UNKNOWN

FEED

Directs the maintenance of required quality control records to ensure the accuracy and precision of the analyzers, troubleshoots quality control issues, and establishes new ranges as necessary for new lots of quality control materials. As a leading global contract research organization (CRO), we partner with researchers to tackle complex scientific challenges, drive innovation, and help build a healthier, safer world.

YEAR

Inotiv

Manager, Clinical Pathology

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About this Job:We are currently seeking candidates with experience in Manufactured Blood Product Development (e.g., using stem cells to generate large-scale blood cell production for transfusion; engineering animal-derived blood products; and developing synthetic blood substitutes to address limitations in human blood donation). The Center's research spans a broad portfolio including advanced imaging, on-demand blood products, organ-on-chip and micro physiological systems, wound care, traumatic brain injury diagnostics, and point-of-need medical devices.

The Geneva Foundation

Research Associate I (Pre-Clinical)

OTHER

The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. The compensation package listed is for 1st year OTE, which are based on a wide array of factors unique to each candidate, including but not limited to skill set, years & depth of experience, certifications and specific office location.

Natera

Clinical Field Specialist

greenhouse_via_bold

Exceptionally bright, flexible, self-motivated, and results oriented with strong interpersonal and analytical skills  Ability to think strategically as well as execute tactically  Must act with a sense of urgency  Have a strong desire to work in a fast-pace environment and must work independently with an internal drive to be successful  Excellent organizational and communication skills (written and verbal) with demonstrated ability to effectively present to both internal and external customers. The compensation package listed is for 1st year OTE, which are based on a wide array of factors unique to each candidate, including but not limited to skill set, years & depth of experience, certifications and specific office location.

Associate Clinical Oncology Specialist

FULL_TIME

Each individual performing high complexity testing must: Follow the laboratory’s procedures for specimen handling and processing, test analyses, reporting and maintaining records of patient test results, Maintain records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens; Adhere to the laboratory’s quality control policies, document all quality control activities, instrument and procedural calibrations and maintenance performed; Follow the laboratory’s established policies and procedures whenever test systems are not within the laboratory’s established acceptable levels of performance; Be capable of identifying problems that may adversely affect test performance or reporting of test results and either must correct the problems or immediately notify the general supervisor, technical supervisor, clinical consultant, or director; Document all corrective actions taken when test systems deviate from the laboratory’s established performance specifications. Have education and training equivalent to an associate’s degree that includes at least 60 semester hours from an accredited institution that, at a minimum, includes either: 24 semester hours of medical laboratory technology courses; or 24 semester hours of science courses that include: six (6) semester hours of chemistry, six (6) semester hours of biology; and twelve (12) semester hours of chemistry, biology, or medical laboratory technology in any combination; AND Have laboratory training that includes either of the following: Completion of a clinical laboratory training program approved or accredited by the ABHES, the CAHEA, or other organization approved by HHS; or At least 3 months documented laboratory training in each specialty in which the individual performs high complexity testing.

The Tatitlek Corporation

Public Health Clinical Laboratory Technician

[AW]-iCims

Under direct supervision, assists Medical Laboratory Scientist by performing routine laboratory support duties and approved testing in any one of various specialized laboratories throughout UMMS: Immunology, Rapid Response (Chemistry/Hematology), Blood Bank, Microbiology, Virology, Molecular Diagnostics, Shock Trauma Stat Lab and Immunogenetics in accordance with departmental procedures and regulations stipulated by Clinical Laboratory Improvement Act. Must possess the skills required for proper specimen collection, including patient preparation, if applicable, labeling, handling, preservation, fixation, processing or preparation, transportation, and storage of specimens.

HOUR

University of Maryland Medical System

Clinical Laboratory Assistant, PRN, Evenings

IRecruitee

A SymphonyAI Group company, GW RhythmX leverages various firm assets, including $1B+ in R&D investment, longitudinal data related to 300 million patients, 4.4 billion total annual claims, and 1.8 million healthcare professionals at more than 3,000 facilities globally. The successful candidate will have a firm grasp of the healthcare services industry, ability to align prospect needs with our Engagement and Experience offerings and demonstrated ability to set and achieve Pod objectives through direct contribution and overall Pod performance.

GetWellNetwork Inc

Senior Director, Pod Leader - Clinical Intelligence (Independent Physician Groups)

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GetWellNetwork, Inc.

Senior Director, Pod Leader – Clinical Intelligence (Independent Physician Groups)

GetWellNetwork

As the industry landscape shifts with new challenges in patient care, quality and compliance requirements, workforce retention, and operational efficiencies, we deliver strategic, data-driven solutions that include redefining workforce management and clinical service delivery. This position serves as a key clinical resource, supporting patient care, clinical research activities, healthcare communications, education, and program development while collaborating with multidisciplinary teams, investigators, and healthcare professionals.

InGenesis, Inc. has achieved national recognition as an industry leader in the delivery of dynamic workforce solutions. InGenesis, Inc. supplies Fortune 500, academic and government clients with advanced workforce management and talent acquisition services. Established in 1998, InGenesis, Inc. has been recognized as one of the fastest-growing privately held companies and one of the top job creators in the U.S. Our national presence, diverse service lines and expansive growth offer employees ample opportunities for professional growth and career development.

InGenesis

Senior Clinical Advisor - (13346)

JobScore

Vacancy NameSenior Manager, Medical/Regulatory Writer Vacancy NoVN831 Employment TypeFull Time Location of roleGaithersburg, MD, Radnor, PA, Remote, US DepartmentRegulatory Affairs Key ResponsibilitiesThe Senior Manager, Medical/Regulatory Writer will be accountable for leading and overseeing the medical and scientific regulatory writing for assigned programs to support submissions from first-in-human studies through product registration. Authoring or supervising the preparation of other regulatory documents required for Health Authority submissions, including but not limited to: Clinical Summaries (Clinical Overview, ISS/ISE, PK/PD summary, Advisory Committee Briefing document), Investigator Brochure(s), DSURs, other regulatory documents including briefing documents for health authorities, responses to Health Authority questions, etc.

Immunocore Holdings Plc

Senior Manager, Medical/Regulatory Writer

Write and edit clinical development documents, including but not limited to, clinical protocols, investigator’s brochures, clinical study reports, subject consent forms, integrated safety and efficacy summaries, Module 2.7.1, 2.7.2, 2.7.3, 2.7.4, and 2.5 documents, presentation materials and publications to medical journals. Our mission is to deliver high-quality service and technology solutions – rooted in strong science and decades of regulatory experience – that will assist our clients in developing and marketing life-changing therapies to positively improve lives worldwide.

Senior Medical Writer (Remote)

partner JazzHR

An innovation leader in every industry we serve, we follow our Purpose and Guiding Principles to help pet owners worldwide keep their companion animals healthy and happy, to ensure safe drinking water for billions, and to help farmers protect livestock and poultry from disease. You will work with a close-knit team of Architects, Developers, Data QA Engineers, DevOps, Product Owners, and Scrum Masters in a variety of remote locations - excellent communication, collaboration and interpersonal skills are important for team success.

7,000 people, one global focus﻿ - enhancing the health and well-being of pets, people, and livestock
We are passionate about what we do at IDEXX – and why wouldn’t we be? When you’re working to raise the standard of care for pets, make drinking water safe for billions and keep our livestock population around the globe healthy and free of disease, it’s no wonder that what we do each day is more than just a job. There’s an energy across IDEXX that is contagious – where caring and committed people come together to make things better.

Idexx Laboratories Inc

Senior Application Developer

The Procurement Manager, Direct Materials is responsible for procurement leadership, sourcing and procuring GMP materials for Catalent Gene Therapy Direct Materials, including defining category strategy, buying channels, and supplier relationship management program, to support our clinical programs effectively. The role: Minimize impact of supplier shortages by proactively identifying and resolving potential material supply issues, timely communication, collaborating with Supply Chain developing inventory management strategies in conjunction with our vendors.

Catalent Inc

Procurement Manager, Direct Materials

The Procurement Manager, Direct Materials is responsible for procurement leadership, sourcing and procuring GMP materials for Catalent Gene Therapy Direct Materials, including defining category strategy, buying channels, and supplier relationship management program, to support our clinical programs effectively. Minimize impact of supplier shortages by proactively identifying and resolving potential material supply issues, timely communication, collaborating with Supply Chain developing inventory management strategies in conjunction with our vendors.

Catalent

Job Description: Parsons is seeking Research Assistants - Microbiology and Molecular Biology to support infectious-disease, genomics, and biosurveillance research at NMRC BDRD. We promote a culture of excellence and close-knit teams that take pride in delivering, protecting, and sustaining our nation''s most critical assets, from Earth to cyberspace.

Parsons is a technology-driven engineering services firm with more than 70 years of experience in the engineering, construction, technical, and professional services industries. The corporation is a leader in many diversified markets with a focus on infrastructure, defense, security, and construction. Parsons delivers design/design-build, program/construction management, systems design/engineering, cyber/converged security, and other professional services packaged in innovative alternative delivery methods to federal, regional, and local government agencies, as well as to private industrial customers worldwide.

Parsons Corp

Research Assistant- Microbiology and Molecular Biology

Job Description: Parsons is seeking Research Assistants - Microbiology and Molecular Biology to support infectious-disease, genomics, and biosurveillance research at NMRC BDRD. We promote a culture of excellence and close-knit teams that take pride in delivering, protecting, and sustaining our nation's most critical assets, from Earth to cyberspace.

Clinical Scientist Jobs in Maryland

Manager, Clinical Pathology Inotiv

Research Associate I (Pre-Clinical) The Geneva Foundation

Clinical Field Specialist Natera

Associate Clinical Oncology Specialist Natera

Public Health Clinical Laboratory Technician The Tatitlek Corporation

Clinical Laboratory Assistant, PRN, Evenings University of Maryland Medical System

Senior Director, Pod Leader - Clinical Intelligence (Independent Physician Groups) GetWellNetwork Inc

Senior Director, Pod Leader – Clinical Intelligence (Independent Physician Groups) GetWellNetwork, Inc.

Senior Director, Pod Leader - Clinical Intelligence (Independent Physician Groups) GetWellNetwork

Senior Clinical Advisor - (13346) InGenesis

Senior Manager, Medical/Regulatory Writer Immunocore Holdings Plc

Senior Medical Writer (Remote) MMS

Senior Application Developer Idexx Laboratories Inc

Procurement Manager, Direct Materials Catalent Inc

Procurement Manager, Direct Materials Catalent

Research Assistant- Microbiology and Molecular Biology Parsons Corp

Research Assistant- Microbiology And Molecular Biology Parsons Commercial Technology Group Inc.

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