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1200 Beaumont Ave, Montreal, QC H3N 1W5, Canada ● Montreal, QC, Canada ● Req #3633Monday, March 27, 2023About The Role As a key member of the Altasciences IT Customer Support function, the IT Technician 3 is responsible for supporting Altasciences’ internal IT service customers in their usage of the tools provided by the Altasciences IT department such as Windows desktop and laptop computers, tablets, desktop and enterprise software, and mobile phones. The IT technician 3 responds to and tracks customer requests and solutions via an IT Service Management system. The IT Technician 3 is expected to ...Read more about IT Technician IIIMore
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About the Role: The Equipment Specialist will ensure that equipment used in the conduct of nonclinical laboratory studies is of appropriate design and adequate capacity to function according to the protocol, and that equipment is suitably located for operation, inspection, cleaning, and maintenance in compliance with the research protocol, Standard Operating Procedures (SOP’s) and Good Laboratory Practice (GLP) regulations.What You'll Do:Ensure equipment is adequately inspected, cleaned, maintai ...Read more about Equipment SpecialistMore
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About the Role: The Biostatistics Manager is responsible for leading the team of Biostatisticians and/or Statistical Programmers in the design, analysis, and interpretation of clinical study data ensuring efficient production of high quality client and internal deliverables. They take accountability for overall planning, organization, and coordination of Biostatistics and/or SAS programming support for all assigned studies and programs. In addition, the Manager, Biostatistics is responsible for ...Read more about Biostatistics ManagerMore
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Cypress, CA, USA ● Req #3500Friday, March 24, 2023About the Role The 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 nee ...Read more about Clinical Research Technician - (CPT1 or MA Required)More
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Kansas, USA ● Overland Park, KS, USA ● Req #3621Friday, March 24, 2023About 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 performed are executed in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOP)s.What You'll Do HereEnsure the confidentiality of clinical trial participants and sponsors i ...Read more about Participant Recruitment AgentMore
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About The Role The Facilities, Housekeeper is responsible for the cleanliness and orderly condition of the site What You'll Do Here Regular cleaning of suites, bathrooms, hallways, lobbies, stairs and other areas so that health standards are met. Perform heavy cleaning tasks, including but not limited to, cleaning floors, washing walls/glass and removing rubbish. Make beds as instructed. Maintain cleaning carts with linens, toiletry items, cleaning supplies a ...Read more about HousekeeperMore
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Kansas, USA ● Overland Park, KS, USA ● Req #3634Thursday, March 23, 2023About 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 an ...Read more about Clinical Quality Control Associate IMore
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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, di ...Read more about Technician, Sample ManagementMore
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About The Role The Proposal Coordinator is responsible for supporting the Lab Proposal and Lab Business Development teams by either facilitating or directly compiling the study specific components required to produce a compelling and winning proposal document, in the established delays. The Proposal Coordinator also supports the Lab Business Development team by coordinating and executing administrative tasks, as needed, in primary support of the Proposal team’s objectives. ...Read more about Proposals CoordinatorMore
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About The Role The Proposal Coordinator is responsible for supporting the Lab Proposal and Lab Business Development teams by either facilitating or directly compiling the study specific components required to produce a compelling and winning proposal document, in the established delays. The Proposal Coordinator also supports the Lab Business Development team by coordinating and executing administrative tasks, as needed, in primary support of the Proposal team’s objectives. ...Read more about Proposals CoordinatorMore
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About the RoleThe Associate Study Manager I will assist with planning and coordinating clinical trials and will work to execute clinical trials. Responsibilities of the Associate Study Manager I include review of clinical trial documentation, resolution of queries and execution of task performed/clinical activities in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs).What You'll Do HereEnsure the confidentiality of clinical trial participants ...Read more about Associate Study Manager IMore
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The Animal Care Tech provides basic husbandry services or perform tasks involved in the care, maintenance, and welfare of animals (non-human primates). What You’ll Do Here: Comply with the appropriate safety and study requirements as described in the Standard Operating Procedures (SOPs), and governmental regulations.Comply with appropriate safety and health practices including personal protective equipment and barrier requirements, as applicable.Recognize animal behavior, health status a ...Read more about Animal Care TechMore
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Kansas, USA ● Overland Park, KS, USA ● Req #3209Wednesday, March 22, 2023About 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
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Kansas, USA ● Overland Park, KS, USA ● Req #3572Wednesday, March 22, 2023About the RoleThe Manager, Participant Relations and Clinical Support is responsible for ensuring that the participant’s experience is positive with the goal to increase repeat participation rate of subjects in studies. Will also coordinate and maintain actions taken with regards to complaints, sanctions and overall status of the participates. The Manager, Participant Relations and Clinical Support will also be responsible for supporting the clinical team with Clinspark (material, setup etc).Wha ...Read more about Manager, Participant Relations & Clinical SupportMore
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Kansas, USA ● Overland Park, KS, USA ● Req #3550Wednesday, March 22, 2023About the RoleThe Associate Study Manager I will assist with planning and coordinating clinical trials and will work to execute clinical trials. Responsibilities of the Associate Study Manager I include review of clinical trial documentation, resolution of queries and execution of task performed/clinical activities in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs).What You'll Do HereEnsure the confidentiality of clinical trial participants ...Read more about Associate Study Manager IMore
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Kansas, USA ● Overland Park, KS, USA ● Req #3535Wednesday, March 22, 2023About the RoleThe Screening Technician III will work with the Screening team to screen participants enrolled in clinical studies. Responsibilities of the Screening Technician III 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)sWhat You'll Do HereEnsure the confidentiality of clinical trial participants and sponsors is ...Read more about Screening Technician III - PhlebotomistMore
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About the RoleThe Study Manager is responsible for the overall supervision, coordination and management of assigned clinical trials in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs). What You'll Do HereEnsure the confidentiality of clinical trial participants and sponsors is respected.Supervise and/or oversee all study related procedures.Act as a resource to indirect reports as well Clinical Operations team members.Oversee trial progression ...Read more about Study ManagerMore
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Kansas, USA ● Overland Park, KS, USA ● Req #3390Wednesday, March 22, 2023About the RoleThe 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 (SOP)s.This will be a night shift position from 7pm-7am.What You'll Do HereEnsure the confidentiality of clinical trial participants and sponsors is respected.Understand pr ...Read more about Clinical Research Tech II - NightMore
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Kansas, USA ● Overland Park, KS, USA ● Req #3388Wednesday, March 22, 2023About the RoleThe 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 (SOP)s.This will be a night shift position from 7pm-7am.What You'll Do HereEnsure the confidentiality of clinical trial participants and sponsors is respected.Unde ...Read more about Clinical Research Technician I - NightMore
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About the RoleThe Clinical Safety Officer 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 HerePerform scheduled inspection of emergency crash carts, inventory/inspect the contents and maintain up to date records. Act as a mentor to Clinical Operations t ...Read more about Clinical Safety OfficerMore
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Kansas, USA ● Overland Park, KS, USA ● Req #3518Wednesday, March 22, 2023The Supervisor, Staff Scheduling is responsible for the supervision and Management of the Staff scheduling team and ensuring the efficient planning and scheduling of staff resources to meet clinical trial activity needs. What You Will do Here: Management of the staff scheduling team, including but not limited to, PTO management, timesheet approval, ongoing and yearly performance reviews, employee hiring, disciplinary actions and termination. Perform, direct and/or ...Read more about Supervisor, Staff SchedulingMore
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Kansas, USA ● Overland Park, KS, USA ● Req #3199Wednesday, March 22, 2023About 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 (SOP)s.What You'll Do HereEnsure the confidentiality of clinical trial participants and sponsors is respected.Understand protocol driven timed study events and acceptable ...Read more about Clinical Research Tech II - PhlebotomistMore
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Kansas, USA ● Overland Park, KS, USA ● Req #3201Wednesday, March 22, 2023About the RoleThe 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 (SOP)s.What You'll Do HereEnsure the confidentiality of clinical trial participants and sponsors is respected.Understand protocol driven timed study events and acc ...Read more about Clinical Research Technician I - NightsMore
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Kansas, USA ● Overland Park, KS, USA ● Req #3206Wednesday, March 22, 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 Technician 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 mentor to Clinical Operations Team Members.Ensure the confidentiality of clinical trial participants and sponsors is respected.Assess Safety improv ...Read more about Clinical Safety TechnicianMore
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About The Role The Senior Analyst is responsible bench work and documentation based on their assignment to the laboratory. Ensures that analyses are performed in accordance with appropriate SOPs What You'll Do Here Technical assay expert in multiple assay types from sample preparation to data generation. Responsible for experiments at the bench based on training and competencies can be assigned conduct, method development, validation and/or sample analysis ...Read more about Senior Analyst, LBAMore