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Search Results for Scientific
Job Title. Location Salary Actions

Pharmacovigilance Regulatory Affairs Advisor Fully Remote

Pharmacovigilance Regulatory Affairs Advisor-Fully remote Our client, a regulatory consultancy organisation are currently recruiting for a Pharmacovigilance Regulatory Affairs Advisor to join their team on permanent basis. This role is 100% home based. Responsibilities Creation & review, with strong emphasis on critical evaluation, of all clinical reports, efficacy & safety summary reports while working collaboratively with clients. Preparation of Risk Management Plans (RMP's), Signal Detection Reports, PSUR's with assessment of ...

Location: Republic of Ireland,
Pharmacovigilance Regulatory Affairs Advisor Fully Remote
Republic of Ireland Not Disclosed

Senior Clinical Data Management Associate

Our client is a Global Biopharma who are establishing a Paediatric Centre of Excellence in Dublin that will be responsible for the management and execution of Paediatric Clinical Trials, across all therapeutic areas, around the world. The Clinical Operations team in Dublin is a pivotal function within this Centre of Excellence. In partnership with Clinical Research, Medical Affairs and other Development Operations functions, Clinical Operations ensures that all clinical trial activities are performed in accordance with applicable SOPs, company policies and regulatory gui...

Location: Dublin,
Senior Clinical Data Management Associate
Dublin Not Disclosed

CMC Development Regulatory Associate

CMC Development Regulatory Associate Our client, a global pharma company are currently recruiting for a CMC Development Regulatory Associate to join their team on a permanent basis.As CMC Development Regulatory Associate you will create and manage submission documents and provide guidance on structure and content placement. You will work within regulations to expedite the registration and lifecycle maintenance of products, to ensure delivery of safe and effective products to patients.The scope of work includes global regulatory requirement assessment and understanding strategy develop...

Location: Cork,
CMC Development Regulatory Associate
Cork Not Disclosed

Clinical Development Director (Oncology)

Our client is a global Biopharma who are establishing a Clinical Trials Centre of Excellence in Dublin, Ireland. They are seeking a qualified Medical doctor (essential), preferably with Oncology clinical trial experience, in the area of Haematology or a related therapeutic area. The successful person shall lead multiple components of clinical trial programs in paediatric oncology clinical development. You may also act as the Physician Responsible on certain projects. For the assigned projects, you will be accountable for various aspects of ongoing clinical trial progra...

Location: Dublin,
Clinical Development Director (Oncology)
Dublin Not Disclosed

Senior Associate (Clinical Data Management)

Our client is a Global Biopharma organisation who have established a Clinical Trials Centre of Excellence in Dublin, responsible for the management and execution of Paediatric Clinical Trials, across all therapeutic areas, around the world. The Clinical Operations team are seeking a Senior Clinical Data Management Associate who will work collaboratively with internal and external colleagues and vendors to support our client’s business objectives by ensuring the accurate and timely acquisition of diverse clinical data through efficient CRF/eCRF design, edit specifications...

Location: Dublin,
Senior Associate (Clinical Data Management)
Dublin Not Disclosed

Clinical Development Director (Oncology)

Our client is a global Biopharma who are establishing a Clinical Trials Centre of Excellence in Dublin, Ireland. They are seeking a qualified Medical doctor (essential), preferably with Oncology clinical trial experience, in the area of Haematology or a related therapeutic area. The successful person shall lead multiple components of clinical trial programs in paediatric oncology clinical development. You may also act as the Physician Responsible on certain projects. For the assigned projects, you will be accountable for various aspects of ongoing clinical trial progra...

Location: Dublin,
Clinical Development Director (Oncology)
Dublin Not Disclosed

Senior EHS Specialist

We’re currently recruiting for an exciting opportunity with an award-winning pharmaceutical organization based in Cork. This is an excellent position for

Location: Cork,
Senior EHS Specialist
Cork Not Disclosed

Clinical Publisher Associate

Clinical Publisher Associate Our client, a global pharma company are currently recruiting for a Clinical Publisher Associate to join their team on a permanent basis. As Clinical Publisher you will create and maintain complex strategic and compliance submissions through collaboration, document management, and internal database maintenance. You will collaborate with Regulatory Associates, Regulatory Scientists, cross-functional contributing/authoring areas, and affiliates to align on submission specific strategies and to ensure adherence to eCTD regulations and guide...

Location: Cork,
Clinical Publisher Associate
Cork Not Disclosed