Top 24 Clinical research Jobs in Joliet Il

Clinical Research Coordinator
Northwestern Memorial Healthcare —Winfield, IL
- $28.55 - $41.40 an hour
- Full-time
- Background check
- Hospital
- Customer service
- Tuition reimbursement
- 401(k) matching
Quick Apply
3d
GWTG-Heart Failure Data Abstractor: Part-Time
Carta Healthcare —Chicago Ridge, IL
- Part-time
- Remote
- US work authorization
- 1 year
- Entry level
- Flexible schedule
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Clinical Research Coordinator
Genesis Orthopedics & Sports Medicine —Oak Brook, IL
- Full-time
- Mid-level
- In-person
- Communication skills
- Opportunities for advancement
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Sr. Clinical Research Coordinator
The University of Chicago —Orland Park, IL
- $70,000 - $85,000 a year
- Full-time
- Background check
- Microsoft Outlook
- 5 years
- Health insurance
- Paid time off
Study Coordinator
Hematogenix Laboratory Sv —Tinley Park, IL
- Full-time
- Bachelor of Science
- Writing skills
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
Clinical Trial Operations Consultant
Cloudbyz —Naperville, IL
- Full-time
- Nursing
- 7 years
- Master's degree
Clinical Project Manager
Hematogenix Laboratory Sv —Tinley Park, IL
- Full-time
- Bachelor of Science
- Mid-level
- 2 years
- Health insurance
- Dental insurance
Quick Apply
Clinical Research Assistant
Illinois Institute of Technology —Bedford Park, IL
- $50,000 - $52,000 a year
- Full-time
- Bachelor of Science
- Analysis skills
- Entry level
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Project Manager
Deciphex —Naperville, IL
- Full-time
- Hybrid work
- Computer literacy
- Mid-level
- Team management
- Opportunities for advancement
Quick Apply
9d
Clinical Research Health Professional
Illinois Institute of Technology —Bedford Park, IL
- $30 an hour
- Part-time
- Mid-level
- 2 years
Quick Apply
Team Lead, Site Operations (Oncology)
ICON Plc —Downers Grove, IL
- $68,616 - $85,770 a year
- Full-time
- Customer service
- Mid-level
- Supervising experience
- Disability insurance
- Health insurance
Medical Assistant
Nephrology Associates of Northern Illinois and Indiana —Westmont, IL
- $18 - $20 an hour
- Full-time
- Patient monitoring
- High school diploma or GED
- Data entry
- Health insurance
- Dental insurance
Quick Apply
Orthopedic APP Clinical Fellowship (Non-Accredited)
Genesis Orthopedics & Sports Medicine —Oak Brook, IL
- Weekends as needed
- Surgery
- BC/BE
- Inpatient
- Paid training
- Disability insurance
Quick Apply
Post Doctoral Fellow, Neuropharmacology- IL- Precision Medicine Program
Midwestern University —Downers Grove, IL
- $61,008 a year
- Full-time
- Microsoft Word
- Microsoft Outlook
- Addiction Medicine
- Paid holidays
- Disability insurance
Post Doctoral Fellow- IL- Physiology
Midwestern University —Downers Grove, IL
- $63,480 a year
- Full-time
- Microsoft Outlook
- Addiction Medicine
- Computer literacy
- Paid holidays
- Disability insurance
Vice President Service Line Clinical Administration Division IL
Advocate Aurora Health —Oak Brook, IL
- Weekends as needed
- Medicine
- BC/BE
- Organizational skills
Post Doctoral Fellow- IL- Pharmacy Practice
Midwestern University —Downers Grove, IL
- Full-time
- Microsoft Outlook
- Computer literacy
- Maintenance
- Paid holidays
- Disability insurance
Medical Assistant - Bilingual
Midwest Allergy Inc —Westchester, IL
- $17.00 - $17.50 an hour
- Full-time
- Spanish
- Vital signs
- Computer literacy
Quick Apply

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Clinical Research Coordinator

Northwestern Memorial Healthcare -
Winfield, IL

Quick Apply

Job Details

Full-time
$28.55 - $41.40 an hour
3 days ago

Benefits

Tuition reimbursement
401(k) matching
Loan forgiveness

Qualifications

Computer operation
Direct patient care
Customer communication
Customer service
Research project coordination
Clinical quality assurance standards
Patient treatment

Full Job Description

Company Description

At Northwestern Medicine, every patient interaction makes a difference in cultivating a positive workplace. This patient-first approach is what sets us apart as a leader in the healthcare industry. As an integral part of our team, you'll have the opportunity to join our quest for better health care, no matter where you work within the Northwestern Medicine system. We pride ourselves on providing competitive benefits: from tuition reimbursement and loan forgiveness to 401(k) matching and lifecycle benefits, our goal is to take care of our employees. Ready to join our quest for better?

Job Description

The Clinical Research Coordinator reflects the mission, vision, and values of NM, adheres to the organization’s Code of Ethics and Corporate Compliance Program, and complies with all relevant policies, procedures, guidelines and all other regulatory and accreditation standards.

The Clinical Research Coordinator is a clinically competent professional responsible for all aspects of coordinating a clinical trial as delegated by the Principal Investigator under all applicable policies, procedures and regulations.

Responsibilities:

Facilitates, maintains, and coordinates the logistical aspects of assigned study protocols with other research staff in accordance with Good Clinical Practice, standard operating procedures and sponsor requirements.
Provides direct patient care pursuant to a study protocol including dispensation of investigational medications and performance of study tests under the delegation and direction of the principal investigator or supervising physician.
Attends investigator's meetings, coordinates and attends pre-study site visits, study initiation visits, and all other study-related visits by Monitors or Sponsor representatives, when required.
Arranges for procedures and necessary visits performed by external vendors that are necessary to the conduct of the study.
Schedules and leads in-house protocol meetings to review study-related procedures, staffing and visit flow.
Schedules and coordinates all medical needs and coverage for protocol related procedures.
Maintains and documents all study-related communication including, but not limited to the principal investigator or supervising physician, study subjects, Sponsor or Sponsor representative(s) and IRB throughout the clinical trial.
Responsible for giving subject instructions for study participation and serves as the primary contact for subjects by being available to handle study-specific questions, concerns, or events.
Ensures all protocol procedures are completed per study requirements.
Obtains and documents all adverse event data on appropriate forms and reports adverse event data to the appropriate parties as outlined by the study protocol, regulations and applicable policies and procedures.
Assures quality and completeness of source documents collected during the course of the study to assist with overall principal investigator review and approval.
Ensures accurate, complete and timely data entry into CRFs using 100% source documentation verification to assist with overall principal investigator review and approval.
Schedules, leads and assists with all study-related visits on site and is readily available during visits for applicable corrections, questions, or other study-related or site needs.
Supervises document retention, security and destruction, where applicable.
Responsible for completing all necessary training for the position, including study protocol specific training and Health System policies and procedures.
Trains other study specific research staff in collection and reporting of required data, where applicable.
Maintains research files, designs forms as needed, reports findings as appropriate, assists in preparation or review of material for submission to an IRB including reviewing and editing protocols and consent documents, where applicable.
Performs all other functions as related to this job and assigned.
Ability to travel between hospital locations where research is conducted.

Qualifications

Required:

Bachelor’s Degree in related field or equivalent experience in in lieu of a degree.
Two years’ experience in managing all aspects of clinical research trials with in-depth knowledge of protocol requirements and Good Clinical Practice.
Intermediate computer and internet knowledge.
Excellent customer service and patient care skills.
Meticulous organizational skills.
Excellent demonstrated written and verbal communication abilities.

Preferred:

Three to Five years’ experience in clinical research trials.
ACRP or SOCRA certification.

Additional Information

Northwestern Medicine is an equal opportunity employer (disability, VETS) and does not discriminate in hiring or employment on the basis of age, sex, race, color, religion, national origin, gender identity, veteran status, disability, sexual orientation or any other protected status.

Background Check

Northwestern Medicine conducts a background check that includes criminal history on newly hired team members and, at times, internal transfers. If you are offered a position with us, you will be required to complete an authorization and disclosure form that gives Northwestern Medicine permission to run the background check. Results are evaluated on a case-by-case basis, and we follow all local, state, and federal laws, including the Illinois Health Care Worker Background Check Act.

Artificial Intelligence Disclosure

Artificial Intelligence (AI) tools may be used in some portions of the candidate review process for this position, however, all employment decisions will be made by a person.

Benefits

We offer a wide range of benefits that provide employees with tools and resources to improve their physical, emotional, and financial well-being while providing protection for unexpected life events. Please visit our Benefits section to learn more.

Sign-on Bonus Eligibility (if sign-on bonus offered for position): Internal employees and rehires who left Northwestern Medicine within 1 year are not eligible for the sign on bonus. Exception: New graduate internal employees seeking their first licensed clinical position at NM may be eligible depending upon the job family.

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Refine Your Search

clinical research jobs in joliet il

Clinical Research Coordinator

GWTG-Heart Failure Data Abstractor: Part-Time

Clinical Research Coordinator

Sr. Clinical Research Coordinator

Study Coordinator

Clinical Trial Operations Consultant

Clinical Project Manager

Clinical Research Assistant

Project Manager

Clinical Research Health Professional

Team Lead, Site Operations (Oncology)

Medical Assistant

Orthopedic APP Clinical Fellowship (Non-Accredited)

Post Doctoral Fellow, Neuropharmacology- IL- Precision Medicine Program

Post Doctoral Fellow- IL- Physiology

Vice President Service Line Clinical Administration Division IL

Post Doctoral Fellow- IL- Pharmacy Practice

Medical Assistant - Bilingual

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