Laboratory Manager
K.A. Recruiting
Laboratory ManagerPosition Highlights:Monday through Friday, Day Shift Position - great for work life balance!Permanent & Full TimeLocated at small community-based general medical and surgical hospitalResponsible for overseeing all staff personnel including evaluating performance, recommends hiring and or firing. Responsible for reviewing and signing out completed lab reports. Follows guidelines set by CLIA, state guidelines etc..Open to both experienced laboratory managers and directors but is also willing to train laboratory supervisors and/or lead technologistsOffering a competitive compensation package and comprehensive benefits package! Sign on and/or Relocation Assistance may also be available to eligible applicants!Requirements:Bachelor's Degree or Masters Degree in Medical Technology or a related fieldMLS/MT ASCP Certification (or equivalent)Area Highlights:Low cost of living area with affordable housing!Proximity to major cities including Harrisburg, Pittsburgh and Philadelphia!Fantastic location for outdoor enthusiasts with camping, hiking, biking, fishing, kayaking nearby!If you are interested in learning more contact Andrea at View email address on click.appcast.io or call/text View phone number on click.appcast.io!
$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...SuggestedFull timeLive inWork at officeLocal area$74.5k - $95k
...Clinical Research Project Manager BThis position is based in the Penn Frontotemporal Degeneration Center (FTDC), part of the Department of Neurology of the University of Pennsylvania's Perelman School of Medicine. The Penn FTDC which is a large translational research center...SuggestedWork at officeLocal areaFlexible hoursAfternoon shift- ...Clinical Research Project ManagerThe Clinical Research Project Manager independently leads and manages clinical trials from study start-up through closeout, ensuring adherence to protocol requirements, institutional standards, and applicable regulatory guidelines. This...SuggestedWork at office
- ...Who We Are TPM Laboratories, Inc. is an independent contract testing laboratory providing personalized analytical services to the pharmaceutical... ...TPM Laboratories is seeking a Chemistry Laboratory Manager to run day-to-day analytical lab execution and provide hands-on...SuggestedContract workShift work
$31 per hour
...clinical research studies conducted at Cooper University Health Care. This role supports study startup, maintenance, and closeout by managing submissions to regulatory agencies, maintaining Investigator and staff documentation, and facilitating communication among...SuggestedFull timePart time- Heartflow is a medical technology company advancing the diagnosis and management of coronary artery disease, the #1 cause of death worldwide, using cutting-edge technology. The flagship product—an AI-driven, non-invasive cardiac test supported by the ACC/AHA Chest Pain...Contract workWork experience placementWork at officeLocal areaWorldwideRelocationShift work
$75.8k - $89.79k
...benefits, a wealth of health and wellness programs and resources, and much more. Posted Job Title Clinical Research Project Manager B (Department of Obstetrics and Gynecology) Job Profile Title Clinical Research Project Manager B Summary The Gynecologic...Full timeContract workLocal areaWork from homeFlexible hours- ...Good Clinical Research Practice (GCP). Performs a variety of research activities in support of clinical trials (including database management, biological specimen processing, and clerical duties) to assist investigators in organizing, gathering and compiling clinical...
- ...activities. This includes, but is not limited to, reviewing coverage analysis, developing and negotiating clinical trials budgets, and managing clinical trial financial accounts.Job DutiesInteracts with co-workers, visitors, and other staff consistent with the values of...
- ...role is ideal for early-career coordinators with some prior research exposure, looking to develop hands-on clinical and protocol management experience.The Clinical Research Coordinator I is responsible for supporting and performing routine clinical research activities...
$46.5k
...participants, obtaining informed consent, facilitating study tasks (training completion, questionnaire administration and interviews), and managing participant remuneration and tracking. Collect and manage study data for the Just ASKTM cluster RCT using REDCap; assist with...Local areaFlexible hours- ...Clinical Trial Manager The role: The Clinical Trial Manager is responsible for the delivery of all clinical aspects of the study. The CTM oversees the clinical portion of the budget, develops monitoring plans & tools, trains CRAs, drives enrolment and study start-up...Local area
- ...Good Clinical Research Practice (GCP). Performs a variety of research activities in support of clinical trials (including database management, biological specimen processing, and clerical duties) to assist investigators in organizing, gathering and compiling clinical...Daily paidFull timeTemporary workPart timeFlexible hoursShift work
- ...Senior Clinical Project Manager - Remote, US ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility...Remote work
- ...organization. This individual will be responsible for overseeing regulatory compliance across clinical research studies, including managing IRB submissions, maintaining regulatory binders and essential documentation, and supporting study startup through closeout. This...
- ...startup to closeout, including protocol coordination (screening, recruiting, enrolling, consenting), feasibility planning, data management, biological specimen management, preparation for monitoring visits, and regulatory and/or IRB document preparation. Ensuring all...Shift work
$47.31k - $53.42k
...facilitate, promote, and ensure good clinical practice in the conduct of all research protocols in the Department/Center. Independently manages different phases of complex clinical trials and mentors coordinators and research assistants. Works with partnering institutions...Full timeLocal areaWork from homeFlexible hours- ...Good Clinical Research Practice (GCP). Performs a variety of research activities in support of clinical trials (including database management, biological specimen processing, and clerical duties) to assist investigators in organizing, gathering and compiling clinical...Shift work
$47.31k - $67.05k
...Responsibilities include study coordination, regulatory support, subject recruitment and enrollment, study visits, data collection and management, and ensuring compliance with institutional, sponsor, and regulatory requirements. The CRC A level will work under close...Local area$63.09k
Clinical Research Coordinator CThe University of Pennsylvania, the largest private employer in Philadelphia, is a world-renowned leader in education, research, and innovation. This historic, Ivy League school consistently ranks among the top 10 universities in the annual...Local areaWork from homeFlexible hours- ...Description Oversees day-to-day clinical trial activities in accordance with Good Clinical Practice (GCP) guidelines. Independently manages or assists with clinical trials from startup through closeout. Coordinates protocol-related activities, including patient...Shift work
- ...Good Clinical Research Practice (GCP). Performs a variety of research activities in support of clinical trials (including database management, biological specimen processing, and clerical duties) to assist investigators in organizing, gathering and compiling clinical...Full timeShift work
- ...intervention, etc. Comply with Institutional policies, standard operating procedures (SOPs) and guidelines, and with HIPAA and management of confidential materials Must comply with federal, state, and sponsor policies For multi-site studies or collaborations,...Full timePart time
$53.42k - $60.81k
...obligations to patients/subjects, Principal Investigator (PI), study team and Sponsor/CRO. This position will report directly to the Program Manager and work directly with PIs and clinical research nurses (CRNs). The CRC is an integral and essential member of the ACC CRU Lymphoma...Full timeLocal areaFlexible hours$47.31k - $67.05k
...Responsibilities include study coordination, regulatory support, subject recruitment and enrollment, study visits, data collection and management, and ensuring compliance with institutional, sponsor, and regulatory requirements. The CRC A level will work under close...Local areaFlexible hours$213.5k - $355.5k
AVEVA is creating software trusted by over 90% of leading industrial companies.Salary Range:$213,500.00 - $355,500.00This pay range represents the minimum and maximum compensation that the position offers, and final compensation can vary within the range depending on work...Full timeWork at officeLocal areaRemote workHome officeFlexible hours$62.9k - $80.2k
...databases, collaborating with sub sites. The ideal candidate is an exceptional communicator with strong organizational and time-management skills. What you will do Applies in depth knowledge of clinical research and independently coordinates the activities of 1...Full timePart timeFor contractorsShift work$53.42k - $63.09k
...Clinical Research Coordinator C In addition to the above, the CRC C will will work with minimal supervision from their project manager and independently manage their assigned clinical trials. The CRC-C may act in a lead capacity in coordination with CRU Research Team...Full timeLocal areaWork from homeFlexible hours- ...Senior Clinical Trial Management ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion...Full time
- ...startup to closeout, including protocol coordination (screening, recruiting, enrolling, consenting), feasibility planning, data management, biological specimen management, preparation for monitoring visits, and regulatory and/or IRB document preparation. Ensuring all...Daily paidFull timeTemporary workPart timeFlexible hoursShift work
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