Data Archive Analyst and Clinical Trials Coordinator

Rockville, Maryland
Apr 06, 2019
Apr 06, 2019
Full Time
The Emmes Cormpany, established in 1977, is a private Contract Research Organization (CRO). Headquartered in Rockville, Maryland, Emmes employs over six hundred staff worldwide with offices located in Frederick, Maryland, Tysons Corner, Virginia, Vancouver, Canada and Bangalore, India. Ranked as a top area workplace of choice by the Washington Post, Emmes fosters an environment of collaboration, professional growth, and exceptional work life balance.

Our studies impact public health initiatives on a global scale occurring in more than sixty countries spanning across six continents. We are dedicated to providing statistical and epidemiological expertise, computer systems deployment, data management, study monitoring, regulatory guidance, and overall operational support to clients engaged in biomedical research. Emmes offers support for the entire process of clinical trials from study design and protocol development through data analysis and manuscript generation.

Primary Purpose

Emmes is seeking a Data Archive Analyst and Clinical Trials Coordinator, to assist with a clinical trial data-sharing project and precision-medicine clinical trials. Major tasks include reviewing data submissions, processing requests for data, and performing project management for clinical trials.

Primary Responsibilities:

Data Archive Analyst Responsibilities:

• Reviewing clinical trial datasets for completeness, clarity, accuracy, and reproducibility.

• Detailing the findings from the dataset reviews in a report.

• Maintaining and organizing data-sharing records.

• Managing daily operations of a data-sharing project, including processing requests for data.

• Generating progress and programmatic reports about the project.

• Tracking submission of clinical trial datasets and publication of clinical trial manuscripts.

• Facilitating review of clinical trial datasets by institutions and collaborators, including identifying relevant agreements affecting the data sharing.

Clinical Trials Coordinator Responsibilities:

• Coordinating scientific working groups and committees of cancer researchers.

• Scheduling and facilitating multi-disciplinary discussions among cancer researchers.

• Creating, maintaining, and refining documents related to research studies and data sharing (e.g., proposal submission forms, process workflows, templates).

• Synthesizing the content of scientific discussions into clearly written summaries.

• Abstracting, compiling, and assessing information from cancer clinical trial protocol documents, manuscripts, and databases.

Primary Requirements

• Bachelor's degree with knowledge of biology required

• Strong writing skills, including the ability to write succinctly, articulately, and professionally

• Knowledge of Microsoft Excel, Adobe, PubMed, and EndNote is desirable

• Good oral communication skills

• Ability to function independently, including anticipating and prioritizing next steps with minimal directions

• Ability to adapt quickly to changing project needs and priorities

• Ability to format documents to achieve a consistent, professional appearance

• Critical thinking and project management skills, especially the ability to apply knowledge and information across a variety of different tasks


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The EMMES Company 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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