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Research Assistant

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Understand the ethical principles and regulatory requirements governing clinical
research, including the principles of Good Clinical Practice (GCP) and the role of the
Institutional Review Board (IRB).
2. Learn the basics of clinical trial design and methodology, including the different phases
of clinical trials, study protocols, and data collection.
3. Develop skills in study coordination, including participant recruitment and enrollment,
informed consent, data management, and regulatory compliance.
4. Understand the role of the CRC in study implementation, including coordinating site
visits, monitoring adverse events, and communicating with study sponsors.
5. Develop skills in communication and teamwork, including effective communication with
study participants, healthcare providers, and study sponsors, as well as collaboration with
other research team members.
6. Develop skills in project management, including managing timelines, milestones, and
deliverables.
7. Understand the importance of continued professional development, including staying upto-
date with new developments in clinical research, attending relevant conferences and
workshops, and maintaining certifications.
8. Develop an understanding of career paths and opportunities for CRCs, including options
for advancement, specialized training, and other professional development opportunities.

GCP certification, Bachelor Degree in science or equivalent, or certified medical assistant with one year experience in clinical research , good communication skills, comfortable with medical terminology.