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

Who we areWorldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Anchored in our company’s scientific heritage, our dedicated therapeutic focus on...

Descrizione Lavoro: EMEA REGULATORY SpecialistDescrizione Lavoro: EMEA REGULATORY Specialist juniorClient DescriptionSiamo alla ricerca di un EMEA REGULATORY Specialist per uno dei nostri clienti in Italia. Il nostro cliente è un'azienda leader nella distribuzione di ingredienti e prodotti chimici speciali e sta cercando una giovane risorsa da inserire in...

Requisition Number7795Employment Type:Regular Who we are Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Anchored in our company’s scientific...

Requisition Number7552Employment Type:Regular Who we are Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Anchored in our company’s scientific...

Job Overview: As a Senior CRA specializing in ophthalmology, you will play a crucial role in the planning, implementation, monitoring, and management of clinical trials related to ophthalmic drugs, devices, or therapies. You will ensure that clinical trials are conducted in accordance with applicable regulatory requirements, protocols, and standard operating...

Descrizione Lavoro: EMEA REGULATORY Specialist Come EMEA REGULATORY Specialist, sarai responsabile della gestione delle attivit regolatorie Sarai coinvolto nella valutazione della conformit normativa dei prodotti e nella gestione delle autorizzazioni di commercializzazione. Candidate Profile Per essere considerato per questo ruolo, dovresti avere una laurea...

azienda leader nella distribuzione di ingredienti e prodotti chimici specialiDescrizione Lavoro: EMEA REGULATORY Specialist Descrizione Lavoro: EMEA REGULATORY Specialist juniorClient DescriptionSiamo alla ricerca di un EMEA REGULATORY Specialist per uno dei nostri clienti in Italia. Il nostro cliente è un'azienda leader nella distribuzione di ingredienti e...

Requisition Number6390Employment Type:Regular Who we are Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Anchored in our company’s scientific...

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...

Abbott Medical is looking for a Specialist Regulatory Compliance EMEA (m/w/d) based in Eschborn near Frankfurt/ Main or other Abbott Medical sites in Europe PURPOSE OF THE JOB The Specialist Regulatory Compliance supports EMEA across the cardiovascular und neuromodulation divisions to comply with regulatory requirements of the MDD, MDR,...

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...

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...

Your Job Prepare, submit and gain approval for regulatory applications to AIFA (MAA, renewal, variations). Assess and respond to regulatory questions to resolve issues. Management of post-approval activities as required. Review and submission (where applicable) of promotional and non-promotional materials. Strategic and operational customer support...

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...

Job Description You will be responsible for supporting the establishment of approaches, processes and information flow, along with building strong relationships to ensure effective collaboration between PSI teams and PSI vendors.  You will Review external vendor quotations Maintain vendor databases and tracking systems Support vendor...

Job Description You will be responsible for supporting the establishment of approaches, processes and information flow, along with building strong relationships to ensure effective collaboration between PSI teams and PSI vendors.  You will Review external vendor quotations Maintain vendor databases and tracking systems Support vendor...

Job DescriptionYou will be responsible for supporting the establishment of approaches, processes and information flow, along with building strong relationships to ensure effective collaboration between PSI teams and PSI vendors. You willReview external vendor quotationsMaintain vendor databases and tracking systemsSupport vendor identification, assessment...

When our values align, there's no limit to what we can achieve.   The purpose of the Global Labelling group is to drive the core labelling strategy and ensure that labelling documents are of high quality and compliant for the safe and effective use of our products for patients and healthcare providers globally. As the Global Labelling Lead , you would...

Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. At least 3 years' experience with submissions....

Job Overview Engage in structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements. Essential Functions • Complete appropriate therapeutic, protocol and clinical...