Celerion

Scientific Report Associate (UK based)

Celerion  •  Belfast, GB (Onsite)  •  1 month ago
Apply
AI can make mistakes so check important info. Chat history is never stored.

Job Description

Scientific Report Associate
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 offers one of the most experienced clinical pharmacology research networks in the industry.   Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you!   Celerion is searching for a full-time Scientific Report Associate for our Belfast, Northern Ireland location. This position will generate, template, and format preliminary and final clinical trial 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.   An attractive salary and benefits package is available.   This position will be a home-based role and candidates must be living in the UK and be eligible to work in the UK.

Criteria

  • A Bachelor's degree OR 1 year relevant experience preferred.
  • Strong proficiency with MS Word and good Business English skills are essential. 
  • The ability to manage multiple priorities and high attention to detail is required.
Celerion is an equal opportunities employer.
Celerion

About 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

Industry
Chemicals & Materials
Company Size
1,001-5,000 employees
Headquarters
Lincoln, NE
Year Founded
2010
Social Media