Clinical Research Data Coordinator I Oncology @ Adventist Health
placeAltamonte Springs, Florida, United States
businessOn Site
scheduleFull-time
Posted 16 days ago
Your Application Journey
Interview
Email Hiring Manager
***** @adventhealth.com
Recommended after applying
Job Details
Overview
Join Adventist Health as a Clinical Research Data Coordinator I (Oncology). You will ensure the accurate, timely, and complete electronic data entry for clinical trials while collaborating with study investigators, coordinators, and sponsors to uphold protocol, FDA regulations, and ICH/GCP guidelines.
Key Responsibilities
- Enter protocol-driven clinical research data accurately and timely.
- Collaborate with study investigators, CRCs, sponsors, and clinical teams.
- Abstract and record essential physical and test data from various sources.
- Maintain participant tracking systems and conduct follow up visits.
Required Expertise & Experience
The candidate should have one of the following qualifications:
- Bachelor’s degree in a health-related or data processing field, or
- Associate degree with 1 year of relevant experience, or
- Accredited allied health certificate with 2 years of experience, or
- 2 years of direct clinical research data entry experience, or
- 3 years of equivalent administrative/professional experience with data.
Benefits & Work Environment
Adventist Health offers comprehensive benefits starting on Day One including paid days off, student loan repayment, and debt-free education opportunities. Experience a supportive community where professional growth meets spiritual wellbeing.
Key skills/competency
- Clinical Research
- Data Entry
- FDA Regulations
- ICH/GCP
- Protocol Adherence
- Data Management
- Tracking Systems
- Collaboration
- Follow-Up
- Customer Service
How to Get Hired at Adventist Health
🎯 Tips for Getting Hired
- Research Adventist Health's culture: Study their mission, values, and news.
- Customize your resume: Emphasize clinical research and data skills.
- Highlight regulatory knowledge: Mention FDA and ICH/GCP understanding.
- Prepare for interviews: Practice operational and team questions.
📝 Interview Preparation Advice
Technical Preparation
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Review FDA and ICH/GCP guidelines.
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Practice using electronic data systems.
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Study protocol and tracking operations.
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Refresh clinical research data procedures.
Behavioral Questions
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Describe team conflict resolution experiences.
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Explain collaboration with clinical teams.
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Discuss managing strict deadlines.
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Share examples of data accuracy focus.
Frequently Asked Questions
What does Adventist Health look for in a Clinical Research Data Coordinator I?
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How important is prior clinical research experience at Adventist Health?
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Can I apply if I have an Associate degree for Clinical Research Data Coordinator I at Adventist Health?
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What are the main responsibilities of the Clinical Research Data Coordinator I at Adventist Health?
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What benefits does Adventist Health offer for Clinical Research Data Coordinator I roles?
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How do I prove my proficiency in data management for Adventist Health?
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What technical skills are needed for a Clinical Research Data Coordinator I at Adventist Health?
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How does Adventist Health support career development in this role?
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Is customer service a key component for the Clinical Research Data Coordinator I?
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What makes Adventist Health a unique workplace for this role?
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