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Clinical Affairs Manager
Our client is a leading medical device company. They have a leadership position in their targeted markets and an established reputation as a leading innovator in the field. The company has premier investors and a strong pipeline. This is a great opportunity for the right candidate. |
New Jersey |
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Regulatory Affairs Manager
Our client is a life science company focused on the development of products that eliminate contagious pathogens. The company has an experienced management team, a varied selection of interesting protocols and an empowering corporate culture that is focused on the long-term development of it's employees. |
Malvern, Pennsylvania |
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Director of Regulatory Affairs
Our client is a pharmaceutical company that develops, manufactures and markets pharmaceutical therapeutics for medical conditions requiring specialized treatment. The company’s prescription drugs are marketed both nationally and internationally. |
Pennsylvania |
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Regulatory Affairs Manager
Our client is a medical device company located in Naples, Florida. They focus on providing the finest quality engineered products and educational services for orthopedic surgeons. With over 3,000 products for arthroscopic and orthopedic surgical procedures (shoulder, knee/hip and small joint), our client has built up a strong customer base across the USA and in 60 countries worldwide. This is a great opportunity for the right candidate! |
Naples, Florida |
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Coordinator of CMC Services, Analytical
Our client is a leading provider of contracted drug development services to the pharmaceutical industry. Their services span from pre-clinical through manufacturing, clinical, regulatory and commercial phases of drug development. Our client’s executive team are accomplished leaders in the full spectrum of drug development and have extensive experience working in and with pharmaceutical, biotech and contract services organizations. |
Cincinnati, Ohio |
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Regulatory Affairs Manager
Our client is a young venture-backed pharmaceutical company headquartered in Massachusetts that is using a science-driven approach to develop novel therapeutics to treat a number of large, poorly served dermatological disorders. The company has premier investors and an experienced management team that is committed to the highest standards of integrity and to improving the lives of patients and their families. This is a strong opportunity for someone that wants to put their drive and initiative to work! |
Massachusetts |
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Director of Regulatory Affairs and Compliance
Our client is a leading global producer of active pharmaceutical ingredients. The company has demonstrated strong growth and profitability in recent years and brings a lengthy history of innovation to each of its products. With a profit sharing program and best-in-class benefits this is a great situation for a candidate that is pursuing a challenging and visible leadership opportunity. |
Connecticut |
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Senior Director, CMC Regulatory Affairs
Our client is a biopharmaceutical company based in San Diego. They focus on in-licensing, developing and commercializing therapeutics for the treatment of cancer and infectious disease. Coupled with these is an experienced management team with significant product development, clinical, regulatory, finance and business management expertise. This is a great opportunity for the right individual to join a dynamic company! |
San Diego, California |
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Senior Director of Global Regulatory Affairs
Our client is an emerging biopharmaceutical company that is focused on the development and commercialization of next generation therapeutics for infectious diseases and cancer. With an experienced CEO and a strong, diverse pipeline, they present a great opportunity for the right candidate! |
Vermont, New Jersey, New Hampshire, New York, California |
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Senior Director of Regulatory Affairs
Our client is an ophthalmic biopharmaceutical company based in Florida. They focus on the discovery, development and commercialization of products to meet the medical needs for the preservation of eyesight. Their corporate headquarters are based in Tampa and they boast a state-of-the-art R&D center in San Diego. With an experienced management team, a robust pipeline and a ‘can do attitude’, this is a great opportunity for the right person to join a rapidly growing company! |
Tampa, Florida |
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Director of Regulatory Affairs
Our client specializes in clinical research and is an expert in a variety of areas including trial design, quality of life and health economics. |
California |
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Associate Director of Regulatory Affairs
Our client is a biopharmaceutical company based in Westminster, Colorado. They focus on the development and commercialization of small molecule therapeutics for the treatment of cancer. Their team is dedicated to patients and the customers they serve. They want to attract, develop and retain world-class talent to build a high-performance organization. This is a great opportunity for the right candidate! |
Westminster, Colorado |
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Senior Regulatory Affairs Manager
Our client is a privately held biopharmaceutical company focused on the treatment of vascular disease. |
Pennsylvania |
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Director of Regulatory Affairs
Our client is a rapidly growing development-stage pharmaceutical company that is focused on the commercialization of therapeutics for patients with unmet needs that are suffering from chronic kidney disease. With offices in Canada and the US the company boasts a world class management team with unparalleled expertise in this area, a varied selection of cutting edge protocols and an empowering corporate culture that is focused on the long-term professional development of it's employees. |
Chicago, Illinois |
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Vice President of Regulatory Affairs
Our client is small private company that specializes in developing therapeutics for endocrinology, bone loss and neuromuscular disease. They have a strong pipeline as well as great leadership and culture. This opportunity is great for someone who is hands-on and is looking for a sense of ownership and accomplishment. |
Cambridge, Massachusetts |
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Regulatory Affairs Manager/Associate
Our client is a privately owned medical device company that is focused on the treatment of vascular disease. The company has an experienced CEO and board, an exciting product candidate and a team that is committed to the highest standards of integrity and to improving the lives of patients and their families. |
Kirkland, Washington |
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Director of Regulatory Affairs
Our client is a successful division of a world-leading medical device company that has developed a reputation for successfully bringing complex products to market in a variety of therapeutic areas. The company has some of the strongest financial indicators in the industry, an experienced management team and a robust pipeline. This is a strong opportunity for someone that wants to put their drive and initiative to work! |
San Jose, California |
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Division Statistical Leader
Our client is one of the world's leading medical device providers. They are a highly profitable, publicly traded company whose products are currently being sold in over 120 countries worldwide. This is a great opportunity for someone to join a company that offers a great corporate culture and is focused on the long-term development of its employees. |
Michigan |
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Manager, ELISA Technology Lab
Our client is a fast growing Contract Research Organization (CRO) located in Central New York State that focuses on conducting research and providing GLP/cGMP compliant analytical testing services for the development of various therapeutics for the Biotech/Pharmaceutical industry. The company has an experienced management team, a varied selection of interesting protocols and an empowering corporate culture that is focused on the long-term professional development of its employees. |
New York |
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Regulatory Affairs Manager/Associate
Our client is a leading medical device company based in the Northeast. They specialize in developing technologies for the treatment of cardiovascular diseases, such as coronary stents and state-of-the-art hernia repair. The company has offices in Australia and The Netherlands and boasts a demand of over 2 million sterile medical products to over 60 countries every year. With emphasis placed on personal development of employees, this is a great opportunity for the right candidate! |
Hudson, New Hampshire |
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Regulatory Submissions Manager
Our client is a rapidly growing biopharmaceutical company based in The Woodlands, Texas. Using their state of the art technology, they have discovered the physiological and behavioral functions of nearly 5,000 genes. They have an exciting goal of advancing 10 drug candidates into human clinical trials by the year 2010. This is a great opportunity for someone looking for personal growth and a challenge! |
The Woodlands, Texas |
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Process Equipment Engineer
Our client is an acute care specialty pharma company based in San Diego. They specialize in a technology that provides sustained-release delivery of medications for post-surgical pain. Our client has two marketed products that are used by professionals in the healthcare industry. The company has premier investors, an experienced management team, a robust pipeline and an empowering corporate culture that is focused on the professional development of its employees. |
San Diego, Southern California |
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Toxicologist
Our client is a global specialty pharma and medical device company located just outside of Chicago, IL. They focus on the design, development, and manufacturing of solutions to improve the safety, delivery and effectiveness of patient healthcare. |
Lake Forest, Illinois |
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Director of Pre-clinical Development/Toxicology
Our client is a global specialty pharma and medical device company located just outside of Chicago, IL. They focus on the design, development, and manufacturing of solutions to improve the safety, delivery and effectiveness of patient healthcare. |
Lake Forest, Illinois |
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Regulatory Affairs Project Manager
Our client is a top 10 pharmaceutical company that has established a reputation as one of the most desirable companies to work for in Canada. With operations around the globe and an empowering corporate culture that is focused on the professional development of its employees, this is a strong opportunity for the right candidate! |
Toronto, Ontario |
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Medical Products Manager
Our client is a rapidly growing company headquartered in Honolulu that is focused on tissue generation for people with illness. The company has an experienced management team and an empowering corporate culture that is focused on the professional development of its employees. |
Honolulu, Hawaii |
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Toxicologist
Our client is a publicly traded provider of personal care products that has established a reputation as one of the best managed companies in North America. With operations in over 120 countries, over $1B in revenue, and an empowering corporate culture that is focused on the professional development of its employees, this is a strong opportunity for the right candidate! |
Illinois |
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Director of Regulatory Affairs
Our client is a dynamic and growing, independent contract drug development and consulting company. Employees at this company are experienced and highly qualified team players, essential to its success. |
West Coast |
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Senior Manager, Regulatory Affairs
Our client is a well established biologics (allergy extract) located in beautiful Western North Carolina. The company, founded in 1904, is a leader in developing and providing allergy immunotherapy products/services for treatment of human beings and animals. In addition to their current product line, they have clinical trials also in process. |
North Carolina |
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Senior Regulatory Affairs Specialist
Our client is a diagnostics company based in California, with their head office in New York. They offer products and services used by the industry to assist with the diagnosis, treatment and management of infectious diseases. The company has an experienced management team, a robust pipeline and an empowering corporate culture that is focused on the professional development of its employees. |
South California |
