As Regulatory Affairs Specialist or Analyst you will assist in the support of the daily operational activities within Regulatory Affairs for the collection, tracking, filing, and storage of clinical trial documents. Moreover, you will support the preparation of regulatory submissions required to market new or existing licensed pharmaceuticals and device

The role of the Clinical Trial Safety Nurse primarily involves the assessment and processing of adverse events received from healthcare professional and clinical trial sites within the US and the tracking, reporting, follow-up to completion and submission of these reports to regulatory authorities on behalf of the clinical trial sponsor. An

As Clinical Trials Financial Analyst you will provide insight and direction related to invoicing and managing clinical trial awards. The candidate should possess thorough understanding of Federal and State laws and regulations related to the provision and reimbursement of healthcare services, clinical research billing, and knowledge of Medicare policy and

As Biomedical Engineer you will work under a quality management system and take an active role in the design and realization of new products and product modifications. Applicants must have good writing skills for the creation of project documents and reports. Responsibilities Quality management Design and realize new products/product modifications

Qualifications MD, DO, RN, PharmD or similar with experience in Oncology clinical development Minimum of 3 years of experience, including 2 years as a medical monitor for clinical trials (Phase I – III) Good verbal and written communication skills essential Experience managing projects, coordinating activities and adhering to tight timelines

Position Overview: Houston company is seeking a Senior Clinical Research Associate (CRA) within the Houston Texas Area. This person would need to have the ability to be approved for a credit card or use existing credit card for hotel, rental car, and other related expenses while traveling. The position would

Vapogenix, Inc., a clinical stage pharmaceutical development company, located near Loop 610 and Highway 288, is seeking an Office Administrator/Executive Assistant to provide general support to all office staff, including C-level executives. Responsibilities involve a wide range of tasks such as scheduling calls and meetings, travel arrangements (domestic and international),

Job Purpose: Work as an integral part of the laboratory production team. Assist in the production of adult stem cell product for banking and for therapeutic use. Job Duties: Conduct hands-on aseptic cell culture Maintain accurate and timely manufacturing records, paper and electronic notebooks, records and logs Document and maintain