
Clinical Research Coordinator
2 days ago
You will work in a clinical research setting, supporting the research team in the management and coordination of health services clinical research projects in Surgery Academic Clinical Programme (Surgery ACP)
You will be responsible for coordinating and implementing various health services clinical research studies in compliance with study protocols, good clinical practices, and regulatory requirements.
Job Responsibilities
- Assist in the planning, implementation, and coordination of clinical research studies, including preparing study documents, coordinating study visits, and managing study timelines.
- Conduct study participant recruitment and screening, obtaining informed consent, and collecting and recording study data accurately and efficiently.
- Ensure compliance with study protocols, good clinical practices, and regulatory requirements, including monitoring and reporting adverse events.
- Maintain study records and databases, and prepare study reports and presentations as required.
- Liaise with study sponsors, study sites, and other stakeholders to ensure effective communication and collaboration throughout the study.
- Ensure that all study-related activities are conducted in accordance with ethical, legal, and regulatory requirements.
Relevant Experience & Skills
· Bachelor's degree in biomedical sciences/Life Science/Nursing or related fields
· At least 2 years of relevant working experience in clinical trials management would be preferred
· Excellent interpersonal and communication (written and verbal) skills
· Strong attention to detail and accuracy
· Bilingual and/or knowledge of local dialects desired
· Proficiency in Microsoft Office applications
Qualities
· Ability to work independently and as part of a team
· Takes initiatives and is self-motivated
· Detail-oriented, with strong administrative, data management and analysis skills
· Able to multi-task and work efficiently with short deadlines
Tell employers what skills you haveAble To Multitask
Microsoft Office
Strong Attention To Detail
Clinical Research
Ability To Work Independently
Surgery
Healthcare
Data Management
Data Entry
Clinical Trials
Protocol
Neuroscience
Verbal Skills
Nursing
Regulatory Requirements
Life Sciences
Screening
Scheduling
Databases
IRB
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