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Company | Jobot |
Address | Aventura, FL, United States |
Employment type | FULL_TIME |
Salary | |
Category | Staffing and Recruiting |
Expires | 2023-08-10 |
Posted at | 9 months ago |
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Why join us?
Why join us?
- Short-Term disability
- Long-Term Disability
- Paid Vacations
- Paid Holidays
- Paid Personal Time
- Dental Insurance
- Company Paid Life Insurance
- 401(k)
- Company Paid Accidental Death & Dismemberment
- Group Health Insurance
- Retirement Plans
- Company Paid Profit-Sharing Plan
- Coordinate and manage all aspects of clinical research studies, including patient screening, enrollment, and follow-up
- Develop and maintain study documentation, including informed consent forms, case report forms, and study protocols
- Assist with data analysis and reporting as needed
- Communicate with study sponsors and regulatory agencies as needed
- Participate in the development and implementation of new research projects
- Attends sponsor Investigator/Study Coordinator meetings as needed for assigned protocols.
- Collaborate with medical professionals and research staff to ensure the smooth execution of clinical trials
- Ensure compliance with HIPAA guidelines and other regulatory requirements
- Strong knowledge of clinical study research processes and procedures
- Ability to manage multiple projects simultaneously and prioritize tasks effectively
- Excellent organizational and communication skills
- 2+ years of experience in clinical research coordination, with a focus on dermatology research (Clinical Research is a must)
- Ability to work independently and as part of a team
- Familiarity with HIPAA guidelines and other regulatory requirements
- Experience with study documentation forms, including informed consent forms and case report forms
- High school diploma or GED
- Proficiency in Microsoft Office and other relevant software applications
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