Candidate Openings

• Chief Medical OfficerThe Chief Medical Officer position will assume a leadership, as well as a hands-on, role in the strategic planning, implementation, and oversight of clinical trials, reporting and potential registration of one or more therapeutic candidates. Specialty training and certification is required. Candidate should be board certified with specialty training and certification with relevant experience in drug development within the pharmaceutical or biotech industry. Strong background and interest in the underlying science and mechanism of action of therapeutic vaccines is required. Prior experience in translational research strongly preferred. Candidate will be responsible for designing and working closely with all functions to enable clinical development goals and deliverables as well as implementation and medical monitoring of clinical trials in early and late stage development. Candidate will be responsible for providing leadership to the program team, principal investigators and other functional groups within clinical development. The clinical operations, safety, regulatory and biostats teams will report into the Chief Medical Officer position.
• Director of Regulator AffairsThe Director of Regulatory Affairs combines knowledge of scientific, regulatory and business issues to enable products that are developed, manufactured or distributed to meet required legislation. This position is responsible for planning, directing, coordinating and controlling the regulatory affairs activities related to all Immgenuity products. Bachelor's Degree in scientific discipline (e.g., Biology, Microbiology, Chemistry, Engineering) PLUS 7-10 years of previous related experience Required OR Master's Degree in Regulatory Affairs and completion of FDA Regulatory Compliance courses. Excellent written and verbal communication skills are required, including negotiating and relationship management skills with ability to drive achievement of objectives. As the Director of Regulatory Affairs, Program Manager, a successful candidate will lead critical tasks in regulatory affairs' subject matter for completing complex tasks within New Product Development
• Virologist, Director of ManufaturingWe are seeking a Virologist with experience in live virus manufacturing and scale-up. The successful candidate will be responsible for using our master cell bank and master virus bank to expand the cell lines and later purify the virus particles via tangential flow filtration and sucrose gradients under cGMP conditions, intercaing with the QA and RA teams. Experience specifically with HIV is preferred. He or she must have the ability to independently execute manufacturing, purification and release testing in a BSL-3 environment as a leader of the manufacturing team. Requires PhD in Virology and 3-5 years' experience in live vaccine manufacturing in cell lines, purification and release testing.
• Immunologist, Director of ResearchWe are looking for an analytical, creative immunologist with a background in HIV immunology to assist us with developing novel immune therapeutics. The immunologist will continuously share findings with management and multidisciplinary teams and collaborate with other scientists in clinical research and development. The successful candidate will have a PhD in Immunology and 2-3 years' experience in research. The candidate must have excellent knowledge of various immune system cells and their assays while providing feedback for clinical teams for best ways to monitor various adaptive and innate cells as well as cytokines they produce. Must have experience in writing grant applications and good interpersonal skills to work with a team of diverse professionals.