Clinical Research Data Coordinator I OncologyAltamonte Springs, FL

Clinical Research Data Coordinator I

At AdventHealth Orlando, what started as a converted farmhouse in rural Central Florida has become Central Florida's major tertiary health care facility. Patients come from the Southeast, the Caribbean and even as far as South America for our proven expertise and compassionate health care.

With a variety of Orlando hospital jobs, we invite you to start or elevate your career with a new job at AdventHealth Orlando. We constantly seek out Orlando nurses, medical assistants, nurse assistants, patient care and health administration professionals who share our passion for whole-person health care.

Every day, our fellow team members show up to work, unified by one shared mission: Extending the Healing Ministry of Jesus Christ. As a faith-based health care organization, our story is one of hope as we strive to heal and restore the body, mind and spirit. Though our facilities are spread across the country, this unwavering belief binds us together. Across every office, exam and patient room, we're committed to providing individualized, holistic care. This is our Christian mission, and it inspires us to help make communities healthier and happier.

The Clinical Research Data Coordinator I is primarily responsible for the completeness, timely delivery, and quality of clinical research data via data entry. In this role, the Clinical Research Data Coordinator I collaborates with study Investigators, Clinical Research Coordinators, study sponsors, and other research and clinical team members in the conduct of Phase I-IV industry-sponsored, grant funded, and/or investigator-initiated clinical trials in accordance with trial protocols, Food and Drug Administration regulations, and International Conference on Harmonization/Good Clinical Practices Guidelines to meet study-specific goals and timelines as well as assist the study team with the operational needs of specific protocols to meet these goals. Actively participates in outstanding customer service and accepts responsibility in maintaining relationships that are equally respectful to all.

The value you'll bring to the team:

• Managing and ensuring the accurate and timely retrieval and electronic data entry submission of protocol driven data points to relevant research sponsors/organizations within the specified time frame.
• Abstracts and records essential physical and test data from internal and external sources.
• Maintains a tracking system of study participants at the relevant time points as deemed necessary.
• Conducts follow up visits and data searches, as assigned, to maintain smooth operational flow.

The expertise and experiences you'll need to succeed:

• Bachelors degree in healthcare related field, data processing or related field, OR
• Associate degree in health science, or related field, and one (1) year of administrative/professional experience with data related responsibilities (e.g. research, statistics, registry) or clinical research experience, OR
• Graduate of an accredited allied health certificate program and two (2) years of administrative/professional experience with data related responsibilities (e.g. research, statistics, registry) or clinical research experience, OR
• Two (2) years of direct clinical research data entry experience OR three (3) years of equivalent administrative/professional experience working with data or medical information to include duties such as data collection, management and verification.

This facility is an equal opportunity employer and complies with federal, state and local anti-discrimination laws, regulations and ordinances.