Patient Recruitment:

• Identify and screen potential study participants based on inclusion and exclusion

criteria as outlined in the study protocol.

• Obtain informed consent from participants, ensuring they fully understand the

study’s purpose, procedures, and potential risks and benefits.

Data Collection:

• Assist in data collection and ensure accurate entry of study data into electronic data capture systems

and clinical databases.

• Maintain detailed and organized records of study-related activities, including patient

information, consent forms, and other relevant documents.

• Conduct regular data quality checks to ensure accuracy and completeness of collected data.

Participant Interaction:

• Schedule study visits and follow-ups with participants, coordinating with clinical staff as

needed.

• Provide support to study participants throughout the study process, addressing any

questions or concerns as needed.

Compliance and Regulatory:

• Follow study protocols and standard operating procedures (SOPs) to ensure compliance

with regulatory and ethical standards.

• Assist in preparing and maintaining regulatory documents, including IRB submissions,

amendments, and approvals.

Communication and Collaboration:

• Work closely with principal investigators and research teams to support study objectives

and ensure seamless operations.

• Communicate regularly with the research team about study progress, participant status,

and any issues that arise during the study.

Quality Assurance:

• Ensure all study procedures are conducted according to protocol and SOPs, contributing to

the overall quality and integrity of the research.

• Assist in preparing for audits and inspections by maintaining accurate and up-to-date study

documentation.

QUALIFICATIONS

Bachelor’s degree in health sciences, Nursing, Biology,
Psychology, or a related field.
Minimum of 1 year of experience in clinical research setting or
related field.

Please refer the Job description for details