Responsibilities. Obtain clinical trial authorisations and ethical approvals. Populate and Manage TMF (Trial Master File) Archival and Storage, Quarterly Reviews, Files documentation of Clinical Study related communications in the TMF- ensuring it is updated for future requirements. Work closely with the study teams to assist with timely uploading of Clinical...

Responsibilities. Obtain clinical trial authorisations and ethical approvals. Populate and Manage TMF (Trial Master File) Archival and Storage, Quarterly Reviews, Files documentation of Clinical Study related communications in the TMF- ensuring it is updated for future requirements. Work closely with the study teams to assist with timely uploading of Clinical...

Responsibilities. Obtain clinical trial authorisations and ethical approvals. Populate and Manage TMF (Trial Master File) Archival and Storage, Quarterly Reviews, Files documentation of Clinical Study related communications in the TMF- ensuring it is updated for future requirements. Work closely with the study teams to assist with timely uploading of Clinical...

A dynamic bio-pharmaceutical company in Cork seeks a Dutch speaker to join its' expanding team of Clinical Associates. All talented candidates are welcome to apply. THE ROLE: * Investigate site activities, including the collection and submission of regulatory documents. * Understand and comply with procurements, * Understand legal and financial...

A dynamic bio-pharmaceutical company in Cork seeks five Flemish speakers to join its' expanding team of Clinical Associates. All talented candidates are welcome to apply. THE ROLE: * Investigate site activities, including the collection and submission of regulatory documents. * Understand and comply with procurements, * Understand legal and financial...

Responsibilities. Obtain clinical trial authorisations and ethical approvals. Populate and Manage TMF (Trial Master File) Archival and Storage, Quarterly Reviews, Files documentation of Clinical Study related communications in the TMF- ensuring it is updated for future requirements. Work closely with the study teams to assist with timely uploading of Clinical...

PE Global are currently recruiting for a Scientific Technical Specialist for a client site in Cork: The Technical Specialist will provide technical process support and expertise to the sterile manufacturing area to manufacture quality pharmaceutical products in accordance to meeting the Priorities of: Compliance, Supply, Strategy and Profit Plan. The...

A dynamic bio-pharmaceutical company in Cork seeks six German speakers to join its' expanding team of Clinical Associates. All talented candidates are welcome to apply. THE ROLE: * Investigate site activities, including the collection and submission of regulatory documents. * Understand and comply with procurements, * Understand legal and financial...

A dynamic bio-pharmaceutical company in Cork seeks French speakers to join its' expanding team of Clinical Associates. All talented candidates are welcome to apply. THE ROLE: * Investigate site activities, including the collection and submission of regulatory documents. * Understand and comply with procurements, * Understand legal and financial requirements...

****this role would suit candidates coming from a scientific or engineering background**** responsibilities. as a manufacturing process specialist, your typical day may include but is not limited to: • supports manufacturing investigations troubleshoot technical issues and provide general technical service support for manufacturing facilities and marketed products. • reviews and...

A QC Laboratory Lead is required by CareerWise Recruitment for our North Cork based Food client. Manage all aspects of a small laboratory in a food company. THE ROLE: * Conduct Q.C. laboratory tests and analysis using provided instruments while adhering to well defined methods and procedures covering the...

This is a great opportunity to join a world leader during a start up phase where you can develop that in depth knowledge that only a start up will afford you. Working on a Technical Transfer project you will be the first port of call for any technical issues associated...

Role Description: Leads early and late phase Technical Transfer activities through generation of protocols/reports, technical writing, execution of laboratory scale studies and participation in manufacturing operations and NPI initiatives. Leads early and late phase product development activities through generation of protocols/reports, execution of laboratory scale studies and participation in Lean...

Our client is a leading pharmaceutical organisation globally. Due to a significant global investment, they are expanding their manufacturing operations in the Cork facility. The role: You will report directly to the Director of Operations and sit on the senior leadership team for the site. The Operations Lead will provide...

Are you ready to take your career to the next level? An innovative bio-pharmaceutical company in Ireland seeks Clinical Research Associates. All talented candidates are welcome to apply. THE ROLE: * Initiate investigator site activities, including collection and submission of regulatory documents, customization and negotiation of informed consent documents. *...