Employment Type:

Full time

Shift:

Day Shift

Description:

GENERAL SUMMARY AND PURPOSE: 

Saint Alphonsus is looking for a Data Coordinator in support of Oncology Clinical Research. This position is accountable for meeting all study-specific data collection goals and data entry timelines. Data will be collected from a variety of sources and recorded into trial specific databases, while simultaneously addressing and amending ongoing data queries from previously reported data. Attention to detail with proven organizational skills across multiple projects is of critical importance to ensure accuracy and integrity of reported data. The position assumes responsibility for coordinating and facilitating all study specific audits and serves as the primary point of contact for data management needs, process and procedure. Effective communication across entirety of research team and external collaborators is necessary to maintain successful collaboration amongst all individuals. Supports clinical research coordinators with regulatory tasks as needed and in accordance with licensure and competency.  

 

SKILLS, KNOWLEDGE, EDUCATION AND EXPERIENCE:  

 - Bachelor's degree preferred or equivalent combination of education and recent experience.  

- Minimum 2 years of experience in clinical research; experience at the site level or within the industry preferred.

- Recent experience in clinical patient care setting with demonstrated proficiency in oncology specific medical terminology and confidence in EPIC navigation.

- Medidata Rave experience is preferred. 

- Certification with Association of Clinical Research Professionals (ACRP) or CRPC (Clinical Research Professional Certification) with Society of Clinical Research Association (SOCRA) preferred

 

ESSENTIAL FUNCTIONS: 

• Knows, Understands, Incorporates, and Demonstrates the Organization's Mission, Vision, and Values in behaviors, practices, and decisions.   

• Facilitates high quality customer service by communicating clearly and efficiently with adherence to identified timelines. 

• Review and support implementation of the Trinity Health Integrity & Compliance policies and procedures pertaining to research (“Trinity Research Compliance Policies”). 

• Continually evaluate and monitor compliance with such policies and procedures on an ongoing basis.   

• Ensures compliance with institutional, federal and state regulation, guidance and policy. 

• Evaluates and analyzes medical records and related source document for case report form completion. 

• Provides efficient and complete data collection, review and reporting. 

• Assures availability of source documentation for all reported data and maintains