ICON Plc
Clinical Research Associate
6 days agoWhat's your preference?
Job Description
- Req#: JR146064
Employer Industry: Clinical Research Organization
Why consider this job opportunity:
- Opportunity for career advancement and growth within the organization
- Competitive salary and comprehensive benefits package, including health insurance and retirement planning
- Flexible country-specific optional benefits, such as childcare vouchers and discounted gym memberships
- Supportive and inclusive work environment focused on employee well-being
- Chance to make a significant impact in the field of oncology clinical trials
- Travel opportunities to various sites, with a preference for candidates in Georgia, Florida, or North Carolina
What to Expect (Job Responsibilities):
- Serve as the primary point of contact between investigational sites and the sponsor
- Conduct site visits, including selection, initiation, routine monitoring, and close-out
- Ensure site compliance with ICH-GCP, SOPs, and regulations
- Monitor patient safety and ensure timely reporting of adverse events
- Collaborate with cross-functional partners to support clinical trial activities
What is Required (Qualifications):
- Bachelor’s degree in Life Sciences or equivalent, or a qualified RN
- 2+ years of on-site monitoring experience in the pharmaceutical or CRO industry
- Experience monitoring hematology oncology clinical trials
- Proficiency in ICH-GCP and clinical systems like CTMS and eTMF
- Willingness to travel up to 50% for on-site monitoring visits
How to Stand Out (Preferred Qualifications):
- Strong communication, problem-solving, and collaboration skills
- Experience in site staff training and compliance record maintenance
#ClinicalResearch #Oncology #CareerOpportunity #InclusiveWorkplace #TravelOpportunities
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