Maryland Oncology
Regulatory Affairs Coordinator (Hybrid Remote)-Ft Worth, Tx
This job is now closed
Job Description
- Req#: 33328
Employer Industry: Oncology Services
Why consider this job opportunity:
- Competitive benefits package, including Medical, Dental, Vision, and Life Insurance
- Generous PTO program and 401k plan with company match
- Wellness program that rewards healthy lifestyle practices
- Tuition Reimbursement and Employee Assistance program
- Opportunity to work within a leading organization in cancer care
- Hybrid remote work option for flexibility
What to Expect (Job Responsibilities):
- Coordinate critical document collection to ensure timely opening of clinical trials
- Maintain protocol regulatory documents in compliance with local and national SOPs
- Develop and implement training materials for staff compliance with regulations
- Oversee preparation of informed consent documents for sponsor and IRB submissions
- Train and mentor research staff on regulatory aspects of clinical research
What is Required (Qualifications):
- Associate's degree required; Bachelor's degree in a clinical or scientific discipline preferred
- Minimum seven years of experience in clinical research, regulatory affairs, or oncology-related fields
- Proficiency in Microsoft Office
- Strong communication skills and ability to multitask
- High level of attention to detail and ability to work in a fast-paced environment
How to Stand Out (Preferred Qualifications):
- Experience in clinical research is preferred
- Experience working with Sponsor Monitor representatives
- Strong time management skills
- Excellent interpersonal skills for effective interaction with diverse teams
#OncologyServices #RegulatoryAffairs #ClinicalResearch #CareerOpportunity #HybridWork
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