ABOUT DAS FEDERAL:
Join our fast-growing Small Business in the heart of Washington DC area, where we're dedicated to supporting government clients and their missions. You'll be working on cutting-edge projects that help keep our country safe and contribute to a greater cause. At DAS Federal, we're committed to creating an inclusive workplace that values diversity and promotes collaboration. We're looking for talented individuals who are passionate about making a difference and eager to work with the latest technologies. In return, you'll be part of a dynamic team that provides industry-leading benefits and a supportive work environment. If you're ready to make a real impact and work on projects that matter, we want to hear from you.
DOCUMENT SPECIALIST OVERVIEW:
In this role, you will collaborate with different teams across the agency and organization to ensure that documents meet quality standards and adhere to regulatory requirements. You will also be responsible for implementing and maintaining document management systems, ensuring that all documents are appropriately indexed and accessible to authorized personnel.
To excel in this position, you should have excellent organizational skills, attention to detail, and a strong understanding of document management best practices. Additionally, you should be able to work independently and prioritize multiple tasks effectively.
We are looking for a candidate who has a passion for process improvement and a commitment to ensuring the highest level of document accuracy and consistency. If you are someone who is interested in making a significant impact in the organization and has a keen eye for detail, we encourage you to apply for this exciting opportunity!
This position shall oversee, and direct management and technical support tasks required for a contract for the National Cancer Institute.
DUTIES:
- Maintain proper records of inquiries about ongoing research
- Provide information, data, reports to formal and informal meetings where research are subject to review
- Communicate internally and externally about aspects of clinical trial information to health professionals and scientists
- Abstract key information to ensure data entry protocols are met and adhere to Standard Operating Procedures
- Support internal projects and initiatives and perform other duties as assigned
MINIMUM QUALIFICATIONS:
- Bachelor's degree from an accredited college or university in a health-related field
- Competency in Microsoft Office software products, including experience with word processing and spreadsheet software
- Excellent verbal and written communication skills
PREFERRED QUALIFICATIONS:
- At least 1 year of experience in the health care/clinical research fields
- Experience with utilization of databases, including data element abstraction, milestone entry, generation of queries and running of canned reports
- Knowledge and experience in clinical trials development processes (both scientific and administrative aspects)
- Knowledge and experience within the oncology community a plus
- Demonstrate experience in dealing with health care professionals at all levels, including effective use of both verbal and written communication skills and ability to assist in providing successful presentations to those professionals
- Must have demonstrated self-motivation, effective communication, organization and process improvement skills
Job Type: Full-time
Pay: $48,000.00 - $52,000.00 per year
Benefits:
- 401(k)
- Dental insurance
- Health insurance
- Health savings account
- Life insurance
- Paid time off
- Vision insurance
Schedule:
- 8 hour shift
Work Location: Hybrid remote in Rockville, MD 20850
