Ich Q10 Jobs in Others

Looking for scientist to work with a growing company that is expanding!!!! Experience in method development and validation Proven laboratory skills in chromatography LC (HPLC or UPLC or UHPLC), and or GC Requied Additional Lab skills KF, FTIR, UV/Vis, DSC/TGA Knowledge of multi-s More...

Documentum Developer - Foster City, CAProject Duration : 2 yearsProject Start date :ASAP, 16-Sep-2019Mandatory Skills :Documentum D2, CARA and LORENZ DocuBridgeRequired skills:Pharmaceutical/ Research and Development/ Regulatory AffairsDocumentum (DFC, DQL)Content Server Administratio More...

Responsibilities:1. Support study feasibility activities and perform database/web searches for sites as needed.2. Work closely with the Site Start Up (SSU) and ensure all study related regulatory and financial documents are collected and reviewed in support of study activation.3. Orga More...

Responsibilities:1. Support study feasibility activities and perform database/web searches for sites as needed.2. Work closely with the Site Start Up (SSU) and ensure all study related regulatory and financial documents are collected and reviewed in support of study activation.3. Orga More...

Sr. Manager / Associate Director Clinical Development Operations Remote but preference is East CoastReport to:Sr. Vice President, Clinical Development Operations (CDO) About Company Company (RTX) is a clinical-phase company. Our core technology combines proprietary dry-powder inhale More...

Responsibilities: Responsible to communicate new regulatory guidelines. Lead the strategic efforts in the interpretation of relevant and new quality guidelines to ensure that the current and phase appropriate requirements and standards are properly and timely implemented Provide su More...

Responsibilities: Manage and prepare IND, NDA, BLA, and DMF regulatory applications in eCTD format for submission to the applicable regulatory authority (FDA/HC) in compliance with required timelines and specifications. Perform quality control procedures to ensure completion, correct More...

Panacea direct is a boutique consulting firm with different LOBs. Professional service is the space where we have been catering Manpower to our different clients in the entire USA. Panacea Direct is an equal-opportunity employer and we are committed to a work environment that supports More...

The Medical and Scientific Writing group has needs forSnr Manager and Associate Director level medical writers with experience writing clinical - each will be an active contributor/lead author of regulatory and scientific documentation, will manage the overall collection of content f More...

Snr Director Regulatory Strategy Oncology with High Profile Oncology Biotech company based in Massachusetts - Position can be remote anywhere on East Coast SUMMARY OF ROLE:Act as responsible for establishment of Global Regulatory strategy and pathway for one/several projects in oncolo More...

Hours: 2nd shift: 2pm to 12:30am Summary: The Quality Lab Associate II will be located at the Drug Delivery Chemistry Laboratories, Round Lake, IL. The Position encompasses the biological, chemical and physical analyses on pharmaceutical products (biologics and drugs) through all sta More...

Director of BiostatisticsExperienced biostatistician who will be responsible for leading, developing and implementing statistical solutions to optimally support all phases of clinical trials and decision making. The successful candidate will function as a lead statistician across assi More...

Director of BiostatisticsExperienced biostatistician who will be responsible for leading, developing and implementing statistical solutions to optimally support all phases of clinical trials and decision making. The successful candidate will function as a lead statistician across assi More...

SAS Developer with Medical Science || Remote ||USA Mandatory Skills: Statistical programmer :- (Experience in SAS, experienced in SDTM and creation of Submission Package) (Experience in SAS, experienced in SDTM and creation of Submission Package)' Plan and lead the development of More...

Senior Director, Clinical OperationsContract to PermPosition DescriptionPrimary ResponsibilityManage end-to-end enrollment process between research sites and CompanyResponsible for collection and review of screen data in a time-sensitive fashion that does not prolong the screening pr More...

JOB SUMMARY: ToxicologyThe candidate will provide scientific oversight and strategic guidance for nonclinical safety evaluation programs from late-stage research through all phases of the drug development process including market application. reporting to the Senior Director Noncli More...

About Company Company is a clinical-phase company. Our core technology combines proprietary dry-powder inhaler device technologies and advanced particle engineering-based inhaled drug formulation approaches to develop novel therapeutics that deliver the drug more directly to the lu More...

Amazing opportunity for a Regulatory Affairs Professional or even someone with a PharmD and Phd and Research experienceLevel of the role can be from Manager level to Associate Director, RA StrategyRegulatory AffairsParamus NJ (Hybrid; 2-day/week onsite)Job SummaryResponsible for devel More...

Responsibilities: Responsible to communicate new regulatory guidelines. Lead the strategic efforts in the interpretation of relevant and new quality guidelines to ensure that the current and phase appropriate requirements and standards are properly and timely implemented Provide su More...

Overview: Tekwissen Group is a workforce management provider throughout the USA and many other countries in the world. The below job opportunity is to one of Our clients who offer biotechnology product development services. The Company focuses on providing laboratory equipment, chem More...