We are seeking a seasoned Clinical Research Associate to join our team in Australia. This role involves monitoring and owning the progress of clinical studies at investigative sites, ensuring compliance with protocols, SOPs, ICH-GCP, and regulatory requirements.
Responsibilities include coordinating study setup and monitoring activities, identifying potential study risks, and proposing mitigation solutions. The ideal candidate will have prior experience as a CRA or Senior CRA in Oncology clinical studies in Australia, with a strong focus on precision medicine.
The successful candidate will be responsible for:
* Monitoring and owning the progress of clinical studies at investigative sites
* Ensuring compliance with protocols, SOPs, ICH-GCP, and regulatory requirements
* Coordinating study setup and monitoring activities
* Identifying potential study risks and proposing mitigation solutions
Requirements:
* Life science degree and/or equivalent experience
* CRA experience within the CRO or pharmaceutical industry (and working in Oncology)
* Availability for domestic travel, including overnight stays, as required
Preferred qualifications include a graduate or postgraduate degree in a scientific or healthcare discipline, two+ years of oncology experience, and study start-up activities experience.
Precision Medicine Group is an equal opportunity employer, committed to providing a supportive and inclusive work environment.
We offer competitive compensation packages, professional development opportunities, and a collaborative team culture.
As a key member of our team, you will have the opportunity to make a meaningful contribution to the advancement of precision medicine and cancer therapies.
We are passionate about fostering a culture that values innovation, teamwork, and customer satisfaction.
Our goal is to deliver exceptional results, exceed client expectations, and drive business growth through strategic partnerships and collaborations.