Description
The
Clinical Development Services division of Quintiles has more depth of
therapeutic expertise and a broader range of services than any other
service provider. We conduct Global trials in all therapeutic areas. In
fact, Quintiles conducts more clinical trials than anyone else in the
world. Become involved in work that improves the quality of life for
people around the globe. We are seeking an enthusiastic Rave Technical
Designer- Global Data and Safety Monitoring to join our team!
Purpose:
Serve as the EDC System Designer for the Rave build team, and produce accurate and complete specifications documents.
Responsibilities:
• Development of eCRF to
meet the needs of the customer and the clinical trial utilizing protocol
and specifications provided at the pre-design meeting. Understand
Quintiles EDC processes and the requirements on the design for reporting
and study management.
• Advise and provide justification for design decisions to Technical Lead and at Design Meeting.
• Responsible for optimal
design reducing the number of edit checks required, ensuring good
system performance, and the utilization of global/client specific
libraries to ensure consistency and efficiency.
• This role will
eventually (3-6 months after starting) be responsible for providing a
draft Edit Check Specification to the DTL.
• Requires good
communication skills and this role will work closely with the Study DTL
and Technical Lead and Validation Team Lead
• Requires a technically
logical thinker to resolve questions and issues with the Technical Lead,
DTL and VTL. This role will need to have a good knowledge of forms
design, data flow, and the impact of design on the system.
The Clinical Development
Services division of Quintiles has more depth of therapeutic expertise
and a broader range of services than any other service provider. We
conduct Global trials in all therapeutic areas. In fact, Quintiles
conducts more clinical trials than anyone else in the world. Become
involved in work that improves the quality of life for people around the
globe. We are seeking an enthusiastic Rave Technical Designer- Global
Data and Safety Monitoring to join our team!
Qualifications
Please read carefully. Candidates who do not meet the minimum requirements will not be considered for this position.
• Bachelor's degree or 3 year Diploma with a minimum of 3 years experience in a clinical data management role.
• Candidates must have prior work experience in CRF design experience.
• Edit Spec writing experience.
• Knowledge of eCRF Help.
• Build Time and Events schedule.
• Excellent communication skills .
• Strong technical skills.
• Excellent leadership skills.
• Candidate must have a thorough knowledge of the clinical trial data management process.
• Knowledge of Medical Terminology, Pharmacology, Anatomy and Physiology.
• Previous experience and
proven competence in managing delivery of project through full data
management study life-cycle (of several large phase I or at least 1
medium size Phase III).
• Excellent organizational, communication, and data management skills (detail oriented).
Primary Location
: United StatesOrganization
: USA02 - US Clinical Development Svcs
We look forward to the prospect of working
with you! Please apply on-line at: http://www.quintiles.com/.
Clinical Data Management Services have higher requirements and have good scope in clinical research industries.
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