REQUIREMENTS:

• Degree in Biomedical Science, Life Sciences, Nursing, Allied Health, Public Health, or a related discipline.
• Minimum 3 to 5 years of experience in clinical research coordination, preferably in investigator-initiated trials.
• Strong knowledge of research ethics submissions (CIRB), regulatory requirements, and visit/audit preparation.
• Proven track record in patient recruitment, participant engagement, and study follow-up.
• Experience managing multiple concurrent studies and ensuring compliance with timelines and protocols.
• Proficient in Microsoft Office applications (Word, Excel, PowerPoint); familiarity with REDCap, SPSS, or R is an advantage.
• Strong administrative and project management skills to support reporting, grant deliverables, and stakeholder coordination.
• Excellent interpersonal and communication skills, with empathy for patients and caregivers.
• Highly organized, detail-oriented, and able to work independently with minimal supervision.
• Proactive problem-solver with the ability to prioritize and manage competing demands.
• Team-oriented, with the ability to mentor junior CRCs/RCs.
• Flexible and adaptable, with willingness to work across sites (e.g., NCCS, SKH, community hospitals).
  Req ID: 4335

• Screen, recruit, and consent participants according to protocol; schedule and manage study visits and follow-ups; engage patients/participants.
• Prepare and maintain ethics submissions, regulatory documents, and Investigator Site Files; support monitoring visits and audits; ensure GCP adherence.
• Administer assessments, collect data, and ensure accurate and timely entry into study databases; assist with data cleaning and query resolution.
• Manage investigational products (e.g., essential oil blends, devices), track inventory, and coordinate transport between study sites.
• Coordinate project timelines, budgets, and reporting; assist in drafting progress reports and grant deliverables.
• Liaise with PIs, clinicians, collaborators, and institutional partners; mentor junior CRC/RCS