Data Manager
Company Name:-
EMMES
Job Location:-
Remote
Job Summary:-
The Emmes Company, LLC.
Emmes is a Contract Research Organization (CRO).
Headquartered in Rockville, Maryland, Emmes employs over seven 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
The Data Manager is responsible for data management activities for research studies.
The Clinical
Data Manager works as an integral part of a cross-functional team through the lifecycle of the research
study from design through final analysis and study closeout.
The Clinical Data Manager is responsible for
the completeness and accuracy of the study data in the electronic database and collaborates with internal
and external project teams on all aspects of data collection.
Responsibilities
Accountable for technical, scientific, fiscal, and overseeing of research projects working with staff at Emmes responsible for research support activities, including but not limited to Clinical Operations, Statistical and Scientific Innovation, Regulatory Affairs, and Pharmacovigilance.
Participates with cross-functional teams in design, documentation, testing, and implementation of clinical data collection studies in an electronic data capture (EDC) system.
Designs and/or develops study-specific electronic or paper Case Report Forms (CRFs), ensuring consistency with study protocol, clinical requirements, and accurate and efficient data collection.
Collaborates with the project team and other study personnel to determine data collection requirements based on the stu
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