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Search Results for Regulatory Affairs for Regulatory Affairs
Job Title. Location Salary Actions

Director, PVE (Risk Management)

Our client is a global Bio-Pharma with a strong pipeline of products across a range of therapeutic areas from Infectious diseases, Inflammation & Oncology. They are seeking a Director of Pharmacovigilance & Epidemiology (Risk Management) to join a new team in Dublin. This team shall be a Centre of Excellence for global Paediatric clinical trials. The ideal person shall have a healthcare degree with a strong drug safety background. Role/Responsibilities: Signal detection and authorship of signal work-up documents in collaboration with a Medica...

Location: Dublin,
Director, PVE (Risk Management) 		Dublin Not Disclosed

Associate Director, Pharmacovigilance & Epidemiology (PVE)

Associate Director, Pharmacovigilance & Epidemiology (PVE) Our client is a Global Biopharma who are establishing a new Centre of Excellence for Clinical Trials in Dublin. They are seeking an Associate Director who will manage Vendor Oversight Operations within PVE. Role/Responsibilities: Oversight of vendor(s) responsible for ICSR processing. This includes, but is not limited to: Scheduled and ad hoc meetings with the vendor(s) Oversight of training and quality metrics Review feedback and performance metrics relating to the vendor(s)f...

Location: Dublin,
Associate Director, Pharmacovigilance & Epidemiology (PVE) 		Dublin Not Disclosed

Director of Clinical Pharmacology (Infectious Diseases)

Our client is a leading Bio-Pharma who are establishing a new office in Dublin in the area of Clinical Research. As a Director within the Clinical Pharmacology Group, the successful person will have ultimate responsibility and accountability for clinical pharmacology programs in the area of HIV and emerging viral infections. As a member of the Clinical Pharmacology team this person shall have unparalleled opportunity to be involved with every aspect of the product development process, from first-in human through approval, including post-marketing activities. In this role, ...

Location: Dublin,
Director of Clinical Pharmacology (Infectious Diseases) 		Dublin Not Disclosed

Director, Quality & Compliance (GCP)

Our client is a global Biopharma organisation who play a crucial role in developing life-saving therapies. They are seeking a Clinical Quality and Compliance Director who is ready to dive-in to support our clients clinical development programs. As a Clinical Quality and Compliance Director, you will support and work with our clinical study management teams and teammates across R&D Quality and Compliance. They need someone with strong leadership skills, expert Good Clinical Practice (GCP) knowledge, audit skills, communication, facilitation skills, and the ability to...

Location: Dublin,
Director, Quality & Compliance (GCP) 		Dublin Not Disclosed

Director, Pharmacovigilance Quality & Compliance (GVP)

Our client is a leading Global Biopharmaceutical organisation who play a crucial role in developing life-saving therapies. They are seeking a Pharmacovigilance Compliance Director who will join their Global R&D Quality and Compliance team. As a member of the global PV management team you will provide leadership in setting the strategic direction of Quality and Compliance PV activities. This role is suited to candidates who possess strong leadership skills and strategic thinking. Utilizing expert Good Pharmacovigilance (GVP) and Good Clinical Practice (GCP) knowledge. The su...

Location: Dublin,
Director, Pharmacovigilance Quality & Compliance (GVP) 		Dublin Not Disclosed

Associate Manager (Technical Training)

Our client is a Global Biopharma based in Limerick. They are currently seeking an Associate Manager for their Technical Training who will focus on Instructional Design. This organistaion seeks people who are excited by a start-up environment, recognize the opportunities that this offers and want to be challenged. The successful person shall be responsible for leading instructional design within Technical Training, managing the eLearning program, training delivery standards, incorporating emerging learning techniques and technologies into the global training program. Role...

Location: Limerick,
Associate Manager (Technical Training) 		Limerick Not Disclosed

Scientific Communications Publication Capability Lead

Our client, a global pharmaceutical organisation are currently recruiting for a Scientific Communications Publication Technical Advisor to join their team. As Publication Capability Lead you will help drive launch and publication capabilities and operational excellence for the Global Scientific Communications Group. Responsibilities Function as an expert on the publication medical writing, publication processes and practices, including authorship, transparency and ethics Consults and advise site publication writers on issue management and escalation Represent the gro...

Location: Cork,
Scientific Communications Publication Capability Lead 		Cork Not Disclosed

Regulatory Scientific Communications Associate

Our client, a global pharmaceutical organisation are currently recruiting for a Scientific Communications Associate to join their newly created Global Scientific Communications team. As Regulatory Scientific Communications Associate you will work with cross-functional, multidisciplinary teams to lead the development of documents intended for regulatory audiences including, clinical study reports, briefing documents, regulatory responses, Investigational New Drug Applications, and marketing authorization applications. Responsibilities Document Preparatio...

Location: Cork,
Regulatory Scientific Communications Associate 		Cork Not Disclosed

Regulatory Affairs Specialist

Our client a medical device early stage company wishes to add a Regulatory Affairs Specialist to our team. The successful candidate will work with the Design, Quality and Regulatory teams to support all regulatory functions for both existing and new products. Role/Responsibilities • Contribute to the regulatory strategy plans for new products, including required Regulatory Agency approvals. • Provide regulatory input into labelling, test strategies for new product development, risk analysis, clinical, preclinical and marketing issues. • Planning,...

Location: Cork,
Regulatory Affairs Specialist 		Cork Not Disclosed

Regulatory Affairs & Quality Manager

Regulatory Affairs & Quality Manager Our client a cardiovascular medical device start-up looking to hire a Quality and Regulatory Affairs manager. The succ

Location: Dublin,
Regulatory Affairs & Quality Manager 		Dublin Not Disclosed
Other Regulatory Affairs Jobs
Job Title Location Salary Actions
Senior Regulatory Affairs Specialist Galway Not Disclosed
Senior Regulatory Affairs Specialist Galway Not Disclosed
Senior Regulatory Affairs Specialist Galway Not Disclosed
Director, PVE (Risk Management) Dublin Not Disclosed
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