!! Need - *Lead Clinical Data Manager *- Start ASAP !!

Position      :      Lead Clinical Data Manager
Location     :      Lexington, MA
Duration    :       6+ Months


*Need Local EAD / Green Card / US Citizens Only *


*Required Skills and Experience :*

   - B.S. degree in Scientific or related field is preferred.
   - Minimum of 5-7 years as a Senior Data Manager within a Data Management
   organization.
   - Experience with leading teams and/or organizations.
   - CCDM certification preferred.
   - Will sit in real world late phase group which runs Non interventional
   trials, safety trials, registry trials.
   - Must have significant Lead Clinical Data management experience Team is
   100% outsourced, meaning candidate will not do actual data work but will
   oversee vendors that do the work Could be working on anywhere from 3-5
   outsourced studies and management of vendors Mostly ongoing long term trials
   - The Clinical Data Manager will have a demonstrated ability to oversee
   the data management activities across a single clinical program or group of
   related studies.
   - Provides Data Management leadership and expertise to project and study
   teams. Will have an good knowledge of the end to end clinical research and
   data management processes, as well as global regulatory and industry rules
   and guidances  (i.e. ICH, GCP) to support drug development processes and
   global project submissions through to approval.
   - Responsible for managing data management components of project and
   study budgets and vendor performance.
   - May mentors team members and more junior staff and may direct
   activities of contract Data Manager staff.
   - Takes leadership role in project implementation As a member of the
   clinical study or project team, ensures oversight of the Data Management
   CRO;
   - Provides status reports/updates, resolves disputes, and ensures timely
   acquisition of high quality deliverables from the CRO Provides Data
   Management expertise to the team in identifying opportunities for process
   and budgetary optimization.
   - Coordinates with Biostatistics and Statistical Programming to ensure
   appropriate design, documentation, testing and implementation of SAS data
   deliverables according to internal and regulatory standards Works with team
   members via matrix relationships (internally or at CROs) by directing work,
   resolving problems and/or providing guidance.





Regards,
Chris Roe - Resource Development Manager
Desk No : 415-251-3968 | Email : ch...@itbtalent.com

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