Covance Associate Drug Safety in Shanghai, China

Job Overview

Are you a Drug Safety Associate who wants to work with one of leading global CROs in the industry? Covance is seeking Drug Safety Associatewith at least 1 year PV experience. Whether you’re ready to make a move or just interested in learning more, apply TODAY and let’s talk together!

Covance China is committed to providing a clinical research career with purpose in a culture that values achievement. By joining our Clinical Trial Operations Team, you will work in a collaborative environment with the flexibility to pursue different clinical trials involving various compounds - giving you an excellent overview of best practices across the industry. Experience the global reach and therapeutic record of success from one of the few truly global drug development companies positioned to provide comprehensive clinical support from First-in-Human studies.

Responsibilities/Duties:

  • Responsible for day-to-day adverse experience case management within the country(ies) covered by the country operation including case intake and follow-up activities in accordance with Global Safety procedures, the review of local literature as per Merck’s procedure and country regulations, and health authority submissions of cases in accordance with Global Safety procedures and health authority requirements.

  • Responsible for aggregate safety report submissions in the country(ies) in accordance with Global Safety procedures and health authority requirements.

  • Responsible for the reconciliation of adverse events reports received from other Merck operating units (e.g., Designated Point of Contact, Medical Information, etc.) and contractual partners, as applicable Responsible for the filing, storage and archiving of safety-related data in accordance with Merck’s policies and local requirements.

  • Serve as the local Deputy Qualified Person for PV (QPPV) / deputy local responsible PV person for the country(ies) when delegated by PV Country Lead.

About Covance:

Covance is one of the world’s largest and most comprehensive drug development services companies, with more than 11,000 employees in 60 countries. We began operations in Asia Pacific in 1988 and today have more than 1000 employees in 14 countries across the region. Through our discovery, nonclinical, clinical and commercialization services, Covance has helped pharmaceutical and biotech companies develop one-third of all prescription medicines in the market today.

Why Covance China?

At Covance China, you will join like-minded professionals who, together, build our reputation as one of the world's largest and most respected contract research organizations. In choosing Covance China, you will be part of a dedicated team that makes a difference in helping to deliver life-saving and life-enhancing medicines to people around the world.

We Offer

Covance’s ongoing success offers team members unsurpassed growth and career development opportunities. At Covance China, we help make the miracles of medicine a reality. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career.

There is no better time and choice to join us!

Education/Qualifications

  • The incumbent must have a health, life science, or medical science batchelor degree or equivalent by education / experience.

Experience

  • He/she should have at a minimum 1 year of pharmaceutical industry experience.

  • He/she must have an awareness of Pharmacovigilance regulations within his/her assigned country(ies).

  • The PV Specialist is expected to have strong communication and time management skills, and have the ability to work independently with minimal supervision.

Job Number 2018-19943

Job Category Clinical Operations

Position Type Full-Time

Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran/Sexual Orientation/Gender Identity). Your confidentiality and privacy are important to us.