NAMSA pioneered the industry, NAMSA was the first independent company in the world to focus solely on medical device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976. We are shaping the industry. NAMSA has been a key contributor to the development of the test methods that govern our industry. We have become the industry's premier provider. We provide support for clients during every step of the product development lifecycle and beyond. Come and work for an organization whose: Mission is to make a scientific contribution to every medical device in the world. Culture is passionately committed to the partnership between one another and our clients to improve and save lives through a respectful, trusting, and collaborative environment. Values have stood the test of time. Above all else, conduct ourselves with integrity Job Description: Develop database specifications based on clinical protocol and/or case report forms. Build and validate clinical databases. Manage and maintain database systems. Create data listings using reporting tools. Provide database training and instruction to team members and study site staff. Contribute to development and improvement of data management processes and procedures. Perform project in compliance with regulations. May take on the Duties and Responsibilities of a 'Clinical Data Manager' as needed. Ensure schedule, budget and quality commitments are met for the client, within the scope of control. Contribute to presentations, including preparation, assembling slides, and speaking. Interact as needed with clients, auditors, inspectors, subcontractors, consultants, and other individuals or departments. Participate in meetings with prospective clients. Provide scope of project and relevant information to support the creation of proposals. Offer opportunities to clients for expansion of MRO services to be provided by NAMSA. Qualifications & Technical Competencies: Bachelor's degree or equivalent experience in a related field, and a minimum of 5 years of relevant experience; or Master's or Doctorate degree or equivalent experience in a related field, and a minimum of 2 years of relevant experience. Fluency in English and local language, if different, required. Experience in clinical database development (iMedNet, Rave or Clindex experience preferred). Advanced knowledge of industry standards and practices in clinical data management, database, and data reporting concepts. Basic SQL and/or SAS programming knowledge. Working Conditions: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to talk or hear. The employee is frequently required to stand; walk; sit; use hands to finger, handle, or feel and reach with hands and arms. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, depth perception, and ability to adjust focus. Extensive use of a computer keyboard.