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Medical Contact Center Assistant I - Swedish speaker

Role overview

Qualifications

  • Fluency in Swedish (C1 or higher) is mandatory
  • A degree in Pharmacy, Life Sciences, MD, VET or related fields is preferred, but equivalent experience is considered
  • Relevant experience includes working in Pharmacovigilance or Drug Safety, Clinical Data Entry/Management, Medical Affairs or Regulatory Affairs, Quality Assurance in the pharmaceutical/biotech/CRO industry

Responsibilities

  • Handle incoming communications via phone, email, fax, etc., providing accurate responses to inquiries
  • Record and report adverse events efficiently and in accordance with regulatory and internal standards
  • Support activities such as data tracking, quality control, training support, and data reconciliation
  • Collaborate across departments and maintain high standards of documentation and communication

Key facts

Other skills

  • Quality Assurance
  • Microsoft Office
  • Communication
  • Detail Oriented
  • Teamwork

About the company

Fortrea logo

Fortrea

Contract Research Organizations (CRO)

We are creative thinkers with decades of clinical trial experience who drive innovative solutions powered by insights from data and technology. As we tackle challenges in today’s world, we know that we need to be nimble and agile. That’s why we work side-by-side with our partners to eliminate inefficiencies from the process so we can help them deliver life-changing therapies faster for patients, caregivers and healthcare providers worldwide.

Company details

Company typeXLarge
IndustryContract Research Organizations (CRO)
Company size10001

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Job description

Your Role at Fortrea:

As a Medical Contact Center Assistant I, you will be the voice of support for healthcare professionals and patients, addressing medical information queries, product quality complaints, and general inquiries. You will also be responsible for receiving, recording, and reporting Adverse Drug Reactions (ADRs) in compliance with regulatory timelines and internal SOPs.

What You Will Be Doing:

  • Handle incoming communications via phone, email, fax, etc., providing accurate responses to inquiries.

  • Record and report adverse events efficiently and in accordance with regulatory and internal standards.

  • Support activities such as data tracking, quality control, training support, and data reconciliation.

  • Collaborate across departments and maintain high standards of documentation and communication.

  • Perform other assigned duties as needed.

What You Bring:

Minimum Qualifications:

  • Fluency in Swedish (C1 or higher) is mandatory.

  • A degree in Pharmacy, Life Sciences, MD, VET or related fields is preferred, but equivalent experience is considered.

Relevant experience includes working in:

  • Pharmacovigilance or Drug Safety

  • Clinical Data Entry/Management

  • Medical Affairs or Regulatory Affairs

  • Quality Assurance in the pharmaceutical/biotech/CRO industry

Safety experience includes:

  • Processing AE/SAE reports

  • Narrative generation

  • Query management

  • Using safety databases

  • Regulatory submissions

Skills & Mindset We Value:

  • Clear written and verbal communication

  • Good grasp of regulatory guidelines (ICH GCP, Pharmacovigilance standards)

  • High attention to detail and accuracy

  • Proficiency with Microsoft Office

  • Team player who can also work independently with moderate supervision

Work Environment:

Remote/ home-based – enjoy flexibility while making an impact.

Learn more about our EEO & Accommodations request here.

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MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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