Clinical Research Associate 1 - CFSP

IQVIA LLC; Lisboa; Presencial; EUR 42 000 - 56 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Career growth resources

Flexible work schedule

Therapeutic knowledge programs

International employer

Mobile phone allowance

Resumo da oferta

IQVIA LLC is seeking a Clinical Research Associate to support site initiation, monitoring and close-out visits, while aiding in recruitment strategy and data integrity. Strong English/Portuguese skills and travel readiness are required.

You will collaborate with study sites and client teams in a dynamic, international environment, contributing to high-quality clinical research operations.

Qualificações

• University degree in scientific discipline or health care.
• Minimum 1 year of on-site monitoring experience.
• Proficient with MS Office.
• Fluent in Portuguese and English.
• Strong organizational, time management and problem-solving skills.
• Ability to establish and maintain working relationships with coworkers, managers and clients.
• Willingness to travel.
• Driver’s license class B.

Responsabilidades

• Performing site selection, initiation, monitoring and close-out visits after training period.
• Supporting the development of a subject recruitment plan
• Evaluating the quality and integrity of site practices per ICH/GCP
• Managing progress by tracking regulatory submissions, recruitment, CRF completion, and data queries
• Collaborating with study-site experts and client representatives

Conhecimentos

Portuguese language

English language

Organizational skills

Time management

Problem-solving

Relationship building

Travel flexibility

Driver’s license

Formação académica

University degree in scientific discipline or health care

Ferramentas

MS Office

Descrição da oferta de emprego

Clinical Research Associate

Your responsibilities

• Performing site selection, initiation, monitoring and close-out visits after completing training period
• 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
• Requires at least 1 year of 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
• 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. 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.