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Global Clinical Trial Managers
3 weeks ago
The primary goal of this role is to oversee the daily activities related to clinical trials. This involves working closely with various stakeholders, including clinicians, researchers, and administrators.
Responsibilities:
- Facilitating the execution of clinical trials by reviewing key documentation and collaborating with project teams
- Assisting in the design and preparation of study and source documentation
- Maintaining accurate records and ensuring that all tracking tools are up-to-date
- Liaising with vendors, pharmacy staff, and Clinical Research Associates regarding IP management and accountability
Key qualifications include a tertiary degree or equivalent experience in a health-related discipline, as well as proficiency in Microsoft Office and other relevant tools.
This is a full-time position requiring flexible hours and ability to work independently. Candidates should possess excellent time management, planning, and organisational skills, with a proven track record in clinical research.
Candidates must also be competent in communication, problem-solving, and emotional intelligence, with a high level of accuracy and attention to detail.
A strong understanding of project management principles and practices is essential for this role. The ideal candidate will have experience working in similar roles within the clinical research industry.
Interested applicants can submit their application via [insert link]. We look forward to hearing from you.