Clinical Data Management

Croissance Clinical Research

• organizing kick-off meetings with the client co-ordination with the functional head.

• responsible for allocating the project/study to team members.

• responsible for review and internal approval of data management plan (dmp), case report form (crf), and edit check specification document (esd).

• responsible for review and internal approval of data entry guidelines, self-evident correction document (sec).

• internal approval of annotated crf (acrf) and functional design specification (fds) document.

• responsible for preparing and training the sop’s.

• responsible for approval of database screens, edit checks designed in database and dcf/query tracker.

• internal quality control for all data management documents like data management plan, annotated crf, functional design specification document, and edit check specification document.

• responsible for issuing the database test certificate.

• responsible for database lock and unlock procedures.

• responsible for exporting the data to sas team for analysis.

• responsible for review and approval of master data management file (mdmf).

• responsible for data management presentation in investigator meeting.

• providing inputs for proposal development in co-ordination with the function head.

• Experience

  2 - 4 Years

• No. of Openings

  4

• Education

  B.Pharma, M.Pharma

• Role

  Clinical Research

• Industry Type

  Call Centre / BPO / KPO / ITES / LPO

• Gender

  [ Male / Female ]

• Job Country

  India

• Type of Job

  Full Time

• Work Location Type

  Work from Office