Clinical Research Project Manager

The University of Kansas Health System

Kansas City, KSFull-time

85K–100K a year

Behavioral Health Market Context

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Job Description

 three years of experience in clinical research, excellent organizational and communication skills, and a strong ability to multitask and prioritize. If you're excited about making a positive impact on patient care and research, then we'd love to hear from you.

Develop research project plans and timelines to ensure successful completion of projects.
Monitor progress of clinical research projects, and provide regular updates to stakeholders.
Manage budget, resources, and personnel for research projects.
Prepare and submit documents for regulatory approval, and ensure compliance with all applicable regulations.
Coordinate with research teams to ensure data is collected accurately and efficiently.
Analyze research data and present results to stakeholders.
Maintain relationships with external research partners and stakeholders.
Develop and implement procedures for quality assurance and risk management.
Provide guidance and training to research staff.
Identify areas of improvement in clinical research processes and procedures.

The University of Kansas Health System is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.

Qualifications

  • The ideal candidate should have a minimum of three years of experience in clinical research, excellent organizational and communication skills, and a strong ability to multitask and prioritize

Benefits

    Responsibilities

    • This role is responsible for the overall planning and execution of clinical research projects, and requires a combination of scientific knowledge, project management skills, and exceptional interpersonal abilities
    • Develop research project plans and timelines to ensure successful completion of projects
    • Monitor progress of clinical research projects, and provide regular updates to stakeholders
    • Manage budget, resources, and personnel for research projects
    • Prepare and submit documents for regulatory approval, and ensure compliance with all applicable regulations
    • Coordinate with research teams to ensure data is collected accurately and efficiently
    • Analyze research data and present results to stakeholders
    • Maintain relationships with external research partners and stakeholders
    • Develop and implement procedures for quality assurance and risk management
    • Provide guidance and training to research staff
    • Identify areas of improvement in clinical research processes and procedures


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