Lead Clinical Project Associate (m/f/d)

60311 Frankfurt am Main, Frankfurt am Main
27.06.2019

Daten dieser Anzeige

Job-ID: 010632498
Lead Clinical Project Associate (m/f/d)

Merz Pharmaceuticals GmbH

Germany

https://merzpharma-openhire.silkroad.com/epostings/index.cfm?fuseaction=app.jobinfo&jobid=813&company_id=30120&version=1&source=ONLINE&jobOwner=992452&aid=1

You will ensure that the operational conduct of our clinical trials meets quality and regulatory requirements You will support the selection, qualification and training of external providers and clinical trial sites You will contribute to the management of site monitoring including centralized monitoring You will take care of a professional document management and inspection-ready Trial Master Files You will perform in-process control of documents and medical review of clinical data.

  ABOUT US: Merz's global leadership in the areas of aesthetics, neurotoxins and consumer care is the result of our innovative, entrepreneurial spirit and the commitment of our colleagues around the world. Our highly attractive portfolio, clear strategic focus and dynamic culture are the keys to our long-term growth and success. Are you ready to become an active contributor to our success story?  Can you see yourself with Merz Pharmaceuticals as   Lead Clinical Project Associate (m/f/d) - part-time (60%) (m / f / d) temporary employment for 1 year Global Clinical Operations       THESE TASKS ARE WAITING FOR YOU:    As Lead Clinical Project Associate you will be a member of the clinical team to strongly contribute to the successful conduct of Merz sponsored clinical trials.   You will ensure that the operational conduct of our clinical trials meets quality and regulatory requirements You will support the selection, qualification and training of external providers and clinical trial sites You will contribute to the management of site monitoring including centralized monitoring You will take care of a professional document management and inspection-ready Trial Master Files You will perform in-process control of documents and medical review of clinical data.       THIS IS WHAT WE EXPECT FROM YOU:    University degree in life sciences or another relevant professional education combined with professional experience In-depth knowledge of clinical trials, relevant regulations (ICH GCP, DIN EN ISO, EU CTR, MDR, FDA, etc.) and processes Strong document management skills Proficiency in MS Office and other relevant applications, e.g., Electronic Data Capture systems High quality commitment, team-orientation and ability to juggle various tasks Fluent business English and knowledge of medical/scientific terminology         INTERESTED? >> Apply here           Merz is a growing international company with its headquarters in the heart of Frankfurt, offering a competitive compensation and benefits package, flexible working environment and numerous professional development opportunities. We look forward to receiving your online application - please be sure to include your salary expectations, your earliest start date and the code 15220.  

Pharma, Chemie, Med.-/ Biotechnologie

Projekt- und Produktmanagement/ Qualitätsmanagement

Forschung & Entwicklung

Chemie/ Pharma/ Biotechnologie

Gesundheits-/ Sozialwesen/ Medizin

Projektleitung/ Stabstelle/ Spezialist

Teilzeit

Befristet

60311 Frankfurt am Main

Frankfurt am Main