1 - 20 of 32 Jobs

Clinical Trial Manager

Axiom Global Technologies, Inc.

Jersey City, New Jersey, USA

Contract, Third Party

Role: Clinical Trial Manager Location: New Jersey Duration: 6+ Months The Clinical Trial Manager is responsible for managing all aspects of clinical trials, from study initiation through to study completion. This includes coordinating cross-functional teams, managing external vendors, ensuring compliance with Good Clinical Practice (Google Cloud Platform) and International Council for Harmonization (ICH) & FDA guidelines, and maintaining adherence to regulatory requirements. Study Planning and

Breeding and Colony Management Technician

Talent Group

Columbus, Ohio, USA

Contract

Key Responsibilities: Perform routine animal care (cage changes, breeding, weaning, health checks).Execute breeding schemes and genetic sampling under IACUC guidelines.Maintain accurate records and adhere to SOPs for personnel and animal safety.Communicate effectively with the team and follow detailed instructions.Qualifications: High School diploma (0-3 years relevant experience).Proficiency in Microsoft Office; strong organizational and communication skills.Passionate about animal welfare and

Sr. Scientist (Bioassay)

IT ENGAGEMENTS, INC.

Arkansas, USA

Contract

Greetings from IT Engagements ! IT Engagements is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. We have an immediate opening for the below position with our premium clients. Job: Sr. Scientist (Bioassay) Location: Remote Duration: 12+ Months Job I'd: 35555597 The ideal candidate is responsible for overseeing the development, validation, and implementation of PK, immunogenicity, and cell based assays in both the regulated and non-regul

Research Associate II (Virology)

Zachary Piper Solutions, LLC

Rockville, Maryland, USA

Full-time

Piper Health and Sciences is seeking a Research Associate II to support a well-known research organization specializing in infectious disease research in the Frederick, MD area. The Research Associate II will be responsible for performing TCID50 and plaque assays. Responsibilities of the Research Associate II include: Design, generate, and characterize recombinant proteins Perform mammalian cell culture, transient transfections, protein expressions, protein purifications, and micro pipetting in

Research Associate II

Software Guidance & Assistance

Tucson, Arizona, USA

Contract

Software Guidance & Assistance, Inc., (SGA), is searching for a Research Associate II for a contract assignment with one of our premier Pharmaceutical services clients in Tucson, AZ. Responsibilities : Responsible for conducting research, development and manufacturing laboratory experimentation and other scientific activities to support the firm's projects. Exercises technical expertise and discretion in the design, execution and interpretation of experiments that contribute to project strat

SharePoint Farm Administrator

LinTech Global Inc.

Frederick, Maryland, USA

Full-time

SharePoint Farm Administrator to support a USAMRIID in Fort Detrick, Maryland. Onsite 3 Days Required and 2 Days Remote Target Salary: $120 to $130K Position Overview: The SharePoint Farm Administrator will be responsible for providing support for all USAMRIID SharePoint servers, both physical and virtual. The SharePoint Farm Administration support for systems include, but are not limited to, Windows Server Operating Systems, IIS, SQL Server, and the Good Laboratory Practice (GLP) Testing & Eval

Analyst, QC

Talent Software Services, Inc

Novato, California, USA

Contract

Analyst, QC IJob Summary: Talent Software Services is in search of an Analyst, QC for a contract position in Novato, CA. The opportunity will be one year with a strong chance for a long-term extension.Position Summary: Join our team in Novato, CA, where you'll have the opportunity to work in a dynamic environment and contribute to cutting-edge projects. We are seeking a dedicated professional to perform essential quality control functions.Primary Responsibilities/Accountabilities: Perform bioch

Senior Lab Supervisor

Software Guidance & Assistance

Santa Clara, California, USA

Contract

Software Guidance & Assistance, Inc., (SGA), is searching for a Senior Lab Supervisor for a contract assignment with one of our premier Pharmaceutical Services clients in Santa Clara, CA. Responsibilities : Ensures the safety, compliance, and smooth operations of research and development laboratories associated with the team. Regulates and maintains the infrastructure of the labs to ensure necessary services are available to scientists. Oversees/coordinates work processes and operation of a

Analytical Process Chemist

Austin Powder Red Diamond

Allensville, Ohio, USA

Full-time

Job DescriptionJob DescriptionAustin Powder Company is seeking an Analytical Chemist to use their knowledge of chemistry, instrumentation, computers, and statistics to solve problems in almost all areas of chemistry for our Red Diamond location. Key Responsibilities and Duties Raw Material Testing when neededField Complaints/ReportsA/QC FunctionsEnvironmental Support both analytical and system designMethod Development/ProceduresInstrumental chemical analysis (FTIR, DSC, HPLC, GC, Colorimetry)Lab

Research Scientist/Study Director - Proteins

Northern Biomedical Research Inc

Portage, Michigan, USA

Full-time

Job DescriptionJob DescriptionRole Summary The Research Scientist (RS) will be engaged in serving as the single point of study control and overall planning and conduct of the study in accordance with applicable regulatory guidelines and contemporary scientific practice. Additionally, the RS will ensure that all Good Laboratory Practices (GLP) are met, and that the outcome of the study is valid and reliable. This role requires experience with LBA method development, GLP-compliant method validatio

Sr. Clinical/Regulatory Affairs Specialist

Cytek Biosciences Inc

Fremont, California, USA

Full-time

Job DescriptionJob DescriptionSr. Clinical/Regulatory Affairs Specialist Lead Clinical Studies. Drive Regulatory Success. Make a Global Impact. We re seeking a Sr. Clinical/Regulatory Affairs Specialist to manage all clinical study activities and regulatory submissions for global product market clearance. If you re passionate about driving clinical excellence, working cross-functionally, and supporting regulatory success, this role is for you. What You ll Do: Clinical Study Management Lead and c

Executive Director, Toxicology

Lifelancer

Remote or Menlo Park, California, USA

Full-time

Job DescriptionJob DescriptionJob Title: Executive Director, Toxicology Job Location: United States Job Location Type: Remote Job Contract Type: Full-time Job Seniority Level: Director Position Summary The Executive Director, Toxicology will provide toxicology expertise to develop and execute non-clinical safety assessment strategies and help to derisk and advance research and development stage programs. The Executive Director will also provide broader non-clinical development expertise in the

Dir./Sr Dir.- Clinical Assays/Bioanalytics

Solid Biosciences

Boston, Massachusetts, USA

Full-time

Job DescriptionJob DescriptionJob Title: Director / Sr Director-Bioanalytics/Clinical Assays Reports to (title): Head of Research, Translational Development Solid Summary: Solid Biosciences is a life science company focused on advancing a portfolio of neuromuscular and cardiac programs, including SGT-003, a differentiated gene therapy candidate for the treatment of Duchenne, AVB-401, a gene therapy program for the treatment of BAG3 mediated dilated cardiomyopathy, AVB-202-TT, a gene therapy prog

Principal HRIS Specialist

TEKsystems

Lancaster, Pennsylvania, USA

Full-time

Job DescriptionJob DescriptionTop 3: 1. 4 years of experience in Lawson HR System 2. 4 years of HRIS maintenance experience 3. Microsoft Excel formulas, pivot tables, analyze data and for uploading spreadsheets US Citizens and GC Holders Plus: --Degree is a plus --Access for reporting Job Description: In a high growth company, the HR System is vital to sustain the growth and allow each facet of HR to continue moving forward. The Principal Specialist will be tasked with responsibilities in all

Research Analyst (BioAnalytical LC-MS/MS)

CMIC, Inc.

Hoffman Estates, Illinois, USA

Full-time

Job DescriptionJob DescriptionCMIC, Inc. is seeking a Research Analyst responsible for conducting lab activities in accordance with applicable Methods, Plans, SOPs/SWPs, GLP regulatory guidelines and 21 CFR Part 11 under guidance from Senior Analysts and Principal Investigator. Conduct Bio-analysis development, validation and sample analysis using mass spectrometry and chromatography for qualitative and quantitative characterization/analysis of small molecules, peptides, proteins in a GLP enviro

QC Specialist, Data Reviewer

Pharmaron

Woburn, Massachusetts, USA

Full-time

Job DescriptionJob DescriptionPosition: QC Specialist, Data Reviewer Department: Quality Control FLSA Status: Exempt Location: Woburn, MA (ON-SITE) Job Overview: The QC Specialist, Data Reviewer will work in a cGxP compliant Laboratory to support quality control of Bioassay and Bioanalytical Assay Validations and Sample Analysis in addition to reviewing controlled documentation and RUO data. Additional tasks: Review SOPs, validation reports, qualification documents, and sample analysis data for

Senior QA Specialist

Global Life Science Hub

Piscataway, New Jersey, USA

Full-time

Job DescriptionJob DescriptionGlobal Life Science Hub is thrilled to partner with a biologics powerhouse on the brink of exponential growth! With 2 commercial products already on the market and a third approval expected any day, they re expanding and renovating their New Jersey facility to scale up production from 50L to 2000L. We re kicking things off by rapidly expanding their quality team with the hire a Senior QA Specialist. The appointed candidate will support the activities of the QA depar

Data Analyst II, Data Integrity

Labstat International Inc.

Kitchener, Ontario, Canada

Full-time

Job DescriptionJob Description Certified Group is a leading North American provider of laboratory testing, regulatory consulting, and certification & audit services. Certified Group includes Food Safety Net Services (FSNS), Certified Laboratories, EAS Consulting Group, Labstat International Inc., Advanced Botanical Consulting & Testing (ABC Testing Inc.), Microconsult Inc., and Micro Quality Labs Inc. Certified Group provides laboratory testing and regulatory consulting services in the food & b

Research & Development Scientist (2-year fixed contract)

Eco Animal Health

Urbandale, Iowa, USA

Full-time

Job DescriptionJob DescriptionSalary: $45,000 - $60,000 dependent on experience RESEARCH AND DEVELOPMENT SCIENTIST 2-YEAR FIXED TERM CONTRACT We have an exciting new opening for a Research & Development Scientist to join our small, dynamic team of R&D specialists. Candidates must be capable of evaluating, recommending, and applying state-of-the-art technology in vaccine research and development. Who is ECO Animal Health? ECO Animal Health (ECO) is a global organisation, headquartered in London (

Senior Quality Specialist

The Rockridge Group

Wilson, North Carolina, USA

Full-time

Job DescriptionJob DescriptionJob Title: Sr. Quality Specialist I Method Validation and Development Chemist Location: Wilson, NC Shift Schedule: Monday-Thursday (10 hours). Hours flexible, typically 7:00am-5:30pm $95k 100k w/ 10% bonus potential (Direct Hire) Primary Responsibilities Serve as an analytical project lead for all assigned products. Project leads ensure all required testing is completed to support the overall project timeline. Perform all assigned testing in a timely and organized m