This is a fully remote position, open to applicants in New Zealand.

📋 Description

• Conduct Pre-Study, Initiation, Interim, and Close-Out monitoring visits either on-site or remotely.

• Ensure that the facilities and personnel at investigational sites are suitable for conducting studies.

• Identify and assess the qualifications, resources, facilities, equipment, and staff of investigators.

• Provide training to investigational site personnel as required.

• Assist in the preparation of regulatory and/or Ethics Committee submissions as needed.

⛳️ Requirements

• Bachelor’s degree in Life Sciences or a comparable combination of education, training, and experience.

• Significant on-site monitoring experience with phase 2/3 clinical trials.

• Preferably, experience with intricate trials such as oncology or rare diseases.

• Proficient in English at a professional level.

• Strong planning, multitasking, and teamwork capabilities in a dynamic environment.

• Excellent communication, collaboration, and problem-solving skills.

• Willingness to travel.

• National travel is a requirement.

🏝️ Benefits

• A collaborative, international team atmosphere.

• Opportunities for career advancement.

• Flexible working options.

• Support for work-life balance.

• Chance to contribute to innovative therapies and enhance patient care.