
Clinical Trials Research Specialist
3 days ago
A highly skilled and experienced Research Associate is required to join our clinical trials unit. The successful candidate will be responsible for coordinating study requirements, organizing informed consent processes, and providing patient care in compliance with protocol requirements.
This is a grant-funded contractual position that requires strong clinical skills, excellent written and verbal communication skills, and the ability to work independently. The ideal candidate will have a degree in Medicine or a relevant health field, current registration with their professional association, and at least one year of research experience.
The successful candidate will also have the opportunity to provide laboratory support services, review clinical trials protocols, and facilitate internal and external audits of the unit. They will be expected to draft and report serious adverse events, annual and periodic reports to regulatory bodies and sponsors.
Key Responsibilities:- Liaise and coordinate study requirements with relevant units and departments of the institution.
- Organize and administer the informed consent process in conjunction with the Principal Investigator.
- Coordinate and provide patient care in compliance with protocol requirements specific to patients screening, recruitment, scheduling, and study visit procedures.
- Degree in Medicine or a relevant health field.
- Current registration with their professional association.
- At least one year of research experience.
- Excellent clinical skills.
- Ability to work independently and versatility to work in a variety of roles.
- Excellent written and verbal communication skills in English.
- Integrity and strong research ethics.
- Efficiency in MS office tools (Microsoft Word, Microsoft PowerPoint and Microsoft Excel).
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