Senior Clinical Trial Associate - Global Trials

Liquidia Corporation; Morrisville (NC); On-site; USD 80,000 - 110,000; Full time

Benefits offered by this job

Medical

Dental

Vision

STD

LTD

401(k)

ESPP

Unlimited PTO

Job summary

Liquidia Corporation invites applications for a Sr. Clinical Trial Associate to join the Clinical Operations team in Morrisville, NC. This role supports execution and management of Phase 2–3 studies, coordinating with internal and external partners and ensuring regulatory compliance.

The candidate will work on study materials, document management, CRO oversight, and trial-tracking systems, with emphasis on accuracy, timeliness, and cross-functional collaboration. Travel up to 15% is required.

Qualifications

• Bachelor’s degree in related discipline and a minimum of 4 years of clinical trials or Sponsor experience.
• Clinical operations experience in Phase 2 to Phase 3 clinical trials including global clinical trials.
• Working knowledge of ICH GCP regulations.
• Previous experience in any group of Pulmonary Hypertension or inhalation research strongly preferred
• Strong initiative and desire to work in a fast-paced, team-oriented, and dynamic environment.
• Excellent written and verbal communication skills and proven ability to multitask.
• Efficient time management and strong organizational skills. Attention to detail and quality are critical to success in this role.

Responsibilities

• Assisting with project start-up, including development of budgets, contracts, financial disclosure statements, and grant payments.
• Collaborating with Program Leaders to develop study-related materials (e.g., informed consent forms, Advertising Materials, sections of study plans, etc.) as required.
• Assist in the oversight, processing, and management of all clinical project-related documents including Investigator Site Regulatory Documents, Case Report Forms (CRF), and Monitoring Reports.
• Reviewing the work of CROs and other vendors (Field Monitors, Central Labs, Clinical Supply Distributors, etc.) assigned to clinical studies to provide feedback to study manager.
• Communicating seamlessly and effectively with internal and external study personnel. Developing and maintaining good working relationships with Investigators and study staff.
• Assist in the routing of Communication Logs, Training logs, and Protocol Deviation Assessments and other documents as required for the study.
• Copy, distribute, and file Serious Adverse Event communications as required.
• Preparation and distribution of project status reports, newsletters, and study event memorandums.
• Provide support for maintaining both electronic and paper document-tracking systems for all documents associated with the start-up and execution of clinical studies.
• Review and verify investigator site visit grant calculations, prepare PO requisitions, and forward invoices, site payment letters, and expense reports.
• Review Investigator and Project files throughout a clinical trial and follow up with CSM on any discrepancy or missing documents.
• Assist in the maintenance of Standard Operating Procedures (SOPs) and Work Instructions.
• Assist in the preparation of an Investigator Meeting.
• Updates internal and external systems in a timely manner (CTMS, clinicaltrials.gov).
• Assists with the maintenance of the Trial Master File.
• Developing and maintaining study trackers and providing metrics as needed.
• Participating in user acceptance testing (UAT) of clinical systems, including EDC and interactive response technology (IRT).

Job description

Liquidia Corporation invites applications for a Sr. Clinical Trial Associate to join the Clinical Operations team in Morrisville, NC. This role supports execution and management of Phase 2–3 studies, coordinating with internal and external partners and ensuring regulatory compliance.

The candidate will work on study materials, document management, CRO oversight, and trial-tracking systems, with emphasis on accuracy, timeliness, and cross-functional collaboration. Travel up to 15% is required.