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Formulation/Process Development Technical Services Quality Assurance & Quality Control Regulatory Affairs Analytical, Bioanalytical, Microbiology & Toxicology Manufacturing & Operations Validation Business Development Medical Writing Clinical Operations, Clinical Research, MD's Clinical Research Associates Pharmacology/ Pharmacokinetics Project Management Other |
Listings posted February 1, 2010
Some of the listings are posted below. We suggest candidates interested in advanciing their career contact us via phone or email with their resume attached. We will contact you as soon as possible to have a confidential conversation. Please know that these listings can change immediately and not all inclusive. The areas we specialize in our listed. Quality Assurance & Quality Control Senior Director , Quality Operations Job Number: 971 Our client located on the west coast has a critical need for a hands-on Senior Director of Quality Operations. Person needs to have a successful track record of ownership in "getting commercial products" out the door. Must have global experience and strong quality operations experience with a major pharmaceutical company. Excellent compensation and benefits with International company. Associate Director/ DIrector, Regulatory Affairs An international company on the east coast has an immediate requirement for a regulatory affairs Associate Director/ Director with submission experience, and experience in advertising and promotional materials. Person must have a minimum of a BS degree and an MS degree is preferred. Experience should include previous contact with the FDA, particularly DDMAC. Exciting growth opportunity for the right individual looking for a new global development environment. Director, CMC Regulatory Affairs Job Number 975 Our client in New Jersey has an immediate need for an experienced leader in Regulatory Affairs with strong CMC strategic experience in branded products. Individual must have a strong scientific background to provide direction to the project teams dealing with regulatory issues. Person should have an advanced degree and a minimum of five years of recent CMC regulatory dealings with the FDA. Company primarily involved in small molecules. Senior Manager/ Associate Director Clinical Regulatory Affairs Job Number 976 International pharmaceutical company that is growing requires experienced individuals in clinical regulatory affairs. Person must operate independently and have direct experience in dealing with the FDA, and preferrably with more than one division. They must be able to contribute immediately in a fast paced environment. A scientific degree is preferred, but experience is key. Dealing with IND, NDA submissions. Client is in New Jersey.
Our client located in the southeast has an opportunity on their pharmaceutical research development and analytical team.. This individual should have a BS degree and a few years experience in HPLC method development. We are seeking individuals looking for an exciting opportunity to be part of a new and changing company environment.
Senior Director, Clinical Project Management Job Number 970 This newly created role with our client in the northeast requires anexperienced person to assist the CMO in the stategic planning to insure success in the clinical development and medical affairs group. Person needs experience in dealing with CRO's, project metrics, clinical trial planning, etc. BS degree with certified project management experience is required. Excellent opportunity with successful biopharmaceutical company. click here to submit resume Our client is looking for an MD, with 3-7yrs experience in pharmacovigilance to develop plans for ongoing or new clinical studies. The focus will be to monitor adverse events of current marketed products. Person will serve as the product safety expert. Must have a strong clinical background. This is a new position located in the northeast. Senior Clinical Research Associate Job Number 974 Client on the East Coast has an immediate opportunity for a Senior CRA with at least 5 years of experience in a lead role. Prefer someone with some operations experience in CNS or Cardio/Renal. Approx. 25-30% travel. Person could be home or office based depending upon individual circumstances. Competitive compensation and benefits.
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