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Reporting to the Clinical Research Program Manager (or local Hospital Administrator/Clinic Director) and Research Programs Office at SC International Headquarters, the CRC II provides support in accordance with SC’s policies and procedures, SC’s hospital regulations, the Code of Federal Regulation, and Good Clinical Practice guidelines, when applicable. Actively collaborates with applicable headquarters departments, including Research Programs, Legal, and Compliance related to protocol reviews, IRB submissions, sponsored contracts, material transfers, data use agreements, and HIPAA compliance for projects conducted within SHC.

Company Overview:
Shriners Children’s is an organization that respects, supports, and values each other. We are engaged in providing excellence in patient care, embracing multi-disciplinary education, and research with global impact. We foster a learning environment that values evidenced based practice, experience, innovation, and critical thinking. Our compassion, integrity, accountability, and resilience define us as leaders in pediatric specialty care for our children and their families. All employees are eligible for medical, dental and vision coverage on their first day! In addition, upon hire all employees are eligible for a 403(b) and Roth 403 (b) Retirement Saving Plan with matching contributions of up to 6% after one year of service. Employees in a full-time or part-time status (40+ hours per pay period) will also be eligible for paid time off, life insurance, short term and long-term disability and the Flexible Spending Account (FSA) plans. Additional benefits available to full-time and part-time employees include tuition reimbursement, home & auto, hospitalization, critical illness, pet insurance and much more! Coverage is available to employees and their qualified dependents in accordance with the plans. Benefits may vary based on state law.

Job Overview:
The Clinical Research Coordinator II is a specialized, independent research professional who ensures oversight and compliance of both system-wide and local SC (Shriners Children's) clinical research activities. Reporting to the Clinical Research Program Manager (or local Hospital Administrator/Clinic Director) and Research Programs Office at SC International Headquarters, the CRC II provides support in accordance with SC’s policies and procedures, SC’s hospital regulations, the Code of Federal Regulation, and Good Clinical Practice guidelines, when applicable. The CRC works closely with the Chief of Staff, SHC scientific and medical staff and other research personnel to ethically recruit and consent SC’s vulnerable pediatric subjects and to appropriately collect and safeguard data. Overall, the CRC II is the site’s primary liaison among research participants, the local investigator(s) and study sponsor(s). This position’s main responsibilities are to help ensure proper study conduct, subject safety, and the quality of data and data safeguards.

Responsibilities:
Study Management and Operations (Good Clinical Practice)<ul><li>Maintains a contemporary knowledge of clinical research regulatory requirements. Has a working knowledge of the complex clinical research process, from protocol development to implementation.</li><li>Supports the investigators’ development of SC investigator-initiated research protocols. Performs critical analysis of proposed research projects in order to determine appropriateness and feasibility at the local site, including the evaluation of resources required, budgeting, and regulatory requirements.</li><li>Supports the implementation of approved research protocols. Ensures studies are conducted in compliance with the approved protocol, Good Clinical Practice (GCP) guidelines, applicable regulatory requirements, SC policies and standards.</li><li>Responsible for tracking all aspects of projects including all study, investigator and Institutional Review Board (IRB) information, patient recruitment activity, and financial management. Actively collaborates with applicable headquarters departments, including Research Programs, Legal, and Compliance related to protocol reviews, IRB submissions, sponsored contracts, material transfers, data use agreements, and HIPAA compliance for projects conducted within SHC. Provides direction and education to clinical research staff on protocol-related activities. </li><li>Works closely with investigators, research leadership, study sponsor and regulatory agencies to conduct and report the results of clinical research.</li><li>Responsible for oversight and documentation of the delivery, storage, and disposition of investigational products at the site, in accordance with federal and state regulations and sponsor requirements. Effectively provides information about the use of investigational products to patients. </li><li>Understands and adheres to safety monitoringand reporting requirements of regulatory agencies that oversee use of an investigational product in research.</li></ul> Data Management and Informatics<ul><li>Coordinates the collection, statistical analysis and dissemination of data results throughout a clinical study. </li><li>Evaluates protocols under consideration for feasibility, including the process for data collection, entry, storage and reporting. Assists in the development of procedures to standardize data collection and management, including the safeguarding of data, for each protocol. Responsible for timely data collection. Ensures accurate entry of research and outcome data into secure research databases. </li><li>Verifies data accuracy through internal quality control measures to confirm reported study data is accurate, complete, and verifiable from source documents. Provides timely responses to data queries; reviews source documents and addresses data discrepancies. Participates in timely and thorough data cleaning and database lock procedures in preparation for data analysis.</li><li>Contributes in compiling, critically analyzing and preparing study results to share with research team. Provides input into the dissemination of research results by verifying all regulatory and compliance criteria are met, confirming that the SC system is credited appropriately, and assisting with abstract and manuscript preparation and submission as applicable.</li></ul> Ethical and Participant Safety Considerations<ul><li>Demonstrates knowledge of ethical standards set forth by the Belmont Report, the Nuremberg Code and the International Conference of Harmonization GCP standards. Exhibits a commitment to human subjects’ protection by providing the highest level of ethical and safety practices to protect all participants involved in research studies supported and approved by Shriners Children's. </li><li>Maintains education in human subject protection and good clinical practice principles, and applies knowledge of those ethical principles when interacting with subjects. Possesses a thorough understanding of the ethical issues involved with vulnerable pediatric populations, and identifies and </li><li>Implements additional safeguards that should be in place for SC’s vulnerable populations. Reports any concerns or issues directly to the Department of Research Programs or other appropriate departments for follow-up.</li><li>Safeguards all participants involved in a research study supported and approved by Shriners Children's. Maintains patient safety and privacy throughout the study. Collaborates with investigators and other research staff to mitigate risk. Protects the rights and well-being of human subjects. Confirms appropriate training and education are in place to safely perform study protocols. </li><li>Adheres to and applies protocol eligibility criteria when recruiting patients. Demonstrates a clear understanding of an ethical and legally effective informed consent process. Effectively communicates with participants/families during the consent</li></ul> Communication, Teamwork, and Professionalism<ul><li>Facilitates the local site’s research programs and projects through collaborative, timely communications and teamwork. Exhibits excellent communication and collaboration in all aspects of the research program within the site; between the site and the sponsor; and with appropriate outside entities. Establishes and maintains collaborative relationships with all involved in clinical research operations. Fosters teamwork by respecting and valuing the contributions of all involved in the clinical research process.</li><li>Works effectively with SC leadership to ensure the research mission is upheld. Maintains scientific integrity, intellectual honesty, and excellence.</li><li>Demonstrates interpersonal and professional skills, including but not limited to, professional appearance, tact, planning, punctuality, dependability and the ability to work effectively with a wide range of individuals in a diverse community.</li><li>Provides expertise consultation and mentorship to site staff, residence, students, and volunteers with respect to research processes, Good Clinical Practices, and regulations governing clinical research. Interacts with other departments in a professional and timely manner to facilitate research coordination.</li></ul> This is not an all-inclusive list of this job’s responsibilities. The incumbent may be required to perform other related duties and participate in special projects as assigned. 

Qualifications:
Required:<ul><li>3 or more years Clinical Research experience, e.g. experience with site management, study management, IRBs, and federal regulations regarding clinical research compliance</li><li>Bachelor's Degree, or 5+ years of specific job-related experience in the administration of clinical research in lieu of degree </li></ul> Preferred:<ul><li>Bachelors degree in clinical research, science or other healthcare related field</li><li>Master’s degree in clinical research, science or other healthcare related field</li><li>CCRP or CCRC certification </li></ul>

Shriners Children's

Clinical Research Coordinator II

Administrative Skills

Budgeting

Certified Clinical Research Coordinator (CCRC)

Clinical Outcomes

Clinical Practices/Protocols

Clinical Research

Clinical Training

Code of Federal Regulations

Communication Skills

Data Analysis

Data Cleaning

Data Collection

Data Entry

Data Management

Data Processing

Data Quality

Documentation

Federal Laws and Regulations

Financial Management

GCP (Good Clinical Practices)

HIPAA (Health Insurance Portability and Accountability Act)

Healthcare

Hospital

Hospital Administration

IRB/IEC (Institutional Review Board/Independent Ethics Committee)

Informatics

Information/Data Security (InfoSec)

Informed Consent

Interpersonal Skills

Investigational New Drug (IND)

Leadership

Legal Research

Maintain Compliance

Medical Records

Mentoring

Operations Research

Organizational Skills

Patient Care

Patient Safety

Pediatrics

Procedure Development

Project Evaluation

Regulations

Regulatory Compliance

Regulatory Reports

Regulatory Requirements

Research Protocols

Risk Management

Safety Training

Safety/Work Safety

Scientific Research

Standards Development

Standards of Care

State Laws and Regulations

Statistics

Student Housing

Team Player

Time Management

[AW]-iCims

KCV empowers ideas that impact lives – by collaborating with higher education institutions across Kentucky to transform research ideas into market-ready products and startups, enhancing the state’s innovation ecosystem and entrepreneurial capacity. Kentucky Commercialization Ventures (KCV) is seeking a Research Development & Commercialization Coordinator to support partner universities across Kentucky in strengthening research capacity, improving grant competitiveness, and advancing innovation and commercialization outcomes.

Supervisor: Executive Director, KCVProgram Areas: KCV EDGE & Licensing and New Ventures TeamAbout KSTC: Since its founding in 1987, the Kentucky Science & Technology Corporation (KSTC) has been a pioneering force in driving science, technology, and innovative economic development throughout Kentucky.Vision and Mission: We envision a future where Kentucky is recognized as a national and international leader, ranks among the top half of states in innovation-driven economic development, and where KSTC is recognized among its peers as setting the benchmark for others to follow. With this vision in mind, our mission is clear: We cultivate knowledge, talent, and investment to propel the state's growth and competitiveness on a national and global scale. Position SummaryKentucky Commercialization Ventures (KCV) is seeking a Research Development & Commercialization Coordinator to support partner universities across Kentucky in strengthening research capacity, improving grant competitiveness, and advancing innovation and commercialization outcomes. This is a unique, multi-institution support role working at the intersection of research development, proposal support, and technology commercialization. The ideal candidate is a strong communicator and problem-solver who can translate complex funding opportunities into clear, actionable guidance while building relationships across varied academic environments. Our team is looking for someone who can think visually, review and produce accessible content, in an environment that fosters positive relationships. Why This Role MattersKentucky Commercialization Ventures (KCV) is a program under the Kentucky Science and Technology Corporation (KSTC) aimed at driving innovation and economic development through the commercialization of research and technology. KCV empowers ideas that impact lives – by collaborating with higher education institutions across Kentucky to transform research ideas into market-ready products and startups, enhancing the state’s innovation ecosystem and entrepreneurial capacity. You will help faculty navigate funding opportunities, build competitive proposals, and connect research to real-world impact, especially in institutions where resources are limited but potential is high. This position will work under the direction of the Associate Director of Research Enterprise, while formally reporting to the Executive Director of KCV. The role will collaborate closely with research administrative personnel to strengthen funding and grant management capacity.What You’ll DoSupport Proposal Development<ul><li>Identify and interpret funding opportunities (e.g., NSF, NIH, EPSCoR, INBRE, State, Foundation, etc.)</li><li>Translate solicitations into clear guidance for faculty and researchers </li><li>Assist with early-stage proposal development, including concept alignment, timelines, and non-technical components </li><li>Develop templates, checklists, and reusable resources to support proposal success Help reduce barriers by simplifying complex application requirements</li></ul>Engage Faculty & Build Research Capacity<ul><li>Conduct outreach to faculty, researchers, and students across partner institutions</li><li>Identify researchers with strong funding and/or commercialization potential </li><li>Support early-career faculty and emerging research programs </li><li>Build relationships that increase participation in research and innovation activities</li></ul>Connect Research to Commercialization<ul><li>Identify research with commercialization potential and connect to KCV programs</li><li>Support development of a pipeline of faculty, technologies, and innovation opportunities</li><li>Assist with preparation for stakeholder engagement</li></ul>Use Data to Drive Strategy<ul><li>Track engagement, funding activity, and pipeline development across institutions</li><li>Identify trends, gaps, and opportunities for targeted support </li><li>Contribute to reporting, dashboards, and program insights </li><li>Construct and run regular reports on the variety of work that is accomplished</li></ul>What We’re Looking ForMinimum Qualifications<ul><li>Bachelor’s degree in a relevant field</li><li>Strong communication and organizational skills </li><li>Ability to translate complex information into clear, actionable guidance </li><li>Experience managing multiple priorities and stakeholders </li><li>US Citizenship or Permanent Residency</li></ul>Preferred Qualifications<ul><li>Experience in research development, grant writing, or proposal support</li><li>Familiarity with federal funding agencies (NSF, NIH, etc.) </li><li>Experience in higher education, research administration, or commercialization </li><li>Experience developing templates, guides, or training materials </li><li>Comfort working with data tracking tools and systems</li></ul>Location & Travel<ul><li>Based in Kentucky (flexible/hybrid depending on candidate)</li><li>Regular travel to partner institutions expected </li></ul>Additional Information: - The above statements describe the general nature and level of work performed by individuals assigned to this job. It is not an exhaustive list of all duties and responsibilities required. Other duties may be assigned as determined by management. - Reasonable accommodations may be made to enable individuals with disabilities to perform essential duties and responsibilities.KSTC is an equal opportunity employer and offers a competitive salary and benefits package. Applications are now being accepted and will be processed as they are received, with screening for interviews beginning immediately.

Kentucky Science & Technology Corporation

Research Development & Commercialization Coordinator

Academic Background

Benchmarking

Content Development

EDGE (Enhanced Data for GSM Evolution)

Economic Development

Ecosystems

Entrepreneurship

Federal Government

Funding

Grant Administration/Management

Grant Writing

Higher Education

Licensing

Market Research

Multitasking

NSF Audio Formats

National Institutes of Health (NIH)

Problem Solving Skills

Proposal Development

Proposal Writing

Reporting Dashboards

Research & Development (R&D)

Research Administration

Sales Pipeline

Startup

Technical Research

Technical Support

Trend Analysis

United States Citizen

User Documentation

Willing to Travel

HiringThing

INTERN

During the school year, students will work part time, but during the summer, the position will work on-site and may include travel to work on clean energy R&D projects at numerous locations across PPL Corporation including Allentown, Pennsylvania, Providence, Rhode Island, as well as Louisville and Lexington, Kentucky. Our high-performing regulated utilities — PPL Electric Utilities, Louisville Gas and Electric, Kentucky Utilities and Rhode Island Energy — provide an outstanding experience for our customers, consistently ranking among the best utilities in the nation.

Company Summary Statement :
As one of the largest investor-owned utility companies in the United States, PPL Corporation (NYSE: PPL), is committed to creating long-term, sustainable value for our 3.5 million customers, our shareowners and the communities we serve. Our high-performing regulated utilities — PPL Electric Utilities, Louisville Gas and Electric, Kentucky Utilities and Rhode Island Energy — provide an outstanding experience for our customers, consistently ranking among the best utilities in the nation. PPL’s companies are also addressing challenges head-on by investing in new infrastructure and technology that is creating a smarter, more reliable and resilient energy grid. We are committed to doing our part to advance a cleaner energy future and drive innovation that enables us to achieve net-zero carbon emissions by 2050 while maintaining energy reliability and affordability for the customers and communities we serve. PPL is a positive force in the cities and towns where we do business, providing support for programs and organizations that empower the success of future generations by helping to build and maintain strong, diverse communities today.

Overview:
The PPL R&D Department is looking for PhD Engineering students from all engineering disciplines to begin in May 2026. We are looking for interns who are passionate about renewable energy, including wind and solar, energy storage, green hydrogen, sustainability, carbon capture and other decarbonization technologies. Ideal candidates will be based in Pennsylvania, Rhode Island, or Kentucky and would be interested in the potential of transitioning to full-time employment with PPL upon graduation. During the school year, students will work part time, but during the summer, the position will work on-site and may include travel to work on clean energy R&D projects at numerous locations across PPL Corporation including Allentown, Pennsylvania, Providence, Rhode Island, as well as Louisville and Lexington, Kentucky. While traveling, all expenses will be paid. 

Responsibilities:
<ul><li>Plans and controls all activities so as to provide an accident-free work place.</li><li>Uses engineering and scientific principles to plan projects, collect and analyze data, and create professional reports.</li><li>Gathers, correlates, and analyzes data using established procedures.</li><li>Coordinates and communicates results and participation in research projects within applicable business units and prepares summaries of value and results to management.</li><li>Identifies opportunities for improvement and/or suggests improved methods.</li><li>Performs detailed and/or engineering assignments involving established calculations, tests and analysis.</li><li>Performs other duties as directed by management.</li></ul>

Qualifications:
Requirements<ul><li>Available part time during the semester and full time during the Summer 2026 semester</li><li>Pursuing a PhD in Engineering from an ABET Accredited program. </li><li>Minimum 3.00 GPA</li></ul>

Research Jobs in Winchester, KY

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Research Jobs in Winchester, KY

Clinical Research Coordinator II Shriners Children's

Research Development & Commercialization Coordinator Kentucky Science & Technology Corporation

Research & Development - PhD Engineering Intern PPL Services Corporation

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