Small Description: The Project Materials Coordinator will oversee and coordinate material procurement and tracking activities for nuclear power plant projects, including refueling outages, forced outages, and on-line maintenance. The role involves tracking material requests, purchase orders, and catalog identifications (CATIDs), verifying incoming materials, coordinating warehouse staging, and maintaining material quality, quantity, and traceability throughout the project lifecycle. The ideal candidate will have experience in materials management, inventory control, procurement coordination, or a technical field, along with familiarity with Asset Suite 9 and Microsoft Office. Candidates must be comfortable using hand and power tools, handling materials, and occasionally lifting up to 50 lbs. or more.

The US Patient Safety Sr. PV Clinical Scientist – Pharmacovigilance (PV) Compliance Team performs tactical and operational responsibilities, including the collection, clinical review, evaluation, and processing of adverse event (AE) information received by US Patient Safety. The Sr. PV Clinical Scientist leads clinical review of USPS cases processed in-house or externally by vendors and supports the US Patient Safety PV Clinical Associate Group Director and PV Clinical Group Director – PV Compliance Team in all activities under the direction of US Patient Safety PV Clinical Management. The role requires in-depth knowledge of Individual Case Safety Reports (ICSRs), the ability to work autonomously with minimal supervision, and the capability to lead projects, coach colleagues, and provide guidance. Working Model: Hybrid, South San Francisco, CA Working Days: Monday through Friday Working Hours: 8:00 AM to 4:30 PM PT Interview Format: Two Rounds 1. Hiring Manager – 30 minutes 2. Upper Management – 30 minutes

Location:-Tucson, AZ 85755 Seeking a detail-oriented Biospecimen Coordinator to support onsite BioSample Management operations. The role will focus on sample intake, triage, accessioning, labeling, QC, tracking, documentation, shipment coordination, and maintaining chain of custody. The ideal candidate will have 1–5 years of relevant sample/specimen handling experience and strong attention to detail, communication, and organizational skills

Location (mandatory): Cambridge, MA 02142 (On-site) We are seeking a highly motivated and creative individual with some process development experience to join our Oligonucleotide/Peptide Purification Development team. This position provides an exciting opportunity to develop robust, high purity, state of the art processes for the purification of oligonucleotides and gain hands-on experience and exposure to the design and development of manufacturing processes for clinical and commercial therapeutics. The individual will contribute to developing new cutting-edge technologies in oligonucleotide and peptide purification.

Location mandatory: Cambridge, MA 02141 (Onsite) The Quantitative Pharmacology (QP) group at Client is seeking a Data Science contractor to develop and enhance Pharmacokinetics (PK)/Pharmacodynamics (PD) modeling, data analysis, and decision-support tools for drug discovery and development. The successful candidate will support the development and enhancement of quantitative pharmacology tools, including PK/PD models, interactive applications using Python and Shiny for Python, automated analytical workflows, model diagnostics and visualization, and agentic AI-enabled workflows to streamline scientific analysis and decision making.

Andover, MA 01810 Monday–Friday Molecular and Cellular Biologist supporting multi-omics and systems biology approaches to improve mammalian/CHO cell culture performance for recombinant protein production. The role is heavily focused on hands-on mammalian cell culture, molecular biology experimentation, sample generation, and downstream data analysis.

Medical Monitor responsible for providing medical monitoring and/or study start-up activities for 1-3 Ophthalmology programs under the direction of the Global Medical Lead (GML). The position requires 20-30 hours per week, with the potential to increase to 40 hours, and includes medical oversight, safety monitoring, clinical trial data review, and support for study-related medical and safety activities.

Location - Tucson, AZ Entry-level Research Associate I role supporting early-phase assay development through laboratory experimentation, scientific activities, technical documentation, quantitative analysis, and basic computational biology tasks. The position requires a Bachelor’s degree in a relevant scientific field and 0–2 years of relevant laboratory or industry experience.

Location : Groton CT 06340 (Onsite) The main function of a Research Associate is to support the execution of health outcomes research studies that evaluate the value of healthcare interventions. This role involves managing study activities, analyzing data, and contributing to the development of scientific communications and strategic planning.