Job Search
-
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
-
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
-
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
-
Harleysville, PA 19438, USA ● Pennsylvania, USA ● Req #3397Wednesday, March 15, 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
-
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
-
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
-
Columbia, MO, USA ● Req #3409Wednesday, March 15, 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
-
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
-
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
-
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
-
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
-
About the Role: The Pathology Associate III will perform duties and tasks related to the post-life portion of research projects. Responsible for oversight and/or performing duties according to study protocol, GLPs and SOPs. Sufficiently knowledgeable and self-reliant to perform a number of research activities without supervision. Has an advanced skillset and takes the lead with routine procedures and tasks. What You'll DoFollow all Standard Operating Procedures (SOPs). Is compliant with GLP, A ...Read more about Pathology Associate IIIMore
-
About the Role: Assist 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. 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 Here:Follow all Standard Operating Procedures ( ...Read more about Research Associate I, Scientific ServicesMore
-
About the Role: Assist the Histology Technician(s), Study Director(s), Study Coordinator(s), and/or Staff Veterinarian(s) in the performance in conducting the post-life portion of research projects. Sufficiently knowledgeable and self-reliant to perform a number of post-life activities without supervision.What You'll DoFollow all Standard Operating Procedures (SOPs). Is compliant with GLP, ALCOA+, USDA, and AAALAC and can identify areas for improvement.Provides high standards of animal care with ...Read more about Histology Technician IIMore
-
About the RoleThe Building Maintenance Technician performs a variety of duties in support of general office/facility maintenance needs. The ideal candidate will be proactive, have strong attention to detail and great organizational skills.What You'll Do Ensure the repairs of damaged walls in the clinic, the laboratory and office spaces. Some places may require working outside of regular business hours Replacement of all non-functioning lighting (neon lights, light bulbs, etc.)Replacement of dama ...Read more about Building Maintenance Technician IIMore
-
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
-
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
-
About the RoleAs a key senior member of our clinical operations facility in Overland Park, KS, the Senior Director, Clinical Operations is responsible for the overall management of the Clinical Operations department including operational execution, quality management and budget adherence. The Senior Director, Clinical Operations will ensure the application and adherence to Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs) regarding ethics, safety and health for clinical sta ...Read more about Senior Director, Clinical OperationsMore
-
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
-
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
-
About the RoleThe Quality Assurance Manager will oversee the activity of the quality assurance department and staff, developing, implementing, and maintaining a system of quality. What You'll Do Here: Manages QA staff and resources to ensure efficiency across functions and sites.Responsible for staff development and align with strategic plan needs.Integrate internal and external quality information to quickly adapt and modulate QA activities.Application of risk assessment approaches within QA o ...Read more about Quality Assurance ManagerMore
-
About the Role: The Necropsy Supervisor is responsible for the leadership and day-to-day management of staff working in the necropsy group. This includes developing, reviewing, and approving planned study events. Actively managing the conduct of study procedures, and ensuring high standards of data quality, procedural compliance, and operational efficiency. Maintaining facilities and equipment in a customer-ready manner. Engaging with staff and driving their technical and professional developmen ...Read more about Necropsy SupervisorMore
-
About the RoleThe Senior Biostatistician is responsible for having expert knowledge of all related processes with the ability to independently lead a study, support analysis, and provide high quality documents to support sponsors' research programs, and deliver a high level of quality and timeliness, resulting in high levels of client satisfaction.What You'll DoFollow department and company standard operating procedures (SOPs), forms, templates and policies.Act as Lead Biostatistician for simple ...Read more about Senior BiostatisticianMore
-
About the RoleThe 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 (SOP)s.What You'll Do HerePerform scheduled inspection of emergency crash carts, inventory/inspect the contents and maintain up to date records.Act as a mentor to Clinical ...Read more about Clinical Research Nurse IIMore
-
The Quality Control Reviewer is responsible for performing quality control (QC) functions including technical and compliance review of data as well as daily pre- and post-activity quality control on various projects. Ensures that all project-related documented is filled out accurately and in a timely manner by study personnel and that all procedures are followed as per protocol, company SOPs and Good Laboratory Practice (GLP) requirements.ResponsibilitiesPerforms QC of data, both paper and elect ...Read more about Quality Control ReviewerMore