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 career advancement
- 401K plan available
- Work in a stimulating environment with a focus on collaboration and innovation
- Flexibility of a home-based position with local or regional travel

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
- Build productive relationships with investigators and site staff to achieve study objectives, including patient recruitment targets
- Perform source data verification and ensure adequate study drug storage and accountability
- Travel to research sites approximately 65% of the time

What is Required (Qualifications):
- B.Sc. in a field relevant to clinical research, nursing degree, and/or equivalent experience
- 2-5 years of experience in conducting on-site clinical monitoring in the biotechnology, pharmaceutical, or CRO industry
- Good knowledge of ICH/GCP standards and applicable regulatory requirements
- Strong verbal and written communication skills in English
- Excellent knowledge of Microsoft Office (i.e., Word, Excel, PowerPoint)

How to Stand Out (Preferred Qualifications):
- Experience in dermatology is an asset
- Strong judgment and problem-solving skills
- Ability to prioritize different assignments and work under pressure while maintaining attention to detail

#ClinicalResearch #Dermatology #CareerOpportunity #RemoteWork #CRO

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