At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring
Our story Strada is a technology-enabled, people powered company committed to delivering world-class payroll, human capital management, and financial management solutions to organizations globally. With a team of more than 8,000 experts and over 30 years
Responsible for leading the team and encouraging changes and challenges, influencing stakeholders inside and outside the company, contributing to the achievement of organizational goals, enhancing performance and productivity, and fostering talent development regardless of whether there
Basic purpose of the job* The Head of Development Regulatory Affairs 1 or 2 has responsibility to develop and implement regulatory strategy for the assigned therapeutic areas (TAs) and exercises activities which include: Guide subordinates on the development
Basic purpose of the job Delivers project management support to the asset team and next–level teams with the focus on asset strategy execution and asset progress. Coordinates the interactions with all key stakeholders, local and Global
Basic purpose of the job Independently writes and manages clinical documents, such as clinical trial reports, Investigation Brochures, Protocols and briefing documents, in both local and global cross-functional project- and study teams, as well as local
1. Basic Purpose of the Position In order to develop veterinary biological products, conduct necessary studies and compile submission dossiers, including CMC part, (under the supervision of superiors, in case of Associate Scientist). In addition, expanding the
Basic purpose of the job To contribute to execute CDMA (Clinical Development & Medical Affairs) activities in Japan according to TA (Therapeutic Area) strategy between start of preclinical development and late stages of commercialization. Accountabilities ・Strengthen
Basic purpose of the job To contribute to execute CDMA (Clinical Development & Medical Affairs) activities in Japan according to TA (Therapeutic Area) strategy between start of preclinical development and late stages of commercialization. Accountabilities ・Strengthen
Basic purpose of the job The manager of RRL JP provides strong leadership to develop and implement regulatory strategy for the assigned products/projects as RRL JP, and exercises activities which include: An integral member of the Regulatory Excellence
Company Description Checkout.com is one of the most exciting fintechs in the world. Our mission is to enable businesses and their communities to thrive in the digital economy. We’re the strategic payments partner for some of
JOB SUMMARY: Briefly state the objective of this position. JCS supports Japan Clinical Lead (JCL) activities in the development and execution of clinical development strategy for target indication(s) in assigned compound(s) to obtain regulatory approval in Japan.
Job Description SummaryThe SSO Associate Clinical Project Manager (aCPM) is accountable for the day-to-day planning, executing and reporting, (from first site initiation visit to and including study site close-out), of assigned Global Drug Development (GDD) studies
We are seeking a dedicated and experienced Japan Clinical Development Lead (J-CDL) to join our Clinical Sciences team. As a key member of the Global Clinical Sub Team (GCST), this role plays a crucial part in
Job Opportunity: Clinical Quality Japan Lead Overview Our client is seeking a Clinical Quality Japan Lead who will play a critical role in ensuring high-quality clinical development programs within Japan. Reporting to the Associate Vice President,
Job Opportunity: Pharmacovigilance Associate - Japan, Osaka About Our Client Our client is a world-leading healthcare intelligence and clinical research organization. They are proud to foster an inclusive environment that drives innovation and excellence, and they
Job Opportunity: Senior Study Start-Up Associate - Japan, Tokyo About Our Client Our client is a world-leading healthcare intelligence and clinical research organization. They are proud to foster an inclusive environment that drives innovation and excellence,
Job Opportunity: Clinical Research Associate (CRA) About the Company Our client, a global, commercial-stage, research-based biotechnology company, is focused on molecularly-targeted and immuno-oncology cancer therapeutics. With a team of over 10,500 employees across the United States,
About Our Client Our client is a world-leading healthcare intelligence and clinical research organization. Proudly fostering an inclusive environment that drives innovation and excellence, the organization welcomes you to join its mission to shape the future
Job Opportunity: Senior Biostatistician Responsibilities * Ensuring that all statistical aspects of documentation pertaining to clinical programs and non-study activities meet required standards and are statistically accurate. * Influencing study design and analysis, and defending statistical
