Oncology Clinical Trials Coordinator
3 weeks ago
Job Overview
We are seeking an experienced research associate specialist to join our team and contribute to the success of our oncology clinical trials. As a key member of our team, you will work on multiple trials, focusing on quality of life initiatives with regional travel.
Responsibilities
- Lead site start-up documents, develop study documents, and mentor junior team members.
- Represent local trial managers or senior monitors on site management teams and take over lead role reports review for sites assigned to other team members.
- Support country budget development and contract negotiation, assist with adverse event reporting, and track metrics and KPIs outlined in the Quality Oversight Plan.
- Collaborate with investigator and site staff to meet all study timelines and operate various systems and databases.
Requirements
- Minimum 2 years' experience in monitoring pharmaceutical industry clinical trials, with at least 1-3 years of experience in oncology trials.
- Bachelor's degree in biological sciences or equivalent, with strong analytical and risk-based monitoring skills.
- Effective communication and influencing abilities, with a willingness to travel up to 50%.
What We Offer
- Competitive salary range of $89,376.00 - $111,720.00 USD per annum, depending on location, experience, education, and skill level.
- Range of benefits, including annual leave entitlements, health insurance options, retirement planning opportunities, and global employee assistance programs.
- Diverse culture that rewards high performance and nurtures talent.
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