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Quality Assurance and Research Education Coordinator

Role overview

Qualifications

  • Certified Clinical Coordinator either through SOCRA or ACRP required
  • Bachelor's degree required
  • A minimum of 3 years of relevant experience required
  • Experience dealing with regulatory agencies required

Responsibilities

  • Ensure the Sponsor, Investigator, and study team adhere to current FDA regulations, applicable ICH/GCP guidelines, local policies and standard operating procedures.
  • Assist in the development and writing of clinical trial monitoring plans based on risk based monitoring.
  • Adhere to monitoring plans; e.g. monitoring visit type, frequency, and required critical monitoring activities.
  • Monitor clinical trial progress through a combination of data review and on site/remote monitoring visits.

Key facts

Hard skills

Other skills

  • Quality Assurance
  • Communication
  • Training And Development
  • Time Management

About the company

Nemours logo

Nemours

Hospitals & Health Care

Nemours is committed to improving the health of children. As a non-profit children’s health organization, we consider the health of every child to be a sacred trust.Through family-centered care in our children’s hospitals and clinics in Delaware, New Jersey, Pennsylvania and Florida, as well as world-changing research, education and advocacy, Nemours fulfills the promise of a healthier tomorrow for all children — even those who may never enter our doors.Nemours began more than 80 years ago with the vision of Alfred I. duPont to improve the lives of children and to do whatever it takes to prevent and treat even the most disabling childhood conditions.Today, through our children’s hospitals and health system, we directly care for 250,000 children annually in Delaware Valley and Florida, including families who travel from across the country and world to see our specialists — treating every child as we would our own.We also reach beyond the walls of our hospitals and clinics to be a voice for children on a national and international level, and to lead the way in prevention, intervention, education, and research.Nemours is growing to better serve the children and families in our care. We have 1.1 million square feet of space currently devoted to providing children’s healthcare or under construction, all designed with significant input and advice from our patients and families.

Company details

Company typeXLarge
IndustryHospitals & Health Care
Company size5001 - 10000

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Job description

Nemours is seeking a Quality Assurance and Research Education Coordinator. The purpose of the Quality Assurance Research Coordinator position is to ensure compliance with respective research protocols, applicable federal and state regulations, ICH-GCP guidelines and all relevant institutional policies and procedures. The Research Quality Assurance and Education coordinator will provide internal monitoring and educational opportunities for Nemours Biomedical Research to support these objectives. 

This is a Hybrid position.  Candidate must be able to be on site in Wilmington, Delaware 30% of the time.

Qualifications:

  • Certified Clinical Coordinator either through SOCRA or ACRP required
  • Bachelor's degree required
  • A minimum of 3 years of relevant experience required 
  • Experience dealing with regulatory agencies required

Primary Responsibilities:

  • Ensure the Sponsor, Investigator, and study team adhere to current FDA regulations, applicable ICH/GCP guidelines, local policies and standard operating procedures. 
  • Assist in the development and writing of clinical trial monitoring plans based on risk based monitoring.
  • Adhere to monitoring plans; e.g. monitoring visit type, frequency, and required critical monitoring activities by utilizing monitoring tracking forms and other monitoring related tools and templates. 
  • Monitor clinical trial progress through a combination of data review and on site/remote monitoring visits. 
  • Verify that trial data is consistent with patient clinical notes and other source documentation (source data verification/review). 
  • Independently coordinate ongoing and upcoming monitoring assignments 
  • Meet expected timelines for completion of monitoring activities and submission of written monitoring reports. 
  • Provide recommendations and guidance to study specific monitoring teams and assist in 
  • audit readiness and preparation. 
  • Provides training programs for clinical research associates developed by the Quality Assurance and Research Program.
  • Participates in education of new team members as well as ongoing education of teams based on gaps identified through internal audits, sponsor monitoring visits, changes in regulations, departmental/corporate policies and other factors as determined by department leadership
  • Must be willing to travel up to 30% of the time as needed
  • Must be able to maintain strict confidentiality.

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MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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