Manager Clinical Trials - Cardiology

Washington University

Northern (KY)

Hybrid

USD 75,000 - 129,000

Full time

13 days ago
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Benefits offered by this job

Vacation leave
Health insurance
Metro U-Pass
403(b) Retirement plan

Job summary

Washington University in St. Louis seeks a senior leader to supervise and educate research coordinators across Functional Research Groups. You will oversee data quality, protocol implementation, and coordination with directors, oncologists, and study teams.

The role involves budgeting, staffing decisions, and strategic planning to ensure successful clinical trials across institutional, cooperative group, and industry-sponsored studies.

Qualifications

  • Education: Bachelor’s degree or combination of education and/or experience may substitute for minimum education.
  • Certifications: Not required for this position.
  • Work Experience: Clinical Research experience preferred (1 year).

Responsibilities

  • Lead the Functional Research Groups and oversee staffing decisions.
  • Orient and train staff; supervise performance and provide feedback.
  • Plan budgets and evaluate new protocols for logistics and finances.
  • Ensure quality data collection and regulatory compliance across studies.
  • Coordinate meetings with directors, oncologists and study teams.

Skills

Clinical Project Management
Clinical Systems
Clinical Trials Administration
Deadline Management
Interpersonal Relationships
Leadership
Microsoft Excel
Microsoft Word
Oral Communications
Prioritization
SQL Databases
Stress Management
Written Communication

Education

Bachelor’s degree
Experience substitution allowed

Tools

SQL Databases

Job description

Location SAINT LOUIS, MO 63110 Scheduled Hours 40

Position Summary

Directly responsible for the supervision, oversight, training and education of research coordinators, and quality assurance monitoring of data in the Functional Research Groups. This position requires the ability to clinically assess protocols for budgetary and logistical issues associated with the coordination and implementation of clinical trials for institutional studies, cooperative group studies, and pharmaceutical industry-sponsored studies.

Job Description
Primary Duties & Responsibilities
  • Leadership of the Functional Research Groups
  • Makes hiring and staffing decisions in the Functional Research Groups with input from the Administrative and Medical Directors of the Core.
  • Orients and trains all staff in the Functional Research Groups, and assists in orienting new staff in the Regulatory and Protocol Development groups.
  • Meet regularly with all staff, providing supervision and training.
  • With the Administrative Director and Medical Director, plan strategically and implement plans for Functional Research Groups, including staffing (setting current and future a appropriate staff levels), education, adherence to federal regulations and standard operating procedures for ensuring quality data collection.
  • Provides feedback and performs annual performance evaluations for Research Coordinators with assistance from Senior Clinical Research Associates and the Administrative Director.
  • Supports Senior Clinical Research Associate through initial performance improvement efforts and directs progressive performance management and disciplinary activities as required.
  • Assesses new protocols for logistical and budgetary issues and creates a plan to address these.
  • Creates budgets for new studies.
  • Assists with evaluating and entering studies into the database.
  • Meets regularly with Administrative Director (at least weekly, but probably more often); represents Functional Research Groups at senior level meetings.
  • Meets regularly with the oncologist to assess the progress and goals of the research program.
  • Leads regular meetings with the study team and members of each clinical area to plan for the successful implementation of upcoming studies.
Oversight of Daily Activities
  • Oversees the daily research activities for Senior Research Coordinators including compliance with protocol criteria and adherence to federal regulations.
  • Oversees daily protocol management activities of Senior Research Coordinators.
  • Monitors collected data for accuracy of objective criteria.
  • Facilitates accrual to high priority research studies.
  • Oversees the quality assurance process for monitoring the collection of data for research, with assistance from the Quality Assurance and Safety Monitoring Committee (QASMC).
Other Functions

Performs other duties as assigned.

Working Conditions

Job Location/Working Conditions Normal office environment Physical Effort Typically sitting at desk or table Repetitive wrist, hand or finger movement (PC Typing) Equipment Office equipment The above statements are intended to describe the general nature and level of work performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all job duties performed by the personnel so classified. Management reserves the right to revise or amend duties at any time.

Required Qualifications
  • Education: Bachelor’s degree or combination of education and/or experience may substitute for minimum education.
  • Certifications/Professional Licenses: No specific certification/professional license is required for this position.
  • Work Experience: Clinical Research (1 Year)
  • Skills: Not Applicable
  • Driver's License: A driver's license is not required for this position.
Preferred Qualifications
  • Education: No additional education unless stated elsewhere in the job posting.
  • Certifications/Professional Licenses: Certified Clinical Research Coordinator (CCRC) - Association of Clinical Research Professionals (ACRP), Certified Clinical Research Professional (CCRP) - Society of Clinical Research Associates (SOCRA), Clinical Research Associate (CRA) - Association of Clinical Research Professionals (ACRP), Clinical Research Professional (CRP) - Association of Clinical Research Professionals (ACRP)
  • Work Experience: No additional work experience unless stated elsewhere in the job posting.
  • Skills: Clinical Project Management, Clinical Systems, Clinical Trials Administration, Deadline Management, Interpersonal Relationships, Leadership, Microsoft Excel, Microsoft Word, Oral Communications, Prioritization, SQL Databases, Stress Management, Written Communication
Grade G14 Salary Range

$75,200.00 - $128,800.00 / Annually The salary range reflects base salaries paid for positions in a given job grade across the University. Individual rates within the range will be determined by factors including one's qualifications and performance, equity with others in the department, market rates for positions within the same grade and department budget.

Benefits Statement
  • Personal Up to 22 days of vacation, 10 recognized holidays, and sick time.
  • Competitive health insurance packages with priority appointments and lower copays/coinsurance.
  • Take advantage of our free Metro transit U-Pass for eligible employees.
  • WashU provides eligible employees with a defined contribution (403(b)) Retirement Savings Plan, which combines employee contributions and university contributions starting at 7%.
  • Wellness: Wellness challenges, annual health screenings, mental health resources, mindfulness programs and courses, employee assistance program (EAP), financial resources, access to dietitians, and more!
Family
  • We offer 4 weeks of caregiver leave to bond with your new child.
  • Family care resources are also available for your continued childcare needs.
  • Need adult care? We’ve got you covered.
  • WashU covers the cost of tuition for you and your family, including dependent undergraduate-level college tuition up to 100% at WashU and 40% elsewhere after seven years with us.

For policies, detailed benefits, and eligibility, please visit: https://hr.wustl.edu/benefits/

EEO Statement Washington University in St. Louis is committed to the principles and practices of equal employment opportunity. It is the University’s policy to provide equal opportunity and access to persons in all job titles without regard to race, ethnicity, color, national origin, citizenship (where prohibited by federal law), age, religion, sex, sexual orientation, gender identity or expression, disability, protected veteran status, or genetic information.

Washington University in St. Louis' collective success is significantly attributed to the passion and outstanding efforts of our community. Our staff, faculty and trainees are committed to excellence and dedicated to carrying out our missions of research, teaching and patient care. WashU prides itself on being a place where people matter, and serious work is done. Our people work together in an inclusive community that celebrates diverse perspectives, collaboration and innovation. We are a community of individuals inspired to work together to develop big ideas and tackle challenging problems. We value the well-being of our people. WashU strives to create a positive employee experience where staff, faculty and trainees thrive, both personally and professionally. Our employees find meaning, connection and vitality in their work and life with a healthy work-life balance and support to learn, grow and make an impact at WashU, the community and the world.

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