Clinical Trial Assistant - Nuernberg, Deutschland - PentixaPharm GmbH

PentixaPharm GmbH
PentixaPharm GmbH
Geprüftes Unternehmen
Nuernberg, Deutschland

vor 2 Wochen

Lena Wagner

Geschrieben von:

Lena Wagner

beBee Recruiter
Beschreibung

Who we are:


Your tasks:


  • Support in the qualityassured and timely planning, coordination, implementation, monitoring and evaluation of international, multicenter studies of phase I to III
  • Helping with the preparation and maintenance of the trial master file(s)
  • Support of Clinical Project Managers with any study activities
  • Updating the Investigator's Brochure(s) as well as the study reports and final reports
  • Track records of study documents
  • Contribution to the overall tasks of the Clinical Research Department
  • Performance of other related duties and responsibilities as assigned
  • Preparation of presentations, also outside of study topics
  • Presentation of the company at scientific congresses
  • Preparation and followup of internal and external meetings
  • Internal and external communication and reporting of project progress

Your profil:


  • Master or Ph.
D. in the medical or natural sciences

  • Fluent English and German (oral and written)
  • Initial industry experience in the field of clinical studies is desirable
  • Proactive, reliable and goaloriented way of working
  • Team player with good negotiating skills
  • Strong communication and persuasion skills
  • Confident handling of MS-Office
  • High willingness to travel and flexibility

We are offering:


  • Familyfriendly orientation with flexible working hours
  • Performancerelated compensation
  • Opportunities for further qualification
  • Pleasant working atmosphere in a committed team
  • Flat hierarchies and short decisionmaking processes

Art der Stelle:
Vollzeit, Festanstellung


Arbeitszeiten:

  • 8Stunden-Schicht
  • Keine Wochenenden
  • Montag bis Freitag

Leistungen:

  • Betriebliche Altersvorsorge
  • Betriebliche Weiterbildung
  • Firmenhandy
  • Flexible Arbeitszeiten
  • Kostenlose Getränke
  • Zusätzliche Urlaubstage

Ausbildung:

  • Bachelor (Wünschenswert)

Berufserfahrung:
Klinische Studien: 1 Jahr (Wünschenswert)


Sprache:

  • Englisch (Wünschenswert)
  • Deutsch (Wünschenswert)

Arbeitsort:
Zum Teil im Homeoffice in 97080 Würzburg
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