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.  

Coordinate clinic staff for clinical study conduct.

• Communicate with staff for availability (10%)
• Coordinate personnel schedules to meet study conduct needs (5%)
• Schedule proper personnel for studies (40%)
• Generate computerized conduct staff schedules (10%)
• Review existing schedules to ensure proper coverage and accuracy (5%)
• Schedule class training (5%)
• Work closely with training coordinators at each site to schedule new associates for training on study conduct
• events (5%)
• Perform conduct events and Clinical Conduct Specialist duties during down time (10%)
• Assist in identifying training needs for clinic
• Assess the need for additional staff using availability reports and study schedules (5%)
• Identify scheduling needs for each study in conjunction with Study Managers
• Attend mandatory meetings - training, weekly initiation, CRD, closing of the books, interim conduct and dry
• runs (5%)
• Provide input on conduct design (set up) and staffing needs/requirements
• May work with study managers to set dosing times for clinical studies in order to most effectively schedule
• staff
• May work with staff managers to

• Associate's degree or equivalent experience required
• Data entry skills
• Internal clinical experience preferred
• **Equivalent education and experience will be considered.

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.