CrawlJobs Logo

Registered Nurse Senior Research Coordinator

advocatehealth.com Logo

Advocate Health Care

Location Icon

Location:
United States , Chicago

Category Icon
Category:

Job Type Icon

Contract Type:
Not provided

Salary Icon

Salary:

35.50 - 53.25 USD / Hour

Job Description:

Cellular therapy research is highly specialized, and ideally, we need licensed RNs — preferably with Oncology experience, and even better if they have Hematology/Oncology or research experience. This position will be onsite located in Midwest Chicago at the Advocate Aurora Research Institute. Hematology/Oncology Cellular Therapy Research.

Job Responsibility:

  • Coordinates the conduct of clinical research protocols/projects with an emphasis on the screening, enrolling, and monitoring of patient candidates/participants
  • Functions as a subject matter expert/resource within Education, Disease Conditions, Computer Applications, Leadership and/or Integration of Research within Clinical Programs

Requirements:

  • Bachelor's Degree in Nursing
  • Typically requires 5 years of experience in Clinical Research enrolling subjects, conducting subject study visits, maintaining source documents and entering data in multiple electronic data systems or critical care or ICU RN Experience
  • Knowledge of Good Clinical Practices, International Conference of Harmonization, FDA Guidance documents, Department of Health and Human Services regulations, standard operating procedures
  • Ability to successfully conduct and manage a research study
  • Ability to provide effective leadership, motivate others and work as a member of a diverse team
  • Ability to mentor staff and to prepare training plans
  • Excellent verbal and written communication skills, organizational and time management skills with ability to work under pressure and meet deadlines
  • Ability to problem solve and work independently with a high degree of accuracy and attention to detail
  • Must be able to establish a good rapport with patients, investigators and sponsors
  • Competency in using Electronic Medical Record (EMR), Microsoft Office Suite, and other computerized programs

Nice to have:

  • Clinical Research Coordinator (CCRC) certification issued by the Association of Clinical Research Professionals (ACRP) when eligible needs to be obtained within 1 year
  • Clinical Research Professional (CCRP) certification issued by the Society of Clinical Research Associates (SOCRA) needs to be obtained within 1 year
  • Oncology experience
  • Hematology/Oncology or research experience
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

Additional Information:

Job Posted:
February 08, 2026

Employment Type:
Fulltime
Work Type:
On-site work
Job Link Share:

Looking for more opportunities? Search for other job offers that match your skills and interests.

Briefcase Icon

Similar Jobs for Registered Nurse Senior Research Coordinator

Senior Research Nurse - Site Manager

This is an exciting opportunity to join EMS Healthcare as a Senior Research Nurs...
Location
Location
United Kingdom , West Kirby
Salary
Salary:
Not provided
ems-healthcare.com Logo
EMS Healthcare
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Registered Nurse with active NMC pin
  • Minimum 2 years’ experience in clinical research nursing
  • Experience supervising or mentoring staff
  • Experience delivering clinical trials in commercial, NHS, or academic settings
  • Strong understanding of ICH-GCP and clinical trial governance
  • Able to work independently, with strong problem-solving and time management skills
  • Comfortable working in a mobile or non-hospital research setting
  • Full UK residency and a valid driving licence
  • Ability to travel within Greater Manchester and surrounding areas if required
  • Willingness to work flexibly, including occasional early starts or late finishes
Job Responsibility
Job Responsibility
  • Lead the day-to-day running of the mobile clinical site, ensuring study delivery meets agreed timelines, quality, and regulatory standards
  • Supervise and support a team of research nurses and site coordinators, fostering a positive team environment and encouraging professional development
  • Act as the senior on-site clinician, providing direct care and support to study participants where required
  • Coordinate and maintain all site documentation, logs, and essential files in line with GCP and EMS SOPs
  • Act as primary liaison for on-site operational matters, escalating issues as required to the Clinical Research & Delivery Manager
  • Oversee scheduling of study visits, staff rotas, and site logistics to ensure smooth and efficient site operation
  • Deliver and/or facilitate protocol and site training for site staff
  • Support recruitment and retention strategies to ensure enrolment targets are met
  • Monitor and maintain high standards of participant care, infection control, and data integrity throughout the study
  • Attend and participate in site initiation visits, monitoring visits, and audits
What we offer
What we offer
  • Bank holidays, plus 25 days annual leave, increasing to 28 after 5 years
  • Buy & Sell Holidays
  • Enhanced Maternity and Paternity Leave
  • 1 Occasion Day each year
  • Healthshield
  • Cycle to Work Scheme
  • Tech Scheme
  • Electric Car Scheme
  • Subsidised company events and gatherings
  • A gift for your birthday
  • Fulltime
Read More
Arrow Right

Senior Research Nurse - Site Manager

This is an exciting opportunity to join EMS Healthcare as a Senior Research Nurs...
Location
Location
United Kingdom , Liverpool
Salary
Salary:
Not provided
ems-healthcare.com Logo
EMS Healthcare
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Registered Nurse with active NMC pin
  • Minimum 2 years’ experience in clinical research nursing
  • Experience supervising or mentoring staff
  • Experience delivering clinical trials in commercial, NHS, or academic settings
  • Strong understanding of ICH-GCP and clinical trial governance
  • Able to work independently, with strong problem-solving and time management skills
  • Comfortable working in a mobile or non-hospital research setting
  • Full UK residency and a valid driving licence
  • Ability to travel within Greater Manchester and surrounding areas if required
  • Willingness to work flexibly, including occasional early starts or late finishes
Job Responsibility
Job Responsibility
  • Lead the day-to-day running of the mobile clinical site, ensuring study delivery meets agreed timelines, quality, and regulatory standards
  • Supervise and support a team of research nurses and site coordinators, fostering a positive team environment and encouraging professional development
  • Act as the senior on-site clinician, providing direct care and support to study participants where required
  • Coordinate and maintain all site documentation, logs, and essential files in line with GCP and EMS SOPs
  • Act as primary liaison for on-site operational matters, escalating issues as required to the Clinical Research & Delivery Manager
  • Oversee scheduling of study visits, staff rotas, and site logistics to ensure smooth and efficient site operation
  • Deliver and/or facilitate protocol and site training for site staff
  • Support recruitment and retention strategies to ensure enrolment targets are met
  • Monitor and maintain high standards of participant care, infection control, and data integrity throughout the study
  • Attend and participate in site initiation visits, monitoring visits, and audits
What we offer
What we offer
  • Bank holidays, plus 25 days annual leave, increasing to 28 after 5 years
  • Buy & Sell Holidays
  • Enhanced Maternity and Paternity Leave
  • 1 Occasion Day each year
  • Healthshield
  • Cycle to Work Scheme
  • Tech Scheme
  • Electric Car Scheme
  • Subsidised company events and gatherings
  • Well being support from our qualified Mental Health First Aiders, as well as via our health scheme
  • Fulltime
Read More
Arrow Right

Oncology Research Nursing Professional

The Oncology Research Nursing Professional (ORNP) –is a Registered Nurse (RN) wh...
Location
Location
United States of America , Palo Alto
Salary
Salary:
83.98 - 111.27 USD / Hour
Stanford Health Care
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • BSN or higher-level nursing degree required
  • 5 plus years nursing experience required OR 3+ years in an oncology research nurse role required
  • 2 or more years of experience in oncology
  • California Registered Nurse (RN) license
  • American Heart Association Basic Life Support (BLS) certification
  • Ability to communicate vetted information at all levels of the organization
  • Ability to be highly- and multi- task focused while managing multiple tasks and projects simultaneously across various platforms
  • Ability to understand information flow and solve problems under pressure
  • Ability to manage conflict resolution
  • Ability to adapt and troubleshoot in a unique and quickly changing, fast-paced environment
Job Responsibility
Job Responsibility
  • Collaborates with the investigator and serves as lead on study patient screening, eligibility determination and enrollment assessments on assigned clinical trials
  • Uses independent judgement to assess, identify, and prioritize clinical information to physician, NP, PA and other clinicians for patients who are being evaluated and/or enrolled in a clinical trial
  • Assesses and documents signs and symptoms of illness, reactions to treatment, changes in physical or psychological condition and general appearance in accordance with the research protocol
  • Manage patient/family phone calls – collaborating with MD, NP and/or PA as needed to obtain orders for the management of the patient
  • Manages and communicates all aspects of care as defined by the research protocol with the physician and other health care professionals and research team members
  • Collaborates with CRC to assure that therapeutic clinical trial flag is placed on the patient during active treatment
  • Plans, coordinates, and completes randomization (if applicable), patient assessments (toxicity assessment, diagnostic tests, and questionnaires), treatments and follow up care according to the defined protocol treatment plan
  • Manages the consent process to ensure it is performed in compliance with institutional, FDA, IRB, clinical trial sponsor and other applicable regulations
  • Oversees and participates in the education of the patient regarding the clinical trial
  • Alerts principal investigator of any concerns raised by the patient during the informed consent process
  • Fulltime
Read More
Arrow Right

Senior Clinical Research Associate

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...
Location
Location
France , Paris Region
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree or Registered Nurse (RN) in a related field or equivalent combination of education, training, and experience
  • Networking and relationship building skills
  • Ability to communicate effectively and appropriately with internal and external stakeholders
  • Ability to adapt to changing technologies and processes
  • Excellent communication (verbal and written), presentation, and interpersonal skills
  • Identifies and builds effective relationships with investigator site staff and other stakeholders
  • Proficiency in local language is required
  • Advanced level or fluency in English is required
Job Responsibility
Job Responsibility
  • Responsible for data integrity, data quality and ensuring compliance with ICH GCP and local requirements at the site level
  • Monitoring will be conducted in line with the Study Monitoring Plan (SMP)
  • Collaborate with the Site Manager to assure that the site complies with the protocol and is inspection ready
  • Coordinate with institutions and investigators at the local level
  • Oversight of Monitoring Responsibilities and Study Conduct
  • Ensuring regulatory, ICH-GCP and protocol compliance
  • Uses judgment and experience to evaluate overall performance of site and site staff
  • Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company Standard Operating Procedures (SOPs)/processes
  • Verifies the process of obtaining informed consent has been adequately performed and documented for each subject
  • Demonstrates diligence in protecting the confidentiality of each subject and assesses factors that might affect subject safety and clinical data integrity
What we offer
What we offer
  • Patient-focused in everything we do
  • Supportive and inclusive environment
  • Career growth and development
  • Flexible work arrangements
  • Diverse therapeutic areas and project exposure
  • Advanced Technology
Read More
Arrow Right

Radiation Therapist Senior

The role is responsible for the provision of services in line with standards of ...
Location
Location
Ireland , Lucan, Co. Dublin
Salary
Salary:
Not provided
hermitageclinic.ie Logo
Blackrock Health Hermitage Clinic
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Possess appropriate qualification in Radiation Therapy: BSc Radiation Therapy
  • Be registered with the Radiographers Registration Board – CORU
  • Have satisfactory post qualification experience and have proven clinical expertise
  • Have experience of or be prepared to participate in research
Job Responsibility
Job Responsibility
  • Demonstrate evidence based practice through decision making and apply it to complex cases
  • Ensure that the Radiotherapy service delivered to patients meets professional and European standards of practice
  • Provide advice and support to Radiotherapy and multidisciplinary colleagues on clinical practice issues
  • Provide clinical leadership and instruction
  • Be accountable for the treatment unit
  • Maintain accurate information systems for clinical data in accordance with departmental and hospital policies
  • Conduct on treatment assessment of patients
  • Assessment of pre-treatment images and approval of verification images
  • In depth assessment of treatment plan
  • Final confirmation of radiotherapy treatment with specified time frame
What we offer
What we offer
  • An Education Support Programme
  • Family Friendly hours available
  • Development opportunities
  • Opportunities for career progression
  • Access to a Pension Scheme
  • Subsidised Restaurant
  • Free staff car parking
  • Employee Assistance Programme
  • Life Assurance
  • Fulltime
Read More
Arrow Right
New

Pediatric Speech Language Pathologist

Baptist Medical Center is currently looking to add a Speech Language Pathologist...
Location
Location
United States , Jacksonville
Salary
Salary:
Not provided
baptistjax.com Logo
Baptist Health (Florida)
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Master's Degree
  • 1 or more years of pediatric acute care experience strongly preferred
  • Speech/Language Experience
  • Voice Experience
  • Neuro Experience
  • Certificate of Clinical Competence in Speech-Language Pathology Required
  • Basic Life Support (BLS) Required
  • Licensed Speech Language Pathologist Required
  • Active BLS from the American Heart Association and licensure from the FL Department of Health required
Job Responsibility
Job Responsibility
  • Evaluates, diagnoses, develops and implements a treatment plan for patients of all diagnoses
  • Provides care for patients who present with a variety of medical conditions and deficits which impact communication, language development, oral motor skills, and feeding safety and efficiency
  • Provides extensive patient/family education
  • Participates in multidisciplinary team care with other rehab professionals, nursing, physicians, dietitians, social services, respiratory, support staff, etc.
  • Works in a fast-paced setting requiring good time management, detailed documentation skills in the EMR, self-directed, and effective communication skills
What we offer
What we offer
  • Up to $1,200 Sign on Bonus
  • Parttime
Read More
Arrow Right
New

Domino’s Delivery Driver

Join our delivery team and bring hot, fresh pizzas to our customers! Earn great ...
Location
Location
United Kingdom , Nottingham
Salary
Salary:
10.00 - 12.21 GBP / Hour
jobs.360resourcing.co.uk Logo
360 Resourcing Solutions
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Full UK or EU driving licence (max 6 points, no recent bans)
  • Own car with valid MOT and insurance
  • Availability for evenings and weekends (required)
  • A positive, can-do attitude and great customer service skills
  • Good local area knowledge
Job Responsibility
Job Responsibility
  • Represent Domino’s with a smile and deliver excellent customer service
  • Deliver products promptly and safely, following all safety procedures
  • Handle payments correctly and securely
  • Support your store team during quieter delivery periods
What we offer
What we offer
  • Flexible working hours to suit your lifestyle
  • Staff discount on all your favourite pizzas
  • Pension scheme
  • You keep all your tips!
  • Excellent training and career progression
Read More
Arrow Right
New

Enterprise Account Executive

This is not your average Account Executive role. At Sigma, we believe that peopl...
Location
Location
United States , San Francisco; New York City
Salary
Salary:
110000.00 USD / Year
sigmacomputing.com Logo
Sigma Computing
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Ideally two or more years of experience closing deals
  • Experience in the data analytics or BI space (Looker, Tableau, Domo, etc.) is preferred
  • Background in high-tech software sales is preferred
  • A track record of success in pipeline generation and quota attainment
  • Partnership and co-selling experience is preferred
  • Team player, hustler, all-around sales superstar
  • Must be based in the San Francisco Bay Area or New York City or be willing to relocate
Job Responsibility
Job Responsibility
  • Maintaining, creating, and updating accurate customer, pipeline, and forecast information in Salesforce
  • Using knowledge of the data and analytics space to interact with a diverse set of businesses in consultative sales
  • Owning your sales process — from first call to demo to proposal to proof of concept to contract
  • Working alongside a team of motivated reps on a high-functioning, energetic team
  • Bringing on new customers and developing advocates for Sigma in the business intelligence market
  • Engaging with partners in the data ecosystem to build pipeline or support specific customer needs and initiatives
  • Generating new revenue for a rapidly growing company
What we offer
What we offer
  • Equity
  • Generous health benefits
  • Flexible time off policy
  • Paid bonding time for all new parents
  • Traditional and Roth 401k
  • Commuter and FSA benefits
  • Lunch Program
  • Dog friendly office
  • Variable pay (based on goal achievement)
  • Stock options
  • Fulltime
Read More
Arrow Right