Senior Clinical Research Associate - Remote & Growth Paths

Medpace, Inc.; Auckland; Remote; NZD 70,000 - 110,000; Full time

Benefits offered by this job

Flexible work from home

Visa sponsorship & transfer

Annual merit increases

Bonus plan based on visits

Fast PACE training program

Cross-functional leadership paths

Airline club allowance

Casual dress code

Job summary

Medpace, Inc. offers flexible work-from-home options and visa sponsorship for qualified candidates in New Zealand.

The role focuses on site qualification, initiation, monitoring, and closeout visits in compliance with protocol, GCP, and regulatory requirements, with opportunities for cross-functional leadership. Responsibilities include ensuring investigator qualifications, maintaining documentation accuracy, regulatory reviews, and data integrity, while supporting patient recruitment and site

Qualifications

• Bachelor's degree in a health or science related field.
• Knowledgeable about Clinical Monitoring practices and procedures to represent the function in internal and external meetings.

Responsibilities

• Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol.
• Communicate with site staff, including coordinators and physicians, to ensure conduct aligns with SOPs, GCP and regulatory requirements.
• Verify investigator qualifications, training, facilities, and staff.
• Verify data accuracy and good documentation practices in source records and CRFs.
• Ensure enrollment of eligible subjects and review regulatory documents.
• Manage investigational product accountability and adverse event review per protocol.
• Assess site patient recruitment and retention and offer improvement suggestions.
• Complete monitoring reports and follow-up letters with clear summaries and actions.

Education

Bachelor's degree in a health or science related field

Knowledgeable about Clinical Monitoring practices

Job description

Medpace, Inc. offers flexible work-from-home options and visa sponsorship for qualified candidates in New Zealand.

The role focuses on site qualification, initiation, monitoring, and closeout visits in compliance with protocol, GCP, and regulatory requirements, with opportunities for cross-functional leadership. Responsibilities include ensuring investigator qualifications, maintaining documentation accuracy, regulatory reviews, and data integrity, while supporting patient recruitment and site