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 : San Francisco, CA 94108 (On-Site) The Associate I, Technical Development Operations will participate in downstream areas of AAV development and production within process development for gene therapy programs and processes. The position supports downstream purification activities, production equipment operations, process development experiments, documentation, and process improvement activities in a collaborative, onsite lab and office environment.

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.

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.

location : Tucson, AZ 85755 Research Associate III supporting Personalized Healthcare Solutions and Ventana projects through research, development, and manufacturing laboratory experimentation. The role requires experience in experimental design, execution and interpretation, quantitative analysis, technical documentation, and regulated laboratory environments.