Clinical Research Coordinator II

Overview

Promotes good clinical practices in the conduct of clinical investigations by possessing an in-depth knowledge of federal regulations and guidance documents for the conduct of clinical trials and human subject protection assuring compliance with protocol and regulatory requirements and by collecting recording and maintaining data and source documentation. This role reviews technical operations ensuring that all processes protocols & procedures are quality controlled & functioning up to standards. This role ensures that all study activities are completed by strictly following Good Clinical Practices (GCP) & all current local state & federal laws regulations guidance policy & procedure developed by the applicable Institutional Review Boards (IRBs) Food & Drug Administration (FDA) Code of Federal Regulations (CFR) & the International Conference on Harmonization (ICH).

Responsibilities

DOCUMENTS AND MAINTAINS ALL STUDY-RELATED PROCEDURES PROCESSES AND EVENTS BY:

Coordinates assigned Research Studies at all levels of acuity within the scope of Licensure.

Plans and designs new forms/source document tools to be used in protocol implementation

Documents protocol deviations and exemptions

Obtains and reviews original source documents (e.g. recordings scans tests procedure results) as needed

Abstracts data from medical records clinic consultation and referral notes to study forms and flowsheets

Records accurate and timely data onto case report forms

Maintains source documentation for all case report entries as applicable

Keys data for electronic submission

Transmits data via fax mail or electronically as requested

Corrects and edits case report form entries as appropriate

Resolves data queries

Completes and maintains the study article dispensing log

Maintains files of all study-related documentation

Prepares case report forms for sponsor/audit review

Collects source documents for sponsor/audit review
PARTICIPATES IN SUBJECT RECRUITMENT ENROLLMENT AND FOLLOW-UP PROCEDURES BY:

Monitors enrollment goals and modifying recruitment plan as necessary

Maintains patient screening/enrollment logs

Follows patient population clinically and maintains documentation supporting study

Reviews inclusion/exclusion criteria with investigator to assure subject eligibility

Reviews and verifies required source documents in subjects medical record to confirm study eligibility

Assures that all screening eligibility and enrollment procedures are performed

Reviews the protocol informed consent form and follow-up procedures with potential study subjects

Conducts interviews to assess the subjects ability and willingness to follow and complete study procedures and visits

Obtains informed consent from research subjects prior to any study-related procedures and documenting appropriately

Follows randomization procedures as per protocol

Assures administration of study article as appropriate

Schedules subjects for follow-up visits

Reviews diaries and questionnaires completed by subject

Ensures appropriate specimen collection batching and shipping as required

Assesses subject compliance with the test article and follow-up visits

Recognizes and reporting common laboratory values and alerts to investigator and sponsor

Protects patient privacy during initial and follow-up interviews

Secures safe storage of study-related documents

Assures appropriate disposal of sensitive documents
COMMUNICATES EFFECTIVELY WITH SUBJECTS RESEARCH TEAM IRB AND SPONSOR BY:

Maintains a list of sponsor/CRO contacts for each protocol

Educate patients on how to use medication or device in study.

Provide management feedback on how to integrate research operations in clinics for most effective workflow.

Provides subjects with information about reporting study-related events to research team

Establishes a mechanism to contact subjects for follow-up visits new information etc.

Utilizes a phone log to document telephone communications

Contacts primary care providers to discuss/inform of patient enrollment and study progress

Meets regularly with investigator and research team to discuss subject participation and protocol progress

Submits protocol amendments and progress reports to IRB in required timeframes

Completes timely notification of the investigator sponsor and IRB of adverse events as outlined in the protocol

Schedules sponsor monitoring visit.

Meets with monitors during routine visits to discuss case report form completion query resolution and other protocol-related issues.
PARTICIPATES IN PROTOCOL ASSESSMENT/PLANNING BY:

Lists and clarifies questions and concerns with the investigator and sponsor regarding enrollment goals sponsor expectations and study procedures

Prepares and submits regulatory documents to sponsor (e.g. Form FDA 1572 laboratory certification and normal values curriculum vitae etc.)

Prepares and submits institutional review board documents

Integrates proposed clinical trial with current research activities

Attends and participates in investigator meetings

Confirms that contact IRB approval of protocol and informed consent have been received prior to study initiation

Completes Sponsored protocol training including (GCP EDC IVRS IRB )

Qualifications

Certifications: Certified Clinical Research Coordinator (CCRC) within 2.5 years - Association of Clinical Research Professionals (ACRP)Association of Clinical Research Professionals (ACRP)Association of Clinical Research Professionals (ACRP) Education: H.S. Diploma/GED; Bachelors Degree: Related Field Work Experience:

Carle Health Company Overview

Find it here.

Discover the job the career the purpose you were meant for. At Carle Health were committed to fostering a workplace where every team member feels valued respected and empowered where passion and purpose come together to positively impact the lives of our patients and our communities. Find it all at Carle Health.

Our nearly 17000 team members and providers work together to support patient care across central and southeastern Illinois. Weve grown to include eight award-winning hospitals and a multispecialty provider group with more than 1500 doctors and advanced practice providers. Were developing the next generation of providers and healthcare professionals through Carle Illinois College of Medicine the worlds first engineering-based medical school and Methodist College. Carle BroMenn Medical Center Carle Foundation Hospital Carle Health Methodist Hospital Carle Health Proctor Hospital Carle Health Pekin Hospital and Carle Hoopeston Regional Health Center hold Magnet designations the nations highest honor for nursing care. We offer opportunities in several communities throughout central Illinois with potential for growth and life-long careers at Carle Health.

We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race color sex age national origin religion sexual orientation gender identity status as a veteran and basis of disability or any other federal state or local protected class. Carle Health participates in E-Verify and may provide the Social Security Administration and if necessary the Department of Homeland Security with information from each new employees Form I-9 to confirm work authorization. For more information:

Salary Range

The compensation range for this position is $24.86per hour - $41.52per hour. This represents a good faith minimum and maximum range for the role at the time of posting by Carle Health. The actual compensation offered a candidate will be dependent on a variety of factors including but not limited to the candidates experience qualifications location training licenses shifts worked and compensation model.

Carle Health offers a comprehensive benefits package for team members and providers. To learn more visit

Required Experience:

IC