Employer Industry: Contract Research Organization (CRO) specializing in Dermatology

Why consider this job opportunity:
- Permanent full-time position with competitive benefits
- Opportunities for ongoing learning and professional development
- 401K plan available
- Work remotely with local or regional travel required to clinical research sites
- Contribute to impactful clinical studies in dermatology and rheumatology

What to Expect (Job Responsibilities):
- Conduct site qualification, initiation, monitoring, and close-out visits for research sites according to the monitoring plan and applicable regulations
- Participate in investigators' meetings and prepare site visit reports and follow-up letters
- Build productive relationships with investigators and site staff to achieve study objectives, including patient recruitment
- Perform source data verification and ensure adequate study drug storage, dispensing, and accountability
- Maintain compliance with ICH/GCP standards and regulatory requirements

What is Required (Qualifications):
- B.Sc. in a field relevant to clinical research, nursing degree, or equivalent experience
- 2-5 years of experience in conducting on-site clinical monitoring in the biotechnology, pharmaceutical, or CRO industry
- Strong knowledge of ICH/GCP standards and applicable regulatory requirements
- Excellent verbal and written communication skills in English
- Ability to prioritize assignments and work under pressure while maintaining attention to detail

How to Stand Out (Preferred Qualifications):
- Experience in dermatology is an asset
- Proficient in Microsoft Office (i.e., Word, Excel, PowerPoint)
- Strong problem-solving skills and excellent judgment

#ClinicalResearch #Dermatology #CRO #CareerOpportunity #RemoteWork

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