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.

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.

Location : Cambridge, MA 02142 The Compound Manager is responsible for the registration, receipt, storage, distribution, inventory control, and quality oversight of chemical compounds supporting discovery research. This role serves as the primary custodian of medicinal chemistry compounds, safeguarding sample integrity, traceability, availability, and accurate documentation. The position partners closely with Medicinal Chemistry, Biology, DMPK, Analytical Sciences, Informatics, and external contract research organizations (CROs) to enable timely project execution and operational excellence.

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.