Ich Q10 Jobs in Others

Director or Associate Director, Clinical Operations (DOE)The Director (or The Associate Director- DOE) of Clinical Operations is responsible for managing clinical operations activities at the project level including coordination of clinical trial activities, directing and supporting t More...

Responsibilities: Provide data management expertise and support to internal project teams, clients, and Clinical Research Organizations (CROs) Plan, perform and oversee development of specifications for eCRFs/CRF, edit checks, electronic data handling, manual review, and execution o More...

Description: Must meet all requirements for Clinical Research Associate position and have demonstrated proficiency in all relevant areas. With limited supervision conducts site evaluations/initiations and closeout visits in addition to routine monitoring visits, as required. Assures More...

Santa Monica, CA Contract Duration: 5-18 months Rate: Negotiable Responsibilities: Excellent employment opportunity for a Clinical Trials Management Associate II in the Santa Monica, CA area. (onsite) Must meet all requirements for Clinical Research Associate position and have de More...

Our client seeks a Clinical Research Operations professional to plan their Phase I Clinical TrialsRequirements Bachelors Degree in life sciences or healthcare field. Additional coursework in clinical trial design.Ability to travel as required (up to 25%).12+ years of proven experience More...

Manager of Regulatory Affairs in Somerset NJ.Fast growing company with great management team. Good writing and communication skills are requiredCMC experience required Experience with ANDA/IND/NDA preferredExperience with eCTD submissionsAnnual reports in accordance FDA and ICH guide More...

Senior Regulatory Associate in Somerset NJ.Fast growing company with great management team. Good writing and communication skills are requiredCMC experience required Experience with ANDA/IND/NDA preferredExperience with eCTD submissionsAnnual reports in accordance FDA and ICH guidance More...

Regulatory PublisherFast growing company with great management team. Good writing and communication skills are requiredCMC experience desired Experience with ANDA/IND/NDA preferredExperience with eCTD submissionsAnnual reports in accordance FDA nd ICH guidanceKnowledge and experience More...

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...

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...

Director, Clinical OperationsContract to PermProvide leadership and manage end-to-end processes involved in outsourced clinical trials, key deliverables are:Maintaining and remediation of operational efficiency at RT and designated CRO demonstrated by meeting development program goal 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: Hands-on experience on validation of enterprise GxP applications systems such as BMRAM. Hands-on experience on validation and qualification of cloud-based applications. Experience on drafting and reviewing Validation Plan, Test Plan , Summary Reports and Traceabil 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...

Responsibilities: Contribute to GRAIL's clinical programs such as MSK and STRIVE studies from a clinical data management perspective. Work closely with GRAIL study team members and strategic partners to ensure that clinical data captured is complete, consistent, and accurate. Perform More...

NAMSA pioneered the industry, NAMSA was the first independent company in the world to focus solely on medical device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976. We are shaping the in 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...

Experience level: Director Experience required: 8 Years Education level: Bachelors degree Job function: Quality Assurance Industry: Biotechnology Compensation: View salary Total position: 1 Relocation assistance: No Visa : Only US citizens and Greencard holdersAt our vision is creatin 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...