Clinical Risk Management Specialist (100% Remote) at Freyr Solutions, Client: Global Pharma company
North Wales, PA 19454
About the Job
Freyr is hiring for a leading pharmaceutical client!!
Job Title: Clinical Risk Management Specialist
Work location: North Wales, PA 19454 (100% remote)
Duration: Long term contract
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.
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.
Responsibilities:
• 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.
For more details and prompt consideration, please share your resume and we can schedule a call to discuss further.
Job Title: Clinical Risk Management Specialist
Work location: North Wales, PA 19454 (100% remote)
Duration: Long term contract
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.
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.
Responsibilities:
• 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.
For more details and prompt consideration, please share your resume and we can schedule a call to discuss further.
Salary
up to 70 /hour
Discounted health insurance, Matching 401(k), Paid sick leaves
Discounted health insurance, Matching 401(k), Paid sick leaves
