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-Bayer	Inquire 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-Quintiles	Inquire 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-GlaxoSmithKline	Inquire 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-MedImmune	Inquire 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 International	Inquire 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-Zeneca	Inquire 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-Idec	Inquire 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 Canada	Inquire 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 Lilly	Inquire 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 Corporation	Inquire 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

showing 1-10 of  512 | Next 10 | Last