Current jobs related to Senior Clinical Research Coordinator - Chicago - Medasource


  • Chicago, Illinois, United States Pillar Clinical Research LLC Full time

    Job SummaryThe Licensed Practical Nurse (LPN) at Pillar Clinical Research LLC is responsible for providing high-quality patient care and supporting the implementation of clinical trials in our inpatient research unit. As a key member of our research team, you will work closely with physicians, nurses, and study coordinators to ensure seamless patient care...


  • chicago, United States US Tech Solutions Full time

    Duration: 12 Months (Possibility of extension)Job Description:The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of clinical trials, recruiting and screening study participants, as well as documenting and reporting on the daily operations of assigned trials. Working in collaboration with the...


  • chicago, United States US Tech Solutions Full time

    Duration: 12 Months (Possibility of extension)Job Description:The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of clinical trials, recruiting and screening study participants, as well as documenting and reporting on the daily operations of assigned trials. Working in collaboration with the...


  • Chicago, United States US Tech Solutions Full time

    Duration: 12 Months (Possibility of extension)Job Description:The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of clinical trials, recruiting and screening study participants, as well as documenting and reporting on the daily operations of assigned trials. Working in collaboration with the...


  • Chicago, Illinois, United States Aquent Full time

    Job Title: Clinical Research CoordinatorJob Summary:Aquent Talent is seeking a highly skilled Clinical Research Coordinator to join our team. As a Clinical Research Coordinator, you will be responsible for managing clinical research studies, adhering to Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs), study protocols, clinical trial...


  • Chicago, Illinois, United States Northwestern University Full time

    Job Summary:As a Clinical Research Coordinator Associate at Northwestern University, you will play a vital role in coordinating non-therapeutic clinical research protocols with direction from the Principal Investigator and/or senior staff in compliance with regulatory laws and institutional guidelines. This position requires strong organizational and...


  • Chicago, United States Aquent Full time

    Job Title: Clinical Research CoordinatorClient Location: Several Onsite locations throughout the US hiring, Chicago, IL Starting: 06/17/2024Salary/Pay Rate: Firm, non-negotiable: NoHours: Full-timeDuration: June 2025Job Description:Our client is seeking a Clinical Research Coordinator to work onsite at their Chicago, IL location.Responsibilities:•...


  • Chicago, Illinois, United States Northwestern University Full time

    Job Summary:**Coordinate Clinical Research Protocols**We are seeking a highly organized and detail-oriented Clinical Research Coordinator Associate to join our team at Northwestern University. The successful candidate will be responsible for coordinating non-therapeutic clinical research protocols with direction from the Principal Investigator and/or senior...


  • Chicago, Illinois, United States Aquent Full time

    Job Title: Clinical Research CoordinatorWe are seeking a highly skilled Clinical Research Coordinator to join our team at Aquent Talent. As a Clinical Research Coordinator, you will be responsible for managing clinical research studies and ensuring compliance with Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs), study protocols, clinical...


  • Chicago, Illinois, United States Aquent Full time

    Job Title: Clinical Research CoordinatorWe are seeking a highly skilled Clinical Research Coordinator to join our team at Aquent Talent. As a Clinical Research Coordinator, you will be responsible for managing clinical research studies and ensuring compliance with Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs), study protocols, clinical...


  • Chicago, Illinois, United States Professional Case Management Full time

    Clinical Research Coordinator **About the Role** At Professional Case Management, we are seeking a skilled Clinical Research Coordinator to join our team. As a Clinical Research Coordinator, you will play a vital role in supporting our mission to deliver care and services that enhance the quality of life of our clients. **Key Responsibilities** * Assist...


  • Chicago, Illinois, United States Northwestern University Full time

    Position OverviewDepartment: MED-Cancer CenterSalary/Grade: EXS/5Role Summary:As a Clinical Research Associate Coordinator, you will be responsible for managing non-invasive clinical research protocols under the guidance of the Principal Investigator and senior team members, ensuring adherence to regulatory standards and institutional policies. You may also...


  • Chicago, Illinois, United States Advanced Clinical Full time

    Senior Program Manager Job DescriptionAt Advanced Clinical, we are seeking a highly skilled Senior Program Manager to join our team. As a Senior Program Manager, you will be responsible for leading and implementing flexible staffing initiatives for our clients, ensuring their needs and expectations are met and exceeded.Key Responsibilities:Develop and...


  • Chicago, United States RPM ReSearch Full time

    Job DescriptionJob DescriptionSenior Manager Microbiology, Research, and Product DevelopmentThe Senior Manager Microbiology, Research has the ability to work in both existing and emerging topical anti-infective technologies and the ability to lead a microbiology group across other medical device applications. This role has responsibility for the scientific,...


  • Chicago, United States ECN Operating LLC Full time

    Job DescriptionJob DescriptionJob Title: Clinical Research CoordinatorDepartment: Site Operations Reports To: Site ManagerLocation: MetroMed Clinical ResearchStatus: Non-exempt (hourly)Compensation: $16.00 - $18.00 Position Summary: We are seeking a reliable and experienced Clinical Research Coordinator to join our growing team at Elite Clinical Network....


  • Chicago, Illinois, United States RPM ReSearch Full time

    Job DescriptionJob SummaryRPM ReSearch is seeking a highly experienced Senior Manager Microbiology, Research and Development to lead our microbiology research efforts. As a key member of our research team, you will be responsible for planning, resource allocation, and management of R&D Microbiology efforts to support our product development and...


  • Chicago, Illinois, United States Professional Case Management Full time

    Job OverviewAbout Professional Case ManagementProfessional Case Management is a dynamic organization dedicated to delivering exceptional care and services to our clients. Our team is passionate about making a difference in the lives of others, and we're seeking a skilled Clinical Research Coordinator to join our Clinical Research division.Key...


  • Chicago, Illinois, United States Northwestern University Full time

    Job Summary:As a Clinical Research Coordinator at Northwestern University, you will play a vital role in the success of our clinical research studies. Your primary responsibility will be to coordinate and manage the day-to-day activities of clinical research trials, ensuring that all studies are conducted in accordance with established protocols and...


  • Chicago, Illinois, United States Northwestern University Full time

    Job Summary:**Coordinate Clinical Research Protocols**We are seeking a highly organized and detail-oriented Clinical Research Coordinator Associate to join our team at Northwestern University. The successful candidate will be responsible for coordinating non-therapeutic clinical research protocols, working closely with the Principal Investigator and senior...


  • Chicago, Illinois, United States Aquent Full time

    About the RoleWe are seeking a highly skilled Clinical Research Coordinator to join our team at Aquent. As a key member of our research team, you will be responsible for managing clinical research studies and ensuring compliance with regulatory requirements.Key ResponsibilitiesManage clinical research studies, including participant recruitment, consent, and...

Senior Clinical Research Coordinator

4 months ago


Chicago, United States Medasource Full time

Tite: Senior Clinical Research Coordinator

Type: 6 month CTH

Years Experience: 5 years of Oncology research experience preferred

Education: Master's or Bachelor's degree required

Location: Lincoln Park area - Chicago, IL

Summary:

Schedule Details/Additional Information:

  • No on-call, no weekends, no holidays
  • Flexibility to stay later based on patient visit and lab schedules, may be asked to cover other sites.

Degrees:

  • Bachelor's Degree (or equivalent knowledge) in Nursing (PREFERRED) OR
  • Bachelor's Degree in Biology or Health science

Major Responsibilities:

  • Performs clinical and administrative coordination of sponsored clinical trials, research protocols/projects, and biospecimen collection studies, as applicable. Provides guidance to physicians, clinical staff and research team members.
  • Coordinates assigned research studies in collaboration with other team members and key stakeholders, including but not limited to; study start-up, review of study CTA/budget/CTMS, IRB submissions, recruitment, screening, and enrollment of research subjects, development of mechanisms to maximize subject adherence to the research protocol, maintain source documentation, data collection (i.e. development, completion and submission of case report forms (EDC), study drug/device accountability, monitoring of subjects, AE/SAE reporting, study close out, and facilitates quality assurance inspections and audits. Acts as a liaison between sponsor and investigators and as the primary protocol/project contact for team members and clinical staff.
  • Plans, develops and implements educational plans to disseminate protocol/project information with research staff, investigators and clinical staff. Reviews protocol amendments and updates, research related orders (in collaboration with Investigational Drug Services), and study-specific workflows.
  • Ensures that laboratory requirements are being met for specimen procurement, proper collection, processing and shipment of specimens.
  • Serves as Primary Research Coordinator on studies across multiple sites guiding research team members involved in the study and coordinates and tracks research activities across sites.
  • Coaches and mentors research team members and other personnel. Assist with implementation of educational training plans including orientation.
  • Maintains competency in research computer applications Attends and participates in educational programs, meetings, and assigned committees.
  • Licensed nurses will utilize advanced assessment skills to identify patient care problems, provide professional nursing care to research patients and support Research Coordinators in performing nursing activities as needed.

Experience Required:

  • 5 years of experience in Oncology Research.

Knowledge, Skills & Abilities Required:

  • 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 mentor team members 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

Physical Requirements and Working Conditions:

  • Must be able to sit, stand, walk, lift, squat, bend, reach above shoulders and twist throughout shift.
  • Must have functional sight and hearing.
  • Ability to function in a latex environment.
  • May be exposed to mechanical, electrical, chemical, and radiation hazards as well as blood and body fluids on a continuous basis; therefore, protective clothing (i.e., gown, mask, goggles, gloves, etc.) must be worn as necessary.
  • Exposed to a normal office environment.
  • Operates all equipment necessary to perform the job.
  • Position may require travel among sites and therefore there is exposure to road and weather conditions.