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Specialist, Data Management

2 weeks ago


Newark, Delaware, United States QPS, LLC Full time $50,000 - $80,000 per year
 

Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you   Specialist, Data Management is a member of the Project Management group within the Bioanalytical Department of QPS. In this entry-level data management position, you will perform and manage electronic inventory and reconciliation for on-site biological samples, pharmacokinetic sample concentration data file creation and delivery, as well as quality control review functions, in order to meet internal and external timeline deliverables in a GLP compliant environment. Please note that this is not an IT role. 

This entry-level role requires advanced skills with computerized databases (i.e., Laboratory Information Management System), statistical data-reduction, an understanding of pharmacokinetic (PK) sample analysis, and an ability to provide detailed customer service. The daily experience involves multiple, extensive, parallel interactions and troubleshooting with QPS operations staff and external study sponsors, clients, vendors, etc. It requires the ability to communicate across many specialties and interests: with scientists, with database experts, with study sponsors, and with regulatory experts. Specialists are trained and supported by process and technical experts.

QPS' Story:

Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of Neuropharmacology, DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II – IV Clinical Research services. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life.

Team members enjoy challenging and rewarding work, and are encouraged achieve their best.  Underpinning the operation is a culture that values diversity, innovation, accountability, team work and a friendly atmosphere where performance is recognized and rewarded.  We provide unique company benefits, training, and advancement opportunities.  Most importantly, we value each of our team members as employees and as individuals.

If this sounds like your ideal work environment, then we would love to speak with you, so apply today

Please visit our website ) for more information and to see all current openings.

The Job

  • Independently organize and prioritize workload to meet internal and client timelines for multiple projects running concurrently
  • Independently extract and correlate sample record databases with data databases and perform custom database record linking
  • Perform the basics of client data management, updating sponsors and/or 3rd party vendors, addressing sample and data reconciliation queries, and making necessary updates
  • Prepare and send interim and final PK sample concentration data files to sponsors and/or 3rd party data recipients.
  • Assist in the management of study timelines and client expectations by actively coordinating with QPS scientists and assessing study status
  • Maintain a working knowledge of current industry guidelines and technology related to bioanalysis and pharmaceutical data management

Work Location

  • This job will be 100% QPS-office/facility based

Requirements

  • High School or GED with 2+ years of relevant industry experience OR
  • Associate's/Bachelor's degree 
    1. A degree in Data Analytics, Analytical Chemistry, Biochemistry, Pharmaceutical Chemistry, Pharmacology, is considered added value 
  • Exposure to FDA Regulated Industry is preferred
  • Bioanalytical CRO experience is considered added value

Why You Should Apply

  • Great learning opportunities, especially for those new to the field.  Our seasoned professionals are here to support and work with you to explore your learning potential and career goals.
  • Structured Career Ladders that provide excellent growth based on your personal aspirations.
  • Bonuses and merit increases are a part of the QPS total rewards approach and are linked to individual, team and company performance.
  • Solid Benefits package, including Company-matched 401(k), and Company-sponsored Group Life/AD&D and Short and Long-term Disability Insurance
  • Park-like setting in Newark, Delaware
  • Internal committees designed with the needs and enjoyment of QPS employees in mind.

QPS, LLC is an Equal Employment Opportunity/Affirmative Action Employer.  In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.