Job Description

Job Summary Essential Requirements:

• Masters Degree in Computer Science, Public Health or related field
• Bachelors or Degree in Medical, Scientific, Biological, Statistical, Computer Science or related field with exceptional work experience
• At least 3 years data management experience working in a clinical research setting
• Experience in data warehousing, databases, software development, open source software, systems administration, software/systems security
• Computer literacy (Proficiency in MS Excel and /or MS Access,SQL, REDCap and/or EDGE)
• Valid GCP Certificate
• Previous research experience
• Familiarity of Research Documentation Standards

Desirable Requirements:

• Knowledge about TB and respiratory infections
• Experience with statistical packages such as R, STATA or SPSS
• Ability to conduct basic statistical analyses and convert them to tables and figures

Responsibilities include (but not limited to):

• Responsible for the day-to-day data collection activities, with the support of all other site staff.
• Manage team of data capturers
• Manage data entry and related databases of existing studies and training databases.
• Design, develop and validate new databases, including those interfacing with electronic CRFs
• Design and implement structures within the database for various analyses and reporting.
• Review and provide input into source documentation templates created by Study Team.
• Develop and provide input into unit SOPs pertaining to all data areas.
• Design a secure data archive and storage solution
• Maintain access control systems, backups, access logs, security checks and software updates of the system
• Develop tools & Infrastructure for mining of datasets (e.g. data warehouses)
• Developing and drafting Data Sharing Agreements
• Preparing and submit application for eletronic equipment calls and other grants
• Involved in the planning stage of research studies by providing input where necessary into design of questionnaires, data collection forms and case report forms (CRFs).
• Monitor adherence of the site to data quality management plans and coordinate activities at the site to ensure timely annual reporting of Quality Management plans.
• Assist in raising source or CRF queries with relevant staff and review that these queries are resolved adequately.
• Evaluate data query rates, response turnaround time and data query trends and assist research staff in formulating responses as necessary.
• Provide training and mentoring for applicable personnel on the different databases/systems.
• Create and produce reports from the training databases as needed.

Additional Information:

• This position will be based between the Old Main Building, Groote Schuur Hospital, and the University of Cape Town Lung Institute, in Mowbray Cape Town
• Working hours 40 hours per week, Monday to Friday
• 12-month contract

Only shortlisted candidates will be contacted. Should you not receive a response within 30 days of the closing date, please consider your application unsuccessful.The University of Cape Town Lung Institute is committed to equity in our employment practices and reserves the right not to appoint.
The selection process will be guided by the Employment Equity Plan and Targets of the University of Cape Town Lung Institute (Pty) Ltd.*Please Note: This Position is not on UCT Conditions of Service.University of Cape Town Lung Institute (Pty) LtdCompany

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