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Clinical Research Coordinator
This job is now closed
Job Description
- Req#: req7107_bzEfuvNOUR76
Employer Industry: Healthcare Research
Why consider this job opportunity:
- Up to 5 remote days per month upon successful completion of training and leadership approval
- Continuing education support for undergraduate and graduate tuition for a maximum of 6 credits per semester
- Comprehensive benefits including medical, dental, vision, and retirement options
- 28 vacation days, 12+ state holidays, and 4 days to volunteer
- Opportunities for professional development and certifications
- Mission-driven work focused on cancer health equity and community-centric healthcare
What to Expect (Job Responsibilities):
- Support Principal Investigators in the activation, execution, and management of clinical research studies
- Assist in assessing study feasibility and determining participant eligibility
- Drive participant recruitment, enrollment, and data collection while ensuring compliance with regulations
- Maintain advanced understanding of clinical research management from initiation to closeout
- Serve as a resource providing information and expert advice on clinical research to the research team
What is Required (Qualifications):
- Must maintain current CITI credentials for Human Subjects Protections and Good Clinical Practice (GCP)
- Strong understanding of federal and state laws and regulations related to clinical research
- Experience in data management, including data entry, quality control, and documentation
- Ability to work collaboratively and independently in a clinical research environment
- Strong communication skills for effective engagement with various stakeholders
How to Stand Out (Preferred Qualifications):
- Previous experience in clinical research coordination or related healthcare field
- Familiarity with electronic clinical research systems such as eMR and CTMS (OnCore)
- Additional certifications in clinical research or related areas
- Experience with community engagement and outreach related to clinical trials
- Knowledge of IRB requirements and human subjects protection regulations
#HealthcareResearch #ClinicalTrials #CancerResearch #ProfessionalDevelopment #RemoteWorkOpportunity
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