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| Job #02100 |
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| About our client |
| Our client is a leading provider of integrated data management solutions for clinical trials and drug safety in North America. |
| Position |
Location |
| Clinical Design Consultant |
Massachusetts |
| Salary |
| Highly competitive package, commensurate with experience |
| Responsibilities |
1) Deliver quality clinical trial design, develop, and consult clients 2) Contribute towards the development and maintenance of work instructions 3) Design and develop eCRFs 4) Work with the study team to design best possible solutions for the trial 5) Review and understand complicated clinical trial protocol 6) Manage customer dialogue for acknowledgement, ownership, commitment, and follow-through 7) Design trial data extract specifications for multiple database configurations 8) Provide innovative solutions to problems based on unique clinical trial requirements 9) Provide input to cross-departmental teams to improve product function 10) Apply clinical knowledge to technical solutions 11) Manage deliverable timelines for the Quality Control Group |
| Requirements |
1) Work independently on less complicated projects, progressing over time to work on more complicated projects 2) Basic understanding of MS Word, Excel, Project and PowerPoint 3) Working knowledge of internet technology 4) Understanding of processes used in clinical data management; clinical trial CRF design, workflow associated with the management of clinical trials and drug/medical device development process 5) 3-5 years’ experience in multiple aspects of clinical trials 6) Working knowledge of GCP and other regulations 7) Knowledge of clinical operations, clinical database structures and implementation 8) Experience in design and implementation of automated, complex, database validation checks |

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