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About the RoleHistology Technicians are required to perform, but not limited to: the preparation of quality tissue samples for histopathologic evaluation; identification of tissue samples for proper embedding orientation; microtomy skills; performance routine hematoxylin and eosin (H&E) staining procedures; knowledge of the use and maintenance of equipment used for the preparation of tissue samples and the ability to maintain a clean and orderly laboratory environment. Evening hours available wi ...Read more about Histology Technician - All LevelsMore
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1200 Beaumont Ave, Montreal, QC H3N 1W5, Canada ● Req #3351Friday, March 31, 2023About The RoleThe Clinical Safety Technician will assist in overseeing the safety of clinical trial participants during study conduct and the maintenance of safety equipment. The Clinical Safety Technician will execute tasks performed in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOP)s.What You'll Do HereAct as a mentor to Clinical Operations team members. Ensure the confidentiality of clinical trial participants and sponsors is respected. C ...Read more about Licensed Practical Nurse (evening and night shift)More
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About the RoleThe Clinical Safety Technician (Research Nurse, LVN) will assist in overseeing the safety of clinical trial participants during study conduct and the maintenance of safety equipment. The Clinical Safety Technician will execute tasks performed in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOP)s.Please Note: This is a part time/variable hour role. Therefore, health benefits are not offered. There is the potential to become a full ...Read more about Clinical Safety Technician (LVN)More
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About the RoleThe Screening Technician I will work with the Screening team to screen participants enrolled in clinical studies. Responsibilities of the Screening Technician I include intake/collection of tasks performed and assessment of overall participant eligibility in regard to tasks performed in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOP)s.What You'll DoEnsure the confidentiality of clinical trial participants and sponsors is respect ...Read more about Screening Technician I - Clinical ResearchMore
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Cypress, CA, USA ● Req #2347Friday, March 31, 2023About the RoleThe Screening Quality Control Associate will perform the quality control of data collected during the screening phase of a clinical trial. The Screening Quality Control Associate will execute all tasks performed and ensure all data is in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOP)s.What You'll DoEnsure and advocate a high level of customer service and quality within the department.Ensure the confidentiality of clinical trial ...Read more about Quality Control Associate - Clinical Research ScreeningMore
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About the RoleThe Screening Administrative Assistant will provide administrative support to the Screening and Recruiting teams and conducting tasks performed in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs). What You'll DoEnsure the confidentiality of clinical trial volunteers and sponsors is respected.Assists in screening admission procedures.Preparation of screening materials.Volunteer identity verification.Update participant managemen ...Read more about Screening Administrative AssistantMore
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About the RoleThe Screening Team Leader will organize screening activities and the Screening Team members to ensure that clinical trial screening activities are conducted within respective trial timelines. The Screening Team Leader will ensure tasks performed and screening activities are executed in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOP)s.What You'll DoEnsure the confidentiality of clinical trial participants and sponsors is respecte ...Read more about Screening Team LeaderMore
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About the RoleThe Clinical Research Technician will work with Clinic Operations teams to execute clinical trial activities. Responsibilities include execution of tasks performed/clinical activities in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOP)s. Please Note: These are variable hour roles therefore, health benefits are not offered. There is the potential to become a full time, regular employee as the opportunity and/or need arises. Wha ...Read more about Clinical Research Technician IIIMore
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About the RoleThe Participant Recruitment Agent will provide volunteers with preliminary clinical trial information and company details as well as pre-screen volunteers to determine eligibility for clinical trial screening. The Participant Recruitment Agent will ensure all tasks are performed are executed in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOP)s. What You'll DoEnsure the confidentiality of clinical trial participants and sponsors i ...Read more about Participant Recruitment AgentMore
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About the RoleThe Sample Management Coordinator is responsible for the management of biological samples collected during clinical trials. The Sample Management Coordinator will ensure tasks performed are conducted within compliance of study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs).What You'll DoEnsure the confidentiality of clinical trial participants and sponsors is respected.Maintain and advocate a high level of customer service and quality within the de ...Read more about Sample Management CoordinatorMore
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About the RoleThe Screening Technician I will work with the Screening team to screen participants enrolled in clinical studies. Responsibilities of the Screening Technician I include intake/collection of tasks performed and assessment of overall participant eligibility in regard to tasks performed in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOP)s.What You'll DoEnsure the confidentiality of clinical trial participants and sponsors is respect ...Read more about Screening Technician IMore
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About the RoleThe Associate Director of Laboratory Operations may be required to perform all the duties described in the job description for Clinical Supervisor, Technical Supervisor, Clinical Consultant, Laboratory Technician and Laboratory Assistant. The Associate Director of Laboratory Operations is responsible for the day-to-day management and oversight of all aspects of laboratory operations as well as personnel performing testing and reporting test results. At present time, the total numbe ...Read more about Associate Director - Laboratory OperationsMore
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About the RoleThis advanced laboratory position includes sample receipt and management, laboratory and equipment maintenance, assisting with the laboratory operation, and collection of data for the Laboratory Sciences laboratory using a variety of equipment and computerized systems. What You'll DoMaintain and document chain of custody for specimens in the laboratory.Perform and document assays such as ELISA, PCR, multiplex and flow cytometry with accuracy.Perform routine laboratory maintenance ( ...Read more about Research Associate IIIMore
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About the RoleWe are looking for talented and enthusiastic people, like you, to join our growing team! The Research Associate II works independently in the day to day laboratory operation, collection and review of data for the Laboratory Sciences department, supports the activities of various service groups including ligand binding, flow cytometry, molecular biology and LCMS/MS, as needed, participates in the creation of study worksheets, SOP’s and other controlled documents as assigned, and pro ...Read more about Research Associate IIMore
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About the RoleThe Facilities Manager is responsible for the management, supervision and coordination of the facilities and transportation teams and the overall upkeep of the Altasciences Clinical Research Site California. What You'll DoManagement of the facilities and transportation teams, including but not limited to, PTO management, timesheet approval, on-going and yearly performance reviews, employee hiring, disciplinary actions and termination.Perform, direct and/or oversee the training of t ...Read more about Facilities ManagerMore
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About the Role: The QA Auditor is responsible for carrying out systematic and independent examination (i.e., audit) of multiple study related activities and documents, to determine whether the evaluated study related activities were conducted, and the data were recorded, analyzed, and accurately reported according to the protocol, standard operating procedures (SOPs), GLP (21 CFR Part 58 and Part 11) and the applicable regulatory requirements. The QA Auditor is responsible for reporting any find ...Read more about Quality Assurance AssociateMore
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About the Role: The Veterinary Technician assists the Animal Technician(s), Study Director(s), Study Coordinator(s), and/or Staff Veterinarian(s) in the performance of animal health care duties and in conducting the in-life portion of research projects. They are responsible for oversight and/or performing duties related to the animal health program. Sufficiently knowledgeable and self-reliant to perform a number of veterinary and research activities without supervision. What You'll Do ...Read more about Veterinary TechnicianMore
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About the Role: Support preclinical toxicologic studies from both the Everett, Washington and East coast and Midwestern sites. What You'll Do Here: Perform macroscopic and microscopic tissue evaluations and interpretation of assigned studiesAssist with necropsy supervision and gross pathology interpretation. Guiding of personal staff for sample collection and technical developmentWrite comprehensive report narratives detailing all test article effectsEnter pathology findings in data capturing s ...Read more about Senior Research PathologistMore
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Harleysville, PA 19438, USA ● Pennsylvania, USA ● Req #3397Friday, March 31, 2023About the RoleThe QA Associate is responsible for carrying out systematic and independent examination (i.e., audit)of multiple trial related activities and documents, to determine whether the evaluated trial related activities were conducted, and the data were recorded, analyzed, and accurately reported, according to the protocol, standard operating procedures (SOPs), GxPs and the applicable regulatory requirements. Responsible for reporting any findings to the Internal Study Team and departmen ...Read more about Quality Assurance AssociateMore
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About the Role We are seeking a motivated and organized individual for a highly respected Contract Animal Research Organization in Scott Township, PA. This individual will be successful at independently performing job-related tasks as well as in a team-oriented environment and will be responsible for data management and project coordination in support of early drug development research projects.What You'll Do Setup and maintenance of the online data collection system, including running data quer ...Read more about Scientific Data OrganizerMore
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About the Role Reporting to the Sr. Manager, Validation and Equipment, the Validation Specialist will assure that equipment and computer systems are validated in accordance with industry best practices (GAMP), regulatory requirements, company policies and procedural operating standards. What You'll Do Here: Author, execute, monitor and/or review Validation documents such as: Risk Assessments, Validation Plans, Test Scripts (IQ/OQ/PQ), Traceability Matrix, and Validation Reports per Standard Oper ...Read more about Validation SpecialistMore
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About the Role The Validation Analyst III is responsible for managing and leading all aspects of a CSV project towards a successful GxP compliant operational delivery and implementation. The Validation Analyst III is responsible for ensuring and developing appropriate mitigations as required to ensure the compliance of software systems. What You'll Do Here: Author, execute, monitor and/or review Validation documents such as: Risk Assessments, Validation Plans, Test Scripts (IQ/OQ/PQ), Traceabi ...Read more about Validation Analyst IIIMore
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Columbia, MO, USA ● Req #3409Friday, March 31, 2023About the Role: The Safety Assessment Data Specialist works collaboratively with designated Study Director(s), Contributing Scientists and Principal Investigators, as appropriate, to provide professional support for data management, analysis, and interpretation, assisting with the reporting process, in compliance with GLP standards. The Safety Assessment Data Specialist assists with administration functions to maximize the business value of internal systems and/or processes (e.g. Ponemah), inc ...Read more about Pre-clinical Safety Pharmacology ECG SpecialistMore
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About the RoleResponsible for all technical aspects of analytical analysis including instrumentation maintenance. What You'll Do Essential functions for this position are not limited only to the tasks and responsibilities which follow: Uses existing company forms and/or creates new forms as per study requirements. Prepares and enters detailed data into laboratory notebooks; reviews data for accuracy. Has knowledge and use of scientific application of computers (e.g., Word, Excel, Chemstation, Ch ...Read more about Analytical ChemistMore
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About the RolePerforms technical aspects of study conduct under general supervision.What You'll DoIndependently train and practice new techniques and procedures as assigned.Perform techniques on various studies (e.g., mouse, rat, rabbit, dog, primates). Observe clinical signs, prepare and enter detailed data in laboratory notebooks, review data for accuracy. Calibrate balances, infusion pumps and other laboratory equipment as required. Assist or perform dose administration by various routes (e.g ...Read more about Research Associate II, Scientific ServicesMore