Junior Study 招聘 在 Shanghai - 16 Job Positions Available

As the Associate Principal Scientist - Sensory, you are part of the Global Science & Innovation Team and play a key role in partnering with Technical Service team in APAC, Global applications & Ingredient Science with

JOB REQUIREMENTS: Academic / Professional Qualification / Working Experience * Advanced SAS programming knowledge * 2 or 5+ years of working experience in Pharmaceutical industry * BSc or higher degree in Mathematical, Statistical, Computer Science or

Responsible for providing technical leadership as compound or indication lead within a cross-functional team to design, execute, analyse and interpret clinical studies. Ensures projects (including multiple studies) adhere to Good Clinical Practice and regulatory requirements. Typical Accountabilities Provides

Build a career with confidence Carrier Global Corporation, global leader in intelligent climate and energy solutions is committed to creating solutions that matter for people and our planet for generations to come. From the beginning, weve

Requisition ID: 100304 Job Category: Engineering Location: Shanghai, 31, China Join a company that is passionately committed to the pursuit of a better world through positive change. With more than 70 years of business and technical

SUMMARY OF THE ROLE You will own key assays and workflows for CAR design, T-cell engineering, and in vitro functional characterization. You will work with project teams to make data-driven decisions to move programs from discovery

Job Overview Acts as Lead Medical Writer on more advanced writing projects (e.g. complex clinical study reports, protocols, more challenging indications, or customers). Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements

When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every

Job Overview: Collaborate with peers across the organization to achieve client-centric delivery in a matrix organization. Collaboration across all stakeholders within Site Readiness. Oversight and accountability of Regulatory Authority (RA), Independent Review Board (IRB)/Ethics Committee (EC)

Job Overview: The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Senior CRA I assure the implementation of

Typical Accountabilities: Takes medical responsibilities to ensures successful conduct and integrity of all in-scope clinical studies Work as China study physician in China-join global studies, PK studies or country-specific clinical initiatives under the supervision from program/study lead physicians. Contributes to study design