Associate Director/Director of Drug Safety(Physician) - Princeton - SystImmune

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 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 responsible for leading Global Safety Teams in developing safety strategies ensuring patient safety and regulatory compliance for products 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 ...

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 ...

· 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 ...

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. · ...

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

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 ...

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 ...

Job Title: Contractor, Global Drug Safety & Pharmacovigilance Medical Writer · Location: Plainsboro, NJ · Type: 6-month Contract (renewable) · Compensation: Up to $73/hr (dependent on experience) · Contractor Work Model: Remote but prefer someone that can come to the office occas ...

· 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. ...

SystImmune is a leading and well-funded biopharmaceutical company that specializes in developing innovative cancer treatments. This job opportunity involves leading medical assessment and interpretation of safety data from multiple sources. The individual will collaborate with cr ...

SystImmune is a leading biopharmaceutical company developing innovative cancer treatments. We offer an opportunity for you to learn and grow while making significant contributions to the company's success. · ...

Job summary · At Genmab we are dedicated to building extraordinary futures together by developing antibody products and groundbreaking KYSO antibody medicines that change lives and the future of cancer treatment and serious diseases. We strive to create champion and maintain a gl ...

We offer an opportunity for you to learn and grow while making significant contributions to the company's success.This individual is to lead medical assessment and interpretation of safety data from multiple sources, including clinical trials, and literature reports. · ...

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 ...

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

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 ...