovigilance activities per project requirement including but not limited to, collecting and tracking incoming Adverse Events(AE)/endpoint information • determining initial/update status of incoming events • database entry • coding AE and Products, writing narratives, Literature related activities. • Assuming other workflow responsibilities for the assigned project as directed by Operations team member or Manager. • Ensure to meet the expec...

 Manager- Drug Regulatory Affairs (R & D). This position will take care of the entire gamut of Regulatory filing, dossier preparation, query response, change controls, variations, preparation, and submission of annual reports. Team Handling skills is mandatory. Must have exposure to working for regulated markets including the EU, Australia, Japan, ROW, and other regulated markets. Desired experience is 10 to 12 years Qualification: M Pharm / Diploma in Regulatory Affairs Location: Bengaluru. Please refer and share the profiles to aravinda.p@medreich.com

 M.Sc. Life Science fresher’s with the specializations like Micro Biology, Biochemistry, Molecular Biology, and Stem Cell Biology & Stem Cell Culture. Good Knowledge related to mammalian cell culture, Real-time polymerase chain reaction (RT-PCR, PCR), flow cytometry (FACS). Location: Bangalore Interested can share the resume on nisha.khan@stempeutics.com

 Hiring at Syncorp Health for the following role:  Clinical Data Management Department: 1. CDP- Candidate should have minimum of 2yrs of experience as a Clinical Database Programmer at a CRO/Pharma,  job location: Bangalore only ____________ Clinical Operations Department: 1. CTL- Candidate should have minimum of 6yrs of experience in Clinical Operations,  Job Location: Bangalore  _____________ 2. Project Coordinator- Candidate from Lifescience/Pharmacy background but compulsory should know Korean Language and have at least 1 yr of working experience.  Job Location: Bangalore only.  Only eligible candidates send cv to I’d: subham@syncorp.in

 Greeting from CBCC Global Research ! Hiring for Experienced CRA - Clinical Research Associate at a Clinical Research Organization. Location : Ahmedabad & Nagpur Experience : at least 3-4 years ( Mandatory On Site Monitoring Experience in Patient based PK studies/BA BE/Clinical trials) No of Vacancies : 03 Interested candidates may share their resume at career@cbcc.global