On-Camera Game Presenter: Energetic Host In Sofia

Cross Border Talents; Lisboa; On-site; EUR 45,000 - 60,000; Full time

Benefits offered by this job

Company car

Mobile phone

Attractive benefits package

Job summary

IQVIA is seeking a Clinical Research Associate 2 based in Portugal. The role focuses on site visits, patient recruitment planning, and ensuring site quality according to GCP/ICH guidelines. You will track submissions, recruitment, data queries, and collaborate with study sites and client teams.

The ideal candidate holds a science/healthcare degree, has 2–4 years of on-site monitoring experience, and is fluent in Portuguese and English, with strong MS Office skills and travel flexibility.

Qualifications

• University degree in scientific discipline or health care.
• 2-4 years of independent on-site monitoring experience.
• Very good computer skills including MS Office.
• Excellent command of Portuguese and English language.
• Organizational, time management and problem-solving skills
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients
• Flexibility to travel
• Driver's license class B

Responsibilities

• Performing site selection, initiation, monitoring and close-out visits
• Supporting the development of a subject recruitment plan
• Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines
• Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions
• Collaborating with experts at study sites and with client representatives

Skills

Portuguese & English fluency

Organizational skills

Time management

Communication skills

Problem solving

Travel flexibility

Education

University degree in science/healthcare

Tools

MS Office

Job description

Clinical Research Associate 2 - Based in Portugal

Lisbon, Portugal
Full time
R
Clinical Research Associate

Your responsibilities will include:

• Performing site selection, initiation, monitoring and close-out visits
• Supporting the development of a subject recruitment plan
• Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines
• Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions
• Collaborating with experts at study sites and with client representatives

Qualifications:

• University degree in scientific discipline or health care
• 2-4 years of independent on-site monitoring experience.
• Very good computer skills including MS Office
• Excellent command of Portuguese and English language.
• Organizational, time management and problem-solving skills
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients
• Flexibility to travel
• Driver's license class B

What you can expect:

• Resources that promote your career growth
• Leaders that support flexible work schedules
• Programs to help you build your therapeutic knowledge
• Excellent working environment in a stabile, international, reputable company
• Company car, mobile phone and attractive benefits package

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.

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.

IQV