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"When I was still in college and working at RTI as an intern, I knew it was somewhere that I wanted to work full-time one day. RTI holds its employees to the highest standards, which allows for continuous growth both professionally and personally. I love being able to walk around campus and be immersed in a community of knowledgeable, hard-working innovators who all have a primary goal of improving the human condition." Lily Duchesneau Financial Analyst- SSES Strategic Pricing Group
"It is a pleasure to be part of a company that has such a positive outreach and works to improve the human condition. With a great reputation in the local community and abroad, it is easy to feel proud of the products and services produced by RTI. I like the variation of my role and that I get to work with a wide variety of people across the globe. I enjoy working at RTI because it is a place that demands excellence while still allowing a healthy work-life balance." Tierra Vazquez Sr. Administrative Assistant-International Education
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Information Technology
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Health Solutions
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190HW Requisition #
Thanks for your interest in the Data Manager position. Unfortunately this position has been closed but you can search our 165 open jobs by clicking here.

 

Qualifications:

   

  

  • Bachelor's level degree in health information management, clinical, biological, or mathematical sciences or related field plus 5 years of data management experience in a professional environment, preferably within a clinical or medical data environment or pharmaceutical company or 10 years of data management experience in a professional environment, preferably within a clinical or medical data environment or pharmaceutical company
  • Direct experience working on prospective observational studies and retrospective medical chart review studies
  • Experience working on multiple simultaneous projects
  • Knowledge of FDA and EU/EMA regulations with respect to data quality and data privacy for the conduct of observational and clinical studies in the US and Europe. Working knowledge of the relevant ICH and GCP guidelines.
  • Demonstrated working knowledge of clinical data management systems and survey data capture systems (e.g., OpenClinica, Qualtrics).
  • Ability to effectively apply knowledge and skills in a highly organized fashion while adhering to regulatory guidelines, SOPs and client expectations
  • Demonstrated written and verbal communication skills 
  • Must be able to set and meet timelines or be able to recognize and schedule changes in response to project demands
  • Ability to maintain a high degree of confidentiality with study data and client's proprietary information
  • Demonstrated organizational and analytical/problem-solving skills
  • Ability to work productively with minimal supervision
  • Ability to work in a team environment and independently as needed

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