PSI is a leading Contract Research Organization with more than 22 years in the industry, offering a perfect balance between stability and innovation to both clients and employees.
We focus on delivering quality and on-time services across a variety of therapeutic indications.
As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.
Based in Sydney / Adelaide / Brisbane / Melbourne
You will :
Conduct and report SIV, RMV, COV onsite monitoring visits
Perform CRF review, source document verification and query resolution
Be responsible for site communication and management
Be a point of contact for in-house support services and vendors
Communicate with internal project teams regarding study progress
Participate in feasibility research
Support regulatory team in preparing documents for study submissions
Prepare and participate on audits and inspections
College / University degree in Life Sciences or an equivalent combination of education, training & experience
At least 2-3 years of independent on-site monitoring experience in Australia or New Zealand
Experience in all types of monitoring visits in all phases of study
Experience in Oncology or Hematology or Gastroenterology therapeutic indications is a plus
Full working proficiency in English
Proficiency in MS Office applications
Ability to plan, multitask and work in a dynamic team environment
Communication, collaboration, and problem-solving skills
Valid driver’s license and ability to travel
Full working rights in Australia
This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.
PSI is an inclusive and equal opportunity employer and is committed to attracting and retaining a diverse workforce that reflects the community we serve.
Applications from Aboriginal and Torres Strait Islanders are encouraged.