Intern - Country Site Activation
IQVIA
Intern - Country Site Activation
Job Description
Intern, Country Site ActivationLocation: PortugalDuration: 3 MonthsHours: 35 hours per weekOverviewThe 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 ResponsibilitiesSupport 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.QualificationsCurrently 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 GainHands-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.
Locations
- Portugal, Lisbon
Skills Required
- Microsoft Office applicationsintermediate
Required Qualifications
- Currently pursuing or recently completed a degree in Life Sciences, Pharmacy, Health Sciences, or a related field. (degree in recently completed a degree in life sciences)
- Strong attention to detail and organizational skills. (experience)
- Good written and verbal communication skills in Portuguese and English. (experience)
- Proficiency in Microsoft Office applications. (experience)
- Ability to manage multiple tasks and work effectively in a team environment. (experience)
- Currently pursuing or recently completed a degree in Life Sciences, Pharmacy, Health Sciences, or a related field. (degree in recently completed a degree in life sciences)
- Strong attention to detail and organizational skills. (experience)
- Good written and verbal communication skills in Portuguese and English. (experience)
- Proficiency in Microsoft Office applications. (experience)
- Ability to manage multiple tasks and work effectively in a team environment. (experience)
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.
- 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.
- 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.
- 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.
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