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Data Manager (Clinical Research)


This is a Full-time position in Tempe, AZ posted October 28, 2021.

Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. Celerion offers one of the most experienced clinical pharmacology research networks in the industry.

Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can’t wait to meet you!

The Clinical Data Manager is responsible for the integrity of the data entered into a Celerion system and/or Sponsor provided system. Ensures database is complete, accurate and consistent and meets quality standards required by Sponsors and regulatory bodies. Collaborates and participates in multidisciplinary teams involved in setting up, conducting and reporting clinical trials. Responsible for Sponsor contact, project communication and timeline management for all data management functions. Manages, organizes, and processes clinical data using a range of computer applications and database systems to facilitate collection and cleaning of subject data.

Essential Functions:

  • Oversight of all clinical data management activities for assigned studies in accordance with SOP’s and Procedure Guides
  • Primary Sponsor contact for data management processes on study
  • Responsible for regular communication of study progress with internal and external project team

Success Factors:

  • Demonstrated client service/communication ability
  • Prior project management experience
  • Understanding of clinical research trials and GCDM practices

This position is based at our Tempe, AZ clinic. The position is expected to work onsite consistently during the training period. Once trained, the position is available to work from home for a significant portion of the week. Fully remote candidates (e.g. those living outside the Phoenix metro area) may be considered if they possess significant experience in the data management of clinical research trials.


  • BA degree in related field.
  • 1-2 years industry experience preferred
  • Knowledge of Good Clinical Data Management Practices, Medical Terminology, GCP, ICH Guidelines, and 21 CFR Part11 preferred
  • Knowledge of SAS preferred
  • Ability to manage multiple projects/priorities required
  • High attention to detail required
  • Excellent oral and written communication skills required
  • Excellent organizational skills required
  • Proficiency in MS office applications required

Celerion Values: Integrity Trust Teamwork Respect

Are you ready to join our team?

Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.