Clinical Research Assistant/ Phlebotomist 227415 - Providence, United States - Medix™

Medix™ Providence, United States

1 month ago

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Engineering / Architecture

Description

Responsibilities:

● Execute all blood draws and phlebotomy 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.

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