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Scientific Report Associate - US

Role overview

Qualifications

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

Responsibilities

  • Generate, template, and format preliminary and final Clinical Study Reports
  • Build appendices and import information from various sources
  • Format the report per client specifications related to margins, fonts, table formats, hyperlinks, bookmarks and styles

Key facts

  • Remote from: United States
  • Full time
  • Junior (1-2 years)
  • Research Associate
  • English

Hard skills

Other skills

  • Microsoft Word
  • Detail Oriented
  • Teamwork
  • Communication
  • Problem Solving

About the company

Celerion logo

Celerion

Contract Research Organizations (CRO)

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

Company details

Company typeLarge
IndustryContract Research Organizations (CRO)
Company size1001 - 5000

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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. 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. 
Requirements:
  • 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.
  • 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.  

    Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as "Not Junk" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.

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    Marcus Rivera

    Chief Revenue Officer

    m.rivera@company.com
    linkedin.com/in/marcusrivera
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