CRA/SCRA

Benefits

Working directly with sponsor

Home based role

Work with a close knit team

Supportive management focused on career development and progression

About the company

This company is an innovative, medium-sized global CRO currently based in over 50 countries. They are well known for their great working culture and dynamic team providing full and functional clinical research solutions to biotech, pharmaceutical and medical device industries.

About the opportunity

The CRA/SCRA is responsible for the preparation, initiation, monitoring and closure of allocated sites. You work in close collaboration with other Monitors and the Local Study Delivery Team to ensure that quality and quantity commitments are achieved in a timely and efficient manner

Duties

Actively participate in local Study Delivery Team meetings.

Drive performance at the sites. Proactively identify study-related issues and escalates as appropriate.

Ensure timely delivery of proper applications/documents for submission to Regulatory Authorities.

Track and manage agreed payments at study site level.

Participate in training and mentoring of new members of the local clinical team ensuring compliance with ICH/GCP

Ensure that all study documents are ready for final archiving and sign-off completion of local part of the Trial Master File.

Contribute to process improvements, knowledge transfer and best practice sharing.

Skills and Experience

Tertiary degree (life science preferred)

Minimum of 18 months independent local clinical monitoring experience

Excellent knowledge of international guidelines ICH/GCP, basic knowledge of GMP/GDP.

Thorough knowledge of monitoring procedures

Good understanding of the clinical trial process

Able to work in fast paced environment

Good communication, interpersonal, analytical and negotiation skills

Culture

Well known for their culture and low turnover, this company provides a close knit and supportive team environment.

How to Apply

Click apply or contact Christine Bristol, Executive Consultant on +61 2 8877 8766 for a confidential discussion.