19 melhores vagas de material specialist para lisboa (Contratando agora!)

Associate/ Study Start Up Manager, IQVIA Biotech
IQVIA —Oeiras
- Período Integral
- Graduação
UAT Tester (10 months project)
TechBiz Global GmbH —Lisboa
- Período Integral
- Teletrabalho
- Graduação
Candidatura rápida
Sr. Spclst, Regulatory Affairs
MSD —Oeiras
- Período Integral
- Modelo Híbrido
Há 3 dias
IT & System Admin
Devote Consulting —1250 Lisboa
SAP LOGISTICS (HYBRID)
iTRTech Group —1050 Lisboa
- Modelo Híbrido
Product/Project Manager
Enkonix —Lisboa
- Modelo Híbrido
Sales Hiring Specialist
Revolut —Lisboa
DORA PROJECT MANAGER (HYBRID)
iTRTech Group —1050 Lisboa
- Modelo Híbrido
Há 6 dias
CLM Solution Engineer
Richemont —Moscavide
Investment Reporting - Analyst / Associate
iCapital —Lisboa
Há 6 dias
Business Analyst
Enkonix —Lisboa
Lead AI Scientist Computer Vision
Siemens Energy —Amadora
- Período Integral
- Modelo Híbrido
Product Growth Specialist
Air Apps —Lisboa
- Período Integral
Project Manager
Enkonix —Lisboa
Product Designer
Enkonix —Lisboa
Graphic Designer (Brand)
Revolut —Lisboa
Programmer SPS / Robot
BENTELER Automotive —Palmela
- Período Integral
Danish Speaking Content Reviewer
Ignite —Lisboa
Candidatura rápida
Há 8 dias
Creator Relations
Air Apps —Lisboa
- Período Integral

More jobs to discover

Find similar jobs that you might be interested in.

UAT Tester (10 months project)
TechBiz Global GmbH —Lisboa
Develop and execute detailed UAT test plans and test cases based on the business requirements. Proficiency in test management software (Sirion) and SQL.
Candidatura rápida

Quero receber o alerta de ofertas mais recentes para material specialist 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

material specialist jobs near lisboa

Ofertas de Sales Specialist em Lisboa

Ofertas de Graphic Designer em Lisboa

Ofertas de Product Manager em Lisboa

Ofertas de Reporting Analyst em Lisboa

Ofertas de Business Analyst em Lisboa

Ofertas de Product Specialist em Lisboa

Ofertas de Social Media Specialist em Lisboa

Ofertas de Sales Specialist em Porto

Ofertas de Sales em Guimarães

Ofertas de Sales Assistant em Coimbra

Ofertas de Regulatory Affairs Specialist em Almada

Ofertas de Public Affairs em Lisboa

Ofertas de Operation Specialist em Lisboa

Ofertas de Supply Chain Specialist em Lisboa

Ofertas de Regulatory Affairs Specialist em Porto

Ofertas de Regulatory Affairs Specialist em Porto Salvo

Ofertas de Sales Specialist em Distrito Do Porto

Ofertas de Regulatory Affairs Specialist em Distrito De Lisboa

Ofertas de Team Manager em Lisboa

Ofertas de Marketing Project Manager em Lisboa

Associate/ Study Start Up Manager, IQVIA Biotech

IQVIA -
Oeiras

Candidate-se agora

Detalhes da oferta

Período Integral

Qualificações

Graduação

Descrição completa da oferta

Oeiras, Portugal | Full time | Home-based | R1543626

Job Overview
Direct and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including pre-award activities, oversight of the scope of work, budget and resources.

Essential Functions

Oversee the execution of Site Activation (including pre-award/bid defense activities) and/or Maintenance for assigned projects in accordance with the agreed RSU site activation strategy, adhering to project timelines.
Develop, implement and maintain the Management Plan according to the Scope of Work and Project Plan, within the agreed project strategy, resolving project related issues where required.
Ensure collaboration across Regulatory & Site Activation, including communication with regions and countries, to successfully deliver the agreed project scope in compliance with the RSU Management Plan.
Create and/or review technical and administrative documentation to support business development and enable study initiation and maintenance, as required.
Provide specialist regulatory and technical scientific support to facilitate efficient business development, initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements.
Provide overall guidance and oversight of multi-regional and multi-protocol programs during initial start-up and maintenance phase as an integral member of the study management team. Determine regulatory strategy/expectations and parameters for submissions and all necessary authorizations
Identify regulatory complexity and challenges and offer creative and practical solutions to support the bid process and subsequent execution of the site activation plan. Assess and review the regulatory landscape and contribute to the collection, interpretation, analysis and dissemination of accurate regulatory intelligence to support assigned studies and wider company, as required.
Execute operational strategy/ expectations for maintenance of clinical study approvals, authorizations and review/ negotiation of contracts and essential documents. Work with Quality Management to ensure appropriate quality standards for the duration of site activation (or Maintenance, as applicable). Mentor and coach colleagues as required. Ensure accurate completion and maintenance of internal systems (with emphasis on CTMS), databases, tracking tools, timelines and project plans with project specific information.
May take a lead role in developing long standing relationships with preferred IQVIA customers. Deliver presentations/training to clients, colleagues and professional bodies, as required. May be involved in activities related to monthly study budget planning and reviews.

Qualifications

Bachelor's Degree Life sciences or related field Req
7 years’ relevant experience in a scientific or clinical environment including demonstrable experience in an international role
Strong negotiation and communication skills with ability to challenge
Excellent interpersonal skills and strong team player
Proven ability to work through others to deliver results to the appropriate quality and timeline metrics on complex projects
Thorough understanding of regulated clinical trial environment and in depth knowledge of drug development process
Demonstrated proficiency in using systems and technology to achieve work objectives
Good regulatory and/or technical writing skills
Strong knowledge and ability to apply Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines and applicable regulatory guidelines
Good leadership skills, with ability to motivate, coach and mentor
Good organizational and planning skills
Ability to exercise independent judgment taking calculated risks when making decisions
Good presentation skills
Proven ability to establish and maintain effective working relationships with co-workers, managers and sponsors.
Excellent understanding of study financial management
Proven ability to work on multiple projects balancing competing priorities

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

material specialist vagas para: lisboa

Associate/ Study Start Up Manager, IQVIA Biotech

UAT Tester (10 months project)

Sr. Spclst, Regulatory Affairs

IT & System Admin

SAP LOGISTICS (HYBRID)

Product/Project Manager

Sales Hiring Specialist

DORA PROJECT MANAGER (HYBRID)

CLM Solution Engineer

Investment Reporting - Analyst / Associate

Business Analyst

Lead AI Scientist Computer Vision

Product Growth Specialist

Project Manager

Product Designer

Graphic Designer (Brand)

Programmer SPS / Robot

Danish Speaking Content Reviewer

Creator Relations

More jobs to discover

Quero receber o alerta de ofertas mais recentes para material specialist 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