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"Clinical Trial Coordinator"

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Clinical Trial Coordinator

Clinical Trial Coordinator

Company:
North Carolina State University

Job Location:
Raleigh, North Carolina

Category:
Laboratory and Research

Type:
Full-Time

Join the Pack! A community with nearly 8,000 faculty and staff, and 30,000 students. NC State is one of the largest employers in North Carolina, offering a large range of career opportunities. Visit us at https://jobs.hr.ncsu.edu/.

Department: 191901 - Research

Location: Raleigh, NC

Essential Job Duties:
Under the direction of the Research Core Director, the Clinical Trial Coordinator plays a key role in supporting clinical research within the Clinical Studies Core (CSC). This position offers the opportunity to work across a varied portfolio of veterinary clinical trials, partnering closely with investigators, clinical teams, and fellow CSC staff.

The Coordinator will contribute to both day-to-day study operations and hands-on clinical and laboratory tasks, helping ensure high-quality execution of ongoing projects. Responsibilities will shift depending on active studies, providing a dynamic and engaging work environment.

Typical activities include patient recruitment and enrollment, animal handling, biological sample collection and processing, and technical assistance for project-specific procedures. The role also requires accurate time tracking, schedule coordination, and occasional bench laboratory work, such as extraction of DNA/RNA, bio specimen database management, and general lab maintenance.

Primary Responsibilities:

Clinical & Technical Duties

  • Perform safe and effective animal handling and restraint for multiple species.
  • Conduct venipuncture and obtain biological specimens (blood, urine, swabs).
  • Process and manage samples, including labeling, storage, and chain-of-custody.
  • Capture and document clinical data according to protocol and regulatory standards.

Research Operations & Compliance

  • Adhere strictly to study protocols across multiple ongoing clinical research projects.
  • Maintain accurate and complete records, ensuring documentation quality and version control.
  • Collaborate with multiple Principal Investigators (PIs) and veterinary specialty teams to support study needs.

Project Coordination & Communication

  • Assist with daily study operations, including scheduling, appointment coordination, and workflow management.
  • Communicate clearly and professionally with PIs, study teams, clinical service units, and external partners.
  • Manage several projects simultaneously, adjusting efficiently to evolving priorities and timelines.

Interpersonal & Organizational Skills

  • Demonstrate strong interpersonal communication when interacting with multidisciplinary teams.
  • Apply effective organizational skills, including time management and prioritization.
  • Multitask confidently in a fast-paced clinical research environment.

Customer/Client Service

  • Provide exceptional customer service to clients, pet owners, and internal stakeholders, fostering a positive and supportive experience.

Key Qualifications

  • Experience in Clinical Research
  • Experience in Veterinary Clinical Medicine
  • Experience in all of the following: animal handling/restraint, venipuncture, biological sample collection and processing

Other Work/Responsibilities:
Other duties as assigned

Minimum Experience/Education:
Bachelor's degree in a discipline related to the area of assignment; or an equivalent combination of training and experience.
All degrees must be received from appropriately accredited institutions.

Required Qualifications:
N/A

Preferred Qualifications:

  • A good understanding or experience with running clinical trials for pivotal submissions to the FDA (FDA or FDA CVM).
  • Experience as a licensed Veterinary Technician.
  • Experience coordinating study operations such as scheduling, appointment coordination, workflow management, and supporting multiple research projects simultaneously.
  • Strong organizational and communication skills, with experience maintaining accurate research documentation and collaborating with investigators, clinical teams, and multidisciplinary partners.

Required license or certification:
N/A

Position Number: 00106330

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