Senior Clinical Research Associate
4 semanas atrás
About IQVIA Portugal
IQVIA is a leading global contract research organization driving human health outcomes forward.
As a sponsor-dedicated CRA, you will enjoy the stability and resources of a global company while gaining direct experience with one of our customers. With access to world-class training and mentoring, you will have the opportunity to put your passions to work in an environment designed to help you gain experience in various therapeutic areas.
Your Key Responsibilities
- Perform site selection, initiation, monitoring, and close-out visits
- Support the development of a subject recruitment plan
- Evaluate the quality and integrity of site practices in accordance with regulatory requirements, including Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Manage progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
- Collaborate with experts at study sites and with client representatives
What We Are Looking For
- University degree in a scientific discipline or healthcare
- 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 English and Portuguese language
- Organizational, time management, and problem-solving skills
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients
- Flexibility to travel
What You Can Expect
- A competitive salary range of $80,000 - $110,000 per year, depending on experience
- Resources that promote your career growth
- Leaders who support flexible work schedules
- Programs to help you build your therapeutic knowledge
- Better work-life balance and optimal DOS
- An excellent working environment in a stable, international, reputable company
- A company car, mobile phone, and attractive benefits package
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