Clinical Study Designer - Lincoln, Nebraska

Posted 23 Days Ago
Be an Early Applicant
Lincoln, NE, USA
Hybrid
Entry level
Pharmaceutical
The Role
Set up and maintain clinical trials in ClinQuick EDC. Create study conduct instruction manuals and detailed timed event schedules for clinic staff and participants. Manage logistical study setup and ensure accurate documentation in a fast-paced clinical research environment.
Summary Generated by Built In
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.
 

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Skills Required

  • Associate's degree in a health-related field or equivalent applicable experience in medical, clinical, pharmaceutical, or laboratory settings.
  • Experience in a medical, clinical, pharmaceutical, or laboratory setting (applicable experience accepted in lieu of degree).
  • Detail-oriented with strong attention to accuracy.
  • Computer literate.
  • Able to work in a fast-paced atmosphere.
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The Company
HQ: Lincoln, NE
1,029 Employees
Year Founded: 2010

What We Do

Celerion, a leader in early clinical research, delivers Applied Translational Medicine. Celerion applies our expertise and experience to translating information gained in research discoveries, to knowledge of drug action and effect in humans to support early drug development decisions and the clinical pharmacology labeling of new medicines. With over 50 years of experience and 600 global clinic beds (including 24 in-hospital), Celerion conducts and analyzes First-in-Human, clinical proof-of-concept, cardiovascular safety (TQT, robust QT), ADME and NDA-enabling clinical pharmacology studies. Celerion provides expertise on modeling and simulation, study design, medical writing (protocols and reports), clinical data sciences, biostatistics, and PK/PD analysis as well as small and large molecule bioanalytical assays through clinical drug development. Regulatory, drug development and program management complement Celerion’s service offerings. Our operations are strategically located in: Lincoln, Nebraska (Corporate Headquarters) Philadelphia, Pennsylvania Phoenix, Arizona Belfast, Northern Ireland,UK Zurich, Switzerland Vienna, Austria Richmond, Virginia Montreal, Quebec, Canada For more information, visit: www.celerion.com

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