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Job Details


Company: Docs Global (Continental Europe)
Location: Budapest,Hungary
Reference: Ref AS-013781
Closing Date: 11 Dec 16
Type: Permanent
Salary (£): Competitive
Benefits: Excellent & Comprehensive

Job Summary:

This is an exciting opportunity to become part of a dynamic and successful international Pharmaceutical organization. The company has seen very large growth on the Hungarian market, thus you will have the chance to become an important part of their future growth and success. If you are looking for a new challenge, the chance to expand your CRA experience and you have the enthusiasm and drive to join a young and dynamic company, then is this is the opportunity for you


Roles & Responsibilities of the position

Conducting site evaluations post-feasibility to determine site suitability
- Performing site initiations
- Building and maintaining solid relationships with investigators and site staff to improve study set-up cycle times
- Developing site logistics and milestone plans
- Developing site visit plans and conducts monitoring visits
- Supporting site with focused patient recruitment strategies
- Coordinating the collection of data and resolution of discrepancies at site
- Coordinating and tracking clinical study and drug supply activities at site
- Providing point of contact for study information exchange and manages site issues
- Ensuring local clinical study compliance with Good Clinical Practice (GCP) and Standard Operating Procedures (SOP)
- Ensuring quality data generation and conducting Source Data Verification (SDV), as required
- Performing site close-out
- Ensuring appropriate safety reporting and management of adverse events and adverse drug reactions
- Sharing study conduct ‘best practice’ to increase site productivity
- Developing action plans to address study related gaps e.g. site failing to achieve recruitment targets
- Preparing sites for audits
- Escalating site-related issues
- Exchanging information on site performance and issues

Job Requirements

BSc in a life science or qualified nurse or relevant experience within a pharmaceutical/biotechnology/CRO organization.
- 1-3 years of CRA/monitoring experience in ONCOLOGY clinical research
- Fluency in Hungarian and English
- Very good time management and organization skills
- Ability to build and maintain strong relationships
- Strong communication skills, both oral and written

Remuneration & other details

Strong, stable position in a large, international Pharmaceutical company
- A dynamic and exciting working environment
- Individualized coaching and development
- Dedicated training and education

Apply for this job: CRA

Contact Information:

Address:  Head Office
2 Globeside, Globeside Business Park
Website:  Visit Our Web Site

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