Senior Clinical Research Associate
CRA04072024_1720077246
Posted: 07/04/2024
- Melbourne, Victoria
- Permanent
Our client seeks an experienced Senior Clinical Research Associate (CRA) to oversee and monitor clinical trials across diverse therapeutic areas.
Founded in the late 1990s, this award-winning firm has established itself as a global leader, operating in over 30 countries.
They offer a supportive work environment with flexible onsite requirements and manageable workloads.
Ideal for a seasoned Clinical Research Associate with a minimum of 2 years' CRO/Pharma monitoring experience.
Key Responsibilities:
- Initiate, monitor, and conclude site visits globally, ensuring adherence to protocols and regulatory standards.
- Identify suitable global clinical trial sites through site selection and qualification activities.
- Collaborate with cross-functional teams, including investigators and project managers, to ensure seamless trial execution.
- Verify clinical data accuracy and compliance with study protocols and regulatory requirements.
- Maintain essential study documentation, including regulatory submissions and monitoring reports.
- Address and escalate issues related to patient safety, data integrity, or study conduct.
- Contribute to protocol development, case report forms (CRFs), and other study-related documents.
- Train and mentor junior CRAs, offering support as required.
Qualifications:
- Bachelor's degree in a scientific or healthcare discipline; advanced degree preferred.
- Minimum 2 years' experience as a Clinical Research Associate, ideally in global clinical trials.
- Proficiency in ICH-GCP guidelines, local and international regulatory requirements, and industry standards.
Position Details:
Title: Senior CRA
Salary: $120,000 - $155,000 plus superannuation
Location: Melbourne, South Australia, Western Australia
To apply for this opportunity, please submit your updated resume or contact Keeley Munday at 02 8310 5854.
Related Keywords: Clinical Research Associate, CRA, Global Clinical Research Organisation, global clinical trials, therapeutic areas, ICH-GCP guidelines, site selection, data integrity, patient safety, regulatory compliance, cross-functional teams, site visits, biotech-sponsored projects, mentoring, junior CRAs, EDC systems, global travel, professional growth, innovation, impactful research, healthcare
Keeley Munday
Principal Candidate Consultant
