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Clinical Conduct Specialist en Celerion

Celerion · Tempe, Estados Unidos De América · Onsite

43.680,00 US$  -  43.680,00 US$

Swift

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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.  

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

We have an exciting opportunity to become a Clinical Conduct Specialist in our Tempe clinic!  In this position you will be assisting Clinical Study Managers with study preparation and set up.  You will work closely with conduct staff to ensure they are trained on study specific duties.  You will be responsible for ordering medical supplies for study set up, preparing clinic flow for smooth conduct, and providing leadership to the team.  You will also participate in client meetings.


Requirements
  • Post high school education in life sciences or medical training preferred
  • At least 6 months of internal and/or relevant external experience preferred
  • Must be able to handle multiple priorities
  • Effective written and verbal communication
  • Organizational skills 
  • Experience working in a medical environment preferred
  • This full-time position includes benefits and requires a flexible schedule including early mornings and occasional weekends.
  • Monday – Friday, 06:30-14:30


    • Essential Functions
  • Work with Clinical Conduct Associates (CCAs), Clinical Conduct Technicians (CCTs), Clinical Services Technicians (CSTs) and Phlebotomists on all shifts to (25%)
  • Develop task lists for work to be done on each shift
  • Identify needed training in areas such as dosing, blood processing, sample shipping, CPR, etc.
  • Communicate study conduct issues, computer changes, etc which impact their ability to work on a study                                                                                                                                               
  • Provide leadership for conduct                                                                                                            
  • Participate in development of new processes
  • Work closely with Study Managers with study preparations and set up (75%)
  • Attend and assist in planning all study meetings, such as initiation meetings, client visits, etc
  • Conduct or assist in study-specific training, such as dry runs, specific training plans, etc
  • Order supplies for studies
  • Check all check-in materials (i.e. books, urine cups, arm bands)
  • Reconcile/ship samples with appropriate documentation
  • Serve as backup for study conduct (CCA, CCT, Dosing Specialists) as needed
  • Enhance the study participant experience
  • Preparation of study conduct stations
  • Ensure adequate study set-up is complete  
  • When necessary, order, label, and reconcile special client specific labels and tubes.                   
  • Perform process audits


    • 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.
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