Must have pulmonary hypertension experience Goal: to supplement monitors (22 sites total; 18 sites enrolling) Duration: Start ASAP Monitoring frequency: CRAs need to be in contact with their sites weekly. CRAs should be on site every 2-3 weeks (to review eligibility for each new subject) Parsippany, NJ

This role will Act as a statistical programming representative in a multidisciplinary study team to ensure timely and quality support for analysis and reporting of clinical trials up to regulatory approval, product launch and annual reports. What You’ll Do Develop, implement, and maintain programs for the activities such as data review and safety signaling analysis on ongoing basis. Work...

The primary responsibility of the Medical Science Liaison (MSL) is to act as a liaison with nationwide and regional key opinion leaders (KOLs) to align interests, discuss research and medical information, and to facilitate both clinical trial efforts of the company and Investigator-sponsored studies in relation to the treatment of pancreatic cancer. This individual’s clinical insights will be...

The primary responsibility of the Medical Science Liaison (MSL) is to act as a liaison with nationwide and regional key opinion leaders (KOLs) to align interests, discuss research and medical information, and to facilitate both clinical trial efforts of the company and Investigator-sponsored studies in relation to Somatuline in the treatment of Gastro-entero-pancreatic neuroendocrine tumors (GEP...

The primary responsibility of the Medical Science Liaison (MSL) is to act as a liaison with nationwide and regional key opinion leaders (KOLs) to align interests, discuss research and medical information, and to facilitate both clinical trial efforts of the company and Investigator-sponsored studies in relation to Somatuline in the treatment of Gastro-entero-pancreatic neuroendocrine tumors (GEP...