Clinical Research Associate
As a key member of our team, you will play a pivotal role in ensuring the integrity and success of clinical trials. Your primary responsibility will be to safeguard the rights and well-being of trial participants, while also guaranteeing the accuracy and completeness of reported data.
Clinical Research Associates work closely with various stakeholders, including Investigational Sites, Sponsors, and regulatory bodies, to ensure compliance with industry standards and guidelines. This involves building strong relationships with site personnel, fostering collaborative environments, and driving site recruitment and engagement initiatives.
Responsibilities include preparing essential documents, supporting ethics and regulatory submission processes, and understanding local and international regulatory requirements for clinical trials. You will also be responsible for monitoring investigational sites as per ICH GCP guidelines.
Our ideal candidate possesses excellent time management skills, attention to detail, teamwork, and computer literacy. A graduate degree in a clinical or life sciences-related field is required, along with relevant experience in the research, pharmaceutical industry, or related field.
Candidates must have full unrestricted working rights in Australia and be committed to upholding our company's values of gender equality and inclusivity. We offer flexible working options, paid parental leave, flexible leave entitlements, wellness programs, and ongoing development opportunities.
Qualifications & Experience
* Graduate degree in a clinical or life sciences-related field
* Excellent time management skills, attention to detail, teamwork, and computer literacy
* Relevant experience in the research, pharmaceutical industry, or related field
What We Offer
* Flexible working options
* Paid parental leave
* Flexible leave entitlements
* Wellness programs
* Ongoing development opportunities