Full-Time Senior Clinical Research Associate

Senior CRA Responsibilities:

Communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in various therapeutic areas.

Building and maintaining relationships with clinical sites and investigators.

Focus on subjects’ rights, safety, well-being and data quality compliance.

On-site Monitoring:

• Conduct and report all types of onsite monitoring visits.
• Be involved in study startup (if applicable).

Data Management & Quality Control:

• 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, including compliance monitoring and reports review.
• Participate in feasibility research.
• Support regulatory team in preparing documents for study submissions.

Experience and Qualifications:

• College/University degree in Life Sciences or an equivalent combination of education, training & experience.
• 5+ years of independent on-site monitoring experience in the USA.
• Experience in all types of monitoring visits in Phase II and/or III.
• Participation in clinical projects as a Lead/Senior Monitor.
• Experience monitoring complex Oncology (breast cancer) trials.
• Full working proficiency in English.
• Proficiency in MS Office applications.
• Ability to plan, multitask, and work in a dynamic team environment.
• Strong communication, collaboration, and problem-solving skills.
• Ability to travel.
• Valid driver’s license (if applicable).

Career Advancement:

Advance your career in clinical research and lead challenging full-service projects on the country/regional level.

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