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Clinical Research Coordinator II - Medical Group

CEDARS-SINAI

Beverly Hills, California • Today

Full-time

Clinical Research Coordinator II - California Heart Center

CEDARS-SINAI

Beverly Hills, California • Today

Full-time

Clinical Research Coordinator II - The Angeles Clinic & Research Institute

CEDARS-SINAI

Los Angeles, California • Today

Full-time

Clinical Research Coordinator I (Hybrid)

CEDARS-SINAI

Los Angeles, California • Today

Full-time

Research Specialist II - Touil Lab - Department of Neurology

CEDARS-SINAI

West Hollywood, California • Today

Full-time

User Study Researcher II

PTR Global

Los Angeles, California • Today

Easy Apply

Full-time

USD 55.00 - 60.00 per hour

Clinical Research Associate I - Heart Institute - Berman Lab

CEDARS-SINAI

Beverly Hills, California • Today

Full-time

Clinical Research Associate I - Heart Institute - Gupta Team

CEDARS-SINAI

Los Angeles, California • Today

Full-time

Heart Institute - Clinical Research Associate I, Susan Cheng Team

CEDARS-SINAI

Los Angeles, California • Today

Full-time

Research Associate II- Dept of Orthopaedics, Metzger Lab

CEDARS-SINAI

Los Angeles, California • Today

Full-time

Heart Institute - Clinical Research Assoc I/CPT, Susan Cheng Team

CEDARS-SINAI

Los Angeles, California • Today

Full-time

Research Associate II - Regenerative Medicine Institute

CEDARS-SINAI

Los Angeles, California • Today

Full-time

Research Associate II - Division of Endocrinology / Department of Medicine

CEDARS-SINAI

Los Angeles, California • Today

Full-time

Senior Clinical Research Associate

EmployVision

Remote • Today

Easy Apply

Contract

$70 - $80

Job Details

Skills

BIND
Logistics
Project Planning
Regulatory Compliance
Scheduling
Forms
Screening
Recruiting
Data Collection
Documentation
Pharmaceutics
Auditing
Facilitation
Reporting
Performance Improvement
Technical Support
Publications
Presentations
Project Budget
Billing
Evaluation
Training
Clinical Research
Collaboration
Research
Microsoft Office
Microsoft Excel
Microsoft Outlook
Microsoft PowerPoint
Laptop
Tablet
Smartphones
Cross-functional Team
Customer Relationship Management (CRM)

BIND
Logistics
Project Planning
Regulatory Compliance
Scheduling
Forms
Screening
Recruiting
Data Collection
Documentation
Pharmaceutics
Auditing
Facilitation
Reporting
Performance Improvement
Technical Support
Publications
Presentations
Project Budget
Billing
Evaluation
Training
Clinical Research
Collaboration
Research
Microsoft Office
Microsoft Excel
Microsoft Outlook
Microsoft PowerPoint
Laptop
Tablet
Smartphones
Cross-functional Team
Customer Relationship Management (CRM)

Summary

Job Description

Are 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; Participates in training and education of new research personnel.

Qualifications

Education:

An Associate Degree/College Diploma is required. Bachelor\'s degree is preferred.

Licenses and Certifications:

Basic Life Support (BLS) from the AHA is required.
Certification in clinical research (SoCRA or ACRP certification) is 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.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id: RTX1d8578
Position Id: 113640875
Posted 10 hours ago

Fitment

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Beverly Hills, California

•

Today

Job Description The mission of the California Heart Center is to integrate quality health care, clinical research, and continuing education to create an environment where advances are fostered for the immediate benefit of patients. The California Heart Center is committed to providing patients with the best medical care and customer service, and to continuously improve the quality of care and service throughout the organization. To learn more, please visit Are you ready to be a part of breakthr

Full-time

Clinical Research Coordinator II - The Angeles Clinic & Research Institute

Los Angeles, California

•

Today

Job Description Grow your career at Cedars-Sinai! The Angeles Clinic & Research Institute has established an international reputation for developing new cancer therapies, providing the best in experimental and traditional treatments, and expertly guiding and training the next generation of clinicians. Our board-certified fellowship-trained medical oncologists, surgeons, immunotherapists, pathologists, and dermatologists work closely together to advance cancer care. We are committed to bringing i

Full-time

Clinical Research Coordinator I (Hybrid)

Los Angeles, California

•

Today

Job Description This role follows a hybrid work schedule, with a minimum requirement of 3 days onsite per week at our Los Angeles work location. Applicants must be able to meet this onsite requirement and, if hired, must reside within a commutable distance of the work location. Join a supportive, collaborative team contributing to NIH-funded studies with partners across multiple institutions. Responsibilities can be aligned with individual skills and interests, with opportunities to grow into n

Full-time

Clinical Research Associate I - Heart Institute - Gupta Team

Los Angeles, California

•

Today

Job Description Grow your career at Cedars-Sinai! . When you join our team, you?ll have access to groundbreaking biomedical research facilities and world-class medical education programs. We take pride in hiring exceptional, dedicated professionals who are passionate about advancing healthcare. Our physicians, nurses, and staff reflect the culturally and ethnically diverse communities we serve and are united by a shared commitment to excellence. Together, we foster a dynamic, inclusive environme

Full-time

Job Details

Skills

BIND
Logistics
Project Planning
Regulatory Compliance
Scheduling
Forms
Screening
Recruiting
Data Collection
Documentation
Pharmaceutics
Auditing
Facilitation
Reporting
Performance Improvement
Technical Support
Publications
Presentations
Project Budget
Billing
Evaluation
Training
Clinical Research
Collaboration
Research
Microsoft Office
Microsoft Excel
Microsoft Outlook
Microsoft PowerPoint
Laptop
Tablet
Smartphones
Cross-functional Team
Customer Relationship Management (CRM)

BIND
Logistics
Project Planning
Regulatory Compliance
Scheduling
Forms
Screening
Recruiting
Data Collection
Documentation
Pharmaceutics
Auditing
Facilitation
Reporting
Performance Improvement
Technical Support
Publications
Presentations
Project Budget
Billing
Evaluation
Training
Clinical Research
Collaboration
Research
Microsoft Office
Microsoft Excel
Microsoft Outlook
Microsoft PowerPoint
Laptop
Tablet
Smartphones
Cross-functional Team
Customer Relationship Management (CRM)

Summary

Job Description

Are you ready to be a part of breakthrough research?

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; Participates in training and education of new research personnel.

Qualifications

Education:

An Associate Degree/College Diploma is required. Bachelor\'s degree is preferred.

Licenses and Certifications:

Basic Life Support (BLS) from the AHA is required.
Certification in clinical research (SoCRA or ACRP certification) is 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.

Dice Id: RTX1d8578
Position Id: 113640875
Posted 10 hours ago

Fitment

Dice Job Match Score™

To see how well you match this job, please log in or create an account.

Once logged in, be sure to complete your profile to get the most accurate match score.

Create job alert

Never miss an opportunity! Create an alert based on the job you applied for.

Beverly Hills, California

•

Today

Full-time

Clinical Research Coordinator II - The Angeles Clinic & Research Institute

Los Angeles, California

•

Today

Full-time

Clinical Research Coordinator I (Hybrid)

Los Angeles, California

•

Today

Full-time

Clinical Research Associate I - Heart Institute - Gupta Team

Los Angeles, California

•

Today

Full-time

Clinical Research Coordinator II - Medical Group

Skills

Summary

Job Description

Qualifications

Dice Job Match Score™

Similar Jobs

Clinical Research Coordinator II - Medical Group

Job Details

Skills

Summary

Job Description

Qualifications

Dice Job Match Score™

Similar Jobs