Clinical Trials Coordinator
3 weeks ago
About the Company:
Clearline Recruitment Ltd is dedicated to connecting talented professionals with leading organizations in the healthcare sector.
Position Overview:
We are collaborating with a prominent global organization committed to fostering a brighter future through innovative healthcare solutions.
If you are seeking a position within a company that values self-drive, dedication, and enthusiasm, you might be the ideal addition to their Medical Clinical Operations team.
Role Summary:
Our client is in search of a Clinical Trials Coordinator. This role offers competitive compensation and an exceptional benefits package, including:
- Comprehensive employee health and wellness support
- Protection during significant life events
- Retirement planning assistance
- Hybrid working model (2 days in the office, 3 days remote)
- Complimentary onsite parking
- Company-sponsored events
- Customized training and development opportunities
Key Responsibilities:
As a Clinical Trials Coordinator, you will demonstrate strong project management capabilities by leading successful study teams throughout all phases of clinical trials.
Your responsibilities will include:
- Managing Investigator Initiated Studies (IIS) and Real World Evidence (RWE) activities, as well as overseeing the country management of global studies.
- Exhibiting creative problem-solving skills and critical thinking while fostering collaborative relationships across the organization and with key stakeholders.
- Ensuring study inspection readiness and overseeing the completion of corrective and preventive action plans following site audits and inspections.
- Supervising study activities from site activation to clinical closure, including monitoring tasks and training.
- Being accountable for vendor deliverables in accordance with timelines, budgets, operational procedures, quality/compliance, and performance standards.
- Maintaining oversight of vendor performance and addressing any issues, ensuring vendors receive appropriate training.
Qualifications:
The ideal candidate will possess experience in managing investigator-initiated and non-interventional studies.
Work Arrangement:
This position offers a hybrid work model, allowing for flexibility between office and remote work.
Contract Type:
This is a temporary position with a duration of 6-12 months.
For further details regarding this Clinical Trials Coordinator role, please reach out to Clearline Recruitment Ltd.
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