Lifelancer is an AI-powered talent hiring platform that connects employers with skilled professionals in the Life Sciences, Pharmaceutical, and IT sectors. It enables individuals to create profiles showcasing their skills, get matched with high-paying international jobs or projects, and facilitates hiring and payroll for employers in multiple countries. The platform aims to streamline the hiring process with efficient AI sourcing and compliance support.
Life Science β’ Freelance β’ Remote Jobs β’ Healthcare β’ IT
51 - 200 employees
Founded 2020
π€ Artificial Intelligence
𧬠Biotechnology
π Pharmaceuticals
π° Pre Seed Round on 2022-03
February 12
Lifelancer is an AI-powered talent hiring platform that connects employers with skilled professionals in the Life Sciences, Pharmaceutical, and IT sectors. It enables individuals to create profiles showcasing their skills, get matched with high-paying international jobs or projects, and facilitates hiring and payroll for employers in multiple countries. The platform aims to streamline the hiring process with efficient AI sourcing and compliance support.
Life Science β’ Freelance β’ Remote Jobs β’ Healthcare β’ IT
51 - 200 employees
Founded 2020
π€ Artificial Intelligence
𧬠Biotechnology
π Pharmaceuticals
π° Pre Seed Round on 2022-03
β’ The Director, Clinical Science will be an essential contributor to the scientific, clinical, and operational scope of clinical development programs with an emphasis on program-specific activities β’ Drive the design, planning, and implementation of study protocols for assigned investigational products β’ Key role in supporting related regulatory activities β’ Work on cross-functional program development and study management teams for the design, execution, and monitoring of clinical trials β’ Assist with data interpretation and communication to both internal and external stakeholders β’ Help support internal process improvement initiatives within the clinical department
β’ PhD degree in health science field, PharmD, or MD or non-US equivalent β’ At least 8+ years of experience in Clinical Science within a CRO or biotechnology company β’ Experience in oncology clinical trials required β’ Late-stage drug development experience required β’ Experience with data analysis and interpretation as an understanding of safety and pharmacovigilance principles required β’ Demonstrated ability to evaluate, interpret and present complex scientific data (preclinical, clinical, translational) to inform scientific hypotheses and development strategy β’ Working knowledge of biostatistics, GCP, and regulatory requirements for clinical studies β’ Must be willing and possess the expertise to work effectively in a fast-paced, team-based matrix environment as well as the ability to function independently as appropriate β’ Flexible to accommodate changes in team and project needs β’ Ability to handle multiple projects at a time and have a strong attention to detail while understanding the higher-level strategy β’ Excellent interpersonal, verbal, and written communication skills β’ Ability to make independent, timely and appropriate decisions
β’ Opportunity to participate in stock programs β’ Performance-based bonus β’ Comprehensive benefits package
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