Associate Director, Global Drug Safety - Plainsboro Township

The Pharmacovigilance Operations Manager plays a critical role in ensuring patient safety and operational excellence across Acadia's global clinical development programs. · ...

The Associate Director will oversee pharmacovigilance operations in North America, ensure compliance with regulatory requirements, and communicate relevant information internally and externally. · Ensure audit preparedness and manage regulatory inspectionsDraft corrective action ...

++The Associate Director will oversee and implement operations of Pharmacovigilance in North America.+ · Responsibilities include the following: · ,+Ensure audit preparedness and manage regulatory and internal inspections,Draft any corrective action/preventative action plans (CAP ...

The Director, Drug Safety Physician is the Lead of the Global Safety Team(s) to develop safety strategies to ensure patient safety and regulatory compliance for products that are in development and / or marketed. · ...

The Director Drug Safety Physician is responsible for leading the Global Safety Team(s) to develop safety strategies ensure patient safety regulatory compliance products in development marketed. · ...

· Kyowa Kirin is a fast-growing global specialty pharmaceutical company that applies state-of-the-art biotechnologies to discover and deliver novel medicines in four disease areas: bone and mineral; intractable hematologic; hematology oncology; and rare disease.  A Japan-based c ...

· Company Description · A Few Words About Us · Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. ...

The Associate Director Drug Safety will oversee Pharmacovigilance in North America. He/She will communicate relevant information internally and with other members of SUN and its affiliates. · The position leads teams based out of USA, Canada & liaise with pharmacovigilance teams ...

The Director Drug Safety Physician is responsible for leading Global Safety Teams in developing safety strategies ensuring patient safety and regulatory compliance for products in development and/or marketed. · ...

Dice is the leading career destination for tech experts at every stage of their careers. Our client, Tandym Tech, is seeking the following. Apply via Dice today · A New Jersey-based biotech company is actively seeking a new Associate Director of Global Drug Safety & Pharmacovigil ...

This role seeks an experienced Pharmacovigilance Systems professional to support Oracle Argus Safety system management. · ...

A New Jersey-based biotech company is actively seeking a new Associate Director of Global Drug Safety & Pharmacovigilance Data Management to join its growing team. · About the Opportunity: · Schedule: · Full-time · Hours: · Standard business · Setting: · Hybrid (at least 2 days a ...

A New Jersey-based biotech company is actively seeking a new Associate Director of Global Drug Safety & Pharmacovigilance Data Management to join its growing team. · About the Opportunity: · Schedule: Full-time · Hours: Standard business · Setting: Hybrid (at least 2 days a week ...

Seeking an experienced Pharmacovigilance Systems professional to support Oracle Argus Safety system management. · ...

This role is critical to ensuring that Argus changes and enhancements perform as intended, meet regulatory requirements and Client business needs, and are supported by high-quality, inspection-ready testing evidence and end-to-end traceability. · ...

We are seeking an experienced contractor to support Oracle Argus Safety System Management activities with a focus on triage and quality review of Argus configuration/change requests. The ideal candidate will have strong knowledge of ICH E2B(R2) and E2B(R3) conventions and practic ...

Responsible for executing US Adverse Event and Pharmacovigilance activities as required by FDA Regulations. · ...

· Full-time · Description · SUMMARY:  · Responsible for executing US Adverse Event and Pharmacovigilance activities as required by FDA Regulations. Provide support and oversight in drug safety related activities including Product Quality Complaints and Medical Information activi ...

Responsible for executing US Adverse Event and Pharmacovigilance activities as required by FDA Regulations. · ...

· Company Description · Artech Information System, a global staffing and IT consulting company. We are constantly on the lookout for professionals to fulfill the staffing needs of our clients and we currently have a job opening that may interest you. · Job Description · Job Tit ...