What are the responsibilities and job description for the Clinical Study Designer position at Celerion?
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.
We are currently seeking a full time Clinical Study Designer at our Lincoln, Nebraska location. As part of our team, you will be responsible for the logistical set up and maintenance of clinical trials in ClinQuick - our electronic data capture system. You will also manage the creation of study conduct instruction manuals and detailed timed event schedules for the clinic staff and study participants.
Requirements:
A minimum of an Associate’s degree in a health related field and/or applicable experience in a medical, clinical, pharmaceutical or laboratory setting is required. You must be detail‑oriented, computer literate, and able to work in a fast-paced atmosphere.
\nCelerion Values: Integrity Trust Teamwork Respect
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.
Salary : $18 - $20
