Research Coordinator 3 Job at Baptist Health (Florida) (Jacksonville)

Clinical Research Coordinator II

Must be comfortable with 50% travel. Highly prefer someone who lives in the Nort...

Location

United States

Salary:

Not provided

Fresenius Kidney Care Eupora

Expiration Date

Until further notice

Requirements

2 to 4 years of clinical research experience, or has successfully performed in the role of Clinical Research Coordinator I for a minimum of 3 years and demonstrated outstanding performance through performance evaluations, certification and other job performance measures
Critical care, nephrology and/ or cardiac experience desirable
Willing to pursue CCRC or CCRP certification when eligible
Current state licensure, if applicable
Good computer skills: Microsoft Office minimally
Excellent communication and organizational skills
Ability to work independently, and exhibit diplomacy and problem solving skills in the performance of this role

Job Responsibility

Assists with the determination of the guidelines for the collection of clinical data and coordinates and implements procedures and processes for data collection
Coordinates all aspects of study subject care from pre-screening through study completion as defined by the protocol and Principal Investigator (PI) delegation
Protect the rights and the well-being of subjects enrolled in studies
Ensures thorough, individualized, protocol-based study subject education on all study process requirements including but not limited to: informed consent, study participation obligations, appropriate use of investigational product, safety, privacy, rights and responsibilities
Develops processes for methodically monitoring the status of study subjects as they progress through the study’s timeline of activities
Regularly evaluates the study subjects’ condition and communicates/documents concerns to PI to ensure subject safety
Accurately documents study subject activities as outlined by the protocol
Maintains documents according to applicable HIPAA and regulatory requirements
Implements study-specific quality goals and practices
Acts as the point of contact or lead person in a facility/practice to oversee protocol compliance

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

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

Sensory Research Coordinator

Spearhead sensory research initiatives to drive product innovation for a leading...

Location

Japan , 東京23区

Salary:

5000000.00 - 7300000.00 JPY / Year

Randstad

Expiration Date

March 23, 2027

Requirements

3-5 years of experience in sensory evaluation or consumer research
Proven ability to design, execute, and analyze sensory studies
Strong understanding of statistical analysis techniques
Excellent communication and collaboration skills in Japanese and English
Proficiency in relevant software (e.g., SPSS, R, TRI*POT)

Job Responsibility

Design and implement sensory research protocols and methodologies
Coordinate research logistics, including participant recruitment and scheduling
Analyze sensory data and generate comprehensive reports
Collaborate with R&D and marketing teams to translate insights into actionable product strategies
Maintain databases of sensory attributes and consumer preferences
Stay abreast of emerging trends and technologies in sensory science

What we offer

健康保険
厚生年金保険
雇用保険
土曜日
日曜日
祝日

Fulltime

Clinical Research Coordinator

At Boston Children’s Hospital, the quality of our care – and our inclusive hospi...

Location

United States , Boston

Salary:

44657.60 - 69773.60 USD / Year

Boston Children's Hospital

Expiration Date

Until further notice

Requirements

Bachelor’s degree required
Bachelor’s degree with at least 3 years of relevant experience
OR Master’s degree with at least 1 year of relevant experience
Strong attention to detail and organizational skills
Ability to work independently and collaboratively within a team
Excellent verbal and written communication skills
Preliminary knowledge of clinical trials research and lab procedures
Proficiency in Microsoft Office (Outlook, Excel, Word)
Professionalism and respect for research participants and their rights

Job Responsibility

Coordinate and execute clinical research studies in accordance with study protocols and institutional policies
Recruit and screen study participants via phone, clinic visits, and other settings
Conduct informed consent procedures and explain study details to participants and families
Schedule and manage study visits, including reminders and follow-ups
Collect and process biological samples (e.g., blood, urine, sputum, stool)
Administer and score questionnaires
perform study procedures such as vital signs, sweat testing, ECGs, and spirometry
Maintain accurate and complete study documentation, including case report forms (CRFs), regulatory binders, and source documents
Assist with IRB submissions, protocol amendments, and regulatory correspondence
Monitor and report adverse events

What we offer

flexible schedules
affordable health, vision and dental insurance
child care and student loan subsidies
generous levels of time off
403(b) Retirement Savings plan
Pension
Tuition and certain License and Certification Reimbursement
cell phone plan discounts
discounted rates on T-passes

Fulltime

Clinical Research Coordinator 2

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

Location

United States , Coral Gables

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
CCRC/CCRP certification preferred
Minimum Required Experience: 2 years
Licenses & Certifications: Basic Life Support

Job Responsibility

Responsible for supporting the Research leadership and Principal Investigator of a designated research project
Performs those functions required by the research protocols with attention to participant safety
Ensures that all requirements of the protocol are met, while meeting compliance with regulatory standards and FDA requirements for each protocol
Must be able to complete detailed paperwork in strict accordance with regulatory requirements and collaborate with physicians, patients, sponsors, and other departments in a service excellence manner

Fulltime

Clinical Research Coordinator

At Boston Children’s Hospital, the quality of our care – and our inclusive hospi...

Location

United States , Brookline

Salary:

44657.60 - 69773.60 USD / Year

Boston Children's Hospital

Expiration Date

Until further notice

Requirements

Bachelor’s degree in psychology, cognitive science, neuroscience, or related field. Master’s preferred
2 years of experience, 3 years of experience or more preferred
Experience working with infants or children in a research setting
Availability for flexible scheduling, including evenings and weekends
2-year commitment to the position
Computer skills including working knowledge of PC and Mac operating systems, as well as statistics software (e.g., Excel, SPSS)
Ability to assist with grant preparation, publications, presentations, and/or applications to an Institutional Review Board
High level of motivation
ability to work independently and as part of a team
excellent communication, organization, and attention to detail

Job Responsibility

Coordinate day-to-day operations and functions for ELEVATE, a study designed to validate a pre-harmonized set of data collection tools to evaluate individual differences in learning and cognition in preschoolers
Working with and coordinating a team of undergraduate students and staff associated with the research project, along with IRB management, and preparing progress reports
Work closely with team members on the development, coordination, and implementation of research procedures and day-to-day operations under the direction of the Principal Investigator and Co-Investigator

What we offer

flexible schedules
affordable health, vision and dental insurance
child care and student loan subsidies
generous levels of time off
403(b) Retirement Savings plan
Pension
Tuition and certain License and Certification Reimbursement
cell phone plan discounts
discounted rates on T-passes

Fulltime

Human Subjects Research Coordinator I

This is a full-time position (40 hrs/wk) in Ob/Gyn to conduct clinical research ...

Location

United States of America , Rochester

Salary:

21.36 - 29.90 USD / Hour

University of Rochester

Expiration Date

Until further notice

Requirements

Bachelor's degree and 3 years’ experience in clinical research coordination
or an equivalent combination of education and experience
Phlebotomy training and certification required
Knowledge of Microsoft Office and Windows software preferred
Experience with data entry or management preferred
Clinical Research Coordinator Certification preferred
Must be able to work occasional weekends and in late afternoons/early evenings on some weekdays
Ability to work independently
Strong organizational and interpersonal skills
Willing to develop the logistics of subject enrollment

Job Responsibility

Engagement and monitoring of study subjects (50%): Schedule and conduct study visits, consenting participants and explaining study protocols to ensure patient compliance
Subject tracking, administering the study vitamin D on the first study day, drawing blood, processing biological sampling, ensuring form completion, and adherence to protocol
Assist in developing protocol with PI, recruitment strategies, and monitors target enrollment numbers
Inform Cornell study team when subjects complete study and need to be reimbursed
Interface with PI at Cornell to update on enrollment status and any issues that arise during the study
Study administration, participates in advertising material development, and coordination of study with PI
Information Management (40%): Completes interviews and phone calls with subjects as required by protocol
Completion of source documents: CRFs, follow up phone calls, and subject mailings
Provide collection, labeling, and coordination of study specimens to be delivered to the core laboratory
Perform chart reviews and information abstraction/recording, phone communications with subjects, fax/mail as necessary as pertains to enrolled subjects at your site

Fulltime

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Research Coordinator 3

Job Description

Job Responsibility

Requirements

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