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Manager of Regulatory Affairs
Our client is a leading privately held pharmaceutical company with operations in over 40 countries. With marketed products, an experienced management team, and an empowering corporate culture that is focused on the professional development of its employees, this is a great opportunity for the right candidate. |
New Jersey |
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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. The company has an established revenue stream, experienced management staff, a robust pipeline and an empowering corporate culture that is focused on the professional development of its employees. |
California |
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Associate Director of 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. The company has an established revenue stream, experienced management staff, a robust pipeline and an empowering corporate culture that is focused on the professional development of its employees. |
California |
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Associate Director/Director, Medical Regulatory Writing
Our client has pioneered a company focused on meeting the growing demand for credible evidence as it believes that this evidence can make a difference when trying to bring a drug to market and that it can enhance healthcare by defining patient requirements, clarifying therapeutic options, and providing patients with appropriate access to the medicines that they need. The company’s comprehensive services cover early-stage product planning through post-approval development. Its depth of industry expertise and a unique operational capability enables the company to demonstrate clinical benefit, manage safety, and minimize risk. The company helps document the economic value of medicines, and develop the evidence that is necessary to secure appropriate coverage and reimbursement. |
Pennsylvania |
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Senior Regulatory Affairs Specialist
Our client is a successful molecular diagnostics business with powerful genomic and proteomic discovery platforms that have identified and validated new drug targets and biomarkers. The company is dedicated to advance the practice of Targeted Medicine. It develops and sells a growing number of molecular diagnostic products with a strategic alliance partner. The company is developing new molecular diagnostics and pharmacogenomic tests, and is also creating additional value through collaborations based on its genomic discoveries, including new druggable targets, new indications for existing drugs, and pharmacogenomic markers for predicting therapy response. The company is also using its high-throughput proteomics discovery platform to identify and validate novel targets in cancer. |
Northern California |
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Senior Manager, Regulatory Affairs
Our client is a successful molecular diagnostics business with powerful genomic and proteomic discovery platforms that have identified and validated new drug targets and biomarkers. The company is dedicated to advance the practice of Targeted Medicine. It develops and sells a growing number of molecular diagnostic products with a strategic alliance partner. The company is developing new molecular diagnostics and pharmacogenomic tests, and is also creating additional value through collaborations based on its genomic discoveries, including new druggable targets, new indications for existing drugs, and pharmacogenomic markers for predicting therapy response. The company is also using its high-throughput proteomics discovery platform to identify and validate novel targets in cancer. |
Northern California |
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Senior Manager, Regulatory Affairs
Our client is a successful molecular diagnostics business with powerful genomic and proteomic discovery platforms that have identified and validated new drug targets and biomarkers. The company is dedicated to advance the practice of Targeted Medicine. It develops and sells a growing number of molecular diagnostic products with a strategic alliance partner. The company is developing new molecular diagnostics and pharmacogenomic tests, and is also creating additional value through collaborations based on its genomic discoveries, including new druggable targets, new indications for existing drugs, and pharmacogenomic markers for predicting therapy response. The company is also using its high-throughput proteomics discovery platform to identify and validate novel targets in cancer. |
Northern California |
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Regulatory Affairs Associate
Our client is a contract drug development company that has established relationships with many pharmaceutical and biotechnology companies in over 17 countries. The company’s services include, early-stage development and trials through late-stage development and trials, CMC and CMO, pharmacokinetics, and CRO services. The company also assists its clients with regulatory consulting, review, and submissions via eCTD. |
Ohio |
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Clinical Compliance Associate
Our client is a leading global health-care supplier and the world’s largest manufacturer of over-the-counter (OTC) pharmaceutical and nutritional products for the store-brand market. The company also develops and manufactures generic prescription (Rx) drugs, active pharmaceutical ingredients (API), and consumer products. |
New York |
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Senior Project Manager
Our client is a leading global healthcare supplier and the world’s largest manufacturer of Over-the-Counter (OTC) pharmaceutical and nutritional products for the store-brand market. The company also develops, manufactures, and markets generic prescription (Rx) drugs, Active Pharmaceutical Ingredients (API), and consumer products. |
New York |
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Director of Clinical Operations
Our client provides professional analysis and consultation in biotechnology, pharmaceutical, environmental, industrial hygiene, and food safety projects. The company has a regulatory compliant contract research facility, providing testing and consulting services in pre-clinical and clinical trials undertaken by pharmaceutical and biotechnology organizations. |
Western Canada |
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Director of Regulatory Affairs and Quality Assurance
Our client is a leading medical device company that engineers and markets safe medication delivery systems. The company is also a champion in its quest to protect healthcare workers, patients, and the environment with innovative medical devices. Our client has developed a patented syringe that offers enhanced infection control and protection for needle-stick injuries. |
Georgia |
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Senior Regulatory Affairs Manager
Our client is a medical device company committed to developing innovative medical technologies that restore function and quality of life to people who suffer from stroke and other neurological disorders. |
West Coast, USA |
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Regulatory Affairs Manager
Our client is a biopharmaceutical company focused on the development, manufacture, and commercialization of biopharmaceutical products such as vaccines and immune globulins that induce the body's immune system to prevent or treat disease. The company operates in two business segments: biodefense and commercial. In its biodefense business the company develops and commercializes immunobiotics for use against biological agents that are potential biological weapons. In its commercial business, the company develops immunobiotics for use against infectious diseases with significant unmet or underserved medical needs. |
Maryland |
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Regulatory Affairs Manager
Our client is a biopharmaceutical company focused on the development, manufacture, and commercialization of biopharmaceutical products such as vaccines and immune globulins that induce the body's immune system to prevent or treat disease. The company operates in two business segments: biodefense and commercial. In its biodefense business the company develops and commercializes immunobiotics for use against biological agents that are potential biological weapons. In its commercial business, the company develops immunobiotics for use against infectious diseases with significant unmet or underserved medical needs. |
Maryland |
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Director of Regulatory Affairs
Our client is a Contract Research Organization (CRO), which manages individual as well as entire development programs for its clients. Using its fully validated systems, the company can customize and accelerate the processing and reporting of clinical data. |
Southeast USA |
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Deputy Director of Regulatory Affairs
Our client is a leading producer of vaccines. The company employs over 8500 people and has a presence in 150 countries. |
Pennsylvania |
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Deputy Director of Regulatory Affairs
Our client is a leading producer of vaccines. The company employs over 8500 people and has a presence in 150 countries. |
Pennsylvania |
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Regulatory Affairs Manager
Our client is a premier molecular diagnostics business that uses proprietary genomics and proteomics discovery platforms to identify and validate novel diagnostic markers. The company develops diagnostic products based on these as well as other known markers. |
California |
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Director of Regulatory Affairs
Our client creates, distributes, and sells topical skin care as well as restoration products. These include prescription creams and liquids for photodamage, hyperpigmentation, wrinkles, and other skin imperfections. The company has more than 70 employees, but is planning to grow its employee strength to 145. |
California |
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Regulatory Affairs Manager
Our client is a leader in the development of compounds used in a variety of clinical indications. Established in 1950s, the company offers the stability of a well-established organization along with the flexibility of a startup. Priding themselves on their aggressive pipeline, the small North American office provides a family environment allowing each individual to be a contributing member of the team. |
Maryland |
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Contract Regulatory Affairs Associate
Our client is dedicated to developing and commercializing novel therapeutic products in the field of oncology. |
New Jersey |
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Director of Regulatory Affairs
Our client is a biopharmaceutical company focused on the development of drugs to treat leukemia, multiple myeloma and osteolytic bone disease. |
New York City, New York |
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Regulatory Affairs Manager
Our client is a leading biomedical company focused on enhancing patient care and improving patient outcome by meeting the physicians’ critical intraoperative diagnostic information needs and patients’ therapeutic treatment needs. |
Dublin, Ohio |
