Clinical Trial Manager at ICON managing trial operations, ensuring high - quality outcomes and compliance with trial protocols for clinical development in Beijing and Shanghai.
FI
Onsite Clinical Research Coordinator II
Posted yesterday
About the role
- Clinical Research Coordinator overseeing research studies at Florida Cancer Specialists. Responsible for implementation and management of clinical trials under medical supervision.
Responsibilities
- Responsible for the performance of the research study under the medical supervision of the Principal Investigator and the research director.
- The research coordinator is responsible for the overall successful implementation and ongoing site management of the research studies.
Requirements
- Candidates must have a minimum of two years prior clinical research experience, preferably with oncology clinical research; or a minimum of three years clinical experience (Medical Assistant, LPN, or RN in an oncology practice).
- Candidates must have effective communication skills, be organized, detail oriented, and strong patient advocates.
- Candidates must be available to travel to investigators meetings.
- Valid Driver’s License in state of residency for travel to clinics.
- Must comply with the Company Driver Safety Operations and Motor Vehicle Records Check Policy.
- SCREENINGS – Background, drug, and nicotine screens.
Benefits
- Medical and Prescription Drug Coverage
- Vision & Dental Insurance
- Employee Assistance Program (EAP)
- Health Savings Account (HSA) & Flexible Spending Accounts
- Paid Time Off (PTO)
- 401(k) Retirement Plan
- Life Insurance
- Tuition Reimbursement
- Disability Insurance
- Accident Insurance
- Critical Illness
- Hospital Indemnity
- Pet Insurance
- Identity Theft
- Legal Insurance
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
No Education Requirement
Location requirements
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