Research Associate - Biotech performs analytical tests and experiments in support of biotech research projects. Operates laboratory equipment and instruments. Being a Research Associate - Biotech utilizes scientific software to interpret and record test results. Experienced with standard chemistry and molecular biology lab practices and techniques. Additionally, Research Associate - Biotech requires a bachelor's degree. Typically reports to a supervisor. The Research Associate - Biotech work is closely managed. Works on projects/matters of limited complexity in a support role. To be a Research Associate - Biotech typically requires 0-2 years of related experience. (Copyright 2024 Salary.com)
Clinical Trial Associate/Clinical Research Coordinator
About Krystal Bio:
At Krystal Biotech, Inc., we bring together the brightest and most eager minds to relentlessly pursue the discovery, development and commercialization of gene delivery medicines for patients with serious and life-threatening genetic diseases. Founded in 2016, Krystal is a leader in gene therapy. Krystal received U.S. FDA approval for the first-ever redosable gene therapy treatment, VYJUVEK™, for the treatment of Dystrophic Epidermolysis Bullosa. Krystal continues to leverage our proprietary platform to develop new treatments across a robust clinical pipeline. Located near Krystal’s headquarters are two state-of-the-art GMP facilities.
Krystal Biotech is based in Pittsburgh, PA which is home to our two state-of-the-art GMP facilities. Additional offices are situated in Boston, MA and in Zug, Switzerland.
Join us on our journey to implement our mission to identify, develop and deliver genetic medicines to patents!
Job Description Summary:
Krystal Biotech, Inc. is seeking a Clinical Trial Associate to support our Clinical Operations Team. The Clinical Trial Associate's responsibilities will entail but not be limited to assisting in the management and inventory of clinical supplies, ensuring proper materials are available at clinical sites in a timely manner, and working with the Clinical Operations team to support multiple Clinical Trials. Conducting reviews of trial data and follow GCP/ICH protocols/guidelines. Will require travel to Clinical sites, including up to 50% of the time, during peak periods.
Primary Responsibilities:
Experience and Skills Desired: