Manager, Data Management

Group: Data Management

Reports to: Associate Director, Data Management

Responsibilities Include:

The Manager of Data Management is responsible for delivering data management
services to clients and project teams, by management of internal clinical data
management staff and clinical data vendors. The Manager, Data Management
maintains optimal department processes and implements excellent project-specific
strategies, and assists with the development and implementation of department
strategies to increase productivity and quality, while decreasing cycle times and
costs. The Manager, Data Management provides oversight of project-related data
management tasks, including contributing to protocol design; development of
project forms to meet project needs; creation, review and finalization of case
report forms (CRFs); database design and preparation of data validation
specifications; and ensuring consistency in database and CRF design. The
Manager, Data Management may directly perform project-related data
management tasks, as required.
The Manager, Data Management develops and maintains a close liaison with
client contacts, project team members, and Project Managers to drive the data
management aspects of project delivery.
The Manager, Data Management provides direct oversight of data management
operations, including hiring personnel, managing personnel matters, and
conducting performance evaluations within clinical data management. The
Manager, Data Management assists with training data management personnel
regarding applicable regulatory guidelines, data management practices, and
computer systems. The Manager, Data Management also assists with resource
allocation in the department.

Minimum Requirements

A BA or BS degree in a health-related field or Registered Nursing degree,
with a minimum of 7 years of directly-related clinical data management
experience and a minimum of 2 years of supervisory experience, to
include data management and/or clinical operations.
· Thorough knowledge of International Conference on Harmonisation (ICH)
Good Clinical Practice (GCP) guidelines and other applicable regulatory
rules and guidelines as well as of medical terminology, clinical trials, and
clinical research.
· Working knowledge of the relationship and regulatory obligation of the
contract research organization (CRO) industry with pharmaceutical /
biotech companies.
. Demonstrated ability to lead by example, and demonstrated skill for
technical and supervisory leadership of staff.
· Skilled in use of computer technology, including clinical trial database s
and applications (e.g., ClinTrial, Inform) and ability to learn new
applications.
· Excellent interpersonal, communication, and organizational skills with the
ability to work independently and in a team environment

Submit Your Resume

If you would like to be considered for a position at Veristat, please submit your resume to Human Resources at hr@veristat.com