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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 ...Read more about Clinical Research Technician IMore
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About The Role The 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 (SOPs). What You'll Do Here Ensure the confidentiality of clinical trial participants and sponsors ...Read more about Screening Team Leader - Clinical OperationsMore
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About the Role Reporting to the Controller, the payroll technician will be a key contributor to the accounting department with the objective of delivering a high level of accuracy, integrity, and timeliness reporting with a focus on supporting the payroll and other accounting processes. What you’ll do here: Validate that all employees have submitted their timesheet and that supervisors have approved all timesheets for their employees. Conduct follow-up with employees and supervisors for missi ...Read more about Payroll TechnicianMore
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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 with ...Read more about Data Coordinator IMore
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Auxvasse, MO 65231, USA ● Columbia, MO, USA ● Req #4364Tuesday, April 23, 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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1200 Beaumont Ave, Montreal, QC H3N 1W5, Canada ● Req #4522Monday, April 22, 2024We are currently looking for a quality Control Associate to join our screening team. Want to contribute to research activities? You are dynamic and have good interpersonal skills? You have a rapid execution, while bringing attention to detail? This position is for you! What you’ll do here: Performing the live quality control (QC) of all data collected as part of screening and to ensure compliance to the study specific protocols and SOPs; Ensuring all corrections to raw data and derived data ...Read more about Quality Control Associate, screening departmentMore
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The Administrative Coordinator supports documentation activities and maintain documentation systems to ensure compliance. What You'll Do Here Maintain computerized files to support all documentation systems including training records and standard operating procedures (SOPs). Assist with notification and distribution of SOPs. Assist with verification of the controlled document binder sets. Assist with maintenance of curricula vitae and job descriptions for the department. Assist Archive staff wi ...Read more about Administrative CoordinatorMore
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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 ...Read more about Client Services Coordinator - HYBRIDMore
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Join Our Team as a Quality Assurance Auditor at our Cutting-Edge Preclinical Facility in Scott Township, Pennsylvania! Are you passionate about ensuring top-notch quality and compliance in a dynamic scientific environment? If so, we invite you to be part of our team at the forefront of scientific innovation. As a Quality Assurance Auditor, you'll play a pivotal role in maintaining our commitment to excellence and regulatory compliance. What You'll Do Here: Dive into the heart of our operations, ...Read more about Quality Assurance Auditor - GLPMore
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About The Role Reporting to the Associate Director, Human Resources, the Human Resources Coordinator is responsible for supporting the HR Department with the daily activities such as Employee lifecycle management (employee hires, transfers, promotions etc.…), creating and maintaining the electronic and hard-copy employee files, aiding in employee status changes, answering inquiries from employees. What You’ll Do Here Maintains human resource information system records and generates reports ...Read more about Human Resources CoordinatorMore
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1200 Beaumont Ave, Montreal, QC H3N 1W5, Canada ● Req #4400Friday, April 19, 2024What you’ll do here; Under the direction of the Cleaning Supervisor; Performs cleaning and housekeeping duties; Cleans and washes floors, walls, furnishings, fixtures, etc; Performs some or all of the additional responsibilities: specialized cleanings (i.e. White Room, Hep-C,etc); inventory management; training; floor stripping/Waxing. What you need to succeed; Bilingual (French/English); High School Degree completed; DEP in building maintenance an asset; Ideally, 3 to 5 years’ experience i ...Read more about Cleaner – level II - evening shiftMore
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About The Role The Study Director, Scientist will have a passion for preclinical research. The Preclinical Study Director represents the single point of control for assigned studies and following confirmation of appropriate education, training and experience. Study Directors are responsible for the interpretation, analysis, documentation, and reporting of study results for GLP and non-GLP studies. What You'll Do Here Performs functions of a Study Director with a full SD workload, including GL ...Read more about Study Director - ScientistMore
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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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About the Role The Scientist II – Laboratory Sciences provides technical and scientific expertise in flow cytometry 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, validation and execution of study samp ...Read more about Scientist II - Flow CytometryMore
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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 ...Read more about Senior Scientist - BiomarkerMore
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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 ...Read more about Senior Scientist - BiomarkerMore
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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 II - BiomarkerMore
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About the role The primary responsibility of the Report Writer will be to draft qualification, validation, and study sample analysis reports for studies performed in the Laboratory Sciences Department, supporting clinical and preclinical (GLP and non-GLP) studies for final review by the Responsible Scientist (e.g., Contributing Scientist, Principal Investigator). The Report Writer will ensure that applicable report sections are accurately completed under the supervision of the Responsible Scient ...Read more about Report Writer - Analytical Chemistry LabMore
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The Specimen Management Technician I, working under direct supervision, is responsible for the timely and accurate receipt, preparation, management, processing, shipping and/or storage of laboratory specimens in compliance with GLP guidelines, study protocols and SOPs. What You'll Do Here Responsible for working in compliance with GLP guidelines, protocols and SOPs. Coordinates and communicates with Study Directors, Coordinators, Pathologists, Laboratory staff and Vivarium Staff. Prepare, rece ...Read more about Specimen Management TechnicianMore
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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 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 ...Read more about Research Associate I, FormulationsMore
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Your Role The PK Scientist is responsible for gathering and synthesizing scientific information, performing pharmacokinetic (PK) and pharmacodynamics (PD) analyses, and providing high‑quality documents to support sponsors' research programs. What you’ll do here Serve as the PK representative or nonclinical principal investigator or contributing scientist (as needed) on assigned project teams. Review of protocols for studies of moderate to high complexity. Contribute to risk assessment and man ...Read more about PK Scientist IMore
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Laval, QC, Canada ● Montreal, QC, Canada ● Ontario, Canada ● Virtual ● Req #4388Wednesday, April 17, 2024Your Role The PK Scientist is responsible for gathering and synthesizing scientific information, performing pharmacokinetic (PK) and pharmacodynamics (PD) analyses, and providing high‑quality documents to support sponsors' research programs. What you’ll do here Serve as the PK representative or nonclinical principal investigator or contributing scientist (as needed) on assigned project teams. Review of protocols for studies of moderate to high complexity. Contribute to risk assessment and man ...Read more about PK Scientist IMore
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About the role The QA Auditor reports to the QA Manager and is responsible for carrying out systematic and independent examination (i.e., audit) of multiple clinical trial-related activities and documents, to determine whether the activities were conducted, and the data were recorded, analyzed, and accurately reported according to the protocol, standard operating procedures (SOPs) and Good Clinical Practices. They are responsible for reporting any findings to the Internal Study Team and depart ...Read more about Quality Assurance AuditorMore
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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 ...Read more about Paramedic - Clinical ResearchMore