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

Clinical Research Nurse Breast Oncology

The Research Nurse in collaboration with the physician, is responsible for the i...

Location

United States , Boston

Salary:

42.65 - 105.81 USD / Hour

Dana-Farber Cancer Institute

Expiration Date

Until further notice

Requirements

Licensed as a registered Nurse in the Commonwealth of Massachusetts, or State of New Hampshire as appropriate
Baccalaureate degree in nursing strongly preferred. If associate degree in nursing, must complete BSN degree within 4 years
Minimum of 1-year recent experience as an RN
Ambulatory and/or oncology experience preferred
Professional nursing certification preferred (OCN, BMTCN, CPHON, AOCNP, CRNI, RN-BC)
AHA BLS required (AHA ACLS accepted as minimum requirement)
Maintains BLS certification

Job Responsibility

Assists principal investigator with protocol development
Assists principal investigator as appropriate with the Institute’s protocol review process
Assists the principal investigator in developing the protocol budget
Collaborates with the Dana-Farber Harvard Cancer Center DFHCC quality assurance of clinical trials office in developing protocol specific materials
Serves as research coordinator for National Cancer Institute, pharmaceutical-sponsored, and National Cooperative Group protocols
Assists with recruitment and registration of patients to clinical trials
Coordinates scheduling of patient’s laboratory and radiographic assessments, admissions and clinic visits
Monitors test results as appropriate
Coordinates protocol data management as necessary
Collaborates with staff within the Institute and with outside organizations in the completion of clinical research trials

Fulltime

Research Coordinator 1 Nurse

Baptist Health is hiring a Research Coordinator 1 Nurse to join the Baptist Heal...

Location

United States , Jacksonville

Salary:

Not provided

Baptist Health (Florida)

Expiration Date

Until further notice

Requirements

Minimum 1 year clinical and/or research experience required
Must have a registered nurse license
Associate's Degree - Nursing
1 year Clinical Experience Required
1 year Clinical Research Experience Required
Licensed Registered Nurse Required

Job Responsibility

Responsible for the conduct of clinical human research activities for Baptist Health Research Institute
Ensures that research is conducted in accordance with established standards by working with clinical investigators to coordinate study-related activities
Coordinates numerous protocols simultaneously
Ensures assigned protocols are consistent with Good Clinical Practice Guidelines (BCP), Federal Food and Drug Administration (FDA), local regulations, institutional policies and procedures, and sponsor specifications
Maintains knowledge of clinical practice standards, nursing practice standards, TJC related safety requirements, OHRP requirements, human subject protection standards, and all institutional policies and procedures

Fulltime

New

Senior Clinical Research Specialist

As a community, the University of Rochester is defined by a deep commitment to M...

Location

United States of America , Rochester

Salary:

60431.00 - 84603.00 USD / Year

University of Rochester

Expiration Date

Until further notice

Requirements

Bachelor's degree and 3 years of relevant experience required
Ability to effectively manage complex research protocols/procedures required
Fully adheres to applicable safety and/or infection control standards
Proficiency in medical terminology, the clinical research process, and applicable regulatory guidelines, standards preferred
Proficiency in managing multiple and competing priorities/demands
Thorough knowledge of and established track record in assuring GCP, Responsible Conduct of Research standards, applicable safety standards, and OSHA guidelines throughout study implementation
Exceptional interpersonal, organizational, and time management skills
highly collaborative, promotes teamwork
Ability to build collaboration among research team members, laboratory staff, patients, and families, clinical services (requires tact, sensitivity, clarity, flexibility, empathy for patients)
Proficient in MS Office (e.g., Word, Excel, and PowerPoint), email, and internet

Job Responsibility

Provides leadership in planning, implementing, monitoring, and evaluating multiple clinical research protocols
Manages the day-to-day operations of multiple studies, carrying out study coordination duties from protocol development and initiation through to study close-out in accordance with regulatory/sponsor guidelines
Monitors and maximizes adherence to research standards, regulatory guidelines, and approved operational procedures
Works closely with study team members and other study sites to ensure the safety and adherence of study participants to the study protocol
Manages study-related administrative and human resources tasks and facilitates across-the-board flow of information, orchestrating study activities and personnel
Coordinates enrollment of participants
Oversees and facilitates eligibility screening and study recruitment activities
Plans study timelines and schedules appointments and study visits
Manages and organizes case report forms, source documents, and research records
Enters research data into data collection forms and/or study databases

Fulltime

New

Research Coordinator 1

Baptist Health is hiring a Research Coordinator 1 to join the Baptist MD Anderso...

Location

United States , Jacksonville

Salary:

Not provided

Baptist Health (Florida)

Expiration Date

Until further notice

Requirements

High School Diploma/GED
1-3 years Clinical Research Experience Required
Must have Clinical Research Experience

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

Research Coordinator 1

Baptist Health is hiring a Research Coordinator 1 to join the Baptist MD Anderso...

Location

United States , Jacksonville

Salary:

Not provided

Baptist Health (Florida)

Expiration Date

Until further notice

Requirements

High School Diploma/GED
1-3 years Clinical Research Experience Required
Must have Clinical Research Experience

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 I

The Clinical Research Coordinator I assists principal investigators or other stu...

Location

United States , Los Angeles

Salary:

61152.00 - 100464.00 USD / Year

Children's Hospital Los Angeles

Expiration Date

Until further notice

Requirements

1+ year experience in clinical trial coordination or computerized databases
High School Diploma or GED required
Bachelor's degree or Associate degree in related scientific field preferred
Certified clinical research associate/coordinator preferred

Job Responsibility

Assists principal investigators or other study team members with research studies
Assists with subject recruitment, data collection, scheduling of study-related activities and follow-up with enrolled subjects

What we offer

Competitive compensation package
Robust benefits program

Fulltime

Clinical Research Coordinator - Breast Oncology Cohort Studies Program

The CRC (Clinical Research Coordinators) work within the clinical research progr...

Location

United States , Boston

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

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 - Cancer Hematology

The CRC (Clinical Research Coordinators) work within the clinical research progr...

Location

United States , Boston

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

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 1

Baptist Health (Florida)

Location:
United States , Jacksonville

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
February 20, 2026

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