CRA II

Phiture; Lisboa; Presencial; EUR 30 000 - 45 000; Tempo integral

Resumo da oferta

Uma organização líder em investigação clínica busca um Clinical Research Associate II para a sua equipe em Portugal. O candidato desempenhará um papel vital na condução de ensaios clínicos e na interpretação de dados médicos. Valorizamos um ambiente inclusivo e diverso que acolhe talentos de alto desempenho.

Serviços

Licença anual diversa

Ofertas de seguro saúde

Planejamento de aposentadoria competitivo

Apoio 24 horas por meio do programa de assistência

Seguro de vida

Benefícios opcionais flexíveis

Qualificações

• Mínimo de 2 anos de experiência como Clinical Research Associate.
• Conhecimento profundo de processos de ensaios clínicos e regulamentos (ICH-GCP).
• Fluente em Português e Inglês.

Responsabilidades

• Conduzir visitas de qualificação, início, monitoramento e fechamento de ensaios clínicos.
• Garantir a conformidade do protocolo e integridade dos dados.

Conhecimentos

Organização

Comunicação

Atenção aos detalhes

Formação académica

Bacharelado em campo científico ou de saúde

Descrição da oferta de emprego

CRA II - ICON Biotech

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team in Portugal for ICON Biotech. As a Clinical Research Associate II Specialist at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. Our biotech division operates with a mindset aligned to small and mid-sized biopharma.

What You Will Be Doing

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborating with investigators and site staff to facilitate smooth study conduct.
• Performing data review and resolution of queries to maintain high-quality clinical data.
• Contributing to the preparation and review of study documentation, including protocols and clinical study reports
  
  

Your profile

• Bachelor's degree in a scientific or healthcare-related field.
• Minimum of 2 years of experience as an independent Clinical Research Associate.
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
• Strong organizational and communication skills, with attention to detail.
• Able to travel across Portugal
• Ability to work independently and collaboratively in a fast-paced environment.
• Fluent Portuguese and English
  
  

What ICON Can Offer You

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our Benefits Examples Include

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
  
  

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply