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Drug Safety Officer
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Drug Safety Officer

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1 Vacancy
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Job Location

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Solna - Sweden

Monthly Salary

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Not Disclosed

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Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Req ID : 2841064

TFS HealthScience is a leading global midsize Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes fullservice capabilities resourcing and Functional Service (FSP) solutions.

The Drug Safety Officer is an integral part of the Project Delivery organization responsible for managing drug safety/vigilance issues in compliance with company policies SOPs and regulatory requirements.

This position is temporary and is available for a duration of one year with the potential for extension based on business needs.

Key Responsibilities:

  • Manage Serious Adverse Events (SAEs) in clinical trials and spontaneous reports from the market ensuring meticulous collection assessment and entry into the safety database.
  • Review and approve processed cases conducting AE/SAE reconciliation.
  • Code adverse events medical history and concomitant medication.
  • Write safety sections in study protocols and clinical trial reports/IBs.
  • Prepare safety documentation for regulatory submissions.
  • Conduct literature searches and contribute to postapproval surveillance plans.
  • Participate in safetyonly project leadership and relevant meetings.
  • Provide internal support contribute to improvement projects and enhance departmental routines.
  • Validate computer applications and stay updated on pharmacovigilance regulations and guidelines.
  • Educate and supervise new Drug Safety personnel and support marketing activities.

Position Requirements:

  • Bachelors Degree preferably in life science or nursing; or equivalent.
  • Relevant experience within the same field.
  • Ability to work in a fastpaced environment with changing priorities.
  • Understanding of medical terminology and science associated with assigned drugs and therapeutic areas.
  • Understanding of Good Clinical Practice regulations ICH guidelines Pharmacovigilance legislation and internal SOPs.
  • Ability to work independently as well as in a team matrix organization with little or no supervision.
  • Excellent written and verbal communication skills.
  • Proficiency in typical word processing; spreadsheets desirable; presentation software a plus.

A Bit More About Us:

Our journey began over 27 years ago in Sweden in the city of Lund. As a fullservice global Contract Research Organization (CRO) we build solutiondriven teams working towards a healthier future. Bringing together over 800 professionals TFS delivers tailored clinical research services in more than 40 countries with flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology Neuroscience Oncology and Ophthalmology.

Our core values of Trust Quality Passion Flexibility and Sustainability are our guiding light serving as the framework for decisionmaking at all levels of the organization. They assist us in attracting and retaining valuable talent who share our sentiments resulting in high employee engagement and satisfaction. By aligning on these fundamental values we cultivate a unified force geared towards innovation and excellence. This collective effort propels us towards our shared goal and fosters a culture of mutual respect and collaboration.

Together we make a difference.


Employment Type

Full Time

Company Industry

About Company

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