
Senior Clinical Research Associate, East Coast
Posted 5 days ago

Posted 5 days ago
This is a fully remote position, open to applicants in New Zealand, +1 more country.
• Conduct on-site or remote monitoring visits for Pre-Study, Initiation, Interim, and Close-Out phases.
• Ensure that investigational facilities and personnel are sufficiently equipped throughout the duration of the study.
• Identify investigators and confirm their qualifications, available resources, facilities, equipment, and staff.
• Provide training to the staff at investigational sites as required.
• Assist in the preparation of regulatory and/or Ethics Committee submissions when necessary.
• Mentor and train new team members.
• Conduct co-monitoring visits to evaluate the performance of junior staff.
• Bachelor's or higher degree in Life Sciences or an equivalent combination of education, training, and experience.
• Significant on-site monitoring experience in Phase 2/3 clinical trials.
• Preferably experienced in handling complex trials related to oncology or rare diseases.
• Proficient in English at a full working level.
• Capable of planning, multitasking, and functioning effectively in a dynamic team environment.
• Strong communication, collaboration, and problem-solving abilities.
• Willingness to travel nationally.
• Full-time employment opportunities.
• Option for remote work.
• Opportunities to mentor and train new personnel.
• Collaborative work environment within the team.
• Engage in work that supports the safe and effective delivery of pharmaceutical treatments for patients.
• Chances to collaborate with experts in clinical research, pharmacovigilance, and quality consulting.
Thermo Fisher Scientific
ICON plc
ICON plc
Clinical Outcomes Solutions
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