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Reminder: This is just a handful of the talent we represent. If you have specific requirements which aren't met by the profiles we have highlighted, please contact us right away so we can send you profiles & resumes that will be a strong match for your specific needs.
sterling Hoffman Life Sciences, Specialists in Pharmaceuticals, Healthcare and BioTech Recruitment
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Are you looking to hire? Here are some of our most recent candidates, currently looking for new positions. To request more information about one of these specific candidates below, click the "Inquire Now" link beside their title.

Senior CRA: ex-BayerInquire Now

20+ years of experience in Clinical Research along with a unique background of medicine, pharmacology & toxicology, preclinical and clinical trials; Developed and implemented site initiation, routine monitoring and closure checklists which improved accuracy by 62%; Successfully managed 45 North American sites along with a start up of phase III international study; Performed drug accountability and reconciled counts with CRF, source data and dispensing logs that increased product quality 80%; Reduced study start-up time by 40% through implementation of new startup procedures and checklists; GCPs, ICH, cGMP, TDP, Pharmacodynamics, Pharmacokinetics, Six Sigma; MS in Biochemistry

VP of Global R&D: ex-QuintilesInquire Now

20+ years of global research experience with multidisciplinary pharmaceutical R&D programs involving medicinal chemistry, pharmacology, enzymology, molecular biology and rational drug design teams; Successfully directed 750 scientists who led 125 R&D programs across the globe worth $21M; Secured R&D collaborations with major pharmaceutical companies which increased revenue by 48%; API supply, Analytical Chemistry, PK/PD, Drug Metabolism; PhD in Chemistry

Director of Toxicology: ex-GlaxoSmithKlineInquire Now

15+ years of progressive experience in managing pre-clinical and clinical studies for drug safety evaluation in various countries, including USA, Canada and China; Prepared regulatory agencies manuals which increased efficiencies by 83%; Designed and implemented 62 clinical safety programs including GLP and non-GLP studies like DMPK, safety pharmacology, pharmacokinetics, mutagenicity and reproductive toxicity studies; Cardiovascular, GLP/non-GLP studies, Immunotherapeutic vaccines, SFDA, PRC; PhD in Toxicology

Director, CRA: ex-MedImmuneInquire Now

20+ years of experience in Clinical Research Management; Reduced single batch costs by more than $10K, an annual cost savings of $700K; Increased revenue of $0.5M to the bottom line of the company; Managed technology transfer to manufacturing and validated the processes; Negotiated site budgets averaging $25K - $40K; FDA, GMP, CAPA, SOP, AOAC, CK-MB, R&D; MS

Clinical Project Manager: ex-PRA InternationalInquire Now

15+ years of experience in Clinical Project Management; Reduced turnover from 45% to less than 12% within 18 months by creating new performance tracking systems; Submitted 100% of monitoring reports within SOP guidelines; Identified and trained 15 regional CRAs and opened 7 of 80 sites within just 4 weeks; Expertise in oncology, cardiovascular, central nervous system, immunology, dermatology and hematology trials; SOPs, GCP, FDA, ICH; PhD in Biochemistry

Regional Sales Manager: ex-ZenecaInquire Now

10+ years of experience; Proven sales record in marketing cardiovascular, pulmonary and oncology products to physicians, medical groups and hospitals; Track record of being in the top 7 for 3 consecutive years; Increased sales revenues by 150% in assigned area by developing a new DTC marketing program; IHC, FCR, PDE, SKU; Bachelor's degree

VP of Quality Systems and Regulatory Affairs: ex-IdecInquire Now

20+ years of experience in Quality and Regulatory Affairs Management; Streamlined the product review and release system from an average QA release time of 15 days to an average of 2 days; Reduced the number of open Change Controls from 168 to 20 by creating tracking and trending system; Designed and implemented a new Chemist and Microbiologist training system which has new analysts prove proficiency against their trainer, which helped drop Laboratory Retest Rate dropped from 8% to 1.9% in just 6 months; Supported company growth from $20M to $100M in less than 5 years while building and training all business disciplines; KPIs, cGMP, FDA, R&D, ISO-9001; MBA, BS in Pathobiology

Senior Manager (National), Clinical Field Operations: ex-Novo Nordisk CanadaInquire Now

20+ years of experience in Clinical Operations Management; Exceeded established productivity goals on over 50 concurrent studies by implementing best practices to increase staff output, regular evaluation of progress to plan and course correction; Improved company’s corporate profitability and field staff productivity by reducing non-enrolling study sites from 20% to less than 5% within 12 months, resulting in $250K cost savings; Increased operational performance by decreasing full IT system access time for new hires from 24 to 6 weeks, allowing staff to assume full case loads faster; Forecasting & Analysis, Quality Improvement, Project Management, Budgeting, Forecasting; BS, RN

VP of Operations: ex-Eli LillyInquire Now

20+ years of experience in Operations Management; Directed actions to support a 100%+ increase in major customer order demand; Planned and implemented a 24X7 operations schedule within 1 week of receiving increased demand; Directed Production records in major product line at 100%+ greater than previous production levels; Credited with 0 environmental spills or releases through career; Increased services and systems speed by 100% at the same annual cost; SAP-ERP/WM, CMMS, TQM, FDA-cGMP, ISO, ERP/MRP, LIMS, PQIP, PSIP; BSME

Clinical Operations Manager (Contract): ex-Sigma-K CorporationInquire Now

15+ years of Clinical experience; Provided clinical operations input in the identification, evaluation and selection of CROs and vendors (central labs, central IRB); Evaluated and selected investigative sites; Developed project budgets and timelines and maintained timelines with respect to milestones and budget; Researched, wrote and prepared patent applications; Identified new investigators for projects; Assisted in the development of innovative devices; HIPAA FDA, GCP, ICH; BS in Molecular Biology

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Executive Search firm announces completed project in New Jersey. Sterling-Hoffman announced today that its search for a Director of Quality on behalf of a local pharmaceutical company in New Jersey is complete. http://www.sterlinglifesciences.com/pr1.html Prestigious recruiting firm solves hiring dilemma for a pharmaceutical company Sterling-Hoffman, briefed industry journalists today that it had completed a Compliance Manager search on behalf of a pharmaceutical company in Indiana. http://www.sterlinglifesciences.com/pr2.html Recruiting firm fills another job opening in New York. Sterling-Hoffman, a prominent executive-search firm, informed the media today that it completed another recruitment project– this time for a Clinical Research Associate http://www.sterlinglifesciences.com/pr3.html Recruiting firm fills another job opening in Florida. Sterling-Hoffman, a prominent executive-search firm, informed the media today that it completed another recruitment project– this time for a Director of Regulatory Affairs. http://www.sterlinglifesciences.com/pr4.html Executive Search firm announces completed project in New Jersey. Sterling-Hoffman announced today that its search for a Director of Quality on behalf of a local pharmaceutical company in New Jersey is complete. http://www.sterlinglifesciences.com/pr5.html http://www.sterlinglifesciences.com/pr6.html Prominent recruiting firm completes search for Vice President of Regulatory Affairs/Quality Assurance for pharmaceutical company in New Jersey. Sterling-Hoffman, a prominent executive-search firm, informed the media today that it completed another recruitment project– this time for a Vice President of Regulatory Affairs/Quality Assurance in New Jersey. Executive Search firm announces completed project in New Jersey; expects strong hiring market in Biotechnology sector to continue. Sterling-Hoffman announced today that its search for a Director of Quality on behalf of a local pharmaceutical company in New Jersey is complete. http://www.sterlinglifesciences.com/pr7.html Executive Search firm announces completed project in New Jersey. Sterling-Hoffman announced today that its search for a Director of Quality on behalf of a local pharmaceutical company in New Jersey is complete. http://www.sterlinglifesciences.com/pr8.html