Clinical Operations Intern

The EMMES Corporation•Rockville, MD

5h•Remote

About The Position

Clinical Operations Intern 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. 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 Clinical Operations intern supports clinical trial activities and works closely with the clinical operations team to ensure department activities are conducted according to required activity quality standard.

Requirements

Undergraduate student; junior or senior preferred.
Knowledge of Word, Excel, SharePoint and PowerPoint.
Strong verbal and written communication skills required.

Nice To Haves

Understanding of study phases and general knowledge of how they apply to clinical development is preferred.

Responsibilities

General administrative support to the clinical operations department.
Assist in managing trial timelines.
Assess and provide feedback on approaches to maximize efficiencies and identify opportunities for improvement.
General administrative support of clinical operations department storage platforms (e.g. Sharepoint, etc.)
Assist in tracking of trial activities which may include but are not limited to feasibility, site selection, participation status, regulatory or ethics status.
Participates in department and/ or clinical trial team meetings and participate in collaborative efforts.