Please send only MATCHING PROFILES.
Location: Groton, CT
Roles and Responsibilities:
As a Consultant, you will be a key player in the consulting team that helps discover and define the problem statement, evaluates the solution options and makes recommendations. You will create detailed design, architecture and process artifacts and implement the deployment plan. You will also support knowledge transfer with the objective of providing value-adding consulting solutions that enable our clients to meet the changing needs of the global landscape.
Desired Skills & Experience
Required
• Bachelor's degree or foreign equivalent required from an accredited institution. Will also consider three years of progressive experience in the specialty in lieu of every year of education.
• At least 4-8 years of experience with Information Technology
Preferred
• At least 4-8 years of experience in Clinical Trial Management, Clinical Data Management, Project Quality Management
• At least 4 years' experience in one or more of the following skills
- End-end Clinical trial management process and related applications.
- Clinical data management applications such as oc/rdc/tms.
- Clinical reporting (internal, FDA) during study start to closeout phases.
- Clinical Data Management processes with knowledge of Clinical DataWarehouse
- Computer systems Validation activities
• At least 4 years of experience in capturing requirements related to internal/external consulting, documenting, and mapping
• Analytical and Communication skills
• Planning and Co-ordination skills
• Experience with project management
• Experience and desire to work in a management consulting environment that requires regular travel
• GCP Certified
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