Clinical Risk Management Associate - I (Assistant) Clinical Risk Management Associate - I (Assistant) - LanceSoft Inc
North Wales, PA 19454-2505
About the Job
Pay Rate : $ 60.00 to $ 65.00 per hour
Location : Remote
Duration : 06 Months +
" Performs primary medical review of serious adverse experience (AE) reports and other AE reports of interest in order to monitor and describe the safety profile of assigned products.
" Takes an active role in the oversight and development of pharmacovigilance and risk management plans (RMPs) of assigned products in collaboration with the CSRM physician.
" Prepares responses to inquiries from health professionals and regulatory agencies regarding adverse experiences reported for assigned products and in collaboration with the CSRM physician, strategizes with the Risk Management Safety Team (RMST) recommending appropriate data to respond to queries and analyze data.
Primary Activities
" Primary activities include, but are not limited to:
" Applies clinical, pharmacological, and epidemiologic knowledge and information technology (IT) skills in order to manage the safety surveillance and risk management of assigned products in collaboration with the CSRM physician.
" In collaboration with the CSRM physician, accountable for monitoring the overall safety profile of assigned products and for describing the safety profile to ensure external communications regarding the safety of these products are accurate.
" Performs safety surveillance review of adverse experience reports for assigned products which includes reviewing individual AE reports, aggregate safety data, published literature, and information from external databases.
" Works with CSRM physician and scientist, if applicable to select and analyze the appropriate data from available IT systems in order to investigate safety issues.
" Prepares responses to safety inquiries from health care professionals, regulatory agencies, subsidiary staff, and other internal customers.
" Demonstrates a working knowledge of pharmacovigilance and risk management; may educate stakeholders outside of CSRM about risk management and the role of CSRM.
" Prepares summaries and analyses of safety related data for regulatory documents such as Periodic Safety Update Reports (PSURs), Developmental Safety Update Reports (DSURs) and summaries in support of regulatory filings.
Interview:
Quals--
Education:
" Graduate degree in nursing, health sciences, pharmacology, epidemiology, public health, or other relevant health-related fields.
" Advance degree like Pharm-D, PHD, MD's -preferred.
Experience:
" At least 3 years of experience in clinical, pharmacological, or related field of expertise.
" Excellent writing and communication skills are a must.
" Experience in data analysis or the interpretation of adverse experience information is a plus.
" Candidates will not be seeing the patients.
" The candidates would not be required to have an active license.
Must have:
" Previous experience in CRO's /academia would be good
" Industry experience is preferred.
" Aggregate review of adverse events reports.
" Review of Individual case safety reports (ICSR).
" Review of adverse event narratives.
" Review of social medial post containing adverse events.
" Therapeutic Areas: Oncology, general medicine. But other Therapeutic Areas experience is fine as well.
" Candidate will be responsible for the Safety & Risk Management for Developmental and Marketed Products.
Software:
" MS office suite, Veeva(SOP's), RXlogix (PV signals platforms)
Important Notes:
" 100% remote.
" Assignment could be extended beyond 6 months.
Location : Remote
Duration : 06 Months +
" Performs primary medical review of serious adverse experience (AE) reports and other AE reports of interest in order to monitor and describe the safety profile of assigned products.
" Takes an active role in the oversight and development of pharmacovigilance and risk management plans (RMPs) of assigned products in collaboration with the CSRM physician.
" Prepares responses to inquiries from health professionals and regulatory agencies regarding adverse experiences reported for assigned products and in collaboration with the CSRM physician, strategizes with the Risk Management Safety Team (RMST) recommending appropriate data to respond to queries and analyze data.
Primary Activities
" Primary activities include, but are not limited to:
" Applies clinical, pharmacological, and epidemiologic knowledge and information technology (IT) skills in order to manage the safety surveillance and risk management of assigned products in collaboration with the CSRM physician.
" In collaboration with the CSRM physician, accountable for monitoring the overall safety profile of assigned products and for describing the safety profile to ensure external communications regarding the safety of these products are accurate.
" Performs safety surveillance review of adverse experience reports for assigned products which includes reviewing individual AE reports, aggregate safety data, published literature, and information from external databases.
" Works with CSRM physician and scientist, if applicable to select and analyze the appropriate data from available IT systems in order to investigate safety issues.
" Prepares responses to safety inquiries from health care professionals, regulatory agencies, subsidiary staff, and other internal customers.
" Demonstrates a working knowledge of pharmacovigilance and risk management; may educate stakeholders outside of CSRM about risk management and the role of CSRM.
" Prepares summaries and analyses of safety related data for regulatory documents such as Periodic Safety Update Reports (PSURs), Developmental Safety Update Reports (DSURs) and summaries in support of regulatory filings.
Interview:
Quals--
Education:
" Graduate degree in nursing, health sciences, pharmacology, epidemiology, public health, or other relevant health-related fields.
" Advance degree like Pharm-D, PHD, MD's -preferred.
Experience:
" At least 3 years of experience in clinical, pharmacological, or related field of expertise.
" Excellent writing and communication skills are a must.
" Experience in data analysis or the interpretation of adverse experience information is a plus.
" Candidates will not be seeing the patients.
" The candidates would not be required to have an active license.
Must have:
" Previous experience in CRO's /academia would be good
" Industry experience is preferred.
" Aggregate review of adverse events reports.
" Review of Individual case safety reports (ICSR).
" Review of adverse event narratives.
" Review of social medial post containing adverse events.
" Therapeutic Areas: Oncology, general medicine. But other Therapeutic Areas experience is fine as well.
" Candidate will be responsible for the Safety & Risk Management for Developmental and Marketed Products.
Software:
" MS office suite, Veeva(SOP's), RXlogix (PV signals platforms)
Important Notes:
" 100% remote.
" Assignment could be extended beyond 6 months.
Source : LanceSoft Inc
