Clinical Research Program Coor - Clinical Research Pharmacy

Overview

Oversees all administrative operations for clinical drug studies that utilize pharmacy services, enhances department and organization reputation by owning and accomplishing program goals with various institutions, vendors, investigators, and study staff.

Why Nationwide Children's Hospital?

The moment you walk through our doors, you feel it. When you meet our patient families, you believe it. And when you talk with anyone who works here, you want to be part of it.

Welcome to Nationwide Children’s Hospital, Where Passion Meets Purpose .

Here, Diversity, Equity and Inclusion are integrated into our core values and practices. We are passionate about building, sustaining and evolving an inclusive and equitable environment.

We are seeking individuals who live these values and want to share their experiences and efforts in support of our collective mission.

We’re 14,000 strong. And it takes every one of us to improve the lives of the kids we care for, and the kids around the world we’ll never meet.

Kids who live healthier, fuller lives because of the knowledge we share. We know it takes a Collaborative Culture to deliver on our promise to provide the very best, innovative care and to foster new discoveries, made possible by the most groundbreaking research. Anywhere.

Ask anyone with a Nationwide Children’s badge what they do for a living. They’ll tell you it’s More Than a Job . It’s a calling.

It’s a chance to use and grow your talent to make an impact that truly matters. Because here, we exist simply to help children everywhere.

Nationwide Children’s Hospital. A Place to Be Proud .

Responsibilities

• Oversees the pharmacy clinical drug study portfolio, responsible for the administrative management of multiple protocols, and acts as a pharmacy liaison.
• Provides administrative management, organization of, and participation in the clinical drug portfolio. Organizes clinical trial fee estimates, and tracks services rendered.
• Manages and tracks projects and initiatives including, the timeline and budget, progress updates, identifying and implementing needed actions, tracking compliance metrics, and preparing presentations.
• Develops and implements template materials required for successful studies, and coordinates personnel needs for the program and projects.
• Provides monitoring, review, and tracking of clinical data, prepares study specific documents according to regulations, including implementation, maintenance, and documentation.
• Collects and controls research data and subject information and tracks screening and enrollment data across multiple sites and projects.
• Remains proficient in regulations, provides guidance to investigators and study team, and monitors, reviews, and tracks clinical data and study specific documents.

Qualifications

Education Requirement :

• Associate’s Degree with equivalent work-related experience, required.
• Bachelor’s Degree, preferred.

Certifications : CCRC or CCRP, preferred.

Skills :

• Demonstrated leadership skills and an understanding of group dynamics.
• Strong critical thinking and organizational skills with demonstrated attention to detail.
• Exceptional interpersonal, written, and verbal communication skills.
• Ability to filter information, discern importance and initiate plan for project completion.

Experience : 2 years of clinical drug study research or project management experience, required.

The above list of duties is intended to describe the general nature and level of work performed by individuals assigned to this classification.

It is not to be construed as an exhaustive list of duties performed by the individual so classified, nor is it intended to limit or modify the right of any supervisor to assign, direct, and control the work of employees under his / her supervision.

EOE M / F / Disability / Vet

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