Perform a variety of routine procedures following established methodologies including in vitro transcription, silica purification, tangential flow filtration, HPLC, cloning, gel electrophoresis, plasmid outgrowth and purification Perform analytical techniques and record quality metrics, with a strong focus on accuracy and reproducibility in work With supervision, develop

Coordinate tasks and activities of the LINC consortium, including sample and data exchange between sites Assist with ex vivo sample preparation and imaging Use image analysis and visualization software to perform data quality assurance and annotation Maintain communication with all LINC teams to track progress towards data acquisition and analysis milestones Assist with c

The Associate Director, Biomarker Operational Quality will provide biomarker quality leadership and oversight across GxPs related to research and development, implementation into clinical trials and potential commercialization of clinical biomarkers into IVDs. This leader will collaborate with business partners and GCP Operational Quality to drive quality outcomes and ope

Great long term contract opportunity for a Clinical Trial Manager with a local pharmaceutical company in Waltham MA. Looking for 5+ years clinical research experience in a pharmaceutical/biotech, CRO setting. Strong knowledge and understanding of GCP/ICH Guidelines for conducting clinical trials. Will be responsible for the oversight, coordination, and execution of clinic

of Position This staff position, reporting to the UNH Biotechnology Innovation Center ( BIC ) Director, provides scientific consulting support to customers of the UNH BIC Pandora Incubator, develops and delivers laboratory skills training curriculum supporting workforce training needs in the biosciences ecosystem, supports the work of doctoral and post doctoral scholars, a

Assist team in the coordination of project related activities (ie. surveys/interviews) at internal or external (on site & off site) study sites. Contact, recruit and enroll research participants, as needed. Maintain databases (including data entry) and project documentation with accuracy, as needed. Maintain the security and confidentiality of all study materials and data

The Director of Pricing and Packaging Strategy at Imprivata is responsible for developing, implementing, and optimizing product packaging and pricing strategies to match customer needs and to maximize revenue while ensuring market competitiveness. Imprivata primarily develops software for healthcare, but also packages services and hardware for full customer solutions. Thi

Operate LCMS, ELISA, PCR, GCMS, and ICP MS equipment to analyze pre clinical samples provided by formulation teams. Prepare pre clinical LCMS and GCMS samples with high precision and quality. Develop bioanalytical methods for the detection of target molecules in complex matrices (plasma, serum, organ tissues, urine, etc). Design automated liquid handling programs for bioa

Assists with coordination of CTNI managed clinical trials Competencies Required Excellent communication skills Sound interpersonal skills and the ability to supervise others Ability to work independently and display initiative to introduce innovations to research study Ability to prepare/monitor budgets Ability to identify problems and develop solutions Ability to priorit

unlocking global understanding. As a unique, world leading provider of technology enabled language, content, and intellectual property services, we remove the barriers to communication to make global connection possible. Our unrivalled experience and deep understanding of language have been developed over more than 60 years. As we look to shape the future, our ambition is

You will be expected to design and execute experiments systematically, analyze and report the results weekly. You willalso work closely with internal and external subject matter experts to identify and understand the nature of nascent technologies, including both characterization and purification systems. Hands on position starting July 2024 to December 2024. Onsite at our

Senior manager role that leads a team (or teams) that develops and introduces new or enhanced products and services in existing markets to strategically manage the product development lifecycle. Delivers enhancements that improve product using contract language, underwriting rules/guidelines, system/platform, automation, and use of pricing/predictive analytics. Creates ins

General Summary of Position Under the direction of the Principal Investigator or designee, the Research Coordinator I is responsible for carrying out multiple complex research protocols. Minimum Qualifications (Required) Bachelor's degree or equivalent in a social, behavioral or health science field plus some working experience in a related field. However, we will conside

The Research Associate I, Next Generation Sequencing (NGS) and Genomics will conduct laboratory functions under general supervision of the Head of NGS and Genomics. She/He will work as part of a team in the operation of the Next Generation Sequencing (NGS) and Genomics laboratory to achieve departmental goals. Responsibilities include hands on preparation of NGS libraries

The Research Associate I will conduct laboratory functions under direct supervision of the supervisor. They will work in compliance with established protocols, procedures, and regulatory requirements to achieve departmental goals. ESSENTIAL DUTIES AND RESPONSIBILITIES Perform day to day experimental activities including human material procurement activities i.e., preserva