Clinical Research Coordinator I

MedStar Health; Akron (OH); Hybrid; USD 50,000 - 70,000; Full time

Job summary

A leading health organization seeks a Clinical Research Coordinator I to facilitate and coordinate daily clinical trial activities. The role involves recruiting participants, ensuring compliance with protocols, and supporting the research team's needs, emphasizing a collaborative approach. Candidates should have a Bachelor's degree in a health-related field and be ready to obtain necessary certifications within 90 days.

Qualifications

• Requires Bachelor's degree in health-related field.
• BLS and CITI certifications needed within 90 days of hire.
• Healthcare experience preferred, along with knowledge of GCP and regulations.

Responsibilities

• Recruit and screen research participants.
• Review regulatory requirements to ensure compliance.
• Collect and document research data accurately.

Skills

Knowledge of clinical trial protocols

Competency in interpreting medical charts

Competency in Microsoft Office

Education

Bachelor's degree in health-related field

Tools

Microsoft Word

Microsoft Excel

Electronic Health Systems

EPIC

Job description

Full-time, 40 Hours/Week

Monday to Friday, 8am - 4:30pm

Hybrid (Onsite 2-3 Days/Week)

Summary:

The Clinical Research Coordinator I (CRC I) is a specialized research professional working with and under the direction of the Clinical Research Support Team Supervisor and Clinical Principal Investigator (PI) on multiple ongoing research studies. While the PI is ultimately responsible for the clinical trial, the CRC I is responsible for the facilitation and coordination of the daily clinical trial activities in accordance with federal, state, and local regulations, Institutional Review Board (IRB) approvals and Akron Children's Hospital (ACH) policies and procedures. The CRC I plays a critical role in the conduct of the study and works collaboratively with the entire ACH Research team, sponsors, and monitors to ensure productivity and timely completion of studies.

Responsibilities:

1. Recruit, screen, enroll and obtain consent/assent from research participants.

2. Utilizing Good Clinical Practice, ensures assigned studies are conducted in accordance with IRB and regulatory agency regulations.
3. Ensures site compliance with research protocols by reviewing all regulatory requirements to confirm implementation of appropriate methods, practices, and procedures for all research activities.
4. Develops source documents, completes timely and accurate data collection, documentation, entry, and reporting in both sponsor and ACH databases.
5. Supports the regulatory document specialist in the maintenance of regulatory documents, study submissions and continuing reviews in accordance with Rebecca D. Considine Research Institute (RDCRI) SOP and policies and applicable regulations.
6. Ensures appropriate credentialing and training of the entire ACH research team.
7. Communicates and collaborates specific study requirements to the research team, including internal and external parties, sponsors, monitors, PIs, and study participants.
8. Ensures proper specimen handling, processing, and shipping according to protocol.
9. Utilizes the Clinical Trial Management System (CTMS) and adheres to protocol specific budgets.
10. Occasional travel to attend sponsor study training meetings (required).
11. Other duties as required.

Other information:

Technical Expertise:

1. Knowledge of clinical trial protocols is preferred.
2. Competency in interpreting medical charts and abstracting data is preferred.
3. Knowledge of GCP, federal, state, and local regulations, including HIPAA policies and procedures.
4. Competency in the use of Microsoft Office, Word, and Excel, Electronic Health Systems, EPIC and databases utilized in research or have a willingness to learn and demonstrate proficiency within six months of hire.

Education and Experience:

1. Education: Bachelor's degree in health-related field is required.
2. Certification: None.
3. Years of relevant experience: None
4. Experience in healthcare is preferred.
5. Basic Life Support (BLS) - Certification is required within 90 days of employment. Akron Children's will facilitate training.
6. CITI Certification - Certification is required within 90 days of hire.
7. International Air Transport Association (IATA)/Dangerous Goods Shipping certification is required within 90 days of hire.
8. Ability to work independently as well as in a team environment.

Full Time

FTE: 1.000000