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Research Associate
2 weeks ago
About the Role:
">The Clinical Trial Coordinator will be working fully embedded within one of our pharmaceutical clients' offices, with the support of ICON right behind you. You will be at the heart of our client's innovation, providing ongoing administrative support to other members of the clinical study team.
Main Responsibilities:
">- Collaborate with site staff to ensure clinical trials are being run according to the protocol
- Document management, tracking, electronic filing and review
- Responsible for IRB/EC as well as RA submission, from initial submission to amendment
- Supporting the study start-up process locally
About Our Team:
">We are a dedicated team of professionals passionate about delivering innovative solutions for our clients. We believe in nurturing talent and promoting a culture of diversity, inclusion & belonging.
Your Benefits:
">- A competitive salary package
- A range of health insurance offerings to suit you and your family's needs
- Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
- Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family's well-being
- Life assurance
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others
About You:
">We are looking for a detail-oriented, passionate and reliable individual with a relevant educational background, either in life-sciences or as a licensed healthcare professional. You should have strong interpersonal skills, proficiency in MS Office and the ability to manage multiple priorities simultaneously.
