Develops and maintains enterprise software applications Collaborates with the product team on requirements elicitation to deliver software Authors and reviews unit/integration test Participates in code and software review processes Collaborates with members of the product, test, and software engineering organizations Develops expertise for all aspects of a software produc

About us SCHOTT is a leading international technology group in the areas of specialty glass and glass ceramics. With more than 130 years of outstanding development, materials and technology expertise we offer a broad portfolio of high quality products and intelligent solutions. SCHOTT is an innovative enabler for many industries, including the home appliance, pharmaceutic

Development of the pharmacometrics strategy of multiple programs Design, perform, interpret and report population PK, PK/PD and exposure response analyses Provide hands on population PK and PK/PD modeling and simulation support for development projects, e.g., dose selection and optimization Clinical study protocol design, data analysis/interpretation, and reporting of stu

Scientist 1 Make an impact. Build a career. At Pace, everything we do is built upon an unwavering commitment to making the world a safer, healthier place. We continually work to develop innovative practices that drive sustainability and empower our partners with accurate, quality data at every critical moment and milestone. That's why we need you your curiosity, your tale

Singular talents thrive as an Associate Director of Medical Writing with Caudex. We advocate. We captivate. We cogently demonstrate. We combine gravitas with that lightness of touch that only comes from genuine, deeply held mastery and passion. We're recognised leaders in our field because we make the extraordinary seem effortless. We are your people. You're a recognised,

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

The Head of Corporate Finance and Treasury reports directly to the CFO and is responsible for the company's corporate finance, treasury, and procurement functions, as well as providing insights to inform our financial strategy, oversight for managing risks, and optimizing the capital structure. This role requires both a strategic mindset and a hands on approach to ensure

Senior Regulatory Affairs Associate Experience Biologic CMC 5+ years of experience Supported the CMC activities related to Vaccine/Biologic manufacturing and control including authoring of submission dossiers related to new application, post approval variations Understanding of EU/CA/WHO/US regulations & guidance allowing appropriate review and compilation of data to appr

/JOB PURPOSE Responsible for managing and maintaining existing investigational new drug (IND) and clinical trial application (CTA) submissions and preparing amendments in compliance with guidelines and regulations. Coordinates, compiles, and tracks product applications to regulatory agencies. Essential Duties And Responsibilities Review clinical site regulatory documents t

Leads multidisciplinary teams in delivering on the design, execution, strategy and management of various development, clinical pharmacology and regulatory engagements, from early translation to late development. Works collaboratively with and leads Certara team members and clients to develop clinical pharmacology and quantitative program strategies that are fit for purpos

At The GIANT Company, we are passionate about building strong families and healthy communities, serving millions of neighbors across Pennsylvania, Maryland, Virginia, and West Virginia. We are committed to being an inclusive place to work and shop. Our shared values of care, courage, integrity, teamwork, and humor guide our work as we embrace the unique talents and differ

PHARMACIST CONSULTANT Job Locations US PA BETHLEHEM | US PA HARRISBURG | US PA WILKES BARRE | US PA PHILADELPHIA ID 2024 143005 Line of Business PharMerica Position Type Full Time Our Company PharMerica Overview Our Pharmacy group focuses on providing exceptional customer service and meeting the pharmacy needs for hospitals, rehabilitation hospitals, long term acute care

include Molecular biological techniques, such as the generation of viral vectors, gene cloning, PCR/RT PCR/qPCR, and protein biochemistry, such as Western blotting and protein purification Rodent related studies in the neuroscience field, including animal handling, surgery, neurological animal models (such as spinal cord injury and optic nerve injury in rodents, and experi

Company Description Today is a new day. At Asbury we're filling it with more laughter, more possibilities, more ways to give back, all backed by support for whatever life brings your way. We are an organization with a mindset to help others, a place where seniors continue to teach, learn, and grow, a certified Great Place to Work where you can build a purposeful career. Le

As the Director of Regulatory Affairs, you will lead a talented team and drive regulatory strategies for our groundbreaking products, focusing on New Drug Applications (NDAs) and Biologic License Applications (BLAs). You will spearhead the preparation and submission of regulatory documents, ensuring compliance with stringent FDA regulations and facilitating productive eng