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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.

Clinical Laboratory Scientist IInquire Now

10+ years of experience in clinical sciences. Performed testing of clinical samples in the chemistry department and supervised lab technicians. Expert in FISH, PCR, ELISA and other molecular techniques. Maintained adequate staffing, scheduled workflow, developed staff and provided technical oversight. AS in Science

Clinical Project ManagerInquire Now

5+ years of experience in monitoring and managing oncology clinical trials (site initiation, contracts, budgets, close-out). Managed several oncology clinical trials (phase I-II) and gained expertise in therapeutic areas such as psychiatry, pediatrics, radiology, infectious diseases and nephrology. Experience with clinical trial protocol development and SAE/AE reporting. Excellent knowledge of ICH and GCP requirements. MD

Clinical Trial Specialist: ex-AmgenInquire Now

Highly qualified clinical research professional with 10 years experience, including phase I-IV studies in a wide range of therapeutic areas. Experienced in all stages of study development from start up to close out and tenure in Amgen, ICON and Pfizer. Provided training during 5 investigator meetings on use of medical equipment and implementation of protocol assessments. BA

International Regulatory Affairs ManagerInquire Now

Experience in domestic and international RA, specializing in product compliance and registration of cosmetics, OTC cosmetics, medicated/functional cosmetics, dietary/health supplements and food products. Assisted in product registrations and labeling compliance for domestic and international markets. 10+ years of experience. BS

Quality Engineer: ex-AlconInquire Now

20+ years of experience with medical device and electronic assembly manufacturing background. Expert in FDA quality system regulation, ISO 13485 medical device, ISO 9001 Quality Management, Lean Six Sigma and validation (IQ, OQ, PQ). Achieved business unit quality metric goals of 20% reduction for return rates and improved customer quality rating by 3 points. BS

District ManagerInquire Now

10 years of experience in sales management. A record of demonstrated management success driving high volume sales results and exceptional talent management. Proven award-winning sales leadership in highly competitive markets. Designed sales plans and programs for maximum ROI to enhance strategic outcomes through business analytics. MBA

Director, Clinical Data Management: ex-PPDInquire Now

15+ years of experience with leadership roles in department management of a full-service data management group with 50 – 70 active projects at any one time in various therapeutic areas. Responsible for management of over $5M in revenue. Developed and reviewed system validation documentation and insured ICH GCP guidelines were observed. BS

Group Leader, Regulatory Operations: ex-GlaxoSmithKlineInquire Now

10+ years of experience in GLP/cGMP audit operations and site quality systems. Led and performed routine internal and external audits and inspections in compliance with FDA and OECD GLP regulatory guidelines and standards, company SOPS, policies, methods and protocols. BS. Registered Quality Assurance Professional

Clinical Studies, Lead: ex-Boston ScientificInquire Now

Managed specific phases of PMA, IDE, and 510(k) studies and worked within the parameters of GCP, ISO Standards and CFR. Managed product inventory and process flow. Participated in phase II study for diagnostic electrophysiology catheter; together with Regulatory Affairs, wrote clinical reports for regulatory IDE submission. MS

Manager, Cellular and Biochemical AssaysInquire Now

10+ years of experience working in both small and large biotechnology companies. Managed R&D and cross-functional operations teams developing and commercializing high throughput cellular and biochemical assays. Led a drug discovery team performing assay development, high throughput screening, lead optimization, and early stage safety evaluation. Manufactured over 600 products that generated $10M in annual revenue. PhD

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