Scientific Data Abstractor - Essex Management
part-time•Rockville
About this role
Overview
Responsibilities
Qualifications
Scientific Data Absractor - Essex Mangement
This is a Part-Time role.
US Remote
This position supports "Essex, an Emmes 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 for clients in the Federal Government, research academia, and private sectors.
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. We’re 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
The team of scientific data abstractors is responsible for abstracting protocol content (e.g., clinical research category, interventions, disease, outcome measures) 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 scientific data, including interpreting protocol data into lay language 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 tasks, as assigned
Qualifications
- Exceptional written and oral communication skills with demonstrated expertise with grammar, syntax, and format
- Able to understand and translate clinical information into lay language
- Able to work in a busy setting, both independently and within a team
- Willing to perform tasks that may fall outside of the normal daily responsibilities
- Able to effectively incorporate diverse feedback from team and user community into a high-quality product
- This position is subject to obtaining a Public Trust Clearance
- Familiarity with area of clinical trials, both interventional and non-interventional (Desired)
- Proficiency with Microsoft® software applications (Desired)
- Knowledge of drug and disease terminology (Desired)
- Possession of a Bachelor’s degree from an accredited college or university in a clinical, biological/biomedical science or healthcare related field
- Two years work experience in clinical trials administration or data analysis
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:
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CONNECT WITH US!
Follow us on Twitter - @EmmesCRO
Find us on LinkedIn - Emmes
The Emmes Company, LLC is an equal opportunity employer and does not discriminate in its selection and employment practices. All qualified applicants will receive consideration for employment without regard to disability or protected veteran status.
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What you'll do
- The primary role involves abstracting protocol content from clinical trials reporting, ensuring timely and accurate data entry while adhering to quality standards. Responsibilities also include completing trial registrations, responding to stakeholder inquiries via a ticketing system, and assisting with SOP improvements.
About The EMMES Corporation
For over 40 years, our team of 1,000+ experienced professionals have provided the full range of Contract Research Organization expertise necessary to conduct clinical research with a firm scientific basis that is fully compliant with national and international regulatory guidelines. With offices throughout the US, Europe, Canada, and India, Emmes supports the advancement of global public health and biopharmaceutical innovation through disciplined science, rigorous research, fact-based decision-making, and operational excellence.
Emmes possesses knowledge across a broad range of therapeutic areas, with specializations in Vaccines and Infectious Diseases, Ophthalmology, Immunology and Neuroscience. From comprehensive support of pandemic research to groundbreaking work in cell and gene therapy across the globe, Emmes has collaborated on clinical research across a wide array of disease states in over 75 nations.
As a strategic collaborator with applied talent in over 2,000 clinical trials and contributions to over 2,500 publications that advance the understanding of medicine and public health, Emmes is committed to expanding the services offered to best meet the changing needs of clients and studies. Ongoing investments in global clinical research capabilities, innovative data management platforms, biostatistics/bioinformatics expertise, and people have enabled Emmes to provide a multi-faceted approach to help you meet your research objectives.
Emmes is a diverse, inclusive, innovative CRO that values integrity, agility, passion for excellence, collaborative partnerships, and intellectual curiosity.
Ready to join The EMMES Corporation?
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Frequently Asked Questions
What does a Scientific Data Abstractor - Essex Management do at The EMMES Corporation?
As a Scientific Data Abstractor - Essex Management at The EMMES Corporation, you will: the primary role involves abstracting protocol content from clinical trials reporting, ensuring timely and accurate data entry while adhering to quality standards. Responsibilities also include completing trial registrations, responding to stakeholder inquiries via a ticketing system, and assisting with SOP improvements..
Is the Scientific Data Abstractor - Essex Management position at The EMMES Corporation remote?
The Scientific Data Abstractor - Essex Management position at The EMMES Corporation is based in Rockville, Maryland, United States. Contact the company through Clera for specific work arrangement details.
How do I apply for the Scientific Data Abstractor - Essex Management position at The EMMES Corporation?
You can apply for the Scientific Data Abstractor - Essex Management position at The EMMES Corporationdirectly through Clera. Click the "Apply Now" button above to start your application. Clera's AI-powered platform will help match your profile with this opportunity and guide you through the application process.