Clinical Research Data Coordinator I Oncology

@ Adventist Health

Benefits and Perks

All the benefits and perks you need for you and your family, including benefits from day one, paid days off, student loan repayment, career development, whole person wellbeing resources, mental health support, and debt-free education opportunities.

Our Promise to You

Joining Adventist Health means being part of something bigger. It is a community that uplifts others in body, mind, and spirit while extending the Healing Ministry of Christ. You will be valued for who you are and the unique experiences you bring to the team.

The Role You’ll Contribute

The Clinical Research Data Coordinator I is primarily responsible for ensuring the completeness, timely delivery, and quality of clinical research data via meticulous data entry. You will collaborate with study investigators, Clinical Research Coordinators, study sponsors, and other research and clinical team members to support Phase I-IV clinical trials in accordance with trial protocols, FDA regulations, and ICH/GCP guidelines.

The Value You’ll Bring

• Manage accurate and timely retrieval of protocol driven data points.
• Abstract and record essential physical and test data from multiple sources.
• Maintain tracking systems for study participants.
• Conduct follow up visits and data searches to ensure smooth operations.

Expertise and Experience You’ll Need

A Bachelor's degree in a healthcare related field, or an Associate degree with one year’s experience, or an allied health certificate with two years’ experience; alternatively, two years of direct clinical research data entry or three years in administrative data roles will suffice.

Key skills/competency

• Clinical Research
• Data Entry
• Oncology
• FDA
• ICH/GCP
• Protocol Management
• Data Management
• Regulatory Compliance
• Tracking Systems
• Team Collaboration