Invites for Senior CDA in MakroCare | 2 Openings
MakroCare has operations and presence in US, UK, EU, and Asia. MakroCare is well positioned to meet the demands of the expanding product portfolio needs of our life sciences clients worldwide. We also understand the demands of an increasingly competitive market.
Post : Sr.CDA (02 posts)
Assume the ability to meet the requirements of a CDA with a high degree of proficiency and autonomy.
Take responsibility for specific tasks on projects, or acts as the main point
Of contact for all the DM deliverables on individual projects.
Train team members on selected tasks.
Develop CRFs, Data Management Plan, eCRF filling instructions, Data Validation Plan.
Develop project specific guidelines, SAE handling, Medical Coding, Third Party data handling and Universal ruling guide lines documents.
Lead UAT activities of Screen Testing & Edit Checks testing.
Lead Data validation and Query Management.
Identifying and reporting protocol deviations and violations.
Conduct reconciliation of SAEs, send out queries as required and notify relevant Safety Groups of possible issues for their action.
If required liaise with 3rd party vendors to clean electronic data.
Perform Interim and final database QC activities.
Update all relevant tracking system on an ongoing basis.
Experience: 4-6 years
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: CDA
End Date: 24th Feb, 2017
E-mail your resume to: firstname.lastname@example.org
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