Job Summary:

As a Clinical Research Assistant, you will play a crucial role in supporting the execution of clinical

research studies and trials. Working under the supervision of the Principal Investigator or Clinical

Research Coordinator, you will contribute to the efficient and ethical conduct of research by performing

various tasks related to data collection, participant recruitment, and study coordination. This position

requires attention to detail, strong organizational skills, and a commitment to maintaining compliance

with regulatory requirements.

Responsibilities:

● Participant Recruitment and Informed Consent:

○ Assist in identifying and recruiting eligible participants for clinical trials.

○ Explain study details to potential participants, ensuring their understanding and obtaining

informed consent.

○ Maintain accurate and up-to-date participant recruitment records.

● Data Collection and Management:

○ Collect and record study data accurately and in accordance with the study protocol.

○ Implement data quality control procedures to ensure accuracy and completeness of data.

○ Maintain organized and secure study-related documentation.

● Clinical Trial Coordination:

○ Assist in coordinating study visits, scheduling participant appointments, and managing

visit logistics.

○ Ensure that all study activities are conducted in compliance with protocol requirements

and regulatory standards.

○ Collaborate with clinical research team members to facilitate smooth study operations.

● Regulatory Compliance:

○ Assist in preparing and submitting regulatory documents to Institutional Review Boards

(IRBs) and other relevant regulatory bodies.

○ Stay informed about changes in regulations and guidelines related to clinical research and

ensure ongoing compliance.

● Communication and Collaboration:

○ Communicate effectively with study participants, healthcare professionals, and other

members of the research team.

○ Collaborate with investigators, sponsors, and other stakeholders to facilitate the progress

of the study.

● Data Analysis and Reporting:

○ Support the analysis and interpretation of study data under the guidance of the research

team.

○ Assist in the preparation of reports, presentations, and publications related to study

findings.

● Professional Development:

○ Stay abreast of developments in clinical research methodologies, regulations, and best

practices.

○ Attend relevant training sessions and workshops to enhance knowledge and skills.