Biostatistician
- Employer
- Thornshaw Recruitment
- Location
- Dublin (City), Leinster (IE)
- Salary
- Competitive
- Start date
- 17 Jun 2019
- Closing date
- 3 Jul 2019
View more
- Discipline
- Data Management / Statistics, Biostatistics, Clinical Data Management, Statistics
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
Job Details
On behalf of my Client, we are accepting applications for the role of Biostatistician - Clinical Assessment.
The role:
As Biostatistician you will use your statistical expertise to review Marketing Authorisation Applications and advise on good drug development, interacting with medical colleagues and multi-disciplinary advisory committees and company representatives as required.
You will work closely and maintain effective working relationships with other members of the Clinical Assessment section, and with members of the department, to ensure effective co-ordination and co-operation across all areas of assessment and to ensure that the objectives of the department are met.
You will maintain effective working relationships with colleagues in other sections and departments, to ensure that issues requiring cross-functional input are conducted effectively and followed up on.
KEY RESPONSIBILITIES
Supporting the Clinical Assessment Manager and other managers in the Clinical Assessment section in the on-going development of the department.
Working with the Clinical Assessment Manager and other managers in the Clinical Assessment section in the preparation of work objectives for the section.
Working with the Clinical Assessment Manager and other managers in the Clinical Assessment section to prioritise work objectives and to ensure that the operational goals of the department are achieved.
Providing support and input to colleagues and others within the Clinical Assessment section.
QUALIFICATIONS AND EXPERIENCE
Have a master’s or PhD in Biostatistics or Statistics with significant experience in clinical trials methodology.
Knowledge and experience of drug development (clinical and post-approval) and understanding drug development as a continuum.
Experienced with ICH GCP, regulatory (e.g. EMA and FDA) guidelines
Sound understanding of a wide range of statistical and clinical trial methodology, including the most up-to-date techniques available that are relevant to the regulation of medicines, as employed across the breadth of the drug development process.
Significant work experience in the design, analysis and interpretation of randomised, controlled clinical trials across all stages of clinical development and in a wide range of therapeutic areas.
The ability to evaluate complex information from a variety of sources and make effective decisions.
For full details contact Tina at +353 1 2784671 or email tdunne@thornshaw.com
Company
Thornshaw Scientific Recruitment was first established in 1999 and since then has become a leader in Scientific recruitment. In 2005 we partnered with Cpl Resources, one of Europe’s most successful recruitment companies.
Our wealth of experience in specialised recruitment allows us to offer the right solution to each employer, whatever their recruitment requirements.
Over the years we have developed strong relationships with our clients in the market and we pride ourselves on our repeat business from clients.
Our Industries
We are a global provider and have been providing a reputable recruitment service to the Biotech, Pharmaceutical, Clinical Research, Medical Device, Engineering and Healthcare industries for over 20 years.
Our Specialities
Clinical Research, Regulatory Affairs, Quality Assurance, Medical Affairs, Pharmacovigilance, Biostatistics, QC, Validation.
Our Mission
For further details on our services contact Tina at +353 1 2784701 or email tdunne@thornshaw.com
- Website
- http://www.thornshaw.com/
Get job alerts
Create a job alert and receive personalised job recommendations straight to your inbox.
Create alert