Regulatory Manager, Clinical Trials Regulatory Management- Home-based, EMEA

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects. RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex Ability to administratively and technically/scientifically review core scientific...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

We are open to hire for this role across Munich, Frankfurt,Berlin-Germany; Amsterdam,The Netherlands; Luxembourg ; London, UK; Dublin, Ireland;The Amazon Security Assurance team is responsible for demonstrating the governance and security controls of services offered by Amazon. At Amazon scale, we must invent new ways to provide the highest level of...

The Manager, Regulatory Affairs International supports ambitious geographical expansion plans. The position will support registration of existing portfolio products into new territories and to register several of development projects into the international region. This role is key to driving both the Regulatory strategy and execution.• Provide...

We are open to hire for this role across Munich, Frankfurt,Berlin-Germany; Amsterdam,The Netherlands; Luxembourg ; London, UK; Dublin, Ireland;The Amazon Security Assurance team is responsible for demonstrating the governance and security controls of services offered by Amazon. At Amazon scale, we must invent new ways to provide the highest level of...

The Opportunity The Regulatory Affairs Specialist is responsible for supporting product commercialization, for GPN owned and contract brands, for all activities involving regulatory compliance from concept to launch. This role will play a critical role in delivery of the growth objectives of the EMEA region.  Ensuring Product Compliance to local...

100,000+ That’s how many patients participate in our clinical trials at any given time. Global Clinical Operations is Novartis’ new powerhouse, redesigned to enable faster trial recruitment and enhanced trial delivery resulting in more timely access for patients to potential novel treatments. Every day, we are the link between science and medicine –...

Regulatory Manager (Cyber Security) (12 Month FTC) Thank you for your interest in working with us. Purpose: The Regulatory Manager will report to the Head of Cyber Security and Resilience. The successful candidate will contribute and support the strategic planning requirements and associated stakeholder relations and will manage, track and report on key...

Description Summary Serves as a key regulatory interface with Global Health Authorities and acts as global regulatory lead for product brand teams to develop, maintain and obtain alignment of global regulatory strategies in accordance with business plans. The incumbent is expected to exhibit leadership behaviors consistent with level and to act with...

What is the opportunity? This is a highly sought-after and topical role within the banking sector which will offer you the opportunity to engage with colleagues across the organisation and also increase their profile with Senior Management. You will become part of a fast-moving team focusing on ensuring the Group is reporting risk-weighted assets & Capital...

What is the opportunity? This is a highly sought-after and topical role within the banking sector which will offer you the opportunity to engage with colleagues across the organisation and also increase their profile with Senior Management. You will become part of a fast-moving team focusing on ensuring the Group is reporting risk-weighted assets & Capital...

Clinical Document Governance Management (CDGM) is accountable for strategy and delivery of clinical document management (CDM) systems, processes, standards and operations of CDM services (including Trial Master File management (TMF), clinical submission readiness, record retention and archiving, Good Documentation Practice capability build) across Novartis...

When our values align, there's no limit to what we can achieve.   Are you an experienced regulatory professional looking for a new opportunity? We are currently seeking a talented CMC Regulatory Manager (Regulatory Affairs Consultant) to join our dynamic team! This is a client dedicated project, and the role can be office or home based in various...

On behalf of our client, an international pharmaceutical, clinical stage drug discovery company, we are currently recruiting for a Clinical Trial Project Manager for the area of rare diseases. This is a 6-9 month contract initially. The role will be predominately based in the Dublin office with approx 5% travel. Main Duties / Responsibilities: The successful...

Role: IRB Regulatory Risk Manager Location: Molesworth Street, Dublin 2 This role is being offered on a permanent basis. Have you experience in interpretating regulation and/or someone with a Credit Risk background with an understanding of regulatory guideline that underpin the Credit Policy suite?Have you a thirst for developing your regulatory...

Regulatory Reporting Manager Dublin, Republic of Ireland | Hybrid Permanent | Full time Closing date: May 16, 2024

Overview Cloud Operations & Innovation (CO+I) builds the physical datacenters, networks, fiber paths, and satellite base stations around the world that support Microsoft’s entire cloud business strategy. The EMEA Regional Compliance Manager is crucial in upholding and enhancing our reputation for compliance and ethical conduct within the...

On behalf of my client, a global pharmaceutical company, we are working with them on a new role for a Pharmacovigilance and Clinical Quality Specialist. This is a full-time permanent role based in Dublin. The Role & Responsibilities: The main purpose of this cross functional position is coordinating and leading a variety of: Pharmacovigilance system quality...

Experienced Clinical Research Associate page is loaded Experienced Clinical Research Associate Apply locations Dublin, Ireland time type Full time posted on Posted 3 Days Ago job requisition id R1415435 Clinical Research Associate (all levels) Sponsor Dedicated, Home Based, Ireland Join us on our exciting journey! Remote/Hybrid/Office based working...

What is the Opportunity? An exciting opportunity to join the Regulatory Reporting Change Team, a sub team within RRCO, is responsible for the development and delivery of strategic reporting solutions to meeting new, and amended, regulatory reporting requirements and to deliver of Bank change projects across regulatory reporting processes. With the ever...