What are the responsibilities and job description for the Protocol Data Abstractor position at The EMMES Corporation?
Overview :
Protocol Data Abstractor
US Remote
Emmes Group : Building a better future for us all.
Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience.
We believe the work we do will have a direct impact on patients lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. Were looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us!
Primary Purpose
This position supports "Essex, a Veridix AI company". Essex is a biomedical informatics and health information technology-focused consultancy founded in 2009 and headquartered in Rockville, MD. The Essex team comprises experts with extensive experience in strategically developing and managing complex health and biomedical information programs as a prime contractor for clients in the Federal Government, research academia, and private sectors.
The team of protocol data abstractors is responsible for abstracting protocol content (e.g., lead organization, participating sites, study status information, IRB, funding) associated with clinical trials reporting. They ensure timely and accurate data entry information, adhering to established program quality standards.
Responsibilities :
- Review documents, validate trial information, abstract relevant protocol data and perform quality control checks following standard guidelines / SOPs
- Complete new trial and amendment registrations and acknowledge trial updates
- Respond to inquiries and resolve issues submitted to an issue / ticketing system by the cancer research community or stakeholders, utilizing effective communication
- Assist to improve Standard Operating Procedures and User Guides
- Troubleshoot and appropriately report unexpected problems that may arise during the data abstraction of clinical trials
- Participate in User Acceptance Testing to support application releases
- Participate in data clean-up related activities
- Perform other related duties, when assigned.
Qualifications :
Proficient with computer usage and Microsoft Office applications
Why work at Emmes?
At Emmes, your actions and hard work will have a direct impact on public health initiatives, both globally and in our local communities with opportunities for volunteerism through our Emmes Cares community engagement program. We offer a competitive benefits package focused on the health and needs of our growing workforce, including :
CONNECT WITH US!
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The Emmes Company, LLC is an equal opportunity affirmative action employer and does not discriminate in its selection and employment practices. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, political affiliation, sexual orientation, gender identity, marital status, disability, protected veteran status, genetic information, age, or other legally protected characteristics.
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