Emmes Group
Location
Rockville, Maryland
The In-House CRA supports site management and monitoring activities to ensure clinical trials comply with protocols, SOPs, and regulatory requirements. Key tasks include maintaining essential documents in the Trial Master File and tracking trial progress via the CTMS.
A Bachelor's degree in a scientific discipline is required, with previous clinical research experience preferred. Candidates must be proficient in MS Office and possess strong organizational, communication, and critical thinking skills.
Be Part of One Team, One Purpose.
At Emmes Group, we’re shaping the future of clinical research—where human intelligence meets cutting-edge technology to drive meaningful advancements in healthcare. With over 47 years of scientific excellence, we’ve led groundbreaking research in cell and gene therapy, vaccines, infectious diseases, ophthalmology, rare diseases, and neuroscience.
Through our two business units—Emmes, a full-service CRO, and Veridix AI, our technology, data, and analytical solutions —we are modernizing clinical trials and accelerating the development of life-changing therapies.
We believe that every clinical breakthrough starts with people—people who are passionate, purpose-driven, and ready to make an impact. At Emmes Group, we bring People, Science, and Technology together to collaborate with our customers and deliver global health impact. Our culture is built on integrity, collaboration, and innovation, ensuring that every challenge is met with perseverance and accountability.
The In-House Clinical Research Associate (CRA) is responsible for assisting with operational activities supporting the site management and monitoring of clinical studies/trials, ensuring clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), and all applicable regulatory requirements. The In-House CRA may also be referred to as a Clinical Trial Associate on some contracts.
Bachelor's Degree Scientific discipline Required less than 1 year Previous clinical research experience preferred (as a CTA, in-house CRA, study coordinator, etc.) Preferred Proficient with MS Office Suite High Good computer and organizational skills High High attention to detail required High Ability to work on varying projects and exercise critical thinking High self starter and a team player who can work cross functionally with heavy oversight High Proficient in organizational, interpersonal, and communication skills both oral and written High Demonstrated problem solving skills, self motivated, and adaptable to a dynamic environment High Knowledgeable in prioritization, problem solving, organization, critical thinking, decision making, time management, and planning activities High Ability to collaborate with internal and external colleagues and work well in a team oriented setting High If you’re looking for a career where your work advances global health and where scientific excellence meets real-world impact, join us and be part of something bigger. One Team, One Purpose.
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