更新于 3月12日

Safety & PV Specialist - 工作時間(周一至周五15:30-0:30)

1.2-1.5萬
  • 大連甘井子區(qū)
  • 1-3年
  • 本科
  • 全職
  • 招2人

職位描述

藥品警戒
工作時間:周一至周五15:30-0:30
主要職責(zé):PV中英互譯,Argus系統(tǒng)中的bookin及其他涉及業(yè)務(wù)
工作地點(diǎn):可全國任何城市homebase

JOB SUMMARY

Assists in all aspects of the collection, processing, and reporting of individual cases safety reports (ICSR), adhering to all data privacy guidelines, Good Clinical Practices (GCPs), Good Pharmacovigilance Practice (GVP), regulatory guidelines, company and project/program-specific procedures for clinical trials and/or post-marketing safety programs.

JOB RESPONSIBILITIES

? Enter information into PVG quality and tracking systems for receipt and tracking ICSR.
? Assists in the processing of ICSRs according to Standard Operating Procedures (SOPs) and project/program-specific safety plans.
o Triages ICSRs, evaluates ICSR data for completeness, accuracy, and regulatory report ability.
o Enters data into safety database.
o Codes events, medical history, concomitant medications and tests.
o Compiles complete narrative summaries.
o Identifies information to be queried and follows up until information is obtained and queries are satisfactorily resolved.
o Assists in the generation of timely, consistent and accurate reporting of expedited reports in accordance with applicable regulatory requirements.
? Ensures all relevant documents are submitted to the Trial Master File (TMF) as per company SOP/Sponsor requirements for clinical trials and the Pharmacovigilance System Master File for post-marketing programs as appropriate.
? Maintains understanding and compliance with SOPs, Work Instructions (WIs), global drug/biologic/device regulations, GCPs, ICH guidelines, GVP, project/program plans and the drug development process.

QUALIFICATION REQUIREMENTS

? Bachelor’s Degree in life science, registered nurse, pharmacist or an equivalent combination of education and experience that gives the individual the necessary knowledge, skills and abilities to perform the job.
? Safety Database systems and knowledge of medical terminology required
? Good understanding of clinical trial process across Phases II-IV and/or post-marketing safety requirements, ICH GCP, GVP and regulations related to Safety and Pharmacovigilance
? Proficiency in Microsoft Office Suite (Word, Excel and PowerPoint), Visio, email (Outlook), TeamShare (or other management/shared content/workspace) and internet.
? Ability to work independently and in a team environment
? Good communication and interpersonal skills, both written and spoken
? Good organizational skills with proven ability to prioritize and work on multiple tasks and projects
? Detail oriented with a high degree of accuracy and ability to meet deadlines

工作地點(diǎn)

大連騰飛園區(qū)在家辦公

職位發(fā)布者

JeremyGu/TA

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Syneos Health賽紐仕醫(yī)藥是一家全面整合生物制藥解決方案的公司,旨在幫助客戶加快推出新療法的速度。我們站在產(chǎn)品研發(fā)的角度,戰(zhàn)略性地融合臨床研發(fā)、醫(yī)學(xué)事務(wù)和商業(yè)能力,以及時應(yīng)對市場變化。Join a game-changing company that is reinventing the way therapies are developed and commercialized. Created through the merger of two companies, INC Research and inVentiv Health, we bring together more than 22,000 clinical and commercial minds to create a better, smarter, faster way to get biopharmaceutical therapies into the hands of patients who need them most. Evolve in a global company that is always looking for ways to work smarter and more efficiently as the only fully integrated Biopharmaceutical Accelerator. You'll be supported with comprehensive resources based on today's emerging technologies, data, science and knowledge- instead of practices from the past. Teaming with some of the most talented professionals in the industry, you'll gain exposure and work in a dynamic environment to over-deliver and outperform. A career with Syneos Health means your everyday work improves patients’ lives around the world.
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