Intern - Country Site Activation

IQVIA; Lisboa; Presencial; EUR 6700 - 10 000; Tempo parcial

Vantagens oferecidas por esta oferta de emprego

Hands-on internship experience

Mentorship & professional development

Certificate of Internship

Resumo da oferta

IQVIA in Lisbon, Portugal, is seeking an Intern for Country Site Activation. The role supports regulatory, contractual, and document-management tasks within clinical trial start-up. The internship offers hands-on experience in a global CRO and exposure to the site activation lifecycle.

The position is part-time, 35 hours per week, for 3 months. Ideal candidates are pursuing degrees in Life Sciences, with strong organizational skills and fluency in Portuguese and English.

Qualificações

• Currently pursuing or recently completed a degree in Life Sciences, Pharmacy, Health Sciences, or a related field.
• Strong attention to detail and organizational skills.
• Good written and verbal communication skills in Portuguese and English.
• Proficiency in Microsoft Office applications.
• Ability to manage multiple tasks and work effectively in a team environment.

Responsabilidades

• Support the preparation and processing of contract addendums.
• Assist with regulatory submissions to relevant authorities and ethics committees.
• Prepare and track regulatory notifications.
• Support implementation and tracking of regulatory submissions and approvals.
• Conduct Trial Master File (TMF) reviews to ensure completeness and compliance.
• Maintain and update clinical trial systems and databases.
• Assist with administrative and operational site activation activities as required.

Conhecimentos

Degree in Life Sciences/Pharmacy/Healt

Attention to detail

Portuguese and English communication

MS Office proficiency

Multitasking & teamwork

Formação académica

Life Sciences/Pharmacy/Health Sciences degree

Ferramentas

MS Office

Descrição da oferta de emprego

Lisbon, Portugal

Part time

R1564897

Intern, Country Site Activation

Location: Portugal

Duration: 3 Months

Hours: 35 hours per week

Overview

The Country Site Activation Intern will support clinical trial start-up activities by assisting with regulatory, contractual, and document management processes. This role offers valuable exposure to the clinical research environment and site activation lifecycle.

Key Responsibilities

• Support the preparation and processing of contract addendums.
• Assist with regulatory submissions to relevant authorities and ethics committees.
• Prepare and track regulatory notifications.
• Support implementation and tracking of regulatory submissions and approvals.
• Conduct Trial Master File (TMF) reviews to ensure completeness and compliance.
• Maintain and update clinical trial systems and databases.
• Assist with administrative and operational site activation activities as required.

Qualifications

• Currently pursuing or recently completed a degree in Life Sciences, Pharmacy, Health Sciences, or a related field.
• Strong attention to detail and organizational skills.
• Good written and verbal communication skills in Portuguese and English.
• Proficiency in Microsoft Office applications.
• Ability to manage multiple tasks and work effectively in a team environment.

What You'll Gain

• Hands-on experience in clinical trial start-up and site activation.
• Exposure to regulatory and clinical research processes.
• Opportunity to develop professional skills within a global clinical research organization.

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.

At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

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