Intern Safety Data Specialist - Pharmacovigilance Management

Data: 2018-12-06

Location: Warsaw, PL

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Requisition ID: CLI008162

Have you heard about MSD? 


MSD is an innovative, global healthcare leader committed to improving health and well-being in 140 countries around the world. We continue to focus our research on conditions that affect millions of people around the world - diseases like Alzheimer's, Diabetes and Cancer - while further expanding our strengths in areas such as vaccines and biologics. 


We aspire to be the best healthcare company in the world and are dedicated to providing leading innovations and solutions for tomorrow. 


MSD’s Global Human Health (GHH) Division abides by a “patient first, profits later” ideology. Results-driven and ambitious, this team of individuals represents a functional balance between meeting company objectives and the needs of people around the world. The division is comprised of sales and marketing professionals who are passionate about their role in bringing MSD's prescription medicines, vaccines, and other medical products to our customers worldwide.


 Opportunity we offer :


 Under the direction of a manager and direct supervision of a SDS/Senior SDS/Lead SDS, the Intern Safety Data Specialist (SDS-Intern) is responsible for analyzing, triaging and processing of all adverse experience information received for investigational products, according to standard operating procedures (SOPs) for further reporting to worldwide regulatory agencies by Global Pharmacovigilance. In addition, the SDS-Intern collaborates with other staff within the organization, as well as cross-functionally.


 Global Pharmacovigilance Case Management (GPVCM) - 100%


 Core activities include, but are not limited to:


  • Performing data entry of adverse experience information from investigational environment or processing another, homogenous type of safety reports (e.g. regulatory forms).

  • Through daily case prioritization activities, completing reports within the established timeframes to ensure compliance with internal, business partner (BP), and regulatory agency reporting requirements worldwide.

  • Participating in training and certification activities for Global Pharmacovigilance Case Management (GPVCM).



Expected Qualification of YOURS :



  • A bachelor's degree and above, preferably in medicine, pharmacy, nursing or biological sciences.




  • Excellent organizational, workload prioritization and time management skills.

  • Excellent overall communication skills with advanced oral and written English skills.

  • Advanced computer skills.

  • Independent, strong analytical and problem solving skills.

  • Good sense and awareness of regulations and policies.

  • Ability to work under time pressure in a changing environment with flexibility.

  • Strong sense of responsibility and accountability


We offer:


  • Competitive remuneration

  • Position in a leading global healthcare company

  • Challenging career

  • Professional growth based on performance



Your role at MSD is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At MSD, we’re inventing for life.



Job: Clinical Data Management
Other Locations:
Employee Status:
Travel: No
Number of Openings:
Shift (if applicable):
Hazardous Materials:
Company Trade Name: MSD

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