上海招聘

1. Support administrative document order
2. Support project responsible colleagues on PSUR submission
3. Protocol notification to healthy authorities
4. Accountable to use TVT and AQWA system for updated BPI/Label implemen-tation
5. Consolidate updates or needed information from DRA project responsible col-leagues
6. Make necessary variation submission and follow up as necessary
7. Take assigned tasks from the line manager and department head instruction
8. Participates in other department activities / initiatives as required
9. Execute daily operation compliance with DRA SoPs/ICC/ACC/NVS code/NP4

RPS Inc. is a next generation global CRO, headquartered in the United States with the operations in 45 countries throughout Americas (US, Canada, Latin America), EMEA and Asia Pacific regions. RPS provides comprehensive global Phase 1-4 clinical development solutions to the pharmaceutical, biotechnology and medical device industries. By combining an experienced clinical research operations infrastructure with the industry’s largest resourcing engines, RPS is uniquely positioned to offer our Clients both integrated and full service global outsourcing solutions. These solutions are powered by highly experienced and seasoned study teams providing innovative, cost-effective and high quality services.


RPS Asia Pacific Headquarters is located in Beijing, China and we have operations in 11 Countries in Asia Pacific region. With the rapid organic expansion of RPS in China & Asia Pacific, we are continuously looking for the experienced industry talents to join us.


Our specialized staff of consultants is eager to discuss your career plans. Tell us about yourself experience, so the appropriate consultant can contact you. RPS is sensitive to your daily responsibilities. Tell us EXACTLY how to contact you and we will. For your convenience, you can also submit your resume. We look forward to discussing the opportunities and benefits of employment with RPS!


For more information, please visit our website www.rpsweb.com.