HN08 - Clinical Research Coordinator
Kelly Services - Diamond Bar, CA

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Job Description:
Clinical Research Coordinator
Every day, Kelly Scientific Resources (KSR) connects
clinical research professionals with opportunities to
advance their careers. We currently have an exciting
contract opportunity for a Clinical Research Coordinator
working with our client based in Diamond Bar, CA.

Job Responsibilities (other duties may be assigned):Phase IV Procedural Outcomes Studies:
  • Works under the direction of the Director, WW Health
Economics, Outcomes Research & Policy and the
Procedure Outcomes Study Manager to assist with the
planning and coordination of Phase IV procedural
outcomes studies that meet company goals and
objectives while adhering to all ethical, medical
and regulatory requirements.
  • Coordinates investigator qualification/site survey
documentation.
  • Manage database for Phase IV study investigator/site
tracking, study start up log, and other study
related information.
  • Coordinates study site NDA and contract
initiation/renewal and payment.
  • Assists with development of and dissemination study
start-up information packets.
  • Establishes and maintains in-house study
documentation and communication files.
  • Prepares and manages updates to study timelines.
  • Develops study status reports and study
communication/educational tools.
  • Organizes investigator meeting.
Health Economics & Policy:
  • Manages CitationPoint published evidence portal.
  • Orders clinical reprints and maintains library.
  • Support the updating/maintenance of an interactive
web-based global value toolkit.
  • Supports the development/dissemination of US
reimbursement materials and educational tools.
  • Coordinates US Health Policy Board and regional
client market access meetings.

Medical Affairs:
  • Organizes logistics and communicate results for
post-market surveillance meetings.
  • Runs and analyzes sales data through Siebel and
Cognos.
  • Spearheads clinical readiness review documentation.
Cross-Department:
  • Issues and manages supplier information in Aravo,
Ariba, Totality, cPDM, and ICD.
  • Manages PO and contract tracking process.
  • Serves as department coordinator for records
management and training.
  • Authors, submits and manages SOP approvals.
  • Manages content updates to company web site and
SharePoint sites.
  • Develops training materials, including PowerPoint
presentations.

Requirements:
  • Good organizational skills.
  • Must be able to prioritize and make quick decisions.
  • Knowledge of data collection practices.
  • Ability to work under deadlines and fast-paced work
environment.
  • High school diploma is required. A bachelor degree
is preferred.
  • Computer literacy required in Microsoft Office
Products such as Word, Excel and Outlook &
SharePoint.
  • Strong Excel background required.
  • Ability to work weekends and “off hours” as needed
to support customer needs.
  • Must be experienced with Siebel data entry.
For immediate consideration, click the Apply Now button,
or refer a friend by clicking the E-mail this job link
provided.
Kelly Scientific Resources® has grown into a $270
million global business as the scientific business unit
of Kelly Services. Our recruiting consultants place
clinical, regulatory and medical affairs, data
management and biostatistics professionals to the
pharmaceutical, biotechnology, medical device, CRO and
university research communities.
We invite you to bookmark our Web site and encourage you

to review it regularly for new opportunities worldwide:
www.kellyscientific.com.
Kelly Services is an Equal Opportunity Employer.
Job Code : BHJOB3479_597234

Kelly Services - 18 months ago - save job - block
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About this company
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Kelly Services, Inc. (Kelly) is a global temporary staffing provider operating in 36 countries and territories throughout the world. The...