Clinical Project Manager – Kansas City – # 9102

Clinical Project Manager – Greater Kansas City area – # 9102

We are seeking an experienced Clinical Project Manager to join a Clinical R& D team.

The Clinical Project Manager

• Supports development and refinement of PM standardizations as assigned
• Reviews the Sponsor contract, protocol/forms, Sponsor study-specific procedures for the study and other documentation required
• Obtains a clear understanding of all aspects of the study and defines the roles of Clinical R&D, the Sponsor and study personnel
• Collaborates with the Sponsor to establish projected study timelines for the study including all activities specified in the contract. Includes responsibility to track timelines, revise as needed to assure milestones are met and to communicate issues/changes to the Sponsor
• Determines clinical project team staffing requirements and communicates necessary resources to the Head of Clinical Services
• Provides oversight to ensure tasks are completed correctly and on time
• Defines the SOPs under which the study will be conducted

• Drafts and finalizes the clinical study monitoring plan, data management plan, transfer of responsibilities, and if appropriate, the safety monitoring plan and IVP/CVP documentation with the Sponsor
• Ensures that Clinical R&D study personnel are trained on the study with documentation of training recorded

Qualifications

• Bachelor’s degree, preferably in a scientific discipline or equivalent experience
• Minimum of 3+ years’ experience in veterinary clinical study project management, data management, Quality Control (QC) and/or Quality Assurance (QA)
• Progression from Clinical Research Associate position or equivalent experience and training
• Experience and skills necessary to monitor a study
• Excellent oral and written communication skills
• Computer proficiency including Outlook & Microsoft Suite and various assigned database platforms and electronic meeting applications
• Valid Driver’s license, passport, and ability to travel to main office as well as to travel to investigator sites to assist as needed
•       Experience with electronic data capture (EDC) systems
•      Thorough knowledge of GCP Protocols, Final Study Reports, and Study Master Files
• Works collaboratively with internal and external key stakeholders to streamline operations for maximum efficiency, automation, and effectiveness where appropriate
• Expresses facts and ideas in writing in a clear, concise, convincing, and organized manner
• Makes clear, concise, and convincing presentations to individuals or groups
• Explains issues and interprets data in understandable terms and adapts communication to target audiences

Compensation is commensurate with experience.

To learn more and/or apply for this exciting opportunity, please apply here: