Clinical Research Coordinator II - Cedars-Sinai Medical Group
Company: CEDARS-SINAI
Location: Los Angeles
Posted on: March 5, 2025
Job Description:
Job DescriptionAre you ready to be a part of breakthrough
research?The Clinical Research Coordinator II serves as the lead
coordinator on an assigned portfolio of research studies,
functioning independently to establish and coordinate logistics and
processes for the conduct of research for the department. This
individual will interact with principal investigators, subjects,
clinic and research staff, laboratory staff, medical professionals,
pharmaceutical staff, and Sponsor representatives to successfully
implement research protocols, in compliance with all applicable
regulatory requirements.Primary Duties and Responsibilities:
- Establishes and executes logistical aspects of clinical
research projects to achieve project objectives, including project
planning, projecting resource requirements, and developing systems
to ensure protocol compliance and patient safety.
- Coordinates administrative functions of research studies,
including scheduling of patients for research visits, procedures,
and labs, and completion and maintenance of consent forms, case
report forms, SAE's, and source documents.
- Responsible for screening and recruitment of potential patients
for protocol eligibility, presenting non-medical trial concepts and
details to the patients, and supporting the informed consent
process.
- Responsible for accurate and timely data collection,
documentation, entry, and reporting, including resolution of
queries from sponsors or regulatory entities.
- Coordinates institutional, pharmaceutical, and internal audits,
including facilitating third-party study monitoring and designs and
implements needed corrective actions.
- Responsible for compiling and reporting on each study including
information related to protocol activity, accrual data, workload,
and other research information; present this information at regular
research staff meetings.
- Responsible for timely submission of adverse events, serious
adverse events, protocol deviations, and Safety Letters in
accordance with local and federal guidelines.
- Identifies quality and performance improvement opportunities
and collaborates with staff in the development of action plans to
improve quality.
- Plans and coordinates strategies for increasing research
participant enrollment, and/or improving clinical research
efficiency as needed.
- Provides technical support for the preparation of grant
proposals, publications, presentations, and special projects.
- Provides assistance with research project budget development,
including identifying and classifying routine care vs.
research-related care, and provides assistance with research
participant research billing and reconciliation.
- Attend meetings and conferences related to research activities,
including research staff meetings.
- Participate in planning, workshops, evaluation meetings, and
seminars, educational or administrative meetings as necessary or
requested; Participate in training and education of new research
personnel.
QualificationsEducation:
- An Associate Degree/College Diploma is required. Bachelor's
degree preferred.Licenses and Certifications:
- Basic Life Support (BLS) is required.
- Certification In Clinical Research (SoCRA or ACRP
certification), Phlebotomy Certification (CA), and Certification as
a Registered Medical Assistant are preferred.Experience and Skills:
- Three (3) years of clinical research coordination or related
experience is required.
- Maintains comprehensive knowledge of assigned research
protocols to coordinate the compliant execution of assigned tasks
in accordance with research governing entity requirements,
including but not limited to Sponsor, FDA, and IRB
requirements.
- Ability to use software applications (MS Office Suite - Excel,
Word, Outlook, PowerPoint) and operate technological devices (e.g.,
computer, laptop, tablet, smartphone, etc.).
- Establishes effective working relationships with
cross-functional team(s).
- Collaborates to solve problems and make decisions to achieve
desired outcomes.
- Cultivates and maintains strong customer relationships and
rapport with stakeholders and/or client groups.
- Identifies and responds appropriately to internal and external
customer needs utilizing available resources.
- Represents the company with external constituents.
About UsCedars-Sinai is a leader in providing high-quality
healthcare encompassing primary care, specialized medicine and
research. Since 1902, Cedars-Sinai has evolved to meet the needs of
one of the most diverse regions in the nation, setting standards in
quality and innovative patient care, research, teaching and
community service. Today, Cedars- Sinai is known for its national
leadership in transforming healthcare for the benefit of patients.
Cedars-Sinai impacts the future of healthcare by developing new
approaches to treatment and educating tomorrow's health
professionals. Additionally, Cedars-Sinai demonstrates a commitment
to the community through programs that improve the health of its
most vulnerable residents.
About the TeamWith a growing number of primary urgent and specialty
care locations across Southern California, Cedars-Sinai's medical
network serves people near where they live. Delivering coordinated,
compassionate healthcare you can join our network of clinicians and
physicians to improve the healthcare people throughout Los Angeles
and beyond.
Req ID : 6853
Working Title : Clinical Research Coordinator II - Cedars-Sinai
Medical Group
Department : Research - CSMN
Business Entity : Cedars-Sinai Medical Care Foundation
Job Category : Academic / Research
Job Specialty : Research Studies/ Clin Trial
Overtime Status : EXEMPT
Primary Shift : Day
Shift Duration : 8 hour
Base Pay : $64,147.20 - $99,424
Keywords: CEDARS-SINAI, Los Angeles , Clinical Research Coordinator II - Cedars-Sinai Medical Group, Healthcare , Los Angeles, California
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