Pharmacovigilance Specialist
Poland
City: Warsaw
Type of Contract: Permanent

Duties:


- Processing adverse events information in a global database based on source data using medical knowledge

- Quality control of entered data, ensuring consistency and compliance with formal requirements
- Substantive cooperation with international teams in order to ensure the highest quality of reporting and work efficiency
- Participation in projects increasing the innovation of the Safety and Clinical Data Management Services
 

Requirements:


- University degree in the field of medicine, pharmacy, nursing, veterinary medicine, dentistry, obstetrics, medical analytics, physiotherapy, medical biology, biotechnology, bioinformatics

- Very good written and spoken English language (B2-C1 level), particularly in usage of medical terminology
- Computer literacy and ease of learning new computer systems and applications
- High level of organizational skills, ability to follow procedures, good time management and ability to set priorities
- Ability to solve problems, person with high analytical skills and detail-oriented who can work independently, ready to adequate feedback reception
- Ability to go extra mile and create friendly working atmosphere based on mutual respect
 

We offer:
 

- Employment based on stable employment contract with trial period
- Attractive private medical care package, sports card, group life insurance and lunch card
- Employee referral bonus
- Entering new growth possibilities as part of the KCR Placement team, cooperating with one of the largest, innovative international pharmaceutical companies with an established position globally.
- Open culture
- Empowering environment to share ideas
- Peer Buddy Mentor introducing you to the organization
- Smooth takeover of duties via 3-step onboarding process
- Remote working options
- Training program and mentoring related to clinical trials, soft skills etc.

 

 

Recruitment process was completed

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