Clinical Informatics Analyst

Overview:

Clinical Informatics Analyst

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 stive 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

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 for clients in the Federal Government, research academia, and private sectors.

The team of Clinical Informatics Analysts are responsible for responding and resolving inquiries, requests or issues submitted by the Clinical Trials Reporting Program user community. They play a critical role working with the larger team to ensure timely delivery and accurate data abstractions, and resolutions of trial related support requests.

Responsibilities:

Respond to inquiries and resolve issues submitted to an issue/ticketing system (e.g., ServiceNow) by the cancer research community and program stakeholders, utilizing clear and effective communication

Manage/coordinate tickets from inception to completion, often requiring input and feedback from several teams.

Manage and perform data reconciliation activities for trial data reported to CTRP

Provide end user application training for new and existing cancer center community

Review clinical trial related documents (e.g., IRB Approval Letter, Protocol Document, Informed Consent Form), to validate trial submissions, abstract relevant administrative data and perform quality control checks following standard guidelines/SOPs

Register trials and amendments in CTRP on behalf of the user community

Review and acknowledge trial updates submitted by the user community

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 quickly learn and understand unique and complex systems and workflows

Able to research and produce results in a fast-paced environment, both independently and within a team effectively and efficiently

Proactive, positive attitude, Team Player

Willing to perform tasks that may fall outside of the normal daily responsibilities

Experience with software ticketing tools, like ServiceNow (Desired)

Proficiency with Microsoft® software applications (Desired)

Possession of a Bachelor’s degree from an accredited college or university in an information technology, clinical, biological/biomedical science, or healthcare related field is strongly preferred; candidates without a Bachelor's degree should possess significant industry experience in healthcare/clinical and Application Support.

Two years work experience in Application Support

Experience with clinical trials domain (highly desired)

Work for this position must be performed in the United States (required). Candidates local to Rockville, MD are preferred.

Applicants selected for this position will be subject to a government security investigation and must meet eligibility requirements for Public Trust positions. Visa sponsorship is not available.

Successful applicants will be required to travel to an NIH-designated facility for security badging within 60 days of hire. Expenses will be reimbursed.

Emmes requires all US based Clinical Research Associate new hires to be fully vaccinated before their first day of employment. All new hires may also be required to comply with other COVID-19 health and safety protocols, such as masking or testing. Emmes complies with all applicable laws regarding reasonable accommodations or exemptions for religious, medical, or other legally protected reasons.

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:

Flexible Approved Time Off

Tuition Reimbursement

401k Retirement Plan

Work From Home Anywhere in the US

Maternal/Paternal Leave

Casual Dress Code & Work Environment

CONNECT WITH US!

Follow us on Twitter - @EmmesCRO

Find us on LinkedIn - Emmes

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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