CrawlJobs Logo
Advocate Health Care Logo Advocate Health Care · Research and Development

Research Coordinator

United States, Charlotte 28.55 - 42.85 USD / Hour · Job Posted January 30, 2026
Apply Position
Job Link Share

Job Description

Join Our Mission to Transform Trauma Care. As a Clinical Research Coordinator on our Trauma & Acute Care Surgery Research team, you’ll be at the forefront of groundbreaking studies that shape the future of critical care. Every day, your work will directly impact the care of critically ill and injured patients, helping advance treatments and improve outcomes for some of the most vulnerable populations. This is a fast-paced, high-impact position. Many of our studies require time-sensitive screening and enrollment, so adaptability and strong organizational skills are key. Our team provides 24/7/365 coverage at the Charlotte campus, ensuring research excellence around the clock.

Job Responsibility

  • Determines protocol-related needs to conduct the trial and orders supplies and equipment
  • Recruits and screens potential patients and obtains informed consent
  • Assists in providing patient education and benefits and risks of participating in a clinical drug trial
  • Designs organizational tools and forms to facilitate accurate data collection and recordkeeping
  • Conducts in-service programs, summarizes study schedule to assist in understanding and implementing a protocol
  • Manages research funds
  • Schedules patient visits and laboratory and diagnostic test procedures
  • Coordinates drug shipments, storage, and accountability with pharmacy
  • Coordinates with Investigational Pharmacy for subjects to receive required drugs
  • Reviews trends, problems encountered, patient adverse events, and patient progress
  • Draws blood or collect other samples as needed and eligible

Requirements

  • Bachelor's Degree and research experience required
  • Master's Degree preferred
  • Phlebotomy certification or venipuncture skills preferred
  • BLS HCP certification from AHA preferred
  • Certification in clinical research (SoCRA, ACRP) preferred
  • Prior experience in clinical trials, especially drug and/or device studies, is strongly preferred
  • Strong communication and teamwork skills
  • Ability to thrive in a fast-paced, high-acuity setting
  • Prepared to take on leadership responsibilities as the Lead Coordinator for a high-priority, Department of Defense–funded Traumatic Brain Injury (TBI) study

What we offer

  • Paid Time Off programs
  • Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability
  • Flexible Spending Accounts for eligible health care and dependent care expenses
  • Family benefits such as adoption assistance and paid parental leave
  • Defined contribution retirement plans with employer match and other financial wellness programs
  • Educational Assistance Program
  • Premium pay such as shift, on call, and more based on a teammate's job
  • Incentive pay for select positions
  • Opportunity for annual increases based on performance
Advocate Health Care - All Job Offers

Looking for more opportunities?

Search for other job offers that match your skills and interests.

Suggested Tags: Frontend Developer Secretary Talent Manager Salesforce Administrator Data Analyst
Similar Jobs for

Research Coordinator

8 matching positions

Research Coordinator

The Research Coordinator provides assistance to the Principal Investigator and S...
Location
Location
United States , Bethesda
Salary
Salary:
55000.00 - 75000.00 USD / Year
genevausa.org Logo
THE GENEVA FOUNDATION
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree or equivalent work experience required
  • 2-4 years’ experience in clinical research preferred
  • 2-4 years’ non-profit, research, or healthcare experience desired
  • Demonstrate competence in oral and written communication
  • Must be organized, attentive to detail, and possess a positive, friendly and professional demeanor
  • Must be flexible with changing priorities and able to communicate in a diplomatic and professional manner
  • Computer skills including at least intermediate level experience with Excel and other Microsoft Office Software
  • Knowledge of CFR, GCP and ICH guidelines
Job Responsibility
Job Responsibility
  • Promote safety and confidentiality of research participants at all times
  • Adhere to Occupational Safety and Health Administration (OSHA), Good Clinical Practices (GCP), Good Laboratory Practices (GLP), and infection control procedures
  • Plan and coordinate the initiation of research study protocol, and the implementation of operating policies and procedures
  • Plan, implement and maintain data collection and analysis systems in support of research protocol
  • may coordinate the collection and analysis of research data
  • Recruit, instruct and coordinate research subjects and/or volunteers, as appropriate to specific study objectives and work scope
  • Coordinate the day-to-day activities of technical support staff specifically engaged in the carrying out of research/clinical protocol, as appropriate to the position
  • may perform aspects of research protocol, as required, in accordance with specified program objectives
  • Organize and facilitate meetings, conferences, and other events associated with research activities
  • may perform and/or coordinate outreach activities, as appropriate to research objectives
What we offer
What we offer
  • medical, dental, and vision healthcare
  • Flexible Spending Account
  • Health Savings account, with employer contribution
  • Short-and long-term disability
  • Employee Assistance Program
  • Life & ADD insurance
  • 403b retirement plan with generous employer match
  • flexible leave options
  • 11 paid holidays per year
  • up to 4 weeks of paid time off in a rolling year
  • Fulltime
Read More
Arrow Right

Research Coordinator

The Research Coordinator provides assistance to the Principal Investigator and S...
Location
Location
United States , Wright Patterson AFB
Salary
Salary:
22.00 - 28.00 USD / Hour
genevausa.org Logo
THE GENEVA FOUNDATION
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree or equivalent work experience required
  • 2-4 years’ experience in clinical research preferred
  • Strong research skills and experience with military populations, preferred
  • 2-4 years’ non-profit, research, or healthcare experience desired
  • Demonstrate competence in oral and written communication
  • Must be organized, attentive to detail, and possess a positive, friendly and professional demeanor
  • Must be flexible with changing priorities and able to communicate in a diplomatic and professional manner
  • Computer skills including at least intermediate level experience with Excel and other Microsoft Office Software
  • Knowledge of CFR, GCP and ICH guidelines
  • Visa sponsorship not available
Job Responsibility
Job Responsibility
  • Participant Coordination: Recruit, screen, and enroll military nursing personnel into the study
  • Serve as the primary contact for participants throughout the study
  • Schedule and manage weekly virtual BSS sessions, including sending Zoom.gov links
  • Data Management: Administer baseline and post-intervention surveys via Max.gov
  • Maintain a secure master list linking participant IDs to contact information
  • Input and manage demographic and survey data in Excel™
  • Compliance & Ethics: Ensure adherence to IRB protocols and consent procedures
  • Monitor attendance and maintain documentation for reporting
  • Coordinate with Chaplain facilitators and civilian team members to avoid coercion
  • Logistics & Communication: Liaise with internal stakeholders to manage study materials and storage
What we offer
What we offer
  • medical, dental, and vision healthcare
  • Flexible Spending Account
  • Health Savings account, with employer contribution
  • Coverage is provided for employees and family members including domestic partners
  • Short-and long-term disability
  • Employee Assistance Program
  • Life & ADD insurance
  • 403b retirement plan with generous employer match
  • flexible leave options
  • 11 paid holidays per year
  • Parttime
Read More
Arrow Right

Research Coordinator

The Research Coordinator provides assistance to the Principal Investigator and S...
Location
Location
United States , Tacoma
Salary
Salary:
55000.00 - 65000.00 USD / Year
genevausa.org Logo
THE GENEVA FOUNDATION
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree or equivalent work experience required
  • 2-4 years’ experience in clinical research preferred
  • 2-4 years’ non-profit, research, or healthcare experience desired
  • Demonstrate competence in oral and written communication
  • Must be organized, attentive to detail, and possess a positive, friendly and professional demeanor
  • Must be flexible with changing priorities and able to communicate in a diplomatic and professional manner
  • Computer skills including at least intermediate level experience with Excel and other Microsoft Office Software
  • Knowledge of CFR, GCP and ICH guidelines
Job Responsibility
Job Responsibility
  • Promote safety and confidentiality of research participants at all times
  • Adhere to Occupational Safety and Health Administration (OSHA), Good Clinical Practices (GCP), Good Laboratory Practices (GLP), and infection control procedures
  • Plan and coordinate the initiation of research study protocol, and the implementation of operating policies and procedures
  • Plan, implement and maintain data collection and analysis systems in support of research protocol
  • may coordinate the collection and analysis of research data
  • Recruit, instruct and coordinate research subjects and/or volunteers, as appropriate to specific study objectives and work scope
  • Coordinate the day-to-day activities of technical support staff specifically engaged in the carrying out of research/clinical protocol, as appropriate to the position
  • may perform aspects of research protocol, as required, in accordance with specified program objectives
  • Organize and facilitate meetings, conferences, and other events associated with research activities
  • may perform and/or coordinate outreach activities, as appropriate to research objectives
What we offer
What we offer
  • medical, dental, and vision healthcare
  • Flexible Spending Account
  • Health Savings account, with employer contribution
  • Short-and long-term disability
  • Employee Assistance Program
  • Life & ADD insurance
  • 403b retirement plan with generous employer match
  • flexible leave options
  • 11 paid holidays per year
  • up to 4 weeks of paid time off in a rolling year
  • Fulltime
Read More
Arrow Right

Clinical Research Coordinator – Neurophysiology Research Core (CNRC)

The Clinical Research Coordinator will play a primary role in collecting data fo...
Location
Location
United States , Brookline
Salary
Salary:
44657.60 - 69773.60 USD / Year
childrenshospital.org Logo
Boston Children's Hospital
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • A Bachelor's degree is required
  • 2 years of experience is required
  • Previous experience with children with autism or other neurodevelopmental conditions is ideal
  • Previous experience working in a research setting (preferably paid professional experience, but may include undergraduate research experiences) is also a plus.
Job Responsibility
Job Responsibility
  • Consents and recruits patients for research studies through personal interviews and written communications with patients/families
  • Provides detailed background information regarding studies to families, communicates all policies and procedures, and responds to all inquiries
  • Evaluates suitability of prospective study candidates and makes selections based upon clinical knowledge of each study
  • Performs EEG and other data collection methods (e.g., ERP, eye-tracking) on participants aged 0-65 years
  • Serves as liaison to the families/patients in the research studies, conducted at both on-site and off-site locations, guiding and advising them during data collection
  • Acts as a resource to study participants, addressing any concerns they may have
  • Troubleshoots resolution of any issues that may arise during data collection
  • Participates in the training of newly hired research study assistants, as required
  • Coordinates activities between the hospital and research laboratories to ensure correct testing/processing and send out instructions specific to the study
  • Communicates project policies and procedures to personnel
What we offer
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
Read More
Arrow Right

Clinical Research Coordinator

Clinical Research Coordinator (contingent workers) ICON plc is a world-leading ...
Location
Location
Poland , Warsaw; Gdansk; Gliwice; Lodz; Zabrze
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in a relevant field such as business administration, project management, or a related discipline
  • Experience in a similar role or environment, with a focus on project support
  • Experience in oncology therapeutic area strongly preferred
  • Strong analytical skills and attention to detail, with the ability to work effectively in a team
  • Excellent communication and interpersonal skills, with a collaborative approach to problem-solving
  • Proficiency in relevant software applications and tools to support project execution
Job Responsibility
Job Responsibility
  • Assisting in the development and implementation of project plans to meet organizational goals
  • Collaborating with team members to identify opportunities for improvement and innovation
  • Gathering and analyzing data to provide insights that support decision-making processes
  • Contributing to the creation of reports and documentation to track project progress
  • Building strong relationships with colleagues to enhance teamwork and communication across functions
What we offer
What we offer
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others
  • Parttime
Read More
Arrow Right

Clinical Research Coordinator II

Job Description Must have RN licensure to qualify. PURPOSE AND SCOPE: Responsi...
Location
Location
United States , Tupelo
Salary
Salary:
Not provided
freseniuskidneycare.com Logo
Fresenius Kidney Care Eupora
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Graduate of a technical program in healthcare, specifically as a Registered Nurse
  • 2 to 4 years of nursing experience, specifically as a Registered Nurse
  • 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
  • Research experience preferred
  • Critical care, nephrology and/ or cardiac nursing 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
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
What we offer
What we offer
  • Healthcare
  • Continuing Education
  • Paid Time Off
  • Collaborative Environment
  • Additional Perks
  • 401(k) Retirement Saving
Read More
Arrow Right

Clinical Research Coordinator

Responsible for supporting the Research leadership and Principal Investigator of...
Location
Location
United States , Boca Raton
Salary
Salary:
Not provided
baptisthealth.net Logo
Baptist Health
Expiration Date
Until further notice
Flip Icon
Requirements
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
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
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
Read More
Arrow Right

Clinical Research Coordinator I

A Clinical Research Coordinator (CRC) I position is currently available within t...
Location
Location
United States , New York
Salary
Salary:
58661.00 - 73530.00 USD / Year
mountsinai.org Logo
Mount Sinai Health System
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelors or Masters degree in Science or closely related field
  • No experience required
  • One year of research experience preferred
Job Responsibility
Job Responsibility
  • Collects and records study data
  • inputs all information into database
  • Under direct supervision of the Principle Investigator(s), obtains informed consent and educates participants regarding study requirements
  • Assists in the activities related to clinical research studies including but not limited to: answering phone calls, screening participants for eligibility, registering subjects with sponsoring agency, and administering lifestyle questionnaires
  • Maintains source documents and subject files in accordance with hospital procedures
  • helps to ensure accurate and complete compilation of subject data through chart reviews
  • Secures, delivers and ships clinical specimens as required by the protocol
  • Responsible for organizing and preparing for monitoring visits
  • Assists with coordination and management of clinical trials including communication with Sponsors
  • Performs other related duties as assigned
  • Fulltime
Read More
Arrow Right