Senior Medical Consultant Kumquat Biosciences Inc San Diego, CA Job Details $175 - $250 an hour 1 hour ago Qualifications Team leadership Pharmaceutical regulatory compliance Identifying new business opportunities Drug regulation Clinical research compliance Business alliance strategy Managing clinical research teams Networking through strategic partnership building Product strategy Business development within healthcare Drug efficacy studies Strategic partnerships Clinical trial support in drug product development Pharmaceutical research experience Senior leadership

Full Job Description Description:

The Senior Medical Consultant (SMC) will work as a strategic partner with members of the senior executive team to develop and advance their clinical development strategy and drive the clinical research vision and regulatory roadmap for the company. The SMC will direct the development of clinical strategies and programs, formulating standards and policies to maximize the potential for success of compounds under development. Primary responsibilities will include developing a target product profile and development plan, executing clinical trials, coordinating with clinical research organizations and other vendors, developing and managing clinical advisory boards, broadening the internal clinical research capabilities, and overseeing all clinical collaboration efforts with partners, principal investigators, and key opinion leaders. Our ideal candidate will have small molecule drug development experience in the fields of Immunology and Inflammation.

Requirements:

Provide insight and guidance with respect to all clinical and medical needs for the strategic direction and new business opportunities across the varied segments of interest for the Company. Provide oversight and leadership of the various functional areas within clinical operations, clinical science, medical monitoring, and regulatory affairs consistent with development goals across the company's portfolio. Drive execution of clinical trial plans to deliver compelling safety, pharmacokinetic, and efficacy data supportive of regulatory and marketing proof-of-relevance. Establish and maintain relationships with principal investigators, consultants and KOLs to ensure that the Company has a clear understanding of clinician needs and requirements, as well as medical practice patterns. Maintain an understanding of competitors and clinical developments in relevant therapeutic areas by attending scientific meetings and tracking literature. Actively assist in seeking product and/or technology alliances with appropriate pharmaceutical company partners to enhance/expedite the development of the company's assets. Help to establish and maintain collaborations with partners in academia, government, and industry.