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 for an internal candidate 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 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 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
Assist 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
Responsible for the regular installation, maintenance and calibration of all clinical equipment
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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