Sr. Manager, ICSR Quality - King Of Prussia - CSL Behring

The Opportunity: · Reporting to the Head of Risk Management, Aggregate Reports & Pharmacovigilance, as the · Senior Manager, ICSR Quality , you will have Individual Case Safety Reports (ICSRs) accountability and you will be responsible for the oversight and control of the operati ...

The Opportunity: Reporting to the Head of Risk Management as the Senior Manager ICSR Quality you will have Individual Case Safety Reports accountability and you will be responsible for the oversight and control of operational management and activities performed by Global Case Man ...

The Opportunity Reporting to the Head of Risk Management Aggregate Reports & Pharmacovigilance as the Senior Manager ICSR Quality you will have Individual Case Safety Reports ICSRs accountability and be responsible for the oversight and control of the operational management and a ...

The Senior Manager, ICSR Quality will have Individual Case Safety Reports (ICSRs) accountability and be responsible for the oversight and control of the operational management and activities performed by the Global Case Management Pharmacovigilance vendor(s) for CSL Behring produ ...

Join CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. · Minimum of 10 years of Clinical Trial and Post-marketing Pharmacovigilance (PV) experience with 5 years of managerial/leadership experience · ...

This role oversees all areas of single case processing in the global pharmacovigilance database from all sources. The Medical Evaluation Lead ensures that the vendor performs case processing in accordance with regulatory guidelines and responds to specific questions or queries ab ...

+We are transforming our R&D organization to accelerate innovation and create greater impact for patients CSL is building a future-ready team that excels in dynamic biotech ecosystems Joining CSL now means being part of an agile team committed to developing therapies that make a ...

CSL is transforming its R&D organization to accelerate innovation and create greater impact for patients. · ...

We are looking for a Senior Director to lead our case management function globally. · Cross-functional collaboration · The incumbent will spearhead strategic outsourcing initiatives,vendor oversight and management applying innovative approaches to achieve case management excellen ...

The Senior Director Global Pharmacovigilance is responsible for leading global medical safety strategy benefit–risk assessment signal detection epidemiology regulatory benefit–risk decision making providing strategic operational leadership across all phases product lifecycle earl ...

The Director, Global Clinical Safety will play a key role in overall clinical safety strategy, · assessing and managing risks of products in various stages of development, · and communicating regulatory safety topics for assigned products.Serve as clinical safety lead for assigne ...

The Director, Global Clinical Safety will play a key role in overall clinical safety strategy and safety assessment of products. · ...

Madrigal is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a serious liver disease that can progress to cirrhosis, liver failure, need for liver transplantation and premature mortality. · Serve as ...

The Director of Global Clinical Safety will play a key role in overall clinical safety strategy, safety assessment, evaluation and risk management of products in various stages of development as well as involvement in all safety surveillance activities and communication of regula ...

At GSK, we're looking for professionals with experience in pharmacovigilance or drug safety to lead ICSR activities within Global Safety. · ...

This role will lead key activities in ICSR management, including intake, triage, case processing, medical review, and reporting to health authorities. · The ideal candidate will have experience in pharmacovigilance or drug safety with hands-on ICSR processing. · Minimum 5 years o ...

Assist with the preparation of adverse event reporting plans and other plans as required. · ...

Mindlance Inc. partners with leading employers across the country. This 6-month contract requires a Safety Scientist to assist in adverse event reporting plans, maintain administrative changes, and process AE reports according to SOPs. · ...

We have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. · We foster a culture ambitious for patients, accountable for impact, and committed to doing the right thing, · making sure that we focus our efforts on acc ...

The Drug Safety Associate will be responsible for case processing, preparation of SUA summary and processes & procedures. · Completion of full case information on the database. · Triage of incoming cases to prioritize for daily workflow management. · Liaison with Case Receipt an ...