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• Participate in study training

• Participate in the translation, testing and review of data collection tools

• Identify, recruit and screen potential study participants

• Conduct and document informed consent process; securely store all informed consent documents per study procedures

• Conduct face-to-face and phone-based interviews with participants (people interested in HIV prevention and site staff), enter data on electronic devices

• Upon learning of any serious adverse event or social harm, complete required forms, enter them in electronic database, and immediately inform Supervisor

• Obtain study forms from health care providers and enter them into electronic database

• Review health facility registers and capture required information into an electronic system

• Provide and document participant reimbursement per study protocol

• Accurately complete and maintain all field logs to track study progress and other files, whether computerized or manual.

• Securely handle and store data collection forms per study procedures

• Identify participants that have missed study appointments; telephone them to conduct follow-up interviews

• Work with the Data Manager and Site Study Coordinator to resolve data queries

• Consult and communicate in a timely manner any challenges encountered during data collection with the Site Study Coordinator

• Flawlessly maintain participant confidentiality

• Implement quality control process throughout the conduct of the study.

• Participate in regular team meetings

• Adhere to the study protocol and all study procedures

• Perform any other related duties

Key Outputs

• Potential study participants identified, screen and recruited.

• Data collection tools translated, tested and reviewed.

• Study protocol and all study procedures adhered to.

• Health facility registers reviewed and required information captured into an electronic system.

• Adverse events effectively documented and reported to the Supervisor.

• Participants that have missed study appointments identified for follow-up interviews.

• Quality control process implemented throughout the study.

• Study Data queries resolved.