Clinical Research Associate II (Contract based)
PSI CRO • Lisbon, Lisbon, Portugal
Há 21 dias
Descrição do cargo
Job Description
As a Contract Clinical Research Associate II, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. You will focus on subjects’ rights, safety and well-being and quality of data compliance.
Home-based (freelance)
You will:
- Conduct and report all types of onsite monitoring visits
- Be involved in study startup
- Perform CRF review, source document verification and query resolution
- Be responsible for site communication and management
- Supervise study activities, timelines, and schedules on the country level
- Be a point of contact for in-house support services and vendors
- Be involved in quality control, such as compliance monitoring and reports review
- Participate in feasibility research
- Support regulatory team in preparing documents for study submissions
Qualifications
- College/University degree in Life Sciences or an equivalent combination of education, training & experience
- A minimum of 1 year of independent on-site monitoring experience in Portugal
- Experience in all types of monitoring visits in Phase II and/or III
- Experience in IBD/Inflammatory Bowel Diseases is mandatory
- Full working proficiency in English and Portuguese
- Proficiency in MS Office applications
- Ability to plan, multitask and work in a dynamic team environment
- Communication, collaboration, and problem-solving skills
- Ability to travel
Additional Information
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