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 Data Coordination Specialist I/II

Details
Country: USA
Location: CT Ridgefield
Total applied: 48

Job Type: Employee
Job Status: Full Time

Data Coordination Specialist I/II

Our Culture - Come Discover Us
Boehringer Ingelheim is a family-owned company that is in the business of providing our customers with pharmaceutical and animal health products that significantly enhance their health and improve their quality of life. Our most important resource is our committed, creative and determined employees whose energy is focused on discovery, development and delivery of our innovative products to those who need them. The employees of Boehringer Ingelheim are our most important competitive advantage. Our global presence and thinking provides the opportunity for employees to work internationally and on teams, offering them visibility and the ability to influence the direction and outcome of critical projects. Competitive benefit and compensation programs reflect the Company's high regard for its employees and enhance each person's ability to balance the demands of work and personal responsibilities. Every employee at Boehringer Ingelheim contributes to the company's uncompromising commitment to quality in our products, excellence in our scientific pursuits and high ethical standards of behavior. The diversity of our employees makes it possible for us to craft unique solutions to today's complex business challenges. We are an equal opportunity employer. M/F/D/V.

Job Description
REQUIREMENTS:

* Bachelor of Science Degree in a Medical or Biological field

* Knowledge of medicine, FDA regulations and clinical trials

* Excellent organizational skills, problem-solving abilities, time management skills and initiative

* Flexible and able to work on several projects simultaneously work independently and as a part of a team

* Good written and oral communication skills

* An understanding of data processing concepts and elementary statistics

* Experience with computers and ability to learn SAS programming

DUTIES AND RESPONSIBILITIES:

* Review protocols, CRFs and database set-up

* Create and maintain data management plan

* Review databases for completeness, accuracy and consistency.

* Prepare/ assist in the preparation of data presentations. Assist in the production of Integrated Clinical Trial Reports

- Apply for Data Coordination Specialist I/II

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