Planet Pharma
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https://www.propharmagroup.com
https://www.propharmagroup.com
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Target Pay Rate: 50-65.36/hr **salary will be commensurate with experience
Job Description:
• 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
• 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.
Qualifications:
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) Day to Day: • Perform Safety Analysis for Clinical and post Marketing Data. • Good Writing Skills. • Candidate may be working with 7 to 8 colleagues on a program or project. • Very collaborative environment. • Working close with Physicians and other groups like Clinical & Regulatory in a very busy space. • Performs primary medical review of serious adverse experience reports and other AE reports of interest to monitor and describes the safety profile of assigned products. • Taking an active role in the oversight and development of pharmacovigilance and risk management plans with direction/guidance from the CSRM team Assists the CSRM team to prepare responses to inquiries from health professionals and regulatory agencies regarding adverse experiences reported for products. • Strategizes with safety team recommending appropriate data to respond to queries and analyze data. **CO/NY candidates may not be considered
Clinical Risk Management Associate - I (Assistant)
351 North Sumneytown Pike North Wales, PA 19454 US
Posted: 11/08/2024
2024-11-08
2025-01-04
Employment Type:
Contract
Job Category: Pharmacovigilance
Job Number: 615385
Is job remote?: Yes
Country: United States
Job Description
Target Pay Rate: 50-65.36/hr **salary will be commensurate with experience
Job Description:
• 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
• 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.
Qualifications:
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) Day to Day: • Perform Safety Analysis for Clinical and post Marketing Data. • Good Writing Skills. • Candidate may be working with 7 to 8 colleagues on a program or project. • Very collaborative environment. • Working close with Physicians and other groups like Clinical & Regulatory in a very busy space. • Performs primary medical review of serious adverse experience reports and other AE reports of interest to monitor and describes the safety profile of assigned products. • Taking an active role in the oversight and development of pharmacovigilance and risk management plans with direction/guidance from the CSRM team Assists the CSRM team to prepare responses to inquiries from health professionals and regulatory agencies regarding adverse experiences reported for products. • Strategizes with safety team recommending appropriate data to respond to queries and analyze data. **CO/NY candidates may not be considered
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Ready to take the next step in your career? Explore job opportunities in North Wales, Pennsylvania, and unlock a world of possibilities right in the heart of Montgomery County! Known for its vibrant community, charming historic district, and proximity to cultural attractions like the Montgomery Mall and Merrymead Farm, North Wales offers an ideal setting for professional growth and work-life balance. With easy access to Philadelphia and its array of museums, theaters, and professional sports teams, you'll enjoy a perfect blend of small-town charm and big-city excitement. Discover your dream job in North Wales today and experience the best that Pennsylvania has to offer!
Although this hasn't been an issue at Planet Pharma, the staffing industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly and never provide banking information during the application process. Candidate safety is a top priority at Planet Pharma.
