Job Description: Clinical Research Assistant

Overview

We are seeking a motivated and detail-oriented Clinical Research Assistant to join our dynamic team. The ideal candidate will support clinical trials and research projects aimed at advancing healthcare outcomes and scientific knowledge. Working collaboratively with a diverse group of researchers, clinicians, and participants, the Clinical Research Assistant will play a critical role in ensuring the success and integrity of studies. This is an excellent opportunity for individuals passionate about clinical research and contributing to meaningful medical progress.

Responsibilities

• Assist in the planning, preparation, and execution of clinical research studies according to regulatory guidelines and protocols.
• Recruit, screen, and schedule participants for clinical trials, ensuring compliance with study inclusion/exclusion criteria.
• Collect, organize, and document clinical data while maintaining confidentiality and accuracy.
• Coordinate with investigators, sponsors, and other stakeholders to manage the daily operations of research projects.
• Prepare and maintain institutional review board (IRB) submissions, informed consent forms, and other regulatory documents.
• Monitor participant status and communicate any adverse effects or unexpected developments to study coordinators or principal investigators.
• Work collaboratively with multidisciplinary teams to ensure compliance with study protocols, Good Clinical Practice (GCP), and ethical standards.
• Maintain tracking systems for study materials, records, and data collection processes.
• Contribute to literature reviews, presentations, and reports for publication or internal use.
• Provide administrative and logistical support to the research team, including scheduling meetings and managing study supplies.

Qualifications

• Education: Bachelor’s degree in Health Sciences, Life Sciences, or a related field. Equivalent work experience will also be considered.
• Skills and Experience:
  • Demonstrated experience or coursework in clinical research, biomedical research, or related fields.
  • Strong understanding of clinical trials and research methodologies.
  • Proficient in data collection, entry, and management with attention to detail.
  • Familiarity with GCP standards and IRB processes is highly desirable.
  • Effective communication and interpersonal skills to work with diverse teams and participants.
  • Ability to manage multiple tasks, prioritize workload, and meet deadlines.
• Technical Expertise: Basic knowledge of statistical analysis software, electronic data capture systems (e.g., REDCap), and Microsoft Office Suite preferred.
• Flexibility: Willingness to work occasional evenings or weekends based on the needs of the research project.