Associate Study Coordinator

North American Science Associates-posted 2 days ago

$18 - $26/Yr

Full-time • Entry Level

Minneapolis, MN

1,001-5,000 employees

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NAMSA pioneered the industry and was the first independent company in the world to focus solely on medical device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976. We are shaping the industry. NAMSA has been a key contributor to the development of the test methods that govern our industry. We have become the industry’s premier provider. We provide support for clients during every step of the product development lifecycle and beyond. Come and work for an organization with the: Vision to inspire innovative MedTech solutions that advance global healthcare, improve patient lives and accelerate Client success and the Mission to deliver best-in-class global MedTech development solutions through our people, expertise and technology by adhering to our core Values: Act with integrity in everything we do. Provide best-in-class customer experiences. Develop superior talent and deliver expertise. Respond with agility and provide timely results. Embrace collaboration, diverse perspectives and ideas. Job Description:

Knows and understands the Animal Welfare Requirements and serves as a support to the Study Directors and/Principal Investigator, when applicable.
Assists Study Directors on select projects under the direction and review of the Study Director team.
Assists in collection, documentation and analysis of pre-clinical data.
Assists in the coordination of study tasks from pre-study initiation to study completion.
Performs accurate and timely record keeping consistent with the maintenance of facility SOPs.
Utilizes computer systems to enter and reference data as needed.
Assists in study planning and design of studies, under the direction and review of the study director team, to meet desired project endpoints, including coordinating pre-study meetings and data review.
Responsible for study planning activities, assists with generating study protocols when directed, coordinates and monitors activities in support of study conduct.
Communicates effectively with Sponsors, Study Directors, Principal Investigators and Testing Facility Management on the progress of all studies.
Assists with data collection, database entry and generating/tabulating data.
Distributes study related documents, i.e. copies of study data sheets
Creates documentation per SOP to assist with test/control article accountability.
May ship specimens, documents, CDs, DVDs etc. per SOP, maintaining accurate chain of custody documentation.
Assists with generating technical reports as directed and assist in identifying issues and recommend solutions.
Maintains client inventory and is required to be familiar with internal and competitor products.
Types correspondence and various types of documentation in proper format and proofreads/distributes as assigned.
Completes special department projects and duties (i.e., data collection, report creation, information maintenance, contacting personnel for routine updates, etc.) as required to support daily business operations.
Other duties as assigned.

One year experience in an administrative position desirable, preferably with an emphasis in a laboratory setting.
Working knowledge of word processing and spreadsheet software.
Requires a minimum of an Associate degree, preferably in a scientific discipline.

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Associate Study Coordinator

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