Asst Manager
Job Responsibilities:
1) Research Administration
-
Assist in grant management and administration e.g. collation and tracking of grant submissions, budget planning and utilization tracking, claims submissions
-
Assist in requests for external collaborations, work with Sr/Manager CRU, Director CRU/ Dy Director CRU/ Specialty Advisory Group Advisors to identify suitable NHGP Principal Investigators
-
Assist in the review of research collaborative agreements, project agreements
-
Coordinate and assist in submission of research proposals for ethics and research funding
-
Monitor research activities and outcomes in NHGP
-
Prepare research reports
-
Assist in supervising temporary research data collection and data entry/ transcription staff
-
Assist in departmental budget planning and utilization tracking
-
Assist in planning and development of clinical research programmes and events.
-
Assist in the implementation of new research policies
-
Build relationships and collaborate with other divisions / departments in NHGP and external partners where relevant to ensure smooth running of clinical research in NHGP, including logistical coordination between study teams and clinics
-
Provide secretariat support to the various Research Committees e.g. Centre Grant Steering Committee and other related committees and workgroups
2. Research Infrastructure Support
-
Assist in the planning and development of research spaces in clinics and office
-
Oversee the maintenance of research drives for storage of research data
-
Oversee the maintenance of the contents on the CRU pages in NHGP website (intranet/ internet)
Job Requirements:
-
Min Bachelor's degree in any discipline, preferably life science related, arts or communications
-
Preferably with about 1-2 years of work experience in operations, administrative work and medical writing
-
High level of computer literacy including proficiency in Microsoft office (Word, Excel, Powerpoint, etc)
-
Advanced English language and writing skills
-
Knowledgeable in Good Clinical Practice, clinical trials and regulatory affairs and medical and research Ethics preferred
-
Knowledge in medical and research terminology preferred
-
Meticulous with good organization, coordination and administrative skills
-
Ability to integrate, interpret and summarize and present data from a variety of sources in a clear, accurate and concise manner
-
Ability to work independently in writing projects
-
Team player with good interpersonal skills