Artech Information System LLC

Clinical Data Manager I

Responsible for providing timely and prefessional ongoing quality management of clinical trial data by identifying errors/inconsistencies in CRF data and ensuring their resolutions in order that databases can be…

Drug Safety Data Management Specialist / Pharmacology Associate

Argus experience is required. • Enter applicable information into the global safety database for initial or follow up cases received via paper, fax or email. Book-in, quality check and initially assess cases from…

Front End Developer - React.js

Agile Angular CSS HTML Java +5 skills

The incumbent should be able to get up to speed on a project with a complex component on the UI side. The UI Developer should have experience in designing applications (require, multiple, UI components, should be able…

Scientific Process Operator

This position is responsible for performing manufacturing procedures and the execution of scheduled tasks within a CGMP environment in the Upstream group. This position is responsible for quality and maintaining the…

EPA OSHA

QC Chemist

• Operate a variety of treatment test equipment, such as HPLC, spectrophotometer, pH meter, filtration devices, hot plates, TDS, Moisture Apparatus, Melting Point, balances, etc. • Conduct a variety of analytical lab…

Bench Scientist

• We are looking for a highly motivated, detail oriented scientist to support antibody drug conjugate (Client) and targeted immunotherapy drug discovery at Pharmaceutical Oncology (ORU) in Pearl River, NY. • The…

Manufacturing Technician I

Operates general manufacturing equipment under close supervision in accordance with current GMPs or standardized procedures and within safety guidelines. Requires good documentation skills and attention to detail.…

Clinical Program Manager

Accessibility Agile Data Quality GCP Networking +2 skills

Leads the cross-functional execution of one or more clinical studies conducted within the Pharmaceutical Clinical Research Unit (PCRU) Accountable to PCRU leadership and the Core Study Team for delivery of a PCRU study…

Clinical Site Manager

North AmericaContract

Contract Negotiation Corrective Action

• Successfully implements and executes client s phase I III clinical trials at their assigned sites • Ensures compliance with regulations, guidelines and policies for studies implemented at their assigned sites. •…

Scientist III (Bioinformatics scientist/computational biologist)

Bioinformatics Java Machine Learning Python

Responsibility The Genetics and Genomics Department in the Genzyme R&D Center seeks a highly motivated bioinformatics scientist/computational biologist to work in a dynamic and cross-functional team involved in…

Manufacturing Technician

North AmericaLead

Work in highly integrated and fast paced interdisciplinary team on process scale up activities, process troubleshooting, and cGMP manufacture of clinical and commercial drug substance. Will work closely with…

Regulatory Manager

Responsible for implementing regulatory strategy and managing operational activities for assigned regions. Provides input into global regulatory strategy, including identification of gaps or risks in global strategic…

Regulatory Compliance

Statistical Programmer III

Responsibilities Coordinate programming activities across several trials with a given compound including publication and regulatory submission activities. Develop programming specifications for analysis datasets,…

GCP SAS Statistics

Laboratory Analyst I

North AmericaJunior

Individual will be primarily responsible for performing all technical laboratory activities involved with processing of clinical trial samples, including: receipt, verification, discrepancy resolution, LIMS entry,…

Statistical Programmer III - Work from Home/Remote 100%

Candidate to provide statistical programming support and validation and help set specifications of analysis datasets, pooled datasets, statistical tables, summaries, figures and listing for Phase II-IV clinical trials.…

GCP SAS Statistics

Associate Director, Global Regulatory Labeling

• Flex position in Global Labeling, for a Global Labeling Product Leader for the Infectious Diseases/Vaccines/Global Public Health Therapeutic Area. The GLPL will have responsibility for: • The creation and maintenance…

Statistical Programmer III

Job Description Min 2-3 years of programming experience in HARP, the GSK programming environment is required. At least 8 years work experience in a Statistical (SAS) programming role preferably supporting clinical…

GCP SAS Statistics

Chemist-II

• Techniques : FTIR, SEM, foreign matter isolation, coursework in analytical chemistry, physical chemistry, and statistics Global Technical Services, part of the Janssen Supply Chain, is currently looking for a…

Documentation Specialist III