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Medical Information Specialist

Lambda Therapeutic Research Sp. z o.o.

  • Warszawa

    Warszawa, Masovian
  • offer expired 22 days ago
  • contract of employment
  • full-time
  • specialist (Mid / Regular)

Your responsibilities

  • Handling adverse events, medical enquiry, product enquiry, product quality complaints received from HCPs/Customers/affiliates/business partners through telephone, letter, fax, e-mail, sales representative or other company personnel, in accordance with company’s controlled documents.

  • Logging and updating of enquiry in medical Information database.

  • Preparation and communication of enquiry response in liaise with designated medical reviewer.

  • Assist designated medical reviewer for follow-up of all medical enquiry.

  • Reconciliation of medical enquires in accordance with Safety Data Exchange Agreements and company’s controlled documents.

Our requirements

  • Degree in pharmacy, nursing, life science or related discipline.

  • 1-year experience in handling medical enquiries- desirable.

  • Strong English skills (written and spoken).

  • Fluency in other European languages would be an asset.

  • Highly process driven with excellent attention to detail and ability to priorities effectively.

  • Motivated self-starter with ability to coordinate diverse priorities.

  • Good computer skills required to develop high level of understanding of Company Safety databases and proficiency in database management and information sourcing.

  • An ability to interact with staff at various levels and in various functional areas to resolve any issues that arise during reviews.

  • Excellent written and oral communication skills.

  • Ability to get on with people and function well within an interdependent team.

What we offer

  • International and dynamic working environment.

  • Employment based on an employment contract.

  • Opportunity to grow professionally.

  • Attractive benefits package.

Lambda Therapeutic Research Sp. z o.o.

Lambda Therapeutic Research Limited is a leading global Clinical Research Organization (CRO) headquartered in Ahmedabad – India, with facilities and operations in Mehsana (India), Warsaw (Poland), London (UK), Pittsburgh (USA), Las Vegas (USA) and Fargo (USA) with approximate 1500 employees across the globe. Lambda offers full spectrum clinical trial solutions and pharmacovigilance services empowered by more than 20 years of service to the biopharmaceutical and generic industry.

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Purpose of the job:

The Medical Information Specialist will act in compliance with Regulation (EU) No 1235/2010 & 520/2012, Directive 2001/83/EC & 2010/84/EU, Applicable National Laws and EMA‘s Guideline on Good Pharmacovigilance Practices (GVP). The Medical Information Specialist will operate in the context of the Lambda Therapeutics Ltd and Marketing Authorisation Holder’s (MAH) controlled documents (SOPs, WIs and Guides), relevant regulations and guidelines.

If you are interested, please send your CV in English via ‘Aplikuj’ button below.