Drug Safety Case Manager

Overview:

We are seeking a dynamic and experienced Drug Safety Case Manager, to join our team in Allschwil, Switzerland. As a Drug Safety Case Manager, you will be responsible for processing adverse event reports in compliance with global regulations and SOPs. This is a full-time position with a desired start date in April/May, for a duration of 12 months.

Responsibilities:

• Manage adverse event case reports, including triaging, data entry, coding of AEs, narrative writing, quality control, and submission of expedited AE reports to health authorities.
• Prioritize cases according to SOPs to ensure timely submission of expedited reports to regulatory authorities.
• Identify missing information and initiate follow-up requests in collaboration with Drug Safety Physician.
• Monitor workflow and work lists to ensure all cases are prioritized and processed appropriately.
• Perform or oversee reconciliation activities

Qualifications:

• University degree in life sciences (pharmacy, nurse), or equivalent education in a health-related field.
• At least 5 years' experience in safety or clinical data management.
• Knowledge of medical terminology and general understanding of disease processes.
• Solid knowledge of coding thesauri and medical/drug dictionaries.
• Good knowledge of EU and US safety reporting requirements.
• Excellent organizational and problem-solving skills, interpersonal skills, and the ability to work under pressure and meet short timelines.
• Fluency in English, both verbal and written.

Day-to-day:

As a Drug Safety Case Manager, you will be responsible for processing adverse event reports, collaborating with the Drug Safety Physician, and ensuring timely submission of expedited reports to regulatory authorities. You will also monitor workflow and work lists to prioritize and process cases appropriately.

Benefits:

• Competitive salary.
• Opportunity to work in a team-oriented environment.
• Gain experience in compliance with global regulations and SOPs.
• Professional development opportunities.

Apply:

If you are a professional with a strong background in drug safety and clinical data management, and are looking for an engaging opportunity in Allschwil, Switzerland, we encourage you to apply for this position. Join our team and make a meaningful impact in drug safety management.

It is essential that applicants hold entitlement to work in Switzerland. Please quote job reference in all correspondence.