- IQVIA (Carlsbad, CA)
- …business management/science/communications Req + 15 years relevant industry experience ( CRO /Pharmaceutical) Req Or + Equivalent combination of education, training, ... and experience Req + Proven track record at developing mid-level and high-level contacts + Solid understanding of commercialization and the principles of drug discovery and development lifecycle + Excellent skills using Microsoft Office Suite: MS PowerPoint… more
- ThermoFisher Scientific (Greenville, NC)
- …Regulatory medical writing projects required + Experience working in the pharmaceutical/ CRO industry preferred + Additional qualifications in medical writing (AMWA; ... EMWA; RAC) advantageous. **Knowledge, Skills, Abilities** + Significant knowledge of global, regional, national and other document development guidelines + Excellent data interpretation and medical writing skills, including grammatical, editorial, and… more
- Taiho Oncology (Pleasanton, CA)
- …in clinical pharmacology part of oncology clinical development with experience in vendor/ CRO relationships. + A working knowledge of the ICH/FDA/EU guidelines for ... DMPK. + Excellence in written and oral communication. + The incumbent in this position may be required to perform other duties, as assigned. The pay range for this position at commencement of employment is expected to be between $194,650 min - $229,000… more
- EMS LINQ (Austin, TX)
- …paid search, paid social, programmatic/display, retargeting, email, webinars/events, website/ CRO , content syndication, and partner channels. + **Full‑funnel campaign ... a collection of information unless such collection displays a valid OMB control number. EOE Statement/Accommodation Notice: LINQ is an Affirmative Action and Equal… more
- Regeneron Pharmaceuticals (Sleepy Hollow, NY)
- …clinical study team meetings, data oversight review sessions, and works closely with CRO medical monitors in support of medical affairs clinical trials. * Oversees ... and provides hands on support in management, generation and dissemination of clinical and non-clinical data that supports the medical strategy and results in high quality publications. * Collaborates effectively within a multifunctional, matrix organization… more
- Charles River Laboratories (Kingston, NY)
- …inventories. + Strictly follow all procedures necessary to maintain the barrier room barrier. + Use supplies according to safety guidelines. Perform all job-related ... **About Charles River** Charles River is an early-stage contract research organization ( CRO ). We have built upon our foundation of laboratory animal medicine and… more
- ThermoFisher Scientific (Suwanee, GA)
- …Experience should be in clinical development in a Pharmaceutical, Biotech or CRO organization + Neurologists with expertise in Pediatric Neurology or Neuromuscular ... diseases are highly preferred. **Knowledge, Skills, Abilities** + Excellent English, both written and spoken is a must, as well as ability to travel + Shown understanding and experience with NDA submission process + Shown understanding of regulatory guidelines… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …validation manuals, database UAT, etc - Trains and support study team and CRO personnel regarding clinical aspects of trial - Assist with medical monitoring, raising ... and responding to investigator queries, writing safety narratives, analysis of trends of safety and efficacy, etc. - Organizes steering committees, advisory boards, and data safety monitoring boards as required - Identifies program, trial or data risks,… more
- Highmark Health (Pittsburgh, PA)
- …(ELT)-qualified initiatives, including but not limited to: + (i) ELT qualified requests of CRO ; + (ii) support of due diligence efforts for Mergers & Acquisitions; + ... (iii) support of enterprise strategic initiatives. + Audit, Risk, and Compliance Strategy & Planning: Directly supports the Director - Enterprise Risk Strategy and the Director - Risk Initiatives with the development of key strategic, administrative and… more
- Grifols Shared Services North America, Inc (Research Triangle Park, NC)
- …study manager in overall study management. Monitors and/or co-monitors as required with CRO and CRA staff to insure study integrity and compliance. Develops ICF ... templates and reviews study specific ICF(s). Participates in CRF development and completion. Reviews monitoring reports and QA reports from site visits. Manages clinical study set-up and follow-up study activities through tracking and review. Assists in the… more