- ThermoFisher Scientific (Greenville, NC)
- …our PPD FSP functional area, allows you to join the renowned PPD CRO and still gain invaluable client dedicated experience. Summarized Purpose: Manages, selects, ... trains, resources, coaches and performance management of respective staff. Focuses on end results using metrics and key performance indicators to manage performance. May lead or contribute to initiatives that enhance the department's performance or lead to… more
- Actalent (Menlo Park, CA)
- …Provides oversight of regional study monitors and/or contract research organizations ( CRO ) to ensure quality, compliance, and timely study execution while ... proactively addressing risk and performance issues. . Facilitate external communication with site staff and pharmaceutical partners (as applicable). . Ensures electronic Trial Master File (eTMF) is current and maintained Skills Clinical trial, Vendor… more
- Eurofins US Network (Lancaster, PA)
- …discipline required + Minimum of 5 years of experience in the biopharma, CRO , CDMO, or laboratory services industry. + Proven success in project/program management ... supporting key accounts. + Experience working in GMP environment strongly preferred. **Skills & Competencies** + Strong understanding of drug development and analytical or manufacturing workflows. + Excellent communication, presentation, and… more
- IQVIA (Durham, NC)
- …managers and internal clients + Fluent English speaker + Pharmaceutical, CRO or related experience/knowledge + Solid understanding of R&D business Qualifications ... MINIMUM REQUIRED EDUCATION AND EXPERIENCE + Bachelor's degree required, and at least 7 years relevant marketing, sales, or design experience; or equivalent combination of education, training and experience PHYSICAL REQUIREMENTS + Extensive use of telephone,… more
- Eurofins US Network (Fremont, CA)
- …+ Experience dealing directly with clients in an industry setting (eg, CRO /client relationship) is highly desirable. + Experience developing assays for neutralizing ... antibody detection is a plus **Additional Information** **Salary Range: $175,000 - $225,000/yr.** The position is full-time, Monday-Friday, 8 am-5 pm, with overtime as needed. + Excellent full time benefits including comprehensive medical coverage, dental, and… more
- Charles River Laboratories (Wilmington, MA)
- …**About Charles River** Charles River is an early-stage contract research organization ( CRO ). We have built upon our foundation of laboratory animal medicine and ... science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products… more
- WuXi AppTec (MA)
- …in chemical or pharmaceutical development and/or manufacturing. Experience in or managing CRO , CMO or CDMOs. + Must be a self-starter, self-motivated, highly ... flexible, with excellent communication skills (verbal, written, and presentation skills). Must be organized and detail-oriented. + Proven experience in creating successful business development plans and processes. Marketing experience preferred but not… more
- WuXi AppTec (Atlanta, GA)
- …of 1 year's relevant experience working in new drug development or CRO /CMO industry (oligonucleotide and peptide strongly preferred) + Must be a self-starter, ... self-motivated, highly flexible, with excellent communication skills (verbal, written, and presentation skills). Must be organized and detail-oriented. + Must have a proven track record of meeting or exceeding sales growth objectives and/or simultaneously… more
- Taiho Oncology (Princeton, NJ)
- …Objectives: + Coordinates cross functional study team meetings and supports study manager with meeting minutes for assigned studies. + Updates internal study ... Monitors Trial Master File related KPIs and performs quality review of the eTMF (per CRO oversight plan) while collaborating with internal and CRO study teams to… more
- Bristol Myers Squibb (Princeton, NJ)
- …enable precision medicine, with a major focus on Companion Diagnostics (CDx) design control , validation, and clinical enablement, and the agility to pivot to GLP ... with Translational Medicine, Clinical Development, Regulatory/QA, Finance/Legal, and external CRO /IVD partners to shorten cycle times, de-risk trials, and improve… more
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