Drug Safety Officer

Phiture; Remote; EUR 60.000 - 80.000; Vollzeit

Zusammenfassung

A global Contract Research Organization is seeking a Drug Safety Officer. The role involves handling SAE in trials, reviewing clinical study protocols, and ensuring compliance with regulatory requirements. Candidates should have 5 years of relevant experience and excellent communication skills. In this home-based position, you will contribute to safety documentation and internal support across departments, enhancing processes in drug safety. This role offers a competitive compensation package and opportunities for growth.

Leistungen

Competitive compensation package

Comprehensive benefits

Opportunities for personal and professional growth

Qualifikationen

• Experience handling SAE in clinical trials.
• Ability to work independently and in a team.
• Proficiency in word processing and spreadsheets.

Aufgaben

• Handle SAE in clinical trials and spontaneous reports.
• Review and write safety sections in clinical study protocols.
• Provide internal support to relevant departments.

Kenntnisse

5 years of relevant experience

Excellent written and verbal communication skills

Understanding of Good Clinical Practice regulations

Able to work in a fast-paced environment

Jobbeschreibung

Drug Safety Officer – home based in US, UK, Poland, Portugal or Sweden

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

As part of our CDSOphthalmology Drug Safety team you will work alongside passionate and innovative professionals to ensure our customers achieve their goals. The Drug Safety Officer is part of the Project Delivery organization and will work on handling of drug safety/vigilance issues according to company policies, SOPs and regulatory requirements.

Key Responsibilities

• Handling of SAE in clinical trials and spontaneous reports from the market, to ensure collection, assessment and entering into the safety database in accordance with the TFS/clients’ SOPs and existing demands of the authorities
• Review and approval of processed cases and AE/SAE reconciliation
• Coding of adverse event, medical history and concomitant medication according to MedDRA and WHO-Drug Dictionary
• QC and approval of coding of adverse event, medical history and concomitant medication
• Review and write the safety section in clinical study protocols
• Review of clinical trial reports/IBs from a safety perspective
• Write the safety parts in the PSUR/PBRER, DSURs, IND, NDA and other safety documents
• Literature search
• Electronic reporting to EudraVigilance
• Contribute to plans/instructions and SOPs for post approval surveillance
• Updating of templates for safety handling in specific studies/projects according to relevant SOPs
• May act as a Project Lead for Safety-only projects
• Participate in relevant meetings. Forward information to relevant members of the department or study team members
• Provide internal support to other relevant departments
• Involved in improvement projects with other relevant departments
• Actively contribute to the organization and development of routines to enhance the work at TFS
• Validation of computer applications specific for the department with respect to drug safety requirements
• Being well‑informed and updated on laws, directives and guidelines concerning handling and reporting of SAEs in clinical trials and serious as well as non‑serious events from the market (pharmacovigilance) and other safety issues
• Education and supervision of new Drug Safety personnel
• Participate in marketing activities

Qualifications

• 5 years of relevant experience
• Able to work in a fast‑paced environment with changing priorities
• Understand the medical terminology and science associated with the assigned drugs and therapeutic areas
• Understanding of the 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
• Demonstrate proficiency using typical word processing; spreadsheets desirable; and presentation software a plus

What We Offer

We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and professional growth in a rewarding environment. You’ll be joining a team that values collaboration, innovation, and making a difference in the lives of patients.

A Bit More About Us

Our journey began over 29 years ago in Sweden, in the city of Lund. As a full‑service, global Contract Research Organization (CRO), we build solution‑driven 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 decision‑making 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.