Employer Industry: Clinical Research Organization (CRO)

Why consider this job opportunity:
- Competitive travel bonus
- Equity/Stock Option program for high-performing CRAs
- Flexible work hours and the opportunity to work from home
- Structured career paths with opportunities for professional growth
- Ongoing therapeutic training by in-house medical and regulatory experts
- Home office support, including a furniture allowance and mobile phone with internet access

What to Expect (Job Responsibilities):
- Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol
- Communicate with medical site staff, including coordinators and clinical research physicians
- Verify investigator qualifications, training, resources, and compliance with protocols
- Perform on-site and remote monitoring activities to ensure site compliance and mitigate risks
- Complete monitoring reports and follow-up letters summarizing findings, deviations, and recommended actions

What is Required (Qualifications):
- Minimum of 1 year of Clinical Research Associate experience
- Must be able to travel 60-70% to locations nationwide
- Bachelor's degree in a health or science-related field
- Proficient in Microsoft® Office
- Strong communication and presentation skills

How to Stand Out (Preferred Qualifications):
- Experience with electronic submission and approval of monitoring visit reports
- Knowledge of regulatory compliance and Good Clinical Practice (GCP) guidelines
- Familiarity with various therapeutic areas, including oncology and cardiology

#ClinicalResearch #CareerGrowth #RemoteWork #CompetitiveBenefits #CRO

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