[Hiring] Senior Clinical Trial Associate @Liquidia

Role Description

Liquidia is deeply passionate and committed to the discovery, engineering, and development required to bring novel therapies to patients who need them most, and to the healthcare providers who care for them. Our current drive is toward improving the treatment of pulmonary arterial hypertension (PAH). We will continue to combine our proprietary, innovative PRINT Technology with new and established medications, offering the potential for both better precision and improved clinical outcomes. Our team members include some of the industry’s top scientists, clinicians, business strategists, engineers, and pharmaceutical executives. We work together to help people lead longer, healthier, and happier lives.

The Sr. Clinical Trial Associate is a member of the Clinical Operations team. The Clinical Operations team is responsible for executing, managing, and conducting studies associated with the company’s clinical development plans. This position requires coordination with all members of the Clinical Operations team as well as other internal and external team members.

Qualifications

• Bachelor’s degree in related discipline
• 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
• Proven ability to multitask
• Efficient time management and strong organizational skills
• Attention to detail and quality are critical to success in this role
• Ability to travel up to 15%

Requirements

• Bachelor’s degree in related discipline
• 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
• Proven ability to multitask
• Efficient time management and strong organizational skills
• Attention to detail and quality are critical to success in this role
• Ability to travel up to 15%

Company Description