Regulatory Documents Jobs in Shanghai

Working with UsChallenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here uniquely interesting work happens every day in every department. From optimizing a production line to the latest breakthrou...

Description Role Summary Responsibilities: You will be working on projects that involve the detailed analysis and creative presentation of clinical trial data for a range of clients including the industrys most successful pharmaceutical and medical technology companies patient and public health bodi...

(Senior) Clinical Research Physician represents frontline scientific expertisefor assigned AbbVie TA development in China. Provides clinical science insights on portfolio assessment developmental plan formation protocol discussion trial quality and safety oversight registration approval and life cyc...

Work Flexibility: HybridPosition summary:Monitors assigned clinical trials to ensure data integrity and adherence to China regulations company policies and any other applicable procedures.Primary point of contact with site staff and is responsible for managing the site throughout all phases of the c...

Context & EnvironmentAs part of China Regulatory Team this position will support the Phileo Regulatory Affairs (RA) Manager and the project director in advancing the regulatory registration process for internal Project (focused on feed products). The role will take charge of preparing regulatory dos...

Work Flexibility: HybridMedical WritingPerform formal literature searches and succinctly summarize scientific content for assigned projects.Participates in post-market surveillance activities by conducting routine systematic literature reviews (e.g. screens articles against inclusion/exclusion crite...

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibilities for clin...

Job Overview:Primary contact with investigative sites during study maintenance and -when assigned- site startup activities with responsibility for collection of the required investigator and regulatory essential documents to ensure EC/IRB/Third body/Regulatory Authority submissions are made within t...

This role is for upcoming future opportunities that may arise at Fortrea.Fortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements well invite you for an interview. If youre pre-selected our recruiter will keep in touch and let you know when t...

This role is for upcoming future opportunities that may arise at Fortrea.Fortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements well invite you for an interview. If youre pre-selected our recruiter will keep in touch and let you know when t...

At Roche you can show up as yourself embraced for the unique qualities you bring. Our culture encourages personal expression open dialogue and genuine connections where you are valued accepted and respected for who you are allowing you to thrive both personally and professionally. This is how we aim...

1.    Supports the TA Head and Global TA Science Lead proposes development strategies and clinical pathways for new compound registrations in China.2.    Acts as China Local Clinical Leader to lead evidence generation working group for excellent delivery for trials in China and to assess new trial o...

BandLevel 5Job Description SummaryAbout the role: In this role you will be responsible for the scientific and medical strategy of assigned China-focused clinical trial(s) responsible for medical and scientific monitoring and reporting of quality data. May take on the duties and responsibilities of t...

Work ScheduleOtherEnvironmental ConditionsOfficeJob DescriptionAt Thermo Fisher Scientific youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier cleaner and safer. We pro...

Description Role Summary Responsibilities: You will be working on projects that involve the detailed analysis and creative presentation of clinical trial data for a range of clients including the industrys most successful pharmaceutical and medical technology companies patient and public health bod...