Job Description

External Required.

• Assist Investigators’ with required research administration; e.g. Institutional Review Board application, draft and review research agreements
• Manage research data, data entry, data cleaning and ethics/legal compliance
• Assist with research such as recruitment, informed consent taking and handle queries by research subjects
• Ensure proper maintenance of study record according to research compliance, protocols and regulations.
• Provide support in grant processing/claims, facilitate grant verification and variation submissions
• Track study expenditure
• Prepare progress and final reports, and ensure proper closure of completed research projects
• Assist PI in preparation of study related presentation/materials
• Coordinate project meetings

• Degree in Life Sciences or related discipline, with a minimum of 5 years of relevant work experience
• Strong administrative and project management skills with ability to manage multiple projects concurrently
• Knowledge in Good CLincial Practice, research ethics, clinical trials and regulatory affairs
• Proficient with MS Office applications
• Responsible and independent.
• Able to work in a team
• Good written and oral communcation skills
• Excellent IT knowledge and skills to provide assistance in data cleaning
• Has experiecne in performing analysis using  scripting programming languages or software (Python, R, Java, C++, C#.Net, SQL).

• Assist Investigators’ with required research administration; e.g. Institutional Review Board application, draft and review research agreements
• Manage research data, data entry, data cleaning and ethics/legal compliance
• Assist with research such as recruitment, informed consent taking and handle queries by research subjects
• Ensure proper maintenance of study record according to research compliance, protocols and regulations.
• Provide support in grant processing/claims, facilitate grant verification and variation submissions
• Track study expenditure
• Prepare progress and final reports, and ensure proper closure of completed research projects
• Assist PI in preparation of study related presentation/materials
• Coordinate project meetings

• Degree in Life Sciences or related discipline, with a minimum of 5 years of relevant work experience
• Strong administrative and project management skills with ability to manage multiple projects concurrently
• Knowledge in Good CLincial Practice, research ethics, clinical trials and regulatory affairs
• Proficient with MS Office applications
• Responsible and independent.
• Able to work in a team
• Good written and oral communcation skills
• Excellent IT knowledge and skills to provide assistance in data cleaning
• Has experiecne in performing analysis using scripting programming languages or software (Python, R, Java, C++, C#.Net, SQL).