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Why this grade This listing scored 27/100, which is an F. It lost the most ground on pay transparency. See the breakdown
- Description depth 20 / 20 How much the posting actually says about the work, measured in characters of real text.
- Remote clarity 8 / 15 Whether "remote" means anywhere, or is quietly restricted to one country.
- Corroboration 5 / 10 Whether more than one source carries this listing.
- Freshness 4 / 15 How recently it was posted. Older postings are likelier to be filled or abandoned.
- Role specificity 0 / 10 Whether the listing is tagged well enough to tell what the role actually is.
- Pay transparency 0 / 25 A published salary range, worth more than any other single factor because it is what a candidate cannot find out without applying.
-10 Ghost-job penalty — Deducted for signals that this posting may not be a real, currently-open role — staleness, repeated relisting, or talent-pool language.
Every figure above is arithmetic over the posting itself — its salary field, its text, its age, its tags and how many sources carry it. How the grades work →
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.
Originally posted on Himalayas
Apply for this role Opens himalayas.app — the link as listed; we have not yet verified it is the employer's own page
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Where this listing came from
- 06 Aug 2026 Himalayas first sighting
Seen on 1 board over 0 days.