Protocol Data Abstractor - Rockville, Maryland, United States - The EMMES Corporation

Description

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 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 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:
Exceptional written and oral communication skills with demonstrated expertise with grammar, syntax, and format

Ability to work in a busy setting, both independently and within a team

Proficient with computer usage and Microsoft Office applications

Bachelor's Degree

A minimum of two (2) years' experience in a pharmaceutical, biotechnology and/or clinical environment which includes medical and regulatory technical writing/editing (Desired)

Familiarity with area of clinical trials, both interventional and non-interventional (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.