Data Management

Current Data Management Pharmaceutical Jobs and Articles

Clinical Research Associate in Czech Republic

My client, an international company, seeks a Clinical Research Associate (CRA) for an urgent permanent position in Czech Republic.  You can be either home based or work from the office in Prague.

CLINICAL DEVELOPMENT and MEDICAL AFFAIRS MANAGER

My Biotech client is now actively looking for a Clinical Development and Medical Affairs Manager You will be joining a dynamic and growing new arm of their business focusing on vaccines. This positio

Medical Director , Oncology

A Medical Director specialising in Oncology is required for a large and friendly company who has recently expanded their operation. RESPONSIBILITIES Provide clinical leadership for Phase II – IV

Medical Advisor, Anti Infectives

A large pharma company is looking to recruit a Medical Advisor specialising in vaccines. This appointment is based in Europe on a permanent basis. RESPONSIBILITIES Reporting to the Therapy Area Di

Epidemiologist

A skilled director of epidemiologist required to be the primary contact person for domestic and external Epidemiologists working for the company on a contractual basis. ROLE This role will require a

Data Management in UK

  An experienced data manager required for a small pharma company in UK, working in Clinical Trials.  This would suit an individual who was motivated by challenge and would like to further

Data Management, Contract in UK

9 month contract for technical data management in North England SKILLS AND EXPERIENCE Working knowledge of Rave, IVR and ePRO SAS programming skills Knowledge of clinical data standards Strong

Senior Regulatory Affairs Manager, Contract in UK

This position is an exciting opportunity for the right candidate, to lead a small team preparing regulatory applications, ensuring compliance with regulatory agencies. This position will also call on

Clinical Specialist in Europe

A fantastic opportunity is available to join a leading international organisation, in Europe, as a feasibility clinical specialist. RESPONSIBILITIES Assessment of sites on a global level Develop

Principle Medical Writer in Europe

A leading pharmaceutical company within Europe and UK is recruiting for a Principle Medical Writer, office based, leading in the creation of regulatory documents. RESPONSIBILITIES Write, edit and

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