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Scientific Report Associate - Lincoln, Nebraska

Celerion

Posted 2 months ago

Full Time

Lincoln, Nebraska

In Person

Smart Summary

Responsibilities

The Scientific Report Associate is responsible for generating, templating, and formatting preliminary and final Clinical Study Reports. This role involves building appendices and ensuring documents meet specific client requirements for styles, fonts, and table formats.

Qualifications

You have a Bachelor's degree or at least 1 year of relevant experience in a related field. You possess strong proficiency with MS Word and Business English. High attention to detail and the ability to manage multiple priorities are essential for this role.

Must Have Skills for ATS

MS Word

Business English

Job Description

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.  

Celerion is searching for a full-time Scientific Report Associate for our Lincoln, NE location. This position will generate, template, and format preliminary and final Clinical Study Reports. This position will build appendices, import information from various sources and format the report per client specifications related to margins, fonts, table formats, hyperlinks, bookmarks and styles. 

\nRequirements:
  • A Bachelor's degree or at least 1 year relevant experience in a related field preferred.
  • Proficiency with MS Word, and Business English are essential.
  • The ability to manage multiple priorities and high attention to detail is required.
\n

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.

Celerion

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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