Clinical Research Assistant

Job Description:

We are seeking a motivated and detail-oriented Clinical Research Assistant to join our dynamic research team. The successful candidate will play a pivotal role in supporting clinical trials and research studies aimed at advancing medical knowledge and improving patient care. The Clinical Research Assistant will work closely with the research team, study participants, and healthcare professionals to ensure the smooth and ethical execution of research projects.

Key Responsibilities:

Participant Recruitment and Screening:Identify and recruit eligible study participants according to study criteria.
Screen potential participants to ensure their suitability for the research.
Data Collection and Documentation:Assist in the collection of clinical data, including medical histories, laboratory results, and vital signs.
Maintain accurate and organized records of all research-related activities.
Ensure data integrity and compliance with study protocols.
Informed Consent Process:Explain the research study to participants and obtain informed consent.
Maintain documentation of informed consent processes.

Clinical Procedures: Assist with clinical procedures, including administering medications, medical tests, and assessments as per the study protocol.
Ensure adherence to ethical and safety standards.

Data Management:Enter, manage, and analyze research data using electronic databases and software.
Generate reports and assist in data interpretation.

Regulatory Compliance:Ensure compliance with regulatory requirements, including Good Clinical Practice (GCP) guidelines.
Assist in preparing and submitting regulatory documents as needed.

Study Coordination:Collaborate with principal investigators, physicians, nurses, and other healthcare professionals involved in the research.
Coordinate study-related activities and scheduling.

Participant Follow-up:Maintain regular contact with study participants to track their progress and ensure retention in the study.

Quality Assurance:Assist in monitoring and auditing study sites to ensure protocol adherence and data quality.

Adverse Event Reporting:Promptly report adverse events and safety concerns to the appropriate regulatory bodies.

Job Type: Full-time

Pay: $12.00 - $16.00 per hour

Benefits:

• Flexible schedule

Schedule:

• Monday to Friday

Experience:

• Clinical trials: 1 year (Preferred)
• Research: 1 year (Preferred)

Work Location: In person