Clinical Research Associate 2 - based in Portugal
Clinical Research Associate
Your responsibilities will include:
- Performing site selection, initiation, monitoring and
- 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
- Requires at least 1 year of
- site monitoring experience. - Very good computer skills including MS Office
- Excellent command of Portuguese and English language.
- Organizational, time management and
- 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 stable, international, reputable company
- Company car, mobile phone and attractive benefits package
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Informações detalhadas sobre a oferta de emprego
Empresa: IQVIA Argentina Localização: Oeiras
Oeiras, Distrito de Lisboa, PortugalPublicado: 16. 3. 2025
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