Principal Investigator

Benefits 12-month contract with very strong likelihood of permanent employment Opportunities for career advancement in clinical research Supportive team environment Engage in multiple clinical trials About the company A prominent multi-site clinical trials network dedicated to delivering exceptional clinical studies.
The company collaborates with top pharmaceutical and healthcare organizations, recognized for its focus on participant care and data integrity in research.
About the opportunity As the Principal Investigator, you will play a key role in conducting and overseeing clinical trials, prioritizing participant safety and well-being.
Responsibilities include contributing to study meetings, reviewing protocols, assessing participant eligibility, and ensuring compliance with ethical and legal standards.
Principal Investigators will also guide sub-investigators to uphold study integrity, essential for the successful execution of trials and advancing medical research.
Duties Conduct clinical trials in accordance with ICH GCP guidelines Oversee participant safety, informed consent, and compliance with study protocols Lead meetings with CROs and sponsors to enhance trial efficiency Ensure medical oversight and maintain quality control of trial data Retain and satisfy study participants Skills and Experience Medical degree (MBBS/MD) General registration (PGY3 and above) Extensive experience in clinical research Phlebotomy skills Culture A collaborative, data-driven, and patient-centered environment committed to clinical excellence.
How to Apply Click apply or contact Rohan Lallbeeharry – Senior Recruitment Consultant at 03 9938 7115 or for a confidential discussion.
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