include but are not limited to Perform analytical testing right first time in order to complete work within the budgeted resource time and in line with agreed project timelines. This includes Stability testing Release testing in support of non GMP and GMP projects Release testing for Clinical Services projects. Fully competent in the following analytical techniques, as dic

The Senior Principal Statistician, Biostatistics will be a lead statistician on individual studies, across related studies, and for integrated summaries and will design and report Phase I to IV clinical studies and regulatory filings under the supervision of a more senior statistician. This role is responsible for all statistical aspects of study design, study analysis an

Work schedule is four days a week Tuesday Friday 10am 8 30pm. Revvity Omics, a division of Revvity, is a clinical molecular and biochemical laboratory offering a variety of different screening and diagnostic testing options. From prenatal screening before birth to newborn screening shortly after birth and whole genome sequencing through one's lifetime. Our goal is to prov

Assist with environmental field surveys including but not limited to wetland and stream delineations, endangered species surveys, environmental inspections, and compliance monitoring. Data collection using handheld GPS. Assist with the preparation of permit applications and associated environmental reports. Assist with transmission line siting investigations and siting do

Write and edit lean clinical regulatory documents companywide for sense, clarity, accuracy. Provide writing support for a wide range of documents, including investigator's brochures, clinical study protocols and reports, integrated summaries, literature reviews, and SOPs. Work with the lead writer to create, manage and communicate the document timeline to ensure all revie

Entry Level Field Survey Technician Job Locations US PA Harrisburg ID 2024 5394 Category Surveying Type Full Time Regular 40 hours Posted Date 2 hours ago (5/13/2024 11 03 AM) Overview Join us as we Rise to the Challenge At KCI, we're building an enduring community that provides unparalleled value to our employee owners. We make our mark designing and delivering our world

Participates on project teams to advance discovery portfolio projects. Presents/defends scientific findings in multi functional project teams/initiatives Independently designs, analyzes, and interprets experimental results and technical reports, etc. Support Molecular Biology experiments for designing expression vectors. Protein expression experience in Mammalian and E.co

The Senior Scientist is a source of scientific and technical medical imaging expertise for Clario customers and internal departments and personnel. Primary Responsibilities The Senior Scientist is a source of scientific and technical medical imaging expertise for Clario customers and internal departments and personnel. Provides guidance to clients and within Clario in the

At TerrAscend , we are on a mission to shape the future of the cannabis industry by creating leading marijuana based therapies for patients and developing premium products for legalized adult recreational use. We are one of the largest and fastest growing multi state, vertically integrated cannabis operators in North America. We're on a roll and are just getting started!

Conduct site visits, surveys and inspections, and assist with data collection and compilation for wastewater treatment projects. Compile and analyze large data sets for wastewater operations parameters. Participate in the planning of wastewater and municipal infrastructure projects. Prepare studies, planning documents, and other written regulatory compliance reports. Prep

Site Name USA Pennsylvania Upper Providence, UK Hertfordshire Stevenage Posted Date Jan 30 2024 Do you share a desire to advance scientific knowledge and capitalise on the revolution in data and predictive sciences to deliver measurable impacts on the success and progression of GSK's medicine discovery portfolio? In this newly created position, you will establish a high p

include but are not limited to Manage all aspects of the preparation of regulatory documents for submission to global regulatory authorities in accordance with ICH and other global guidelines, standards and processes, and AMA Medical Writing styles, as applicable, in adherence with study/project timelines and corporate objectives. Manages EU regulatory submissions in colla

The Director will be responsible for managing the product leaders and external FSP personnel, overseeing all ongoing clinical studies, and planning the operational aspects of all new clinical studies. The Director will support Integrated Data Analytics and Statistical Programming in statistical analysis and oversee statistical programming activities for all clinical studi

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting opera

Provide archaeological support which may include archaeological surveys, testing, or excavations, and corresponding documentation. Adhere to strict safety standards. Essential Roles and Responsibilities Follow safety rules, guidelines and standards for all projects. Participate in pre task planning. Report any safety issues or concerns to management. Be responsible for ma