Clinical Research Associate 2 – CFSP
IQVIA
full-time
Posted on:
Location Type: Office
Location: Madrid • Spain
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About the role
- 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
Requirements
- University degree in scientific discipline or health care
- Experience in Pharma Industry, and/or Clinical Trials environment
- Very good computer skills including MS Office
- Excellent command of Spanish 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
Benefits
- 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
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
site selectionsubject recruitment plan developmentregulatory submissions trackingcase report form completiondata query resolutionGood Clinical PracticeInternational Conference on Harmonization guidelines
Soft skills
organizational skillstime managementproblem-solving skillseffective working relationshipsflexibility
Certifications
university degree in scientific disciplineuniversity degree in health caredriver’s license class B