Clinical Research Associate 2 - Based in Portugal

IQVIA; Oeiras; Presencial; EUR 30.000 - 50.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Company car

Mobile phone

Attractive benefits package

Descripción de la vacante

A global clinical research provider is seeking a Clinical Research Associate 2 based in Portugal. The role involves performing site selection and monitoring visits, supporting subject recruitment, and ensuring regulatory compliance. Candidates must have a relevant university degree and a minimum of two to four years' experience in monitoring. Excellent communication skills in Portuguese and English, along with strong computer skills, are essential. The position offers career growth resources and a flexible work environment.

Formación

• Minimum of two-four years of on-site monitoring experience or equivalent combination of education and experience.
• Driver's license class B is required.
• Effective working relationships with coworkers, managers, and clients.

Responsabilidades

• Perform site selection, initiation, and monitoring visits.
• Support development of subject recruitment plans.
• Evaluate quality and integrity of site practices.
• Track regulatory submissions and recruitment progress.
• Collaborate with experts at study sites.

Conocimientos

Monitoring experience

Excellent command of Portuguese

Excellent command of English

Computer skills including MS Office

Time management skills

Problem-solving skills

Ability to establish relationships

Flexibility to travel

Educación

University degree in scientific discipline or health care

Descripción del empleo

Clinical Research Associate 2 - Based in Portugal

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.

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


• Minimum of two-four years of on-site monitoring experience alternatively an equivalent combination of education, training and 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

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.