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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.

Director of Quality Assurance & Regulatory: ex-DraegerInquire Now

Expertise in: FDA Regulation; ISO 9001, ISO 13485 and QSR 21CFR Compliance; Six Sigma Lean Manufacturing Techniques; Root Cause Analysis; Risk Management; Internal & External Auditing; Budget Management; Training; CAPA system; MS, BS in Business Administration

Clinical Research Associate: ex-Warner ChilcottInquire Now

Expertise in: ICH, GCP Guidelines; Regulatory Submissions; Study Start-Up Processes; Clinical Trials; Site Inspections; Maintaining Compliance with Protocols; CRF Development; Maintaining Corporate Guidelines; Conducting Clinical Testing and Statistical Analysis; Life Cycle Development; BS in Biology

Quality Assurance Specialist: ex-PatheonInquire Now

Expertise in: Draft, Review and Product Releases; Validation Protocols; SOPs Writing; GMP/GLP/GCP Guidelines Compliance; Project Management; HPB, FDA and EMEA Regulatory Submissions; PhD in Production Management, MS in Metallurgical Engineering

Vice President, Clinical Operations: ex-ParexelInquire Now

Expertise in: Clinical Outsourcing and Supplier Management; FDA/ICH Regulation Compliance; Program Budgeting; P&L Management; Product Life Cycle Management Strategies; Process Analysis; PhD in Neuroscience and Anatomy; BA in Zoology

In-House Clinical Research Associate: ex-QuintilesInquire Now

Expertise in: ICH, GCP Guidelines Compliance; Documenting Guidelines; CRF Completion and Submission; Regulatory Document Review; Tracking and Reporting Critical Data Elements; Data Query Generation; Degree in History

Senior Quality Engineer: ex-HospiraInquire Now

Expertise in: Statistical Analysis; FDA Audits; Writing Quality Assurance Protocols; SAP; Program Management; Process Validation; Lean Manufacturing and Six Sigma Techniques; GMP and SOP compliance; BS in Food Science

Senior Director, Clinical Data Management: ex-BayerInquire Now

Processes involved in: Introducing data standards for eCRF development; Reviewing and preparing sections of clinical study reports; Establishing budgets and providing estimates for data management; Managing system development lifecycle of global R&D financial applications; Directing all data management NDA activities; Expertise in: Financial Controlling and Analyses; ICH / GCP Guidelines, 21CFR Part 11 Regulations Compliance; Budgeting; Strategic and Resource Planning; SOPs Compliance; MBA in Management Information Systems, BS in Biology and Computer Science

Quality Manager: ex-PPDInquire Now

Process involved in: Release Testing; Review of Stability Studies Data and Reports; Method Validation and Qualification; Protocol/Method Review; Expertise in: Laboratory and Quality Management; Root Cause/CAPA Analysis; Data Analysis; ISO/HACCP Implementation; Regulatory Reporting; Risk Management; External/Internal Auditing; MS in Pharmacy Administration

Consultant, Pharmaceutical Regulatory Affairs: ex-TibotecInquire Now

Processes involved in: Managing regulatory documents; Reviewing clinical trial documentation; Developing strategy for Phase III clinical trial development; Updating periodic adverse drug experience reports; Compiling IND, NDA submissions; Reviewing advertising and promotional materials for new products; Expertise in: Regulatory Submission Planning and Scheduling; SOPs Compliance; Risk Management Programs; Updating Global Labeling; PhD in Biochemistry, MS

Senior Clinical Research Associate: ex-MDS PharmaInquire Now

Processes involved in: Site Management as per the Project Plans; Maintenance of Study Files; Writing Clinical Trial Reports; Maintaining Trial Master Files; Identifying Potential Qualified Investigators and Clinical Sites; Expertise in: AE and SAE Reporting; GCP, ICH, FDA Regulations and Company SOP Compliance; Mentoring Newer CRAs; Managing Multiple Studies and Investigators; Bachelor’s degree in Health Information Management

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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