Fortrea job vacancy for Safety Science Analyst- B Pharma/ M Pharma Freshers apply now
Safety Science Analyst
Safety Science Analyst (Contract – 6 months)
Bangalore India
Education :
B Pharma/ M Pharma
Qualification :
We require fresh graduates and post graduates who are available to join immediately
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
These statements are intended to describe the general nature of the job and are not intended to be an exhaustive list of all responsibilities, skills and duties*.
Perform case intake and triage of the incoming safety information or reports from various sources either spontaneously or from a clinical trial
Assist with processing of the adverse events, including but not limited to:
Data entry of safety data onto adverse event tracking systems
Write patient narratives & code adverse events accurately using MedDRA (for Marketed products, if applicable)
Assist in the listedness assessment against appropriate label (for Marketed products, if applicable)
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Assist in generation of queries and collection of missing or discrepant information in consultation with medical staff, if needed
Submission of expedited SAE reports to clients, regulatory authorities, ethics committees, investigators, 3rd party vendors, Partners and Company project personnel, as required within the agreed timelines
Assist with processing and submission of expedited and periodic reports to worldwide regulatory agencies or other recipients (Clients, Regulatory Authorities, Ethics Committees, investigators and company project personnel etc), and prioritize the reports for processing and submission within the regulatory and/or study specific applicable timelines
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