Laboratory Manager
$78.1k - $145.25kAdventHealth
Our Promise to You Joining UChicago Medicine AdventHealth is about being part of something bigger. It’s about belonging to a community that believes in the wholeness of each person, and serves to uplift others in body, mind and spirit. UChicago Medicine AdventHealth is a place where you can thrive professionally, and grow spiritually, by Extending the Healing Ministry of Christ. Where you will be valued for who you are and the unique experiences you bring to our purpose‑minded team. All while understanding that together we are even better. All the benefits and perks you need for you and your family Benefits from Day One: Medical, Dental, Vision Insurance, Life Insurance, Disability Insurance Paid Time Off from Day One 403‑B Retirement Plan 4 Weeks 100% Paid Parental Leave Career Development Whole Person Well‑being Resources Mental Health Resources and Support Pet Benefits Schedule and Location Schedule: Full time Shift: Day (United States of America) Address: 5101 WILLOW SPRINGS RD, LA GRANGE, Illinois, 60525 Job Description Other duties as assigned. Follows safety policies including the use of PPE, handwashing, and hazardous chemical handling, and completes required training for handling hazardous waste. May include transport of hazardous waste from the point of generation to a designated secure storage area; employee will be required to complete initial training (prior to handling hazardous waste) and refresher training to include proper handling and transport of hazardous waste, and proper selection, use and disposal of personal protective equipment. Provides orientation and training to new employees and medical technology students, documenting the process appropriately. Leads and participates in laboratory performance improvement activities, promoting team building, employee engagement, patient satisfaction, and safety. The expertise and experiences you’ll need to succeed Qualification Requirements: Bachelor’s (Required) Clinical Laboratory Supervisor (SU) – EV Accredited Issuing Body, Medical Laboratory Scientist MLS (ASCP) – EV Accredited Issuing Body, Medical Lab Scientist (MLSAMT) – EV Accredited Issuing Body, Medical Technologist (MTAAB) – EV Accredited Issuing Body Pay Range $78,100.78 – $145,253.04 This facility is an equal opportunity employer and complies with federal, state and local anti‑discrimination laws, regulations and ordinances. #J-18808-Ljbffr
- ...program. We are looking for candidates with prior clinical research experience who thrive in a fast-paced environment, can independently manage multiple studies, and are passionate about patient care and advancing clinical research. Responsibilities Coordinate and manage...SuggestedFull timeMonday to Friday
- ...regulations, and Loyola University policies. The role involves overall management and implementation of assigned research protocols across... ...specimens and processing. Collect and manage patient and laboratory data; maintain research project databases and develop study documents...SuggestedFull timeWork experience placementWork at officeLocal area
- ...participants according to inclusion and exclusion criteria. Coordinate collection of study specimens and processing. Collect and manage patient and laboratory data for clinical research projects. Manage research project databases, develop flow sheets and other study related...SuggestedFull timeWork experience placementLocal area
$31 per hour
...Clinical Research Coordinator II is responsible for the overall management and implementation of an assigned set of multiple research... ...study specimens and processing. Collects and manages patient and laboratory data for clinical research projects. Manages research project...SuggestedHourly payFull timeWork experience placementLocal area- ...Clinical Research Coordinator II is responsible for the overall management and implementation of an assigned set of multiple research... ...study specimens and processing. Collect and manage patient and laboratory data, manage research project databases, develop flow sheets and...SuggestedWork experience placementLocal area
- ...criteria using clinical judgment and protocol knowledge. Coordinate collection and processing of study specimens. Collect and manage patient and laboratory data for clinical research projects; manage research project databases, develop flow sheets and other study documents,...Full timeWork experience placementLocal area
$28 per hour
...Clinical Research Coordinator I is responsible for the overall management and implementation of an assigned set of multiple research... ...study specimens and processing. Collect and manage patient and laboratory data for clinical research projects. Manage research project...Hourly payFull timeWork experience placementWork at officeLocal area$28 - $40 per hour
...and patient privacy requirements. Training in Good Clinical Practice (GCP). Strong organizational skills with the ability to manage multiple tasks and timelines. Ability to engage confidently and professionally with participants and research staff. High attention...Full timeContract workTemporary workMonday to Friday- ...Clinical Research Coordinator I (CRC) reports to the Regional Manager and is responsible for coordinating and implementing assigned... ...medical history and medication lists Phlebotomy and basic laboratory tests Processing & shipping labs for central and local labs...Private practiceWork at officeLocal area
$25 - $35 per hour
...clinical trial. This contractor will function as one of the primary CRCs for the study and must be able to work independently while managing multiple study activities. The ideal candidate has hands-on clinical research experience, strong organizational skills, and the...Contract workTemporary workFor contractorsImmediate start$23.32 - $43.37 per hour
...] Exhibits technical skills and aptitudes related to specific laboratory specimen collections as performed in department or work area assigned... ...or Equiv [Required] Work Experience 1+ years of leadership/management experience 2+ years of related laboratory experience [Required...Full timeWork experience placementLocal areaShift work- ...About the job Medical Laboratory Manager Our client is a rapidly growing, Chicago-based clinical laboratory and we're driven to set a new standard in healthcare for patient care and customer support. This means developing the most efficient processes, monitoring...
$94.4k - $293.8k
...edge technology. We help our clients envision and achieve Digital Laboratory Transformation through co-creation and application of digital... ...scientific user experience to help our clients better capture, manage, integrate, and analyze complex scientific data. We help...Live inWork at officeLocal area- ...Job Description Be a part of a world-class academic healthcare system, UChicago Medicine , as a Laboratory Manager in the Clinical Microbiology and Immunology Laboratory department. Here, you will be responsible for planning, organizing, and managing all technical...Full timeLocal areaRelocation packageShift workDay shift
- Revival Research Institute, LLC is looking for a full-time Clinical Research Coordinator in Elgin, Illinois. The ideal candidate will have a background in clinical research, organizational skills, and a strong desire to learn. This entry-level position offers room for ...Full time
$70k - $85k
...The Biological Sciences Division at the University of Chicago is looking for a Senior Clinical Research Coordinator to manage complex clinical trial activities. This role includes oversight of compliance, coordination of data collection, and acting as a liaison within...$26 - $43 per hour
...interpersonal skills to work in a team environment Working Conditions and Environment: • Work is performed in an office/ laboratory and/or a clinical environment. • Exposure to biological fluids with potential exposure to infectious organisms. • Exposure to...Hourly payTemporary workWork at office- ...cities but not limited to: Chicago, Illinois; Minneapolis, Minnesota; Dallas, Texas; Houston, Texas; Austin, Texas. The Clinical Trial Manager (CTM) is responsible for oversight and management of all clinical operational activities at the trial and site level. The CTM will...Work experience placementWork at officeLocal areaRemote workRelocationShift work
- ...Research Assistant – Job Description Manage the front desk including reception/screening/scheduling/reminder calls. Provide assistance to research site staff by organizing files, projects, data, etc. Provide general office management to keep operations running smoothly...Interim roleInternshipWork at office
- Clinical Research Coordinator (Full‑time) We are seeking a full‑time Clinical Research Coordinator with a minimum of 1 year of clinical experience. Someone with a strong interest in the clinical research field would be an excellent fit for our entry–level position, with...Full timeWork at office
$46.28k - $75.67k
...monitoring, and close‑out visits; attend investigator meetings as needed. Assist with literature searches, QA/AC procedures, and data management tasks such as coding, updating spreadsheets, and importing/exporting data. Perform other job functions as assigned....Flexible hours$60k - $75k
...to follow the clinical protocol. While the Principal Investigator is primarily responsible for the overall design, conduct, and management of clinical trials, the CRC2 is delegated to perform study related tasks across the life cycle of the study. The CRC2 plays a critical...Work experience placementWork at office$60k - $75k
...PI) and under the direction of a departmental or lab research manager. While the Principal Investigator is primarily responsible for... ...Collects, processes, ships and stores specimens to appropriate laboratory according to established aseptic techniques. Identifies and...Contract workWork experience placementWork at office- ...a specialized researcher partnering with the clinical Principal Investigator (PI) and under the direction of the Clinical Research Manager within the Section of Gastroenterology in the Department of Medicine. While the Principal Investigator is primarily responsible for...Full timeWork experience placement
- ...A leading research university in Chicago is seeking a Clinical Research Coordinator I to manage multiple research protocols, ensuring compliance with clinical guidelines and regulations. The role involves working closely with participants, collecting data, and coordinating...
- ...specific required certification for participating study staff. Manage all clinical trial patients enrolled in studies, discuss protocols... ...team player working with physicians, nurses, non‑clinical, laboratory and ancillary staff Capability to meet data deadlines and maintain...Temporary workInterim roleLocal area
- ...and other research visit needs.] Collects AE’s, SAE’s, concomitant medication, and other relevant medical data needed per protocols Manages research workflow components, collects, prepares, processes, and submits participant data and samples to appropriate entities,...Contract workWork experience placementMonday to Friday
$49.92k - $81.62k
...administrative data tasks varies according to the specific requirements of each research program.**Essential Job Functions:*** Coordinates and manages the initiation and regulatory compliance of clinical research studies, including preparing all necessary documents for IRB and...Hourly payFull timePart time- ...Senior Clinical Project Manager (Chicago, IL) Responsibilities Contribute to our cutting-edge radiopharmaceutical development program Conceptualize, plan, design, place, execute, and summarize clinical trials Drive daily vendor and site management, including collaboration...Work at office
- ...strive for an environment in which inclusiveness drives productivity and results. Some responsibilities will include coordinating and managing multiple studies. They are also responsible for assisting the Principal Investigators and other clinical staff with any study...Work at office
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