(M.S., MPH, Ph.D., or similar degree) in the health sciences, life sciences, clinical sciences or biomedical engineering...
degree (M.S., MPH, Ph.D., or similar degree) in the health sciences, life sciences, clinical sciences or biomedical...
relevant experience in lieu of Bachelor's Degree or international equivalent. 3+ years of experience in the life sciences...
working environment Bachelor's degree in a relevant field, such as life sciences, regulatory affairs, or a related discipline...
. Bachelor's or Master's in Computer Science, Information Systems, Life Sciences, Bioinformatics, or similar. Experience..., review, and approve GxP Computerized Systems Validation life cycle and Change Control documents. Qualifications: 10...
execution. Worked in Life Sciences vertical both GxP and non GxP space. Familiar with Life science business process flow... with hands on testing deliverables. 5 years Hands On - POMS MES and Integration in Life Sciences. 2 years Life Sciences...
's or master's degree in Immunology, Cell Biology or a related Biological Sciences field, with 3-5 years of relevant hands...
solutions tailored exclusively for the dynamic life science industry. We provide a full spectrum of services, including...
clinical development life cycle Compile, coordinate and review applications to Regulatory Authorities including...
, and management of the clinical study database throughout its life cycle, from CRF design, database development and testing...
Responsibilities: The Regulatory Coordinator is responsible for the coordination, preparation, and maintenance of regulatory documentation and compliance for clinical trials. This role ensures adherence to local, state, and federal regul...
Job description: Our client is seeking an experienced Regulatory Operations Consultant to support Veeva Vault RIM, with a primary focus on archiving legacy regulatory content and mitigating documentation into Veeva Vault. This role will p...
Roles & Responsibilities: Must have basic knowledge or understanding of Pharmaceutical/Medical Device compliances like 21 CFR Part 11 Compliance, GAMP, GDP etc. Previous work experience in MES implementation using any platform. Must hav...
Summary : The Sr. Quality Manager is an advanced technical resource in the principles and application of quality assurance and compliance. The Sr. Quality Manager coordinates or executes activities on multiple complex projects and takes ...
Responsibilities: Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s) Produces and delivers CDISC and regulatory compliant SDTM, and ADaM standard datasets. Cre...
Roles & Responsibilities: Serve as the subject matter expert for planning, setup, and acquisition of external clinical data at the study level, managing study startup, conduct, and closeout activities. Create external data transfer agree...
Summary : Strong experience holding the responsibility and relevant experience in the global pharmaceutical industry in functions such as Clinical Operations, Data Management and Statistics, with at least 5 years of experience in GCP Qual...
Job Description: We are currently seeking a highly motivated and passionate scientist to join our team in Immunology Discovery department based in Cambridge MA. The candidate will focus on generating biology data packages to help advance t...