Principal Clinical Database Programmer
- Employer
- Parexel
- Location
- United Kingdom
- Salary
- Competitive
- Start date
- 17 Oct 2019
- Closing date
- 16 Nov 2019
View more
- Discipline
- Data Management / Statistics
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
Job Details
The Principal Database Programmer will be recognized as a subject matter expert, providing technical support and expert advice to internal and external sponsors. In addition, the Principal Database Programmer can fill the Database Primary (late phase) or Technical Lead role on projects; liaise with sponsors, Data Management Leads and other functional areas as required.
General areas of responsibility also include eCRF design, edit check programming and integration of third party systems with the EDC databases. Further, the Principal Database Programmer will monitor quality, timelines, resource allocation, and productivity in relation to budgets. All tasks should be performed in accordance to corporate quality standards, SOPs/Work Instructions/Guidelines, ICH-GCP and/or other international regulatory requirements.
Qualifications
Skills:
- Excellent English written and oral communication skills.
- Demonstrate ability to learn new systems and function in an evolving technical environment.
- Attention to detail.
- Ability to work together with a team (including international teams as required) as well as independently.
- Work effectively in a quality-focused environment.
- Demonstrate strong organizational skills, ability to manage competing priorities, and be flexible to change.
- Business/Operational skills that include customer focus, commitment to quality management and problem solving.
- Good business awareness/business development skills (including financial awareness).
- Work effectively in a quality-focused environment.
- Strong leadership ability.
- Ability to create, maintain and define strategies to improve the efficiency of running a clinical trial.
- Demonstrate commitment to refine quality processes
- Demonstrated application of CRS concepts to achieve best practice and promote continuous improvement.
- Excellent analytical skills.
- Good presentation skills.
- Tenacity to work in an innovative environment.
- Ability to negotiate and influence in order to achieve results.
Knowledge and Experience
- Proficiency in at least two programming environments (e.g., SAS, CDMS, EDC, SQL, VB, Java).
- Extensive experience working with RAVE and a preference for additional experience with at least one other system used within the Clinical Trial process (e.g. SAS, CDMS, CTMS, Medical Safety Reporting).
- Relevant Clinical Trial industry experience.
- Knowledge of SOPs/Guidelines/Work Instructions/System Life Cycle methodologies, ICHGCP and any other applicable local and international regulations such as 21 CFR Part 11 and proven practical application.
Company
Parexel International Corporation is a leading global biopharmaceutical services organization, providing a broad range of knowledge-based contract research, consulting, and medical communications services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, Parexel has developed significant expertise across the development and commercialization continuum, from drug development and regulatory consulting to clinical pharmacology, clinical trials management, medical education and reimbursement. Parexel Informatics, Inc., a subsidiary of Parexel, provides advanced technology solutions, including medical imaging, to facilitate the clinical development process.
Mission: Parexel’s mission is to combine the strength of our expertise, experience and innovation to advance the worldwide success of the bio/pharmaceutical and medical device industries in preventing and curing disease.
- Website
- http://www.parexel.com/
- Telephone
- +44 1895 238000
- Location
-
The Quays
101-105 Oxford Road
Uxbridge
Middx
UB8 1LZ
GB
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