Header Job Summary We are seeking a highly motivated and experienced Clinical Research Principal Investigator to lead and oversee groundbreaking medical research initiatives. This pivotal role involves designing, implementing, and managing clinical trials with a focus on advancing scientific knowledge and improving patient outcomes. The ideal candidate will possess a strong background in molecular biology, immunology, and clinical research practices, coupled with excellent leadership and communication skills. As a key driver of research excellence, you will ensure compliance with regulatory standards while fostering innovation within the research team. This paid position offers an exciting opportunity to contribute to impactful medical discoveries in a dynamic research environment. Responsibilities Lead the planning, coordination, and execution of clinical trials in accordance with FDA regulations and ICH Good Clinical Practice (GCP) guidelines Develop detailed study protocols, ensuring scientific rigor and adherence to ethical standards Oversee patient monitoring activities, including recruitment, informed consent processes, and ongoing safety assessments Supervise laboratory research activities utilizing techniques such as tissue culture, protein purification, ELISA, Western blotting, flow cytometry, PCR, microscopy, chromatography, and immunological assays Review and validate research documentation including case report forms (CRFs), regulatory submissions, and study reports for accuracy and compliance Analyze complex bioinformatics data sets using R, Python, SAS, or other statistical tools to derive meaningful insights Publish research findings in peer-reviewed journals and present at scientific conferences to disseminate knowledge Experience Extensive experience in clinical trials management within a biomedical or pharmaceutical setting Proven expertise in laboratory research techniques including cell & molecular biology research, transfection methods, mammalian cell culture, in vivo studies, and assay development Strong background in immunological laboratory techniques such as flow cytometry and ELISA Demonstrated ability to analyze research data using statistical software like SAS or R for rigorous scientific interpretation Familiarity with FDA regulations related to clinical research and laboratory practices including HIPAA compliance for patient data security Experience securing research grant funding and managing project budgets is preferred Prior involvement in publishing papers in peer-reviewed journals and contributing to academic or medical research initiatives Join us to be at the forefront of innovative medical research! Your expertise will drive meaningful discoveries that can transform healthcare practices worldwide. We value your dedication to advancing science while ensuring the highest standards of safety and compliance. This is your chance to lead impactful projects that make a difference—apply now to become part of our vibrant research community!

Pay:

From $166.00 per hour Expected hours: No less than 10.0 per week

Work Location:

Hybrid remote in Minneapolis, MN 55447