Safety Science Analyst-Covid19 Study Jobs in Bangalore,Mumbai,Pune - Covance India Pharmaceutical Service Pvt.
Job Description
SAFETY SCIENCE ANALYST (6m Contract) Covid-19 Study
You should be a qualified BDS/BHMS/BAMS/B.Pharm/M.Pharm/Pharm.D from the batch of 2018/2019/2020. No experience required. This is a 6-month contract role.
Responsibilities:
You should be a qualified BDS/BHMS/BAMS/B.Pharm/M.Pharm/Pharm.D from the batch of 2018/2019/2020. No experience required. This is a 6-month contract role.
You will be required to join immediately in November 2020, if selected.
Responsibilities:
• Assist in the processing of expedited safety reports (ESRs). This includes, but is not limited to: maintenance of adverse event tracking systems set-up and maintenance of project files, core process files and central safety files reporting of ESRs to clients, regulatory authorities, ethics committees, investigators and Covance project personnel, if required, within study specified timelines.
• Provide administrative support to PV&DSS personnel (e.g. proof-reading and editing correspondence/documents, mailings, filing, faxing, photocopying and archiving etc).
• Ensure all incoming faxed Serious Adverse Event (SAE) reports are appropriately stamped, logged into the departmental tracking application and forwarded in a timely manner to the designated Drug Safety Associate (DSA)/Senior Drug Safety Associate (Sr. DSA).
• Ensure submission of client-related documents is sent to the client within designated timeframes (e.g. SAE reports, ESRs, Safety Management Plans (SMPs)).
• Where applicable, check the PV&DSS hotline mailbox regularly for reported SAEs and forward messages to the designated DSA/Sr. DSA.
• Assist in the maintenance of files regarding adverse event reporting requirements in all countries.
• Coordinate shipments of safety documents.
• Prepare and coordinate safety study files for archiving at the completion of projects.
• Arrange and schedule internal and external meetings/teleconferences.
• Train and mentor the PV&DSS Support Specialists in their day-to-day activities.
• Work within the Standard Operating Procedure (SOP) system, including departmental Work Instructions (WIs).
• Build and maintain good PV&DSS relationships across functional units.
• Any other duties as assigned by management.
PS: Depending on business requirement and your performance, at the end of 6 months, this contract role may either be extended or converted to a full-time role or may also end the contract.
• Provide administrative support to PV&DSS personnel (e.g. proof-reading and editing correspondence/documents, mailings, filing, faxing, photocopying and archiving etc).
• Ensure all incoming faxed Serious Adverse Event (SAE) reports are appropriately stamped, logged into the departmental tracking application and forwarded in a timely manner to the designated Drug Safety Associate (DSA)/Senior Drug Safety Associate (Sr. DSA).
• Ensure submission of client-related documents is sent to the client within designated timeframes (e.g. SAE reports, ESRs, Safety Management Plans (SMPs)).
• Where applicable, check the PV&DSS hotline mailbox regularly for reported SAEs and forward messages to the designated DSA/Sr. DSA.
• Assist in the maintenance of files regarding adverse event reporting requirements in all countries.
• Coordinate shipments of safety documents.
• Prepare and coordinate safety study files for archiving at the completion of projects.
• Arrange and schedule internal and external meetings/teleconferences.
• Train and mentor the PV&DSS Support Specialists in their day-to-day activities.
• Work within the Standard Operating Procedure (SOP) system, including departmental Work Instructions (WIs).
• Build and maintain good PV&DSS relationships across functional units.
• Any other duties as assigned by management.
PS: Depending on business requirement and your performance, at the end of 6 months, this contract role may either be extended or converted to a full-time role or may also end the contract.
Job Particulars
Who can apply Freshers and Experienced (0 to 1 Years )
Hiring Process Written-test, Face to Face Interview, Telephonic Interview
Employment TypeFull Time
Job Id1039088
Job Category Pharma
Locality Address Hinjewadi
State Karnataka, Maharashtra
Country India
About Company
Covance, a business segment of LabCorp, is recognized as a leader in drug development, medical device, diagnostics, crop protection and chemical testing because of our exceptional people. We embrace and celebrate the different strengths, experiences and perspectives of our nearly 65,000 enterprise team members across the globe. Our team is driven by our mission to improve health and improve lives. Here, you can play a role in bringing new scientific discoveries to life and make a difference in the lives of millions. And, with our comprehensive service portfolio, you’ll have the opportunity to explore diverse projects and unique career paths across life science. Join us and discover your extraordinary potential.
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