Job Description:
CLINICAL DATA MANAGER
Kelly Clinical Research has an immediate need for a
Clinical Data Manager in Hazelwood, MO area. The
Clinical Data Manager (CDM) is a member of the clinical
research team responsible for data management activities
across multiple trials. Activities include assisting in
data entry, query processing, site management, data
reporting and other data management activities in
support of clinical trial projects. The CDM performs
data management activities on both paper based and
electronic data capture EDC studies. This is a 6-12
month contract position for someone who can start ASAP.
Job duties include:
CRF data review, preparation for entry, query
processing, discrepancy management, ad hoc reporting
and listing generation.
Develop study specific database requirements and
edit check requirements with the help of Clinical
Research Associates CRA and field monitors.
Create and maintain data management trackers and
checklists for multiple projects.
Set-up and keep track of new sites, users across
studies for EDC studies.
Assist in CRF design/development.
Assist with database design and validation
activities for paper based trials.
Support with EDC study validation, user acceptance
testing and implementation.
Assist in development of data verification audit
listings and other audit activities.
Design case report forms.
Build database using ORACLE Clinical and Remote Data
Capture.
Assist in overall project tasks such as generating
CRF completion guidelines, process flowcharts,
Standard Operating Procedures SOPs, work
instructions and training guidelines.
Support the team in any study startup and closeout
activities including final report data QC.
Participate in project meetings to give a status
update to project managers and upper management.
Assist in preparation of study material for
investigator, study coordinator and monitor
meetings.
Requirements:
Bachelor’s degree in sciences or health profession
or combined education and CDM experience equivalent.
5-8 years CDM experience.
Computer literacy in MS Word, Excel, PowerPoint,
Access, ORACLE Clinical, RDC and CRF design tools.
Ability to speak, write and understand English to
comply with written procedures, instructions, SOPs
and other documents.
Excellent organizational skills and attention to
detail.
Ability to prioritize and multitask is a plus.
Ability to speak, write and understand English to
comply with written procedures, instructions, SOP’s.
Must be immediately eligible to work for any
employer in the U.S. without restriction.
If you are a Clinical Data Management professional
looking to make a move, please APPLY NOW and be sure to
include a MS Word resume.
Note: All work must be done on-site, no work-at-home or
telecommute option. No relocation assistance will be
provided.
Kelly Clinical Research specializes in delivering
clinical research workforce solutions to the world’s
leading pharmaceutical, medical device, and
biotechnology companies, as well as contract research
and site management organizations. We provide contract,
temp-to-hire and direct hire opportunities. Areas we
specialize in include Clinical Research Associates
(In-house and Field-based), Data Management, U.S. and
International Regulatory Affairs, Biostatistics and
Analysis, Medical Writing, Project Management, GCP Audit
and Quality Assurance, Clinical Operations and Support.
Kelly Services, Inc. is an Equal Opportunity Employer
Job Code : BHJOB3479_436851
Kelly Scientific Resources - 14 months ago
- save job
-
block
