Project Assistant
Kendle International
Munich, Germany
Ref: EP141-03
Kendle International

The Role


The Role


An entry level position that provides basic administrative, clerical, and communication activities necessary to support assigned Project Teams that result in meeting client expectations, project goals and timelines

Requirements


Requirements


Education: Minimum of Associate’s degree (AA/AS) or equivalent in office administration, business/secretarial field or related discipline.
Experience: 0-12 months or equivalent administrative experience

An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.

Candidate should be able to prioritize work. Candidate/incumbent should have attention to detail and good proofreading skills. Candidate should be proficient in word processing (able to type 50-60 wpm), use of spreadsheets (e.g. Excel), and presentation software (e.g. PowerPoint). Candidate should possess the ability to learn and function proficiently in multiple types of databases. Candidate must be able to work concurrently on several projects, each with specific instructions that may differ from project to project. Candidate should have knowledge of basic English/grammar and should be familiar with medical terminology

About the Company


About the Company


Kendle is a leading global clinical research organization providing the full range of early– to late–stage clinical development services for the world's biopharmaceutical industry. Our focus is on innovative solutions which reduce cycle times for customers

Kendle was established in 1981. A founder run company, Kendle is currently ranked as the 4th largest Contract Research Organisation (CRO) for Phase II-IV studies. Employing in excess of 3,000 Associates globally, Kendle spans 6 continents with global locations across North America, Europe, Asia/Pacific, Latin America and Africa.

Kendle’s Corporate Headquarters are in Cincinnati, USA and the its UK offices are in Glasgow, Edinburgh and Camberley, Surrey.

We are always keen to hear from clinical professionals, particularly within the following disciplines; Clinical Trial Administrators, Clinical Research Associates, Clinical Project Managers, Regulatory Affairs Consultants/Managers, Biostatisticians, SAS Programmers, Data Managers, Pharmacovigliance professionals and Medical Writers.

In June 2009 Kendle was again named among the top two providers in the 2009 CenterWatch Survey of US investigative sites, making us the only CRO to have been ranked consistently among the top two providers in the 2009, 2008 and 2007 CenterWatch Surveys of US and European Investigative Sites.

Successful applications to Kendle will be rewarded with a highly competitive compensation and benefits package including; 25 days annual leave, contributory pension, private medical insurance, life assurance, permanent health insurance, Kendle College e-training & bonuses!! Car allowances will be offered for certain roles.