
Clinical Trials Site Monitor
2 weeks ago
Pharmaceutical Career Opportunity
A career that makes a meaningful difference in the lives of patients is now available at a world-leading pharmaceutical company.
You will be part of a talented team that leverages cutting-edge science to create positive impact in therapeutic areas such as cancer, cardio-metabolic diseases, vaccines, and oncology.
Key Responsibilities:
- Conduct site monitoring from selection to close out.
- Monitor clinical trial progress and escalate any deviations or risks that may impact timely completion of study milestones.
- Submit visit reports to the Clinical Trial Manager on time.
- Collaborate with cross-functional teams including site staff, PI, CTM, CTA, contracts, and SSU teams.
- Perform monitoring activities in global oncology studies including on-site and remote visits.
Required Skills and Qualifications:
- Hold a tertiary degree in Life Sciences.
- Have 2+ years independent site monitoring experience.
- Ideal candidates have experience working within the CRO/Pharma industry.
Benefits Package:
We offer a competitive salary, annual leave entitlements, health insurance options, retirement planning, and other benefits focused on employee well-being and work-life balance opportunities for you and your family.
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