Clinical Research Associate

ALDAPH Alger, Algérie
Postuler
  • Secteur d'activité Industries
  • Date d'expiration 19 Mars
  • Nombre de postes 01 poste ouvert
  • Niveau de poste Confirmé / Expérimenté
  • Niveau d'étude (diplome) Licence (LMD), Bac + 3| Master 1, Licence Bac + 4

 

Join Clinical operation department and become part of a fast-changing environment where engaged people do their best every day to get Novo Nordisk’s medicines approved across the globe.

  • Our people have a unique combination of scientific insight, patient focus and the ability to navigate many agendas and stakeholders.
  • That makes Clinical Research a truly interesting and challenging place.
  • We are currently looking for a Clinical Research Associate an interest in working, join our Clinical operation department.

 

About Novo Nordisk Algeria

  • Novo Nordisk Algeria belongs to International Operations, Region Asia Africa Middle East Oceania (AAMEO), and is one of the largest and most dynamic affiliated worldwide.

 

About the department:

  • The Clinical operation department is part of the Clinical, Medical and Regulatory organization.
  • We are a dedicated team who are responsible for the Clinical research project

 

Work:

  • Role is critical to the success of an affiliate increasingly strategy for Novo Nordisk. You will report directly the Clinical Research Manager.
  • The Clinical Research Associate is the primary point of contact between site staff and Novo Nordisk. In this role the you acts as ambassador for the company.
  • You are responsible for taking leadership of site management for the selection (if applicable) and initiation of sites as well as conduction and closing activities of the appointed studies in compliance with local regulations, ICH- GCP, NN procedures and protocol requirements to ensure data quality and study subject protection. You are responsible for recruitment at site level. The Clinical Research Associate thereby delivers results that have a direct impact on the successful completion of the clinical program
  • You coordinates with the team and communicates to them progress and critical issues that may impair trial progress. In some cases, you may have direct contact with the ITM

 

Qualification:

  • Degree or higher qualifications with scientific background
  • At least 5 years of experience in conducting clinical trials as CRA and/or Trial company
  • High commitment to quality of all projects. A “do what it takes” mindset and positive attitude
  • IT Capabilities with specific knowledge : e-system (EDC, IMPACT, IVWRS, Clinphone)
  • Mastery  in Clinical trials execution, ICH GCP
  • The ability to cope and work effectively within an environment that has quickly changing processes and procedures
  • The ability to manage multiple projects simultaneously
  • The ability to work effectively and efficiently under deadlines
  • Willingness and ability to implement action plans without being told to do so
  • Fluency in written and spoken Arabic, French and English is a must.

 

 Working at Novo Nordisk:

  • At Novo Nordisk, your skills, dedication and ambition help us change lives for the better for patients around the world.
  • As their needs evolve, so does our challenge to find better and more innovative ways to improve their quality of life.
  • In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.



Clinical Research Associate

ALDAPH Alger, Algérie
Postuler

Partagez vos avis

Participez à l'amélioration du site en envoyant vos commentaires:

Vous êtes ?