Location (mandatory): Fully Remote (EST Preferred) Contract (mandatory): 04 Months Contract + (Highest possibilities of extension) Clinical Program Sourcing & Contract Management (CPSCM) Manager is responsible for leading end-to-end study-level contracting execution for complex clinical vendor categories supporting global clinical trials (Phase I–IV). Reporting to the Sr. Manager, CPSCM, this role serves as the contracting lead for high-value and high-impact service areas such as CRO services, central laboratories, clinical technology providers, and other large functional service categories. This role works exclusively with established preferred vendors operating under existing Master Service Agreements (MSAs) owned by Category Management. This role is accountable for managing the specification intake process with Clinical Trial Leads (CTLs) and Study Teams, developing and negotiating vendor budgets, ensuring scope accuracy, preventing duplication of services, and executing Statements of Work (SOWs), amendments, and closeout documentation in alignment with study timelines and Vendor Sourcing Timelines (VSTs). The Manager serves as a key procurement partner to Clinical Operations, Category Management, Finance, and Legal to ensure study timelines, commercial frameworks, and governance requirements are met while delivering compliant, commercially sound, and predictable contracting outcomes.

Location : Tucson, AZ 85755 We are seeking a Clinical Lab Scientist I to join our team in Tucson, AZ. This is a first-shift, 12-month contract opportunity supporting clinical laboratory and medical research activities. The ideal candidate will have 1–3 years of clinical laboratory experience, with histology or immunohistochemistry (IHC) experience preferred. Candidates who are detail-oriented, collaborative, and passionate about advancing clinical research are encouraged to apply.

location : Groton, CT 06340 We are seeking a Lab Technician to support necropsy and histology activities for rodent and non-rodent safety studies. This role is responsible for laboratory support functions, specimen handling, equipment maintenance, and ensuring compliance with GLP, SOPs, EHS standards, and animal welfare regulations. Candidates with a background in Histology or Animal Science are encouraged to apply, including entry-level professionals with relevant education

Location : Cambridge, MA 02140 Seeking a Comparative Medicine Trainer to provide hands-on training in laboratory animal techniques, coordinate training programs, support vivarium operations, and ensure compliance with animal welfare regulations. The ideal candidate will have experience working with rodents, laboratory animal training, and regulatory standards in a research environment.

Location (mandatory): Tucson, AZ 85755 (Onsite) This is an onsite position for a Research Associate II in Research & Early Development supporting Ventana projects. The role is responsible for conducting research, development and manufacturing laboratory experimentation and other scientific activities. The primary focus is on slide imaging and image acquisition using systems such as the DP600s, 200s, VS200, and multispectral flash instruments. The individual will perform repetitive, well-defined tasks including virtual staining and assembling slide cohorts to enable the development of AI algorithms while ensuring compliance with GMP, GLP, Design Control, and company procedures.

Location (mandatory): San Diego, CA 92121 The Bioinformatics RA III or Scientist I (AI/ML – Assay Design) is responsible for developing AI and machine learning solutions to optimize assay and primer design for diagnostic platforms. This role combines bioinformatics, molecular biology, and data science to build intelligent pipelines that analyze high-throughput PCR and sequencing data, enabling data-driven assay development and improved diagnostic performance.

Location (mandatory): Portsmouth NH Looking for a candidate with science degree and some manufacturing experience

Location (mandatory): Vacaville CA The Manufacturing Associate is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. Level I associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique in handling of products and materials.

Location (mandatory): Vacaville CA We are seeking a highly motivated and experienced Quality Systems Support Specialist to join our team in Vacaville, CA. In this role, you will provide essential support to the Quality System Management process with document control and PQS integration, ensuring compliance with cGMP and global requirements.