20 melhores vagas de clinical trials para lisboa (Contratando agora!)

Associate Clinical Trials Regulatory Manager, EMEA
IQVIA —Oeiras
- Período Integral
- Graduação
Cell and Organoid Culture Research Technician (Botton-Champalimaud Pancreatic Cancer Centre)
Champalimaud Foundation —Lisboa
- Doutoramento
- Mestrado
- Graduação
Country Activation and Submissions Representative_(Home-Based, Portugal) - IQVIA Biotech
IQVIA —Oeiras
- Período Integral
- Graduação
Há 9 dias
Analyst in UK Health Technology Assessment Strategy and Implementation - Portugal (Hybrid/Home-based)
IQVIA —Oeiras
- Período Integral
- Modelo Híbrido
Bioinformatician (Cancer Genomics Lab - Botton-Champalimaud Pancreatic Cancer Center)
Champalimaud Foundation —Lisboa
- Doutoramento
- Mestrado
Clinical Trial Manager
ICON Plc —Lisboa
- Período Integral
- Graduação
Há 3 dias
Clinical Trial Manager - IQVIA Biotech
IQVIA —Oeiras
- Período Integral
- Graduação
Tech Systems/Support Analyst - English + Dutch, French or German (Portugal Homebased)
IQVIA —Oeiras
- Período Integral
Senior Site Contract Associate - IQVIA Biotech
IQVIA —Oeiras
- Período Integral
- Graduação
Clinical Data Management Lead
IQVIA —Oeiras
- Período Integral
- Teletrabalho
- Graduação
Pathology Research and Macroscopy Technician
Champalimaud Foundation —Lisboa
- Doutoramento
- Mestrado
- Graduação
Contact Center Analyst - Fluent Spanish and English (Portugal Homebased)
IQVIA —Oeiras
- Período Integral
Site Enrollment and Engagement Lead
IQVIA —Oeiras
- Período Integral
- Graduação
Laboratory Technician – Advanced Omics Platforms
Champalimaud Foundation —Lisboa
- Doutoramento
- Mestrado
Associate Director - Clinical Project Management (IQVIA Biotech)
IQVIA —Oeiras
- Período Integral
- Graduação
13 h
Regulatory Medical Writer III
Fortrea —Oeiras
- Período Integral
- Doutoramento
- Mestrado
Há 13 dias
(Senior) Clinical Project Manager - Global Study Leadership
IQVIA —Oeiras
- Período Integral
- Graduação
Há 8 dias
Clinical Embryologist
Ovom Care GmbH —1050 Lisboa
- Mestrado
Candidatura rápida
Junior Clinical & Translational Pathologist – Pancreatic Cancer & Biobanking
Champalimaud Foundation —Lisboa
- Doutoramento
- Mestrado
Senior/ Medical Writer - FSP
IQVIA —Oeiras
- Período Integral
- Modelo Híbrido
- Doutoramento
- Mestrado
- Graduação
13 h

Quero receber o alerta de ofertas mais recentes para clinical trials em lisboa

Ao iniciar sessão na sua conta, concorda com os Termos de Serviço do SimplyHired e consente com a nossa Política de Privacidade e Cookies.

Explorar ofertas em mais locais

clinical trials jobs near lisboa

Associate Clinical Trials Regulatory Manager, EMEA

IQVIA -
Oeiras

Candidate-se agora

Detalhes da oferta

Período Integral

Qualificações

Graduação

Descrição completa da oferta

Oeiras, Portugal | Full time | Home-based | R1556227

Associate Clinical Trials Regulatory Manager

EMEA

Homebased

Job Summary

The Associate Clinical Trials Regulatory Manager provides regulatory support and oversight for clinical trial submissions across global programs. This role is responsible for preparing and reviewing regulatory documentation, managing submissions, ensuring regulatory compliance, and supporting clients and internal stakeholders throughout the clinical trial lifecycle. This is not a people manager role, but a process management position.

Key Responsibilities

Serve as the Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects and programs.
Provide regulatory oversight and strategic guidance to internal and external stakeholders.
Review scientific and regulatory documentation, conduct gap analyses, and provide recommendations.
Author and/or review key regulatory documents, including Investigational Medicinal Product Dossiers (IMPDs) and clinical trial justifications.
Coordinate and support European centralized submissions and global country submissions.
Ensure project deliverables are completed on time, within scope, and in compliance with regulatory requirements.
Maintain accurate records in internal systems, databases, and tracking tools in accordance with SOPs.
Support business development activities by providing regulatory expertise.
Deliver regulatory training and presentations as required.
Mentor junior team members and contribute to departmental knowledge sharing initiatives.

Qualifications and Experience

Bachelor's degree in Life Sciences, Pharmacy, Regulatory Affairs, or a related field.
Typically 3–5 years of experience in Regulatory Affairs within the pharmaceutical, biotechnology, CRO, or clinical research industry.
Experience supporting clinical trial submissions and regulatory documentation.
Strong scientific writing, document review, project management, and stakeholder engagement skills.
Advanced knowledge of clinical trial regulations and regulatory submission processes.

Knowledge & Competencies

Advanced knowledge of regulatory affairs and clinical trial submission requirements.
Strong analytical and problem-solving skills.
Excellent communication and collaboration abilities.
Ability to work independently and manage multiple priorities in a fast-paced environment.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Candidate-se agora

Refine sua pesquisa

clinical trials vagas para: lisboa

Associate Clinical Trials Regulatory Manager, EMEA

Cell and Organoid Culture Research Technician (Botton-Champalimaud Pancreatic Cancer Centre)

Country Activation and Submissions Representative_(Home-Based, Portugal) - IQVIA Biotech

Analyst in UK Health Technology Assessment Strategy and Implementation - Portugal (Hybrid/Home-based)

Bioinformatician (Cancer Genomics Lab - Botton-Champalimaud Pancreatic Cancer Center)

Clinical Trial Manager

Clinical Trial Manager - IQVIA Biotech

Tech Systems/Support Analyst - English + Dutch, French or German (Portugal Homebased)

Senior Site Contract Associate - IQVIA Biotech

Clinical Data Management Lead

Pathology Research and Macroscopy Technician

Contact Center Analyst - Fluent Spanish and English (Portugal Homebased)

Site Enrollment and Engagement Lead

Laboratory Technician – Advanced Omics Platforms

Associate Director - Clinical Project Management (IQVIA Biotech)

Regulatory Medical Writer III

(Senior) Clinical Project Manager - Global Study Leadership

Clinical Embryologist

Junior Clinical & Translational Pathologist – Pancreatic Cancer & Biobanking

Senior/ Medical Writer - FSP

Quero receber o alerta de ofertas mais recentes para clinical trials em lisboa

Related Searches

Explorar ofertas em mais locais

Where you'll work

Home-based

Culture

Ferramentas para Candidatos

Ferramentas da empresa

Procurar

Mantenha-se em Contacto