Clinical Research Assistant - #236902 - Medix™ : Job Details

Position Overview:

We are seeking a dedicated and detail-oriented Clinical Research Coordinator Assistant to support the execution of clinical trials. In this role, you will play a vital part in patient recruitment, screening, enrollment, and data coordination, ensuring compliance with study protocols and regulatory requirements.

Key Responsibilities:

• Patient Recruitment & Enrollment: Identify, recruit, and screen potential study participants in alignment with eligibility criteria.
• Participant Interaction: Obtain informed consent, schedule study visits, and ensure participants adhere to visit timelines.
• Assessments & Data Collection: Perform basic assessments, such as vital signs and questionnaires, and document findings accurately.
• Data Coordination: Maintain and update clinical trial databases, ensuring accuracy and timely entry of participant data.
• Protocol Compliance: Assist in monitoring study conduct, ensuring all activities are performed according to the protocol, Good Clinical Practice (GCP), and regulatory guidelines.
• Administrative Support: Coordinate study visit logistics, prepare study materials, and support site audits or monitoring visits as needed.
• Communication: Act as a liaison between participants, clinical staff, and investigators to address concerns and provide updates.

Qualifications:

• Bachelor's degree in a health-related field or equivalent experience in clinical research or patient care.
• Prior experience in clinical research, patient recruitment, or data entry preferred.
• Strong interpersonal skills with the ability to engage and build rapport with participants.
• Excellent organizational skills and attention to detail.
• Familiarity with clinical trial regulations and GCP is a plus.
• Proficiency in [Insert tools/software, e.g., EDC systems, Microsoft Office].