The EMMES Corporation employs professionals in the following areas. If you are interested in working for a reputable research firm with a great environment and excellent benefits, please send your curriculum vitae or resume and letter of interest to:

The EMMES Corporation
401 N. Washington Street, Suite 700
Rockville, Maryland 20850
Fax to: 301-251-1355 or
e-mail to: careers@emmes.com

POSITIONS AVAILABLE

STATISTICIAN
Ph.D. or experienced Master's level biostatisticians with experience in clinical trials methodologies. Successful applicants will show a proficiency with data analysis, scientific reporting and standard statistical computing methods. Initiative, leadership and excellent interpersonal and communication skills are essential for interacting with and supporting the needs of clients and colleagues.

PROGRAMMERS/ANALYSTS
Duties include: Customize and support Java Web-based clinical data entry systems used in clinical studies. Develop custom modules using J2EE, SQL and Java technologies, maintain clinical trials database, ensure database integrity and provide data changes.

DATA MANAGER AND PROTOCOL MONITOR
Dependable, detail oriented individual with a minimum of a B.S. degree or equivalent experience in a medical/biologic or other health related field to conduct database management and protocol monitoring for multi-center NIH clinical trials. The ideal candidate must have strong data management/computer skills and be able to effectively communicate and coordinate with internal and external clients and colleagues. Experience in clinical research is helpful. Position will involve general database management support activities including report generation, data entry, filing, and may involve some travel.

CLINICAL INFORMATION SPECIALIST
Individuals must be independent with excellent team building, communication, and organizational skills. Strong scientific/medical writing skills and graduate training in a health/medical/biologic field, or equivalent experience in oncology required. Responsibilities include support and collaborate with NCI investigators on cancer therapy clinical trials, database management, literature & database searches, preparing summaries of scientific meetings, and other program activities as needed. It is especially important for this individual to take initiative and to be responsive and adaptable to the changing needs of our clients. The ability to prioritize multiple tasks is essential. Experience with MS Office, Access, and Medline helpful.

ADMINISTRATIVE COORDINATOR
Self-motivated, organized, and detail oriented with a minimum of 2 years experience and excellent computer skills with proficiency in MS Word to assist project teams with clinical trials research. Responsibilities for administrative assistants include typing correspondence and memorandum for team members, facilitating production of policy and procedure manuals, coordination of large and small meetings and many other duties. We prefer applicants with some college.

SYSTEMS COORDINATOR
The Systems Coordinator is the liaison between project and programming teams to ensure project requirements and corporate applications are integrated/configured effectively. We seek a bachelors degree with 2 yrs experience in systems implementation or data management. Education/training in rational database design, MS, SQL, JavaScript and VBA programming and experience in biology or other applied research a plus.
Excellent verbal and written communication and interpersonal skills.

EMMES is an Affirmative Action/Equal Opportunity Employer.