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

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...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programs RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may act as a Regulatory Oversight for a key customer Ability to...

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...

We are currently partnering with a Galway based medical device start-up who are looking to hire a Senior Clinical Trial Specialist as they expand. Job Summary: The Senior Clinical Trial Specialist you will be responsible for planning, executing, and overseeing clinical trials to ensure they are conducted in accordance with regulatory requirements,...

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...

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...

The candidate will support the development and execution of regulatory strategies for biologic products and combination products for the portfolio assigned and perform the duties outlined below In this role, a typical day might include the following: • Support CMC/Combination product development activities from a regulatory standpoint during early...

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 –...

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...

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 in...

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...

Why Patients Need You We're looking to bring medicines to the world faster and we are not willing to compromise on excellence and integrity. Adhering to local and global regulations is essential and the ever-changing regulatory environment requires forward thinking and attention to detail. Your dedication and expertise will help expand and accelerate...

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...

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...

Clinical Research Associate (all levels) Sponsor Dedicated, Home Based, Ireland Join us on our exciting journey! Remote/Hybrid/Office based working options. Our Sponsor Dedicated (cFSP) team are growing, join us on our mission to drive healthcare forward! As Clinical Research Associate you will be responsible perform monitoring and site management...

Are you looking for an opportunity to join a growing and dynamic organisation? Do you want an opportunity to use your skills to enhance Network Security in Ireland? Would you like the chance to challenge and develop yourself while working with a great group of colleagues? Look no further....Job Title: Regulatory Manager (Cyber Security)Starting Salary:...