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About The Role The Laboratory Specialist I is responsible for the processing 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).The work hours of this position are: Monday - Friday 2200-0630 with occasional weekends. What You'll Do Here Ensure the confidentiality of clinical trial participants and sponsors ...Read more about Laboratory Specialist IMore
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Everett, WA, USA ● Req #4470Wednesday, April 17, 2024About the Role The Research Associate Intern is responsible for performing laboratory benchwork and documentation based on their laboratory assignment using a variety of laboratory methods including LCMS, ELISA, PCR and flow cytometry. Train and assist in the daily operations of the Laboratory Sciences Department including learning the scientific and technical concepts of laboratory assays, operation of laboratory equipment and instruments, and overall care in the laboratory environment. Wh ...Read more about Research Associate, Laboratory Sciences - Summer InternMore
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Laval, QC, Canada ● Req #3790Tuesday, April 16, 2024About The RoleFor this position we are looking for a Scientist that is experienced in developing flow cytometry antibody panels as well as Elispot method development and conducting GLP Bioanalytical sample analysis for either non clinical or clinical studies. The candidate will have experience in Fortessa and Diva software or equivalent and familiar with Elispot and fluoroSpot instrument acquisition and data analysis. It is of added value if the candidate also has experience in supporting Bioa ...Read more about Scientist, Flow Cytometry and Cell Based AssaysMore
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Laval, QC, Canada ● Montreal, QC, Canada ● Ontario, Canada ● Virtual ● Req #4269Tuesday, April 16, 2024You are an experienced Statistical Programmer that has understanding of clinical research and the role of data management, programming and statistics in the clinical study process and you want to make a difference by helping to improve people's quality of life, our opportunity will surely interest you! At Altasciences, you will have the opportunity to develop your skills and advance your career. If you stand out for; your client-focused approach to work, your ability to prioritize workload and y ...Read more about Senior Statistical ProgrammerMore
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Auxvasse, MO 65231, USA ● Columbia, MO, USA ● Req #4165Tuesday, April 16, 2024About The RoleJoin our team at Altasciences Preclinical Columbia as a Veterinary Technician and play a crucial role in facilitating and supporting the work and research of our veterinarians, study directors and clients. As a Veterinary Technician, you will be responsible for a wide range of animal health activities, including medicine, surgery, and drug therapy. Working closely with our dedicated vet services staff, you will be instrumental in the treatment of all on-site ill and injured anima ...Read more about Veterinary TechnicianMore
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1200 Beaumont Ave, Montreal, QC H3N 1W5, Canada ● Req #4452Monday, April 15, 2024About the RoleYou have experience in customer service in a call center and 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 good communications skills, your professionalism and your dynamism; send us your application! As a Customer Service Representative, your main responsi ...Read more about Bilingual Customer Service RepresentativeMore
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1200 Beaumont Ave, Montreal, QC H3N 1W5, Canada ● Req #4451Monday, April 15, 2024About the Role; The Clinical Research Technician will work with Clinic teams to execute clinical trial activities. Responsibilities of the Clinical Research Technician include execution of tasks performed/clinical activities in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOP)s. What you’ll do here; Ensure the confidentiality of clinical trial participants and sponsors is respected; Understand protocol driven timed study events and acceptabl ...Read more about Clinical Research TechnicianMore
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1200 Beaumont Ave, Montreal, QC H3N 1W5, Canada ● Req #4436Monday, April 15, 2024About The RoleThe licensed practical nurse will assist in overseeing the safety of clinical trial participants during study conduct and the maintenance of safety equipment. The licensed practical nurse will execute tasks performed in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOP)s. What You'll Do Here Act as a mentor to Clinical Operations team members; Ensure the confidentiality of clinical trial participants and sponsors is respected; ...Read more about Licensed Practical Nurse (Day, evening or night shifts available)More
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About The RoleWe are seeking a Scientist for our Ligand Binding Department (immunogenicity Unit) located in Laval. The Scientist will be responsible for the oversight of immunogenicity study conduct from assay development and optimization based on study requirement, to validation and sample analysis. The Scientist will be the primary contact to the client for all scientific discussions pertaining to all study phases. The Scientist will review all data generated and communicates results to clien ...Read more about Scientist, ADA, immunogenicityMore
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About the Role We are looking for a highly skilled Talent Acquisition Advisor to join our US team and help us find the right people for the right roles. The ideal candidate will have a deep knowledge of the screening, interviewing and hiring process in order to support our internal clients through the full cycle of the recruitment process across the assigned Altasciences sites. We're seeking someone who's passionate about discovering talent and helping people develop successful careers. Your ...Read more about Talent Acquisition AdvisorMore
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About the role The Proposal Coordinator 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 Scientific Services ...Read more about Proposals CoordinatorMore
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About the role The primary function of this position is to provide administrative and organizational support in coordination, compilation, and quality control of study data and documentation management; assist with compliance of Good Laboratory Practices (GLP) with preparation and quality control of data for reporting and study audits; prepare necropsy and post necropsy forms and obtain Study Director approval as necessary; verification of raw data and organization of necropsy notebooks; maint ...Read more about Pathology CoordinatorMore
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Are you ready to embark on a dynamic and stimulating career in research? Altasciences invites you to join our team as a Research Associate at our cutting-edge Preclinical site in Everett, Washington. Immerse yourself in a fast-paced, innovative environment where you'll play a pivotal role in the daily operations of the Laboratory Sciences laboratory. About The Role As a Research Associate III, you will be at the forefront of groundbreaking research, contributing to the success of our labora ...Read more about Research Associate PCR - Laboratory SciencesMore
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About the role The Data Coordinator I is responsible for the correlation and/or entry of clinical trial data into electronic data capture (EDC) software. The Data Coordinator I will conduct tasks performed within compliance of 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. Maintain and advocate a high level of quality and customer service within the ...Read more about Data Coordinator - Clinical OperationsMore
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About the RoleThe Technician, stockroom & Supplies is responsible for reception of all commodities ordered or imported, proper storage (both on and off site), inventory, distribution to operations groups, on site stockroom. What You'll Do Here Responsible for preparing operation’s orders, storage, and inventory tracking of the laboratory and operational supplies. Responsible for carrying out receiving duties including, un-packing, product abd count verification, reception processing, and storin ...Read more about Technician, Stockroom and SuppliesMore
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About The RoleReporting to the Director of Infrastructure & Operations the Database Administrator (DBA) will have and maintain a very sound knowledge of Oracle, Microsoft SQL, and other popular databases, the DBA is responsible for maintaining, updating, and managing databases and the information that is stored within them, while ensuring compliance of pertinent regulations and procedures. The DBA will assist and provide guidance and best practices in the creation of Views, appropriate indexes, ...Read more about Database AdministratorMore
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About The RoleReporting to the Director of Infrastructure & Operations the Database Administrator (DBA) will have and maintain a very sound knowledge of Oracle, Microsoft SQL, and other popular databases, the DBA is responsible for maintaining, updating, and managing databases and the information that is stored within them, while ensuring compliance of pertinent regulations and procedures. The DBA will assist and provide guidance and best practices in the creation of Views, appropriate indexes, ...Read more about Database AdministratorMore
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About The RoleThe primary responsibility of the Report Coordinator will be to write research reports for studies performed at APC, both GLP and non-GLP studies. The Report Coordinator will ensure that all reports accurately depict the conduct of the study according to the raw data and protocol and will require a reasonable amount of supervision. The Report Coordinator will assist the Study Director throughout the lifetime of the study report from study termination through report finalization. Wh ...Read more about Report Coordinator I - RemoteMore
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About The Role The Clinical Quality Control Associate I is responsible for the quality control (QC) review of clinical trial data and assisting the Quality Systems team with QC related tasks. The Clinical Quality Control Associate I will conduct tasks performed within compliance of 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. Maintain and a ...Read more about Clinical Quality Control Associate IMore
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About the Role The Pharmacist is responsible for the execution of tasks performed and the handling of Investigational and Non-Investigation Products (IP/NIP) 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. Maintain and advocate a high level of customer service and quality within the department. Oversee and/or perform pharmacy relat ...Read more about PharmacistMore
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About The RoleThe lead archive activities and implement archive systems to ensure compliance with GLPrequirements. They will perform all necessary lead functions to effectively and efficientlycoordinate personnel assigned. Oversee training of Archive personnel for consistency with procedures. The Lead Archivist will provide feedback to supervisor on employee performance. What You'll Do Here Develop and maintain computerized files to support and maintain archive processes. Coordinate the receipt ...Read more about Lead ArchivistMore
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About The Role The Training Specialist (TS) works closely with the In Vivo Management Team and Training Program Manager to develop training standards and produce material to support the training and education of staff. You will also act as a certified trainer, training personnel to be competent in skills and knowledge. As a TS, you will serve as a role model to staff facility wide, promoting Alta’s high standards of animal welfare, technical proficiency, and data quality. What You'll Do Here ...Read more about Training Specialist - Preclinical LaboratoryMore
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About The Role The responsibilities of the Sample Management Specialist are to oversee tasks completion by Sample Management Technicians Service group, to ensure that sample management activities are provided to the laboratories with quality and efficiency, and to ensure integrity of study samples and material at all time. What You'll Do Here Be responsible for monitoring tasks conducted in the Sample Management Technicians Service group. To report major issues to the supervisor in a timel ...Read more about Sample Management SpecialistMore
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About The RoleParticipate in the day-to-day planning and organization of studies by working with multiple departments and coordinating activities. Oversee the conduct of animal research according to regulatory guidelines, protocols, and standard operating procedures (SOPs). Responsible for assisting Study Director (SD) in monitoring of studies and reporting directly to Study Coordinator Supervisor. The Study Coordinator I is involved in all areas of the study and is available for all questions r ...Read more about Study Coordinator IMore
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About The Role The Laboratory Specialist I is responsible for the processing 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).The work hours of this position are: Monday - Friday 1400-2230 with occasional weekends. What You'll Do Here Ensure the confidentiality of clinical trial participants and sponsors ...Read more about Laboratory Specialist IMore