At SGS Consulting, we go beyond resume-job matches, creating meaningful connections and pathways for individuals to thrive in defining careers.
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SGS_JOB_2145
Contract - 12 Months (possible extension)
Location - South San Francisco, CA 94080. Cell Line Development Research Associate is involved in the creation of stable cell lines for the recombinant adeno-associated viral vector (rAAV) production processes. He/she executes experiments, produces relevant documentation, and works under supervision. He/she will be responsible for: Culturing mammalian cells for viral production in shake flasks, spinner flasks, spin tubes, deep well and automation platforms. Performing experiments in the development, optimization and scale-up of AAV producer cell lines. Preparing process development protocols, data analysis summaries, technical reports, and other relevant process documentation. Optimization of transfection and transduction protocols for newly engineered cell lines. Maintaining an accurate laboratory notebook. Ensuring work conforms to applicable quality and safety standards. Participating on project teams (as needed). Must be able to lift 25 pounds. Due to the inherent nature of cell culture, some weekend work and/or work on holidays may be needed. On occasion, long work hours may be required depending upon the experiment schedule. Handling large volumes of cell culture or related materials, such as tens of liters, may be required. Also, several viral materials, including AAV, may be involved in the work.
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.
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
At SGS Consulting, we go beyond resume-job matches, creating meaningful connections and pathways for individuals to thrive in defining careers.