Senior Clinical Research Associate

November 10

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PSI CRO AG

Number One Patient Enrollment CRO • Clinical Research • Clinical Trials • Oncology • Hematology

1001 - 5000

Description

• Conduct and report all types of onsite monitoring visits • Be involved in study startup (if applicable) • Perform CRF review, source document verification and query resolution • Be responsible for site communication and management • Be a point of contact for in-house support services and vendors • Communicate with internal project teams regarding study progress • Participate in feasibility research • Support regulatory team in preparing documents for study submissions

Requirements

• College/University degree in Life Sciences or an equivalent combination of education, training & experience • Independent on-site monitoring experience in Peru • Experience in all types of monitoring visits in Phase II and/or III • Availability to travel • Full working proficiency in English and Spanish • PC skills to be able to work with MS Word, Excel and PowerPoint • Ability to plan, deal with different tasks and work in a dynamic team environment • Communication, collaboration, and problem-solving skills

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