Job Vacancies at Aga Khan University Hospital

Computer Science jobs, Information Technology jobs, Statistics jobs, Medical jobs, Healthcare jobs, Nursing jobs, Research jobs

Data Associate, Provost Office COE

Job Summary

The Data Associate will be required to support the review of the design and development of the study databases and data collection tools. He/she will also be involved in study team activities related to data collection, participant ID management, tracking of participant follow-up, management of all data & IT devices, management of user accounts, and supporting IT infrastructure at the recruitment sites. His/her role will involve coordinating data management activities. He/she will also be the point person in interactions with the AKU ICT team, data teams from other research projects in CoEWCH, and the collaborating institutions.

Responsibilities:

• Contribute to the design and set up of study databases in collaboration with collaborators at Indiana University and other collaborating institutions.
• Manage all study data handling systems: both paper and electronic.
• Testing and troubleshooting data handling systems.
• Development and piloting of data collection tools.
• Alongside the study coordinator oversee all study data related activities.
• Prepare training schedules synchronized with other training activities and guided by the study coordinator.
• Conduct training related to data entry and data quality and use of devices eg. Tablets, bar code scanners.
• Provide approval for staff to participate in data entry after achieving desired proficiency in data entry.
• Continuously assess training needs for the team and arrange appropriate refresher training as needed.
• Co-supervise clinical and research teams in their data handling tasks.
• This includes enumerators and nurses.
• Ensure that the generation, printing and allocation of IDs is done in a timely and accurate manner with no duplications and conflicts.
• Ensure that the above is well documented.
• Support the selection, purchase, setup and maintenance of data collection devices: including computers, tablets and bar code readers.
• Supervise the inventory keeping for study ICT equipment and accessories.
• Set up specific user profiles for each user and assign and manage user access rights.
• Support the development of site-specific SOPs, policies and processes for data collection and handling.
• Set up systems to ensure continuous data cleaning by the study teams.
• Develop, test and apply data quality assessment tools.
• Continuously monitor and advise the research team on data quality issues, including discrepancies, errors and missing data.
• Respond to queries and data errors and implement corrective actions to clean the data.
• Participate in standardization of data collectors for specific activities eg. anthropometry measurements.
• Identify errors or potential sources of error in data collection systems, databases and applications.
• In liaison with the data manager, test and implement modifications to the study database.
• Contribute to periodic and ad hoc data analysis of study data to support study activities or answer specific research questions.
• Respond to data requests from study investigators and analysts.
• Preparation and compilation of reports for data as agreed with supervisors.
• Provide data exports in desired format to study investigators.
• Liaison with the data teams in partnering institutions.
• Be the study contact person with the Aga Khan University’s ICT team in tasks related to data management, internet and intranet connectivity, user accounts and logins and device setup.
• Liaison with the County health records departments.
• In collaboration with AKU ICT team and other providers – Ensure the network set up, running smoothly and is of sufficient capacity to handle study needs.
• Implement and enforce regular data security activities such as backups, archiving and user administration.
• With necessary approvals, establish appropriate linkage between the databases for other research studies in AKU.
• Facilitate data sharing where appropriate and with necessary approvals.
• Support the setup and running of other sub-studies and/or related studies as allocated by the Principal Investigator.
• This may include responsibilities in other studies/projects within the CoEWCH.

Requirements:

• Bachelor’s Degree in any of the following or closely related fields: Computer Science, Information Technology, Statistics.
• Training and/or demonstrable competence in any/most of the following: MS-Access, SQL-Server, MySQL, Oracle, DHIS-2, ODK, and ODK-Tracker, REDcap.
• Training and/or demonstrable competence in any of the following statistical packages Stata, SPSS, R. Python.

Relevant Experiences:

• At least 2 years of data management experience.
• Relevant experience in a health research environment including community and public health facility settings will be an added advantage
• Relevant experience in multi-centre / multi-country projects will be an added advantage
• Demonstrable programming proficiency in at least 2 of the following: MS-Access, SQL-Server, MySQL, Oracle, DHIS-2, REDCap, ODK
• Proficiency with data management procedures: data cleaning, manipulation, summarization, tables, listings, graphics and report generation
• Experience in programming and troubleshooting electronic field data capture platforms
• Experience in data analysis will be an added advantage
• Excellent written and verbal skills in English

Personal Characteristics:

• Good organizational and management skills
• Attentive to detail and quality
• Ability to work independently/ with minimum supervision and within stipulated deadlines and schedules
• Excellent interpersonal and communication skills
• A team player and able to work in a multicultural environment

Closing Date: 18/03/2025, 7:59:00 PM

Clinical Practice Educator, OR Recovery

Responsibilities

• Lead the team in development, implementation and monitoring of unit based clinical policies and procedures
• Take lead in identification, definition and monitoring of unit based clinical indicators
• Responsible for continuing education/training for nurses in assigned unit
• Participate in evaluation of care and outcomes through Mortality and Morbidity discussions, clinical incidence trends and clinical indicators
• Participate in establishment of standards of care with unit staff, and monitors delivery of care according to established standards.
• Together with the Nurse Manager, conduct regular evaluation of nurses and designs individual development plans based on identified learning/training needs
• Ensure  monthly report of learning activities and spot checks are  submitted to the relevant persons on time
• Communicate effectively with the multidisciplinary team about all clinical matters such as infection control in assigned unit, spot checks and documentation.
• Guide nurses to evaluate effectiveness of  care given through re-assessments
• Ensure patients receive appropriate teaching about their condition and treatments
• Provide leadership of the multidisciplinary team and ward management in the absence of the nurse manager.
• Design a plan for continuing unit based learning and works with the nurse manager to ensure participation of all nurses
• Maintain records of all learning activities for the unit and individual nurses participation
• Designs methods to motivate nurses in assigned unit to pursue individual professional growth and development
• Participate in evaluation of nursing documents to ensure their appropriateness in capturing patient information
• Ensure nursing staff are familiar with the documentation policy and train nurses on the use of all nursing forms/charts
• Ensure compliance to documentation policy through spot-checks on nursing forms such Initial assessment, Vital signs chart, Patient Education Record, and fluid chart, treatment sheet and progress notes chart
• Take lead in unit based Continuous Quality Improvement (CQI) projects, Clinical Care Program Certification (CCPC) and ensures participation by   nurses.
• Guide nursing staff in initiation of and participation in unit based as well as hospital wide nursing research projects.

Requirement

• Registered nurse (KRN/M; KRCHN) with a BSc-Nursing degree
• Current licensure with the Kenya Nursing Council
• Certification in BLS
• Minimum 5 years continuous nursing experience in Operating Theatre unit in an acute care hospital.
• Possess teaching abilities, leadership qualities, professional judgment, critical thinking and problem-solving abilities, and a sense of professional development
• Demonstrate evidence-based knowledge of current practices in nursing

Closing Date: 27/03/2025, 7:59:00 PM

Manager, Research Administration, Department of Haematology/Onclogy

Job Summary

• The Department of Haemato-Oncology is seeking a Research Administration Manager, to ensure that the studies conducted by the Clinical Research Unit (CRU) meet the standards governed by regulations, laws, and guidelines both locally and internationally for clinical trials. One of the objectives of the organization is to become a center of excellence in conducting clinical trials. This position contributes by ensuring that CRU studies are conducted at high standards in accordance with the applicable local and international regulations, laws, and guidelines. Data Management and Front Office report to the Research Administration Manager.

Responsibilities

• Preparation, review, and submission of all components of ethical and regulatory submissions for new and ongoing clinical trials (new protocols, amendments, safety reports, annual reports, etc.)
• Filling all documents required in an investigator site file.
• Coordinating the preparation and training of SOPs and maintaining the review cycle.
• Assist the investigators and study team in the development and review of study documents (i.e., Protocol, informed consent forms, source documents, site specific addendums, study logs, etc.).
• Maintain up-to-date understanding of the Institutional Ethics Research Committee, Pharmacy and Poisons Board, National Commission of Science, Technology, Innovation, US Department of Health and Human Services, Office of Human Rights Protection, Food and Drug Administration, and European Medicines Agency’s policies by reading articles/publications and attending trainings/seminars.
• Reviewing and monitoring study procedures and documentation to ensure that the trial is conducted according to protocol, Good Clinical Practices, SOPs, and regulatory requirements.
• Responsible for onboarding, ongoing training, and evaluation of all staff in the CRU Data Management section and Office Administrator(s).

Requirements

• Bachelor’s degree in related field, Master’s degree is an added advantage.
• At least four (4) years’ experience in research and project management.
• Proficiency in office software, learning management platforms, office management systems and procedures.
• Strong organizational skills with ability to work with minimal supervision.
• Exceptional interpersonal and communication skills both written and verbal communication.
• Demonstrates supervisory skills and ability to work in a multicultural environment.
• Ability to independently prioritize work, critical thinking and problem-solving skills.
• Adaptability to new or changing situations, work under pressure and to meet tight deadlines.
• Ability to maintain confidentiality.

Closing Date: 27/03/2025, 7:59:00 PM

Method of Application

Use the link(s) below to apply on company website.

• Data Associate, Provost Office COE
• Clinical Practice Educator, OR Recovery
• Manager, Research Administration, Department of Haematology/Onclogy