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Participate in protocol, standard operating procedures (SOPs) or any other study trainings

Participate in study site entry visits and engage with management of study participants. These include but not limited to patient enrolment, as guided by the protocol.

Obtain written informed consent for those eligible and are willing to participate in the study

Administer all study procedures like sample collection, data collection and entry, patient follow-up and treatment to patients recruited into the study as guided by the protocol and in accordance to set standards of Good Clinical Practice

Perform patient safety monitoring for any adverse events, offer care and referral as needed

Provide counselling and pyscho-social support to study participants where needed

Conduct assessment of maternal hemodynamics and maternal hemodynamics data collection under guidance of coordinator.

Perform first-level quality assurance and quality control (QA / QC) to ensure all fields in the consent forms and case report forms (CRFs) are complete and accurate

Offer support to the community health workers and research assistants for the follow- up of study participants.

Assist in generating study progress reports as needed.

Perform any other duties assigned by the Project Manager and principal Investigator, as deemed necessary for study activities