Our client, a rapidly expanding pharmaceutical firm in the Raleigh area, has an immediate need for a highly competent and knowledgeable industry professional, with background working with Regulatory Submissions, for contract opportunity expected to last 2+ months. Role will involve reviewing completed and new Regulatory Submission Documents for key details to be organized and entered into a newly-created Access database. This is detailed and critical work and requires a candidate with impeccable proofreading skills and a strong compliance orientation. Company will pay an excellent wage to attract and retain an excellent person. Key details are below. Role: Compiling data and documents for Regulatory Submissions Access database Schedule: 40 hours/week (flexible daytime hours); ASAP for approximately 2 months Location: North Raleigh Rate: $20 - $35/ hour (depending on experience) Requirements: Knowledge of the content of Regulatory Submission Documents such as INDs and NDAs; excellent attention to detail and organizational skills; experience with Access a plus. If you are interested, please apply for further consideration.