Laboratory Manager
Cleveland Clinic
Laboratory Manager
Join Cleveland Clinic Mercy Hospital and experience world-class healthcare at its best. Officially becoming a full member of the Cleveland Clinic Health System in 2021, Mercy Hospital offers a wide variety of medical specialties to the communities in and around Stark County. Here, you will work alongside passionate and dedicated caregivers, receive endless support and appreciation, and build a rewarding career with one of the most respected healthcare organizations in the world.
A Laboratory Manager is responsible for the technical and scientific oversight of the laboratory, including day-to-day operations, supervision of personnel performing testing, and the accuracy and timeliness of test result reporting.
A caregiver in this position works days from 8:00AM – 5:00PM.
A caregiver who excels in this role will:
- Participate in verifying test procedures performed and establishing laboratory's test performance characteristics, including the precision and accuracy of each test and test system
- Ensure enrollment and participation in an HHS approved proficiency testing program commensurate with the services offered.
- Establish a quality control program appropriate for the testing performed, establish the parameters for acceptable levels of analytic performance and ensure that these levels are maintained throughout the entire testing process from the initial receipt of the specimen, through sample analysis and reporting of test results.
- Resolve technical and operational problems and ensure that remedial actions are taken whenever test systems deviate from the laboratory's established performance specifications.
- Ensure that patient test results are not reported until all corrective actions have been taken and the test system is functioning properly.
- Identify training needs and ensure that every performing tests receives regular in-service training and education appropriate for the type and complexity of the laboratory services performed.
- Evaluate the competency of all testing personnel and assure that the staff maintain their competency to perform test procedures and report test results promptly, accurately and proficiently.
- Ensure the competency of testing personnel in areas of responsibility i.e. moderately complexity and/or high complexity testing.
- Ensure that the staff maintain their competency to perform test procedures and report test results promptly, accurately and proficiently.
- Evaluate and document competency assessment of testing personnel in laboratory area of responsibility at least semiannually during the first year the testing personnel tests patient specimens and annually thereafter.
Minimum qualifications for the ideal future caregiver include:
- Pattern I: In areas that support Clinical Pathology:
- Bachelor's degree in a chemical, biological, clinical or medical laboratory science, or medical technology from an accredited institution
- 5 years of clinical laboratory training or experience, or both, in high complexity testing
- 3 years of clinical laboratory management or supervisory experience
- Laboratory training or experience and can be met by any combination of years of clinical laboratory training or experience
- Clinical laboratory training or experience can be met by:
- Medical technology internship
- Full time experience performing non-waived testing for the required number of years
- Part-time experience performing non-waived testing, with 2080 hours equivalent to one year.
- In areas that support Anatomic Pathology (depending on department):
- Bachelor's degree from a four-year college or university
- Education and training equivalent to meet ASCP Board of certification qualifications for Histotechnologist (HTL)
- OR
- Education and training equivalent to meet ASCP Board of Certification qualifications for Cytotechnologist (CT)
- AND
- Meets the requirements and training of a Cytotechnologist (CT) as dictated by most current CLIA regulations.
- Diploma and/or transcripts must be provided
- Education will be verified
- Education outside of the United States requires diploma/transcripts translated into English and proof of foreign equivalency from a NACES (National Association Credential Evaluation Services, Inc) member
Physical Requirements:
- Visual acuity to study specimens under a microscope.
- The ability to distinguish colors.
- Fine motor skills and manual dexterity to handle specimens and lab equipment required to process specimens and repair equipment.
- May be required to stand for long periods of time.
- Light lifting may be required.
- May be exposed to hazardous chemicals, biohazards, radioactive materials, etc.
Personal Protective Equipment:
- Follows standard precautions using personal protective equipment as required.
The policy of Cleveland Clinic Health System and its system hospitals (Cleveland Clinic Health System) is to provide equal opportunity to all of our caregivers and applicants for employment in our drug free environment. All offers of employment are followed by testing for controlled substances.
Cleveland Clinic Health System administers an influenza prevention program. You will be required to comply with this program, which will include obtaining an influenza vaccination on an annual basis or obtaining an approved exemption.
Decisions concerning employment, transfers and promotions are made upon the basis of the best qualified candidate without regard to color, race, religion, national origin, age, sex, sexual orientation, marital status, ancestry, status as a disabled or Vietnam era veteran or any other characteristic protected by law. Information provided on this application may be shared with any Cleveland Clinic Health System facility.
If applying for a Florida position, please see the following website for more information on the background screening requirements required by the Agency of Health Care Administration:
Please review the Equal Employment Opportunity poster.
Cleveland Clinic is pleased to be an equal employment opportunity employer.
$83.4k - $108.42k
...Description The Clinical Research Supervisor oversees daily supervision of clinical research staff and provides support to Research Manager / Director and Principal Investigator of designated research projects. He/she performs functions required by the research protocols...SuggestedWork at office- ...cancer therapies. Excellent communication - verbal and written, interpersonal and organizational skills, and a collaborative management style. Ability to effectively communicate and interact with physicians and other clinical staff. Ability to engage in critical...SuggestedFull timeWork at officeLocal areaWorldwide
- ...entry-level clinical research professional that has a foundation in clinical research through assigned responsibilities in data management or implementing clinical research protocols. The incumbent is responsible for simple clinical research protocols and timelines.CORE...SuggestedFull timeTemporary workWork at officeLocal areaWorldwide
$25 per hour
...consent, and potential risks/benefits. Study Operations & Data Management Organize and maintain all clinical trial documentation and... ...sponsors, and study monitors. Track and manage study supplies, laboratory kits, and equipment inventory. Assist in organizing investigator...SuggestedHourly payFull timeWork at officeMonday to FridayFlexible hours- ...implementation of multiple complex clinical research protocols. Develops SOPs and templates with guidance from the PI/Clinical Research Manager. Oversees and facilitates eligibility screening and study recruitment activities; implements strategies to increase accrual....SuggestedFull timeLocal areaNight shiftWeekend workAfternoon shift
- ...providing leadership in the planning, implementing, monitoring, and evaluating of multiple clinical research protocols. This role manages multiple studies’ daily operations, carries out study coordination duties from protocol development and initiation to study close-out...Full timeLocal area
- ...providing leadership in the planning, implementing, monitoring, and evaluating of multiple clinical research protocols. This role manages multiple studies' daily operations, carries out study coordination duties from protocol development and initiation to study close-out...Full timeTemporary workLocal areaWorldwide
- ...in clinical research through assigned responsibilities in data management or implementing clinical research protocols. This role... ...support with study related procedures as required, i.e., EKG, laboratory and tumor assessment studies. Ensures timely IRB submissions...Full timeTemporary workWork at officeLocal areaWorldwideNight shiftWeekend workAfternoon shift
$59.83k - $99.96k
...ensure consistency among staff across all participating sites. Leading Meetings: The hired candidate will take a leadership role in managing project meetings for the Duke site as well as larger, cross-site meetings. They will work closely with project leadership to...For contractorsWork experience placementRemote workWorldwide- ...Coordinator is responsible for the overall coordination, organization, management, and efficient implementation of clinical trials. The CRC... ...medical terminology to communicate with physician office and laboratory staff. Demonstrate the initiative to act independently,...Work at office
- ...‑level clinical research professional that has a basic foundation in clinical research through assigned responsibilities in data management or implementing clinical research protocols. This role exhibits increased learned skills and flexibility in performing duties, and...Full timeLocal areaNight shiftWeekend workAfternoon shift
- ## Clinical Research CoordinatorApplylocations: Miami Beach, FLtime type: Full timeposted on: Posted Yesterdayjob requisition id: JR102403**As Mount Sinai grows, so does our legacy in high-quality health care.**Since 1949, Mount Sinai Medical Center has remained committed...
- ...The Clinical Research Coordinator will perform and manage tasks that are critical to clinical research studies. The Clinical Research... ...effectively with study sponsors, CROs, monitors/CRA's, IRBs, laboratories, and clinical personnel within the research industry. Be...Contract workWork at officeFlexible hours
- Current Employees: If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click here to log in to Workday to use the internal application process. To learn how to apply for a faculty or staff position, please review this tip sheet...Full timeTemporary workPart timeWorldwideNight shiftWeekend workAfternoon shift
- Clinical Research Coordinator 2 (A) The Surgery department has an exciting opportunity for a Clinical Research Coordinator 2 (A) position. The incumbent serves as a mid-level clinical research professional that assists in the planning, coordinating, implementing, monitoring...Full timeLocal area
- Clinical Research Coordinator 2 The University of Miami, Bascom Palmer Eye Institute, has an exciting full time opportunity for a Clinical Research Coordinator 2 in Miami, Florida. The Clinical Research Coordinator 2 serves as a mid-level clinical research professional...Full timeWork at officeLocal areaWorldwide
- Clinical Research Coordinator 2 The Bascom Palmer Eye Institute is currently seeking a full time Clinical Research Coordinator 2 to work at the McKnight Vision Research Center in Miami. The Clinical Research Coordinator 2 serves as a mid-level clinical research professional...Full timeLocal areaNight shiftWeekend workAfternoon shift
- ...Sr. Clinical Research Coordinator - Neurology - Onsite (Full Time, Days) Under direction of the Senior Manager of Clinical Trial Operations, the Senior Clinical Research Coordinator, CTO (SCRC) works independently on complex projects/assignments and manages and conducts...Full timeWork at officeFlexible hours
- ...entry-level clinical research professional that has a foundation in clinical research through assigned responsibilities in data management or implementing clinical research protocols. The incumbent is responsible for simple clinical research protocols and timelines....Full timeWork at officeLocal area
- ...entry-level clinical research professional that has a foundation in clinical research through assigned responsibilities in data management or implementing clinical research protocols. This role exhibits increased learned skills and flexibility in performing duties and...Full timeTemporary workLocal areaWorldwideNight shiftWeekend workAfternoon shift
- ...Miami is looking for a full-time Clinical Research Coordinator 1 (A) to work on-site at UHealth. This entry-level position involves managing simple clinical research protocols, coordinating participant activities, and maintaining accurate research records. The ideal...Full time
- Dormont Manufacturing Co is seeking a Full-time Clinical Research Coordinator 1 in Miami. This entry-level position involves performing chart reviews, coordinating clinical research protocols, and ensuring compliance with regulations. The ideal candidate will have a Bachelor...Full time
- The University of Miami, Bascom Palmer Eye Institute, is seeking a full-time Clinical Research Coordinator 1 in Miami, Florida. This role involves coordinating clinical research protocols, conducting patient screenings, and supporting data collection activities. Ideal candidates...Full time
- ...Manufacturing Co is seeking a Clinical Research Coordinator 2 to support clinical research studies within the Department of Pathology and Laboratory Medicine at the University of Miami. The role involves assisting in study planning, participant recruitment, and adherence to...
- Direct Jobs is seeking a Senior Clinical Research Coordinator in Miami, Florida. In this role, you will manage daily activities of complex research studies ensuring compliance with protocols and regulations. The ideal candidate has substantial pediatric clinical research...
- ...amendments and follow ups to IRB. Help process patient specimens (e.g., blood) to be stored and shipped to the central research laboratory. Core Qualifications Bachelor’s degree in a relevant field. Minimum 2 years of relevant experience. Knowledge, Skills and Attitudes...Full timeLocal areaNight shiftWeekend workAfternoon shift
- ...outreach activities to recruit populations historically underrepresented in genetics research. Schedule and enroll participants, manage calendars and coordination with other staff. Coordinate enrollment activities, set up local and remote trips, including overnight...Full timeLocal areaRemote workNight shift
- The University of Miami is looking for a Clinical Research Coordinator 2 for the Bascom Palmer Eye Institute in Miami, FL. This full-time position involves assisting in the planning, coordination, and implementation of clinical research studies. Responsibilities include...Full time
- Study coordinator to support ongoing large clinical study in US. Completes all paperwork required to capture all data as specified by a study protocol, and for ensuring subject safety, understanding, and cooperation during the study process. Interacts with the research ...Local area
- ...projects in Miami, Florida. The SCRC will ensure that research studies adhere to protocols, regulatory standards, and GCP, while also managing patient recruitment and data integrity. Successful candidates will have a Bachelor's degree with relevant experience, possess...
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Laboratory Manager. Be the first to apply!

