Clinical Research Coordinator 1 Job at Baptist Health (Florida) (Jacksonville)

Research Coordinator 1

Sets up and performs routine clinical trial related activities • Collects, enter...

Location

United States , Jacksonville

Salary:

Not provided

Baptist Health (Florida)

Expiration Date

Until further notice

Requirements

High School
Clinical Research Experience
Driver's License - DMV

Job Responsibility

Sets up and performs routine clinical trial related activities
Collects, enters and summarizes clinical trial data, monitors patients, their results, detects and reports all events per protocol, applicable policies and applicable regulations
Dedicated to excellence in all aspects of clinical research with keen focus on ethics, safety, quality, compliance, and stewardship
Understands and demonstrates Baptist Health System- Research objectives and mission
Impacts research throughout the institution
Other duties as assigned

Fulltime

Clinical Research Coordinator

Responsible for supporting the Research leadership and Principal Investigator of...

Location

United States , Boca Raton

Salary:

Not provided

Baptist Health

Expiration Date

Until further notice

Requirements

Associate's of arts degree is required
In lieu of Associates degree, 3 years of research experience is required OR, a Foreign Medical Degree with 1 year of experience required
Advanced computer literacy in Microsoft Office
Proven ability to manage multiple assignments systematically
Excellent interpersonal, collaborative, and team-building skills are required
Must be able to work in a high-demand environment with the ability to take responsibility in meeting deadlines
Strong verbal and written communication skills
Minimum Required Experience: 2 Years

Job Responsibility

Supporting the Research leadership and Principal Investigator of a designated research project
Performing functions required by the research protocols with attention to participant safety
Ensuring that all requirements of the protocol are met, while meeting compliance with regulatory standards and FDA requirements for each protocol
Completing detailed paperwork in strict accordance with regulatory requirements
Collaborating with physicians, patients, sponsors, and other departments in a service excellence manner

What we offer

Career growth and development opportunities, with clear pathways and ongoing support
Comprehensive health and wellness resources that go beyond traditional benefits
A wellness program that can help employees eliminate their medical plan deductible, reducing out-of-pocket healthcare costs
Tuition reimbursement to support continued learning and advancement

Fulltime

Clinical Research Coordinator II - Precision Medicine

A Clinical Research Coordinator II (CRC II) position is available for the Precis...

Location

United States , BOSTON

Salary:

56000.00 - 63700.00 USD / Year

Dana-Farber Cancer Institute

Expiration Date

Until further notice

Requirements

bachelor's degree or 2 years of experience as a Dana-Farber Clinical Research Coordinator
1-3 years of relevant experience
preference for those with a background in medical or scientific research or a technology-oriented business environment
excellent organization and communications skills
strong interpersonal skills
detail oriented
ability to effectively manage time and prioritize workload
must practice discretion and adhere to hospital confidentiality guidelines
computer skills including the use of Microsoft Office

Job Responsibility

liaise between the LSP, DF/HCC hospitals, and external investigators to facilitate highly collaborative translational biomarker driven research
facilitate the emerging fields of cancer spatial biology
work closely with principal investigators, program managers, biomarker researchers, and data scientists
primary data collection and management of patient clinical information as it pertains to participation in clinical trials and patient consent
ensure timely facilitation of trial assessments per protocol and collection of protocol related samples including shipment to outside entities
support and maintain participant/subject trial binders and maintain regulatory binders
ensure study compliance with all state, federal, and IRB requirements
screen patients for protocol eligibility
obtain informed consent for non-treatment trials
register study participants with the clinical trials management system, ONCORE

Fulltime

Clinical Research Coordinator - Immune Effector Cell Therapy Program

The CRC (Clinical Research Coordinator) will work within the Immune Effector Cel...

Location

United States , Brookline

Salary:

48100.00 - 54400.00 USD / Year

Dana-Farber Cancer Institute

Expiration Date

Until further notice

Requirements

Excellent organization and communications skills required
Strong interpersonal skills – ability to effectively interact with all levels of staff and externals contacts
Must be detail oriented and have the ability to follow-through
Ability to effectively manage time and prioritize workload
Must practice discretion and adhere to hospital confidentiality guidelines at all times
Must have computer skills including the use of Microsoft Office
Bachelor’s Degree or 1 year of Dana-Farber Associate Clinical Research Coordinator experience required
0-1 years of experience working in a medical or scientific research setting or comparable technology orientated business environment preferred

Job Responsibility

Support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator and the Clinical Research Manager
Responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials
Ensures timely facilitation of trial assessments per protocol and collection of protocol related samples including shipment to outside entities as required
Support and maintain participant/subject trial binders and may maintain regulatory binders, to ensure study compliance with all state, federal, and IRB requirements
May be responsible for pertinent IRB protocol submissions
Screen patients for protocol eligibility, obtain informed consent for non-treatment trials, and register study participants with the clinical trials management system, ONCORE
Oversight of the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities
Responsible for data reporting and management, collection of source documents, use and development of case report forms, adverse events reporting, filing, and archiving of study records, and resolution of data queries
May prepare and or complete regulatory related reports and IRB submissions
Maintain and organize study participant/subject trial binder and regulatory binders, enter all required study data on an ongoing basis and as applicable

Fulltime

Clinical Research Coordinator - Thoracic Oncology

The CRC (Clinical Research Coordinator) will work within the Thoracic Oncology c...

Location

United States , Brookline

Salary:

48100.00 - 54400.00 USD / Year

Dana-Farber Cancer Institute

Expiration Date

Until further notice

Requirements

Bachelor's Degree or 1 year of Dana-Farber Associate Clinical Research Coordinator experience required
0-1 years of experience working in a medical or scientific research setting or comparable technology orientated business environment preferred
Excellent organization and communications skills required
Strong interpersonal skills – ability to effectively interact with all levels of staff and externals contacts
Must be detail oriented and have the ability to follow-through
Ability to effectively manage time and prioritize workload
Must practice discretion and adhere to hospital confidentiality guidelines at all times
Must have computer skills including the use of Microsoft Office

Job Responsibility

Oversight of the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities
Responsible for data reporting and management, collection of source documents, use and development of case report forms, adverse events reporting, filing, and archiving of study records, and resolution of data queries
May prepare and or complete regulatory related reports and IRB submissions
Maintain and organize study participant/subject trial binder and regulatory binders, enter all required study data on an ongoing basis and as applicable
Ensure all study related samples are collected, properly prepared, and shipped according to the protocol requirements and IATA/DOT regulations
Collaborate with other departments such as Protocol Scheduling, Materials Management, the Clinical Research Laboratory, Pharmacy, Research Nursing, and other departments, as needed per the requirements of the clinical trial
Responsible for organizing and preparing for both internal and external auditing and study monitoring visits
Coordination and management of clinical trials throughout the trial life cycle, including communication with sponsors and regulatory authorities
Close-out of clinical trials, including contributing to research articles, audit preparation, and communication with regulatory agencies and other disciplines involved
Interact with study participants as directed/required by the protocol and/or study team

Fulltime

Clinical Research Coordinator - Tumor Institute

This is a combined posting for Associate Clinical Research Coordinator, Clinical...

Location

United States , Seattle

Salary:

27.92 - 57.71 USD / Hour

Providence Swedish

Expiration Date

Until further notice

Requirements

Bachelor's Degree preferably in Science, Healthcare, or other related field., Or Significant experience in research coordination may be substituted for educational requirements
Within 60 days of hire: Washington Medical Assistant Registration
1 year of experience in related area
Bachelor's Degree preferably in Science, Healthcare, or other related field, Or Significant experience in research coordination may be substituted for educational requirements
3 years of experience in related area
Bachelor's Degree preferred fields: Science, Healthcare, or other related field, Or Significant experience in research coordination may be substituted for educational requirements
Within 60 days of hire: Washington Medical Assistant Registration
5 years of experience in related area

Job Responsibility

Independently coordinates research and administrative tasks in support of one or more research studies
Works with study investigators and supervisor to address study-related issues
Backs up other coordinators as needed
Supports department financial performance through budgeting, billing and as directed
May develop specialized research instruments and assist in the preparation of scientific manuscripts or presentations
May entail regular after-hours support, occasional on-call work and occasional overnight business travel
Trains other research coordinators in the proper conduct of research studies and participates in quality control activities, as directed
Assists manager or supervisor in providing oversight of financial and quality initiatives

What we offer

Retirement 401(k) Savings Plan with employer matching
Health care benefits (medical, dental, vision)
Life insurance
Disability insurance
Time off benefits (paid parental leave, vacations, holidays, health issues)
Voluntary benefits
Well-being resources

Fulltime

Clinical Research Coordinator

We are looking for a Clinical Research Coordinator to support clinical research ...

Location

United States , Anaheim

Salary:

Not provided

Robert Half

Expiration Date

Until further notice

Requirements

At least 2 years of relevant experience, including a minimum of 1 year working in a Clinical Research Coordinator or closely related clinical research role
High school diploma or equivalent required
a bachelor's degree is preferred
Working knowledge of regulations and ethical standards governing human subject research and clinical trial conduct
Ability to manage scheduling, administrative support tasks, and detailed documentation in a fast-paced research setting
Strong verbal and written communication skills with the ability to interact professionally across teams and with external partners
Demonstrated problem-solving skills, sound judgment, and composure when responding to urgent or unexpected situations
Comfortable working independently while also contributing effectively within a collaborative team environment
Proficiency with Microsoft applications and general administrative coordination tools

Job Responsibility

Coordinate participant-related study activities from enrollment through closeout, helping keep each trial on schedule and aligned with approved protocols
Maintain organized research records, track study documentation, and support accurate preparation of materials required for clinical trial operations
Arrange visits, assessments, and data collection appointments while ensuring timelines are followed and information is recorded appropriately
Monitor study participants during assigned activities and assist with compiling research findings, summaries, and required reports
Record adverse events, protocol departures, and unexpected study issues in a timely manner to support regulatory compliance and quality standards
Assist with administrative and regulatory tasks tied to active studies, including maintaining files and supporting protocol-related processes
Provide clear explanations to prospective participants and caregivers regarding study expectations, procedures, and visit requirements
Perform protocol-directed procedures such as vital signs, EKGs, blood draws, and other assigned safety or efficacy assessments
Collaborate with research staff and leadership on additional study development or coordination activities as needed

What we offer

medical
vision
dental
life and disability insurance
401(k) plan

Fulltime

Clinical Research Coordinator

CRC monitors and coordinates multiple research projects in order to assess the n...

Location

United States , Madera

Salary:

35.85 - 53.35 USD / Hour

Valley Children's Healthcare

Expiration Date

Until further notice

Requirements

Equivalent Experience Three (3) years research experience (required)
College Degree - 4 year (preferred)
CCRP - Certified Clinical Research Professional - SOCRA - Society of Clinical Research Associates (preferred)
Minimum one (1) year Research (required)
Minimum two (2) years Related experience (preferred)
Experience with clinical trials is strongly preferred
Knowledge of Institutional Review Board (IRB) policies and procedures
Knowledge of the scientific method and statistical analysis techniques preferred
Computer Skills Microsoft Office

Job Responsibility

Monitor and coordinate multiple research projects
Assess the need for and implement strategies to ensure the conduct of quality research
Achievement of expected timelines and deliverables and efficient use of resources
Assist PIs with study protocol development, ICFs, and required study documents in preparation for IRB submission
Assist with recruitment activities, consents patients, ensures eligibility prior to enrollment, and randomizes patients to study
Abstract data, complete case report forms and maintain research record and data integrity
Schedule and meet with study monitor for site visits
Maintain data in an audit ready state
Ensure study meets the requirements of executed contract and budget
Ensure compliance to the research protocol, appropriate SOPs, policies and federal regulations

Fulltime

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Clinical Research Coordinator 1

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Job Responsibility

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