Senior Clinical Research Associate – Sponsor Dedicated
IQVIA
full-time
Posted on:
Location Type: Office
Location: Madrid • Spain
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Job Level
Tech Stack
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 (GCP) and International Conference on Harmonization (ICH) guidelines
- Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
- Collaborating with experts at study sites and with client representatives
Requirements
- University degree in scientific discipline or health care
- At least 2 years of on-site monitoring experience
- Good knowledge of clinical research regulatory requirements
- 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
- Better Work-Life balance, optimal DOS
- 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 & Tools
on-site monitoringclinical research regulatory requirementsGood Clinical Practice (GCP)International Conference on Harmonization (ICH)data query resolutioncase report form (CRF) completion
Soft Skills
organizational skillstime managementproblem-solving skillseffective working relationshipsflexibility