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

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

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

This individual will support analytical development activities conducted at Sarepta Andover facility in the field of in vitro potency of AAV based Drug products. The individual will help in the development and validation of cell based in vitro potency assays. The position requires a strong background in cell culture, sample preparation and protein analysis. The work involv

Site Name USA Pennsylvania Upper Providence, Durham Blackwell Street, UK Hertfordshire Stevenage, Waltham Posted Date May 3 2024 The Strategic External Development (SED) team is an empowered, innovative, and agile CMC development organization within MDS that will unlock the potential to rapidly deliver an increased number of transformative medicines to patients through ex

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

Coordinates the implementation, both internally and externally, of sponsored clinical research studies. Initiates and maintains contact with study participants. Help screen applicants, ensuring they meet appropriate criteria, and makes independent judgment as to the suitability of their participation. May be required to perform clinical tests such as phlebotomy, EKGs, etc

Principal duties may vary over time with grant funding and project demands, and with skill level of other staff assigned to projects. Evaluates and recruits potential study participants. Interacts with potential study participants, educating them about the studies including the possible risks/benefits, procedural details, and significance of the studies. Obtains informed

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

Sarepta is seeking an experienced psychometrician to join our Patient Centered Outcomes Research Team. As a psychometrician in this role, you will be instrumental in designing, developing, and validating patient reported outcomes measures and assessment tools to evaluate the impact of our portfolio of products on patients' outcomes. Your work will directly contribute to ou

Provides assistance on clinical research studies as per study guidelines and protocols. Recruits and evaluates potential study patients. Per protocol instruction, conducts telephone interviews or schedules patient for study visit and screening. May be required to perform clinical tests such as questionnaires, phlebotomy, EKGs, etc. if certified and as needed. Will work in

At Oxford Instruments, we enable the world's leading industrial companies and scientific research communities to image, analyse and manipulate materials down to the atomic and molecular level. With a sixty year history, and fourteen Queen's Awards for Enterprise, our world class products and technologies are helping our customers to address the greatest challenges of the

Quantitative Research Assistant, International Development (U.S.) Job Location US Remote | US VA Arlington | US DC | US IL Chicago | US MD Rockville | US MA Waltham Job ID 13009 Job Location United States Category Research Overview Join AIR as a Quantitative Research Assistant with our International Development Division (IDD) and make a difference, improving the quality o