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  • Laval, QC, Canada ● Req #4459
    Tuesday, June 18, 2024
    About The Role We 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 Here Responsible for sample control activities including the receipt, invento ... More
  • Sacramento, CA, USA ● Req #4735
    Monday, June 17, 2024
    About the role Do you love working with animals? Do you want to contribute to advancing human health science research? Do you like to work in small teams? Altasciences is seeking Research Associates at all levels of experience that have a passion for scientific research. In this position your focus will be working directly with larger animals in the collection of data and in support of the development of human medicine. You will perform technical procedures to support advancements in pharmaceuti ... More
  • Columbia, MO, USA ● Req #4444
    Monday, June 17, 2024
    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 ... More
  • Laval, QC, Canada ● Req #4730
    Friday, June 14, 2024
    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 ... More
  • Seattle, WA, USA ● Req #4739
    Friday, June 14, 2024
    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 ... More
  • Laval, QC, Canada ● Req #4620
    Friday, June 14, 2024
    About The Role The Marketing Manager, Preclinical Services collaborates with multiple subject matter experts to coordinate and execute a fully integrated marketing strategy for the Preclinical services, including creative campaigns, events, and digital marketing. The Marketing Manager, Preclinical Services must remain abreast of the latest market/industry trends, as well as understand the Altasciences value proposition and customer base, in order to build brand awareness and support internal ... More
  • Everett, WA, USA ● Req #4315
    Friday, June 14, 2024
    About the role Provides support to Client Managers, Business Development and Proposals staff. Coordinate onsite meetings client's and staff, prepares client agendas, prepare client conference rooms, attends meetings as needed. Support Proposals with Salesforce data entry. What You'll Do Here Comfortable with client interactions and strong customer service abilities and to advocate on client’s behalf. Support Client Managers and Business Development in the coordination of onsite meetings with st ... More
  • Columbia, MO, USA ● Req #4504
    Friday, June 14, 2024
    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 ... More
  • 1200 Beaumont Ave, Montreal, QC H3N 1W5, Canada ● Req #4452
    Friday, June 14, 2024
    About 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 ... More
  • 1200 Beaumont Ave, Montreal, QC H3N 1W5, Canada ● Req #4451
    Friday, June 14, 2024
    About 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 ... More
  • Columbia, MO, USA ● Req #4665
    Friday, June 14, 2024
    About the Role The Construction Technician (also known as Facilities Assistant III) role is an advanced level of technician classification and will be proficient in all FA I, II, and III skills. The FA III is expected to perform a full range of duties. The FA III requires specialized knowledge and complex construction related work. The FA III will provide direction to lower-level technicians and requires general supervision from the Director of Facility Operations. The FA III may manage invento ... More
  • Cypress, CA, USA ● Req #4646
    Friday, June 14, 2024
    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 Do Here Ensure the confidentiality of clinical trial volunteers and sponsors is respected. Assists in screening admission procedures. Preparation of screening materials. Volunteer identity verification. Update particip ... More
  • Everett, WA, USA ● Req #4687
    Friday, June 14, 2024
    About the role The Training Lead works under limited supervision and supports the Invivo Operations department by providing the development, coordination, and assurance of GLP compliant training procedures and practices. Works, as delegated by department management, to ensure the successful completion of training activities and maintenance of technical skills. Provides administrative and organizational support in training planning, scheduling, coordination, document management and reporting. Per ... More
  • Overland Park, KS, USA ● Req #4595
    Friday, June 14, 2024
    About 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 ... More
  • Everett, WA, USA ● Req #4653
    Friday, June 14, 2024
    About the role   The Research Associate Lead will provide technical leadership in the assigned area (e.g., chromatography, ligand-binding assay, flow cytometry, molecular biology). Trains junior staff and oversees their activities, including instrument operation, troubleshooting, and maintenance. Executes projects, and identifies and acquires the necessary facilities, equipment and procedures performing the below duties.   What You’ll Do Here Oversee and perform study activities according to th ... More
  • Columbia, MO, USA ● Req #4628
    Friday, June 14, 2024
    About The Role In the performance of their respective tasks and duties, the Associate Scientist, Dose Concentration Analysis are expected to be engaged in the conduct of or responsible for the supervision of a nonclinical laboratory study shall have the education,training and experience, or combination thereof, to enable that individual to perform their assigned functions. They will also need to comply with Good Laboratory Practices (GLP), and all regulatory requirements applicable to the posit ... More
  • Auxvasse, MO 65231, USA ● Columbia, MO, USA ● Req #4643
    Friday, June 14, 2024
    About The Role Altasciences is looking for a Quality Control Coordinator to ensure all study and facility data is in accordance with APC Standard Operating Procedures (SOP's), the study protocol, and Good Laboratory Procedure (GLP) requirements.  What You'll Do Here Maintain competency in the current APC Standard Operating Procedures (SOPs), GLP regulations, and ALCOA+. Reviews protocols and study schedules for all studies prior to data collection. Suggests areas of improvement to the protocol ... More
  • Everett, WA, USA ● Req #4654
    Friday, June 14, 2024
    The QC Reviewer II is responsible for performing quality control including daily in-process quality control on various projects and training employees in Laboratory Sciences, including other QC Reviewers. The QC Reviewer II ensures that all project related documentation is filled out accurately and in a timely manner by the analysts and that all procedures are respected as per the company’s SOPs. What You'll Do Here Trains new QC reviewers and other Laboratory Sciences staff on how to QC table ... More
  • Columbia, MO, USA ● Req #4636
    Friday, June 14, 2024
    About The RoleThe Animal Care Technician is be responsible for the coordination, movement, and maintenance of facility equipment and supplies. Participate in sanitation through the central cage wash/ In-life and performs monthly environmental tasks for the facility. What You'll Do Here Handle, restrain, and manipulate animals consistently, professionally, and with empathy. Completes training focused on general core skills for the area of work. Understands the importance of the work done at a CR ... More
  • Overland Park, KS, USA ● Req #4594
    Friday, June 14, 2024
    About the Role The Clinical Safety Officer (Paramedic) will oversee the safety of clinical trial participants during study conduct and the maintenance of safety equipment. The Clinical Safety Officer will execute tasks performed in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOP)s.   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 ... More
  • Cypress, CA, USA ● Req #4604
    Friday, June 14, 2024
    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 Do Ensure the confidentiality of clinical trial participants and sponsors is re ... More
  • Overland Park, KS, USA ● Req #4508
    Friday, June 14, 2024
    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 ... More
  • Overland Park, KS, USA ● Req #4529
    Friday, June 14, 2024
    About the Role The Clinical Research Technician I will work with Clinic Operations teams to execute clinical trial activities. Responsibilities of the Clinical Research Technician I 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 eve ... More
  • Everett, WA, USA ● Req #4559
    Friday, June 14, 2024
    About the role   The Senior Scientist – Laboratory Sciences provides technical and scientific expertise in biomarker assays for method development, validation/qualification and execution of analytical projects in support of preclinical /clinical studies.   What You'll Do Here   Perform all study work in compliance with GLP regulations and maintain all related documentation in accordance with SOPs, Study Protocol, and Analytical Project Plans. Method development, qualification, validation and ex ... More
  • Columbia, MO, USA ● Req #4424
    Friday, June 14, 2024
    About The RoleThe Research Associate I, Formulations will prepare dose formulation and other study related materials in compliance with relevant regulations including GLP. Be responsible for test/control article receiving, tracking, returning and/or disposition. The Research Associate I, Formulations will also monitor laboratory supplies and cleanliness to provide a clean and regulatory compliant laboratory. What You'll Do Here Follow all Altasciences Standard Operating Procedures (SOPs) and is ... More