Clinical Research Coordinator I- Precision Medicine
Not Disclosed•Full-TimeOn-site
location_onTwo City Center, 645, Hamilton Street, Center City, Allentown, Lehigh County, Pennsylvania, 18101, United States
About St. Luke's
St. Luke's University Health Network is proud of the skills, experience, and compassion of its employees, who are our most valuable asset. Individually and together, our team is dedicated to satisfying our organization's mission: an unwavering commitment to excellence as we care for the sick and injured, educate physicians, nurses, and other healthcare providers, and improve access to care in the communities we serve, regardless of a patient's ability to pay.
About the Role
The Clinical Research Coordinator (CRC) assumes a critical role in our research process. This position is responsible for the screening, enrollment, consenting, and coordination of clinical trials, ensuring strict compliance with the protocol and all local, state, ICH/GCP Guidelines, and Federal regulations. The CRC ensures the sound conduct of clinical trials, including recruitment, screening, enrollment, and follow-up of eligible subjects according to protocol requirements. A key part of this role is maintaining high-quality data for all patients enrolled in assigned trials, ensuring timely and accurate data entry and documentation.
Application Instructions
To apply, please complete your application using your full legal name and current home address. Be sure to include your employment history for the past seven (7) years, including your present employer. We encourage you to upload a current resume detailing all work history, education, and any applicable certifications or licenses. It is highly recommended that you create a profile at the conclusion of submitting your first application.
Equal Opportunity
St. Luke's University Health Network is an Equal Opportunity Employer.
Work location
Work model: On-site
Two City Center, 645, Hamilton Street, Center City, Allentown, Lehigh County, Pennsylvania, 18101, United States
Allentown, Pennsylvania
Key Responsibilities
- check_circleConduct clinical trial procedures including recruitment, screening, enrollment, and subject follow-up
- check_circleObtain informed consent from participants and document the consent process as required
- check_circlePrepare research charts for monitoring visits and audits and respond to data queries
- check_circleReview patient charts for adverse events and submit appropriate documentation
- check_circleReview medical charts to extract data and determine patient eligibility for assigned protocols
- check_circlePrepare and ship laboratory specimens to central laboratories while maintaining certifications
- check_circleProvide direction and training to other research staff on case report form completion
- check_circleComplete case report forms, enter data timely, and report adverse drug events
- check_circleScreen, enroll, and consent patients for clinical trials in compliance with protocols and regulations
- check_circleCoordinate long-term survival follow-up by acquiring medical records and contacting patients
- check_circleMaintain accurate documentation including regulatory files, source data, and study logs
Requirements
- verifiedBachelor's degree required; Associates or High School with 3 years clinical research experience
- verified2 years experience in health-related field
- verified1 year clinical research experience preferred
- verifiedKnowledge of Microsoft Office (Word, Excel, Access, Outlook)
- verifiedFamiliarity with medical terminology
- verifiedKnowledge of ICH/GCP guidelines, HIPAA, and confidentiality policies
- verifiedIATA training certification for laboratory specimen shipping
Nice to Have
Associates degree or High School degree with equivalent clinical research experience (3 years) with 1-2 years coordinator and/or data management experience. One year experience in clinical research.
Similar Job Opportunities
Skills, education and keywords
Skills: Ich/gcp Guidelines, Hippa Regulations, Case Report Forms, Microsoft Office, Word, Excel, Access, Outlook, Internet Functions, Medical Terminology.
Education: Bachelor's degree required, but Associates or High School with experience accepted; Associate's degree accepted with equivalent clinical research experience; High School degree accepted with equivalent clinical research experience.
Frequently asked questions about Clinical Research Coordinator I- Precision Medicine at St. Luke's University Health Network
What does a Clinical Research Coordinator I- Precision Medicine at St. Luke's University Health Network do?expand_more
Day-to-day, the Clinical Research Coordinator I- Precision Medicine at St. Luke's University Health Network will conduct clinical trial procedures including recruitment, screening, enrollment, and subject follow-up; obtain informed consent from participants and document the consent process as required; prepare research charts for monitoring visits and audits and respond to data queries; and review patient charts for adverse events and submit appropriate documentation.
What are the requirements for this Clinical Research Coordinator I- Precision Medicine role?expand_more
To qualify for the Clinical Research Coordinator I- Precision Medicine at St. Luke's University Health Network position, applicants should have: Bachelor's degree required; Associates or High School with 3 years clinical research experience; 2 years experience in health-related field; 1 year clinical research experience preferred; Knowledge of Microsoft Office (Word, Excel, Access, Outlook); Familiarity with medical terminology; and Knowledge of ICH/GCP guidelines, HIPAA, and confidentiality policies.
Where is the Clinical Research Coordinator I- Precision Medicine role at St. Luke's University Health Network located?expand_more
Clinical Research Coordinator I- Precision Medicine at St. Luke's University Health Network is based in Two City Center, 645, Hamilton Street, Center City, Allentown, Lehigh County, Pennsylvania, 18101, United States. This is a on-site role.
Is this Clinical Research Coordinator I- Precision Medicine job remote, hybrid, or on-site?expand_more
St. Luke's University Health Network has listed this Clinical Research Coordinator I- Precision Medicine role as on-site.
How much experience is required for this Clinical Research Coordinator I- Precision Medicine role?expand_more
Clinical Research Coordinator I- Precision Medicine at St. Luke's University Health Network typically requires 2+ years of relevant experience at the mid level level.
What skills do you need for the Clinical Research Coordinator I- Precision Medicine role at St. Luke's University Health Network?expand_more
Key skills for Clinical Research Coordinator I- Precision Medicine at St. Luke's University Health Network include Ich/gcp Guidelines; Hippa Regulations; Case Report Forms; Microsoft Office; Word; Excel; Access; and Outlook.
What education is required for Clinical Research Coordinator I- Precision Medicine at St. Luke's University Health Network?expand_more
Educational requirements for this role: Bachelor's degree required, but Associates or High School with experience accepted; Associate's degree accepted with equivalent clinical research experience; and High School degree accepted with equivalent clinical research experience.
What category does the Clinical Research Coordinator I- Precision Medicine role belong to?expand_more
Clinical Research Coordinator I- Precision Medicine at St. Luke's University Health Network is part of the scientific & qa job category on Recrutus.