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Laval, QC, Canada ● Req #4264Monday, March 25, 2024About the role The Operator Specialist is responsible for performing daily batch injections in validation, production, and method development in Mass Spectrometry. The Operator Specialist monitors the injection performance and troubleshoot difficult issue in Mass Spectrometry. Act as a mentor for the operators’ team. Optimizing injection schedule to meet clients’ deadlines. The Operator Specialist will work during the evening shift; Monday to Friday 2pm to 10pm What You’ll Do Here Starts the ...Read more about Operator Specialist, Instrumentation, Injection in Mass SpectrometryMore
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About The Role The Technician, Instrumentation is responsible for performing routine maintenance and preventative maintenance on non-chromatographic laboratory and clinical equipment. Technician, Instrumentation also provides coaching and training for laboratory and clinic employees. What You'll Do Here To perform calibration, routine and preventative maintenance of non-chromatographic laboratory and clinical equipment; To perform troubleshooting and repair on non-chromatographi ...Read more about Technician, InstrumentationMore
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About The RoleThe Research Scientist is assigned to projects based on scientific competency and training. The Research Scientist will plan and/or perform laboratory bench work and ensure the overall integrity/quality of assigned method development and/or studies. The Research Scientist can also support client interactions for their assigned projects. What You'll Do Here: Plans and perform laboratory bench work for method development and method qualification studies, interpretation of results, d ...Read more about Research Scientist , LBA , ADAMore
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About The Role The Research Associate II, Laboratory Sciences role works independently in the day-to-day laboratory operation, collection, and review of data for the Laboratory Sciences department. Support and perform data collection activities including ligand binding assays, and/or flow cytometry, and/or cell-based assays, and/or mass-spectrometry, and/or as assigned. Participates in the creation of study worksheets, SOPs and other documents as assigned. Provides support for general laboratory ...Read more about Research Associate II, Laboratory SciencesMore
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About The Role The primary function of this position is responsible for providing estimated pricing for client requested quotes based on the Study Design Documents as provided by the Preclinical Business Development team and the Client Managers. Communication, via email, phone or Teams with Preclinical Business Development and Client Management is required to establish accurate Study Design documents to meet the clients preclinical study needs. Communication with the Bio Analytical and Scientifi ...Read more about Proposals ManagerMore
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About The Role The QC Reviewer is responsible for performing quality control including daily in-process quality control on various projects. Ensures that all project-related documentation is filled out accurately and in a timely manner by the analysts/scientists, and that all procedures are respected as per the company’s SOPs. Assist in daily activities of the Laboratory Sciences department including stocking supplies and general cleaning and/or as assigned. What You'll Do Here Follow Alta’s St ...Read more about QC ReviewerMore
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About The Role Primary responsibilities include proficiency in performing test and control article formulation, dose preparation and dispensing. Proficient in documentation of formulation procedures. Also responsible for receiving test and control article materials and maintaining chain of custody documentation associated with test and control materials, including inventory. Additionally, maintaining accountability and reconciliation of test materials is required. Responsible for reviewing prot ...Read more about Research Associate II, FormulationsMore
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Everett, WA, USA ● Req #4323Friday, March 22, 2024Are you ready to step into a leadership role that fuels scientific innovation and drives success in laboratory endeavors? Look no further! Altasciences is on the lookout for an exceptional individual to fill the pivotal position of Research Associate Supervisor. If you have a passion for managing talented teams, optimizing laboratory resources, and contributing to cutting-edge studies, this is your golden opportunity! About the Role As the Research Associate Supervisor, you will be the linchpi ...Read more about Research Associate, Laboratory Sciences SupervisorMore
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About The Role This is a mid-level associate position that works both independently and under minimal supervision. Working closely with veterinary and behavioral management, the enrichment associate supports the physical and psychological wellbeing of the animal colony through various daily enrichment. What You'll Do Here Documents compliance with environmental enhancement Standard Operating Procedures (SOPs). Assists with training of staff on enrichment SOPs. Prepares, distributes, and maint ...Read more about Environmental Enrichment AssociateMore
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About The Role Works under the guidance of designated Study Director(s), Contributing Scientists and PrincipalInvestigators, as appropriate, to provide administrative and professional support for accuratestudy progression based on Protocols and Method Validation Plans, organization, scheduling,reporting, client relations and operations. What You’ll Do Here Assist with the preparation and distribution of Protocols, Analytical Study Plans andAmendments/Amended Protocols. Schedule and/or help co ...Read more about Study CoordinatorMore
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Are you a detail-oriented individual with a passion for safety and compliance? Do you thrive in a fast-paced environment and want to contribute to the well-being of our employees? Our Preclinical site in Everett, WA, is seeking a dedicated Environmental Health and Safety Coordinator to join our team and ensure the highest standards of safety and regulatory compliance. As an Environmental Health and Safety Coordinator , you will play a vital role in maintaining our commitment to employee safety a ...Read more about Environmental Health & Safety CoordinatorMore
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About The RoleWe are currently seeking a dynamic, teamwork-oriented person to fill a Technician, Sample Management position in our Technical Support department. Want to contribute to pharmaceutical research activities? You have a great ability to concentrate? You have a rapid execution, while bringing attention to detail? This position is for you! Do not hesitate and send us your resume immediately. What You'll Do HereResponsible for sample control activities including the receipt, inventory, d ...Read more about Sample Management TechnicianMore
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1200 Beaumont Ave, Montreal, QC H3N 1W5, Canada ● Req #4458Tuesday, March 19, 2024About the Role If you're looking for new challenges in a completely different working environment and want to make a difference by helping to improve people's quality of life, our opportunity is sure to interest you! At Altasciences, you'll be able to develop your skills and advance your career. If you stand out for your dynamism, interpersonal skills, customer service, speed of execution, attention to detail and flexibility, send us your application! What you’ll do here: Perform screening ...Read more about Licensed Practical Nurse - Screening DepartmentMore
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About the Role The role of the Clinical Laboratory Scientist is responsible for analyzing specimens, verifying reports, performing quality assurance, and reviewing results for validity. What You'll Do Here Follow established procedures for obtaining and processing biological specimens for analysis in the department. Analyzes clinical laboratory specimens Performs data entry into the computer Verifies and reports laboratory results Follows procedures approved by the Laboratory Director (or ...Read more about Clinical Laboratory ScientistMore
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At Altasciences Clinical Los Angeles , we're looking for a dedicated Validation Analyst to join our dynamic Validation department. As a key player, you will be involved in the entire lifecycle of computerized system validation, playing a crucial role in planning, execution, and documentation. If you're ready to be part of a team that values innovation, regulatory excellence, and professional growth, this opportunity is tailor-made for you.. What You’ll Do Here Implement industry-leading practic ...Read more about Validation Analyst III - HybridMore
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About The Role The Advisor, Internal Communications will be a key contributor to the Internal Communications department. Reporting to the Senior Advisor, Internal Communications, their role will consist of implementing plans and tools that support the various employee communications strategies in order to help achieve the company's business strategies, promote its organizational culture and increase employee engagement On a day-to-day basis, the Advisor, Internal Communications will be resp ...Read more about Advisor, Internal Communications (Hybrid)More
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Auxvasse, MO 65231, USA ● Columbia, MO, USA ● Req #4364Monday, March 18, 2024About The Role Altasciences Preclinical Columbia (APC), a leader in the medical research field, is looking for a talented and visionary Clinical Pathology Manager to spearhead our department. We offer an exciting opportunity to not only lead but also innovate in a cutting-edge environment that is expanding its capabilities and is continuously expanding! This is a great leadership opportunity, where you will have the opportunity to facilitate innovation, manage change, and foster teambuilding to ...Read more about Clinical Pathology ManagerMore
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You want to make a difference by helping to improve people's quality of life? Our opportunity will surely interest you! As a fast-growing contract research organization, you will have the opportunity to develop your skills and advance your career. If you stand out for your organizational skills and your attention to details; don't hesitate to send us your application! About The Role The Associate Scientist is the right hand help for the scientist. As such, their responsibility is mainly to as ...Read more about Associate ScientistMore
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About The Role The QC reviewer is responsible to perform the quality control for data generated and work conducted in the laboratory. What You'll Do Here Ensures that all batch related documentation is completed accurately and in a timely manner by the analysts and that all procedures are respected as per the company’s SOPs. Based on training QC reviewer can draft study documents for BPI review such as Memo to File, SOP/Protocol/Study Plan deviations., perform quality control batch r ...Read more about QC Reviewer, LC-MS/MSMore
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About the Role The Analyst is responsible bench work and documentation based on their assignment to the laboratory. Ensures that analyses are performed in accordance with appropriate SOPs What You'll Do Here Responsible for experiments at the bench based on training and competencies can be assigned conduct validation and/or sample analysis. Execute appropriately method standard operating procedure (SOP), ensure completeness and accuracy of documentation Follow general SOP and good laboratory ...Read more about Analyst I, LC/MSMore
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About the RoleThe Data Manager II supports sponsors’ research programs by contributing to the data cleaning efforts needed to provide clean, analyzable clinical data proficiently and independently. What You'll Do Here Performs data management cleaning activities including listing review, issuing and closing queries, and external vendor data reconciliation per protocol, department and client standards, and International Conference on Harmonization (ICH) Good Clinical Practice (GCP) guidelines. E ...Read more about Data Manager IIMore
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About the RoleThe Data Manager II supports sponsors’ research programs by contributing to the data cleaning efforts needed to provide clean, analyzable clinical data proficiently and independently. What You'll Do Here .Performs data management cleaning activities including listing review, issuing and closing queries, and external vendor data reconciliation per protocol, department and client standards, and International Conference on Harmonization (ICH) Good Clinical Practice (GCP) guidelines. ...Read more about Data Manager IIMore
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About the Role The Clinical Research Nurse will oversee the safety and consent of clinical trial participants during study conduct and the maintenance of safety equipment. The Clinical Research Nurse will execute tasks performed in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs). What You'll Do Here Perform scheduled inspection of emergency crash carts, inventory/inspect the contents, and maintain up to date records. Act as a mentor to ...Read more about Registered Nurse - Clinical ResearchMore
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Overland Park, KS, USA ● Req #4420Wednesday, March 13, 2024About the Role The Clinical Research Technician II will work with Clinic teams to execute clinical trial activities. Responsibilities of the Clinical Research Technician II include execution of tasks performed/clinical activities in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs). What You'll Do Here Ensure the confidentiality of clinical trial participants and sponsors is respected. Understand protocol driven timed study events and ac ...Read more about Phlebotomist - Clinical Research Technician IIMore
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Auxvasse, MO 65231, USA ● Columbia, MO, USA ● Req #4018Tuesday, March 12, 2024About The Role Join a dynamic team at the forefront of scientific research! As a Research Associate, you'll embark on an exciting journey where you'll perform cutting-edge procedures, collaborate with renowned experts, and contribute to groundbreaking discoveries. From caring for animals and collecting data to operating state-of-the-art laboratory equipment, you'll be an integral part of our mission to advance scientific knowledge. If you're ready to make a significant impact and thrive in a fas ...Read more about Research Associate - Laboratory AnimalsMore