What are the responsibilities and job description for the Clinical Study Designer - Lincoln, Nebraska 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.
Celerion 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.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
Salary : $20 - $21