Clinical Research Coordinator II

DM Clinical Research
Chicago, IL, US
Full-time

Clinic Research Coordinator II The Clinical Research Coordinator II , will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH / GCP guidelines and to provide the best quality data to the sponsor.

The CRC I will also ensure study enrollment meets or exceeds Sponsors' expectations. To ensure company goals are achieved on a timely basis.

Duties & Responsibilities : Completing all the DMCR-required training, including but not limited to ICH-GCP Certification and IATA Certification on a timely basis.

Completing all the relevant training prior to study-start and on a continued basis in a timely manner. This will include but is not limited to : a.

Sponsor-provided and IRB-approved Protocol Training b. All relevant Protocol Amendments Training c. Any study-specific Manuals Training, as applicable d.

Sponsor-specified EDC and / or IVRS and any other relevant Electronic Systems training. Conducting study subject visits, and all other relevant protocol-required procedures and documenting these in a timely manner.

Adherence to ALCOA-C Standards with all the relevant clinical trial documentation. Completing data entry and query resolution in a timely manner as per internal company guidelines and as per sponsor expectations.

Demonstration of appropriate and timely follow-up on the action items, at their respective sites. Demonstrated understanding and implementation of Laboratory Manuals and protocol-specified laboratory procedures, storage, temperature monitoring, equipment calibration and laboratory kit inventory, under the direction of the Site / Study Management Team, for assigned protocols.

Liaising with Laboratory team, Data team, Administrative staff, Clinical Investigators, Research Participants and Sponsor / CRO representatives, under the direction of the Site / Study Management Team, for assigned protocols.

Submitting required administrative paperwork per company timelines. Participating in subject recruitment and retention efforts.

Engaging with Research Participants and understanding their concerns. Any other matters, as assigned by management. Knowledge & Experience : Education : High School Diploma or equivalent required Bachelor's degree a plus Foreign Medical Graduates preferred Experience : At least one years of experience as a CRC, preferably with practice coordinating industry-sponsored vaccines in a private setting.

At least two years of experience as a research assistant, data coordinator, laboratory personnel, or equivalent experience in a clinical research setting Credentials : ACRP or equivalent certification is preferred Registered Medical Assistant certification or equivalent is preferred Knowledge and Skills : Be an energetic, go-getter who is detail-oriented and can multi-task.

Be goals-driven while continuously maintaining quality. Bilingual in Spanish is preferred Powered by JazzHR

30+ days ago
Related jobs
Promoted
UIC Ophthalmology & Visual Sciences
Chicago, Illinois

Clinical Research Coordinator within the Ophthalmic Clinical Trials and Translational Center (OCTTC) is responsible for managing, coordinating, and implementing all components of clinical research protocols, including pre and post-research activities both within and outside the clinical setting. Cli...

DM Clinical Research
Chicago, Illinois

Clinic Research Coordinator II   The  Clinical Research Coordinator II , will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. ...

Regulatory Affairs Professionals Society
Chicago, Illinois

Clinical Research Coordinators, Research Associates, Graduate Students, Students, Volunteers. The UIC Office of the Vice Chancellor for Health Affairs - Office of Population Health Sciences seeks Visiting Clinical Research Compliance Coordinator. The UIC Office of the Vice Chancellor for Health Affa...

Ann & Robert H. Lurie Children’s Hospital of Chicago Foundation
Chicago, Illinois

Certification as a Clinical Research Professional (SOCRA) or Clinical Research Coordinator (ACRP) preferred. Assists clinical research personnel in the implementation of clinical research projects. High School Diploma with five to seven years clinical research experience -or- Associates/two years of...

University of Chicago
Chicago, Illinois

Acts as a resource on clinical research and related aspects of clinical study for other clinical research staff. CRC) is a specialized researcher partnering with the clinical Principal Investigator (PI) and under the direction of the Section Administrator and/or Clinical Research Manager within the ...

Ann & Robert H. Lurie Children’s Hospital of Chicago Foundation
Chicago, Illinois

Certification as a Clinical Research Professional (SOCRA) or Clinical Research Coordinator (ACRP) preferred. Promotes the ethical conduct of research and Lurie Children’s by serving in a leadership/appointed role of an internal/external clinical research committee (e. High School Diploma with five t...

University of Chicago
Chicago, Illinois

The Clinical Research Coordinator 1 provides support to the faculty of the Section of Hematology/Oncology within the Biological Sciences Division. Uses knowledge of clinical studies to coordinate the collection of analyzable clinical research data and/or samples. BSD MED - Hematology and Oncology - ...

Northwestern University
Chicago, Illinois

Completion of a research certification through accredited research professional organization such as ACRP. Previous clinical research experience involving direct interaction with participants including consenting. Background in healthcare and/or clinical research with experience collecting medical h...

Ann & Robert H. Lurie Children’s Hospital of Chicago Foundation
Chicago, Illinois

Assists clinical research personnel in the implementation of clinical research projects. Based on specific research program needs, patient facing vs. Adheres to research protocol in compliance with applicable institutional, local and feral regulations (OHRP, FDA, GCP, etc. Seizes opportunities to en...

University of Illinois Chicago
Chicago, Illinois

The Division ofGastroenterology and Hepatology is seeking an academic hourly Clinical ResearchCoordinator who will manage and coordinate the timely handling of allcomponents of clinical research protocols, including pre and post researchactivities, internal and external to the clinic setting. Certif...