Drug Safety Case Manager — Idorsia Pharmaceuticals
- Location
- Allschwil
- Contract
- full-time
- Posted
- 34 days ago
Role overview
Are you passionate about patient safety and ensuring that medicines are monitored to the highest standards?
As a Drug Safety Case Manager, you will play a critical role in safeguarding patients by ensuring accurate and timely management of safety information throughout the product lifecycle.
Working within a collaborative and highly skilled Drug Safety team, you will take ownership of adverse event case management activities while partnering closely with physicians, clinical teams, regulatory colleagues, and external partners to ensure compliance with global pharmacovigilance requirements.
- Are you passionate about patient safety and ensuring that medicines are monitored to the highest standards?
- As a Drug Safety Case Manager, you will play a critical role in safeguarding patients by ensuring accurate and timely management of safety information throughout the product lifecycle.
- Your Responsibilities: Case Management & Safety Reporting
- Manage adverse event cases from receipt through submission, including triage, data entry, medical coding, narrative writing, quality review, and expedited reporting for both clinical trial and post-marketing cases
Main responsibilities
- Your Responsibilities: Case Management & Safety Reporting
- Manage adverse event cases from receipt through submission, including triage, data entry, medical coding, narrative writing, quality review, and expedited reporting for both clinical trial and post-marketing cases
- Prioritize and process safety cases in accordance with global regulations, SOPs, and reporting timelines
- Identify missing or incomplete information and coordinate follow-up activities with Drug Safety Physicians and other stakeholders
- Monitor case workflows to ensure efficient and compliant case processing
- Support or oversee reconciliation activities to ensure data consistency across systems Clinical Trial & Cross-Functional Support
- Contribute to the successful set-up of new clinical studies by providing safety reporting documentation, reconciliation plans, monitoring guidance, and TMF documentation
- Support SAE reconciliation activities between clinical and safety databases
- Coordinate SUSAR notifications to investigators and Ethics Committees
- Collaborate with internal and external stakeholders, including CROs, to establish and maintain safety agreements and processes What You'll Bring:
Application process
- We encourage all potential candidates with diverse backgrounds of race, color, religion, sexual orientation, gender identity, age, national origin, and disability to submit their job applications.
- All applicants will receive consideration.
- We are committed to fostering respect, fairness, and equal opportunities for all job applicants and our employees.
- Please be informed that if you are selected for this position, your employment will be subject to a pre-employment background screening process, of which you would be informed in greater detail in due course.
- Idorsia Pharmaceuticals Ltd ("Idorsia") is committed to a fair and transparent application process.
- In order to avoid any conflict of interest in line with Idorsia Code of Business Conduct, which would undermine such a commitment, the applicants must disclose any personal, financial, or other outside interests interfering with the interests of Idorsia.
- Further, the applicant is obliged to disclose any and all relationships with close or affiliated persons, who are employees of Idorsia or are collaborating with Idorsia in any other contractual relationship.
- Please note Idorsia operates a strictly controlled list of preferred recruitment partners.
Contacts
- For those partners who have no valid, signed Master Service Agreement in place with Idorsia, all unsolicited resumes, CVs, anonymous profiles, or any other candidate details submitted through our website or to personal e-mail accounts of employees of Idorsia Pharmaceuticals (including any of its subsidiaries, affiliates, or related companies) are considered the property of Idorsia Pharmaceuticals and are not subject to payment of any form of introduction, placement or referral fees. now Find similar jobs: R&D Functions Technical Support
Company and context
- Excellent organizational skills with the ability to manage multiple priorities and meet tight deadlines
- Strong attention to detail, problem-solving abilities, and a collaborative mindset Fluent English, both written and spoken
- EU/EFTA citizenship is required due to permit restrictions
- Why Join Us?
- This role offers the opportunity to make a direct impact on patient safety while working in a dynamic, international environment.
- You will collaborate with experienced professionals across clinical development and pharmacovigilance, contribute to innovative clinical programs, and play a key role in ensuring the safe use of medicines. Work Location: Allschwil, Switzerland
- Business Area: Global Business Development, Drug Safety Schedule: Fulltime Job Type: Permanent Job ID : 4790
- At Idorsia, we harness the power of difference, authenticity, and inclusion to achieve business success.
Additional details
- Your Responsibilities: Case Management & Safety Reporting
- Support or oversee reconciliation activities to ensure data consistency across systems Clinical Trial & Cross-Functional Support
- Collaborate with internal and external stakeholders, including CROs, to establish and maintain safety agreements and processes
- Strong attention to detail, problem-solving abilities, and a collaborative mindset Fluent English, both written and spoken
- You will collaborate with experienced professionals across clinical development and pharmacovigilance, contribute to innovative clinical programs, and play a key role in ensuring the safe use of medicines. Work Location: Allschwil, Switzerland
- Business Area: Global Business Development, Drug Safety Job Type: Permanent
- For those partners who have no valid, signed Master Service Agreement in place with Idorsia, all unsolicited resumes, CVs, anonymous profiles, or any other candidate details submitted through our website or to personal e-mail accounts of employees of Idorsia Pharmaceuticals (including any of its subsidiaries, affiliates, or related companies) are considered the property of Idorsia Pharmaceuticals and are not subject to payment of any form of introduction, placement or referral fees.
Notes and original content
- Your Responsibilities:
- Case Management & Safety Reporting
- Support or oversee reconciliation activities to ensure data consistency across systems
- Clinical Trial & Cross-Functional Support
- What You'll Bring:
- Strong attention to detail, problem-solving abilities, and a collaborative mindset
- Fluent English, both written and spoken
- You will collaborate with experienced professionals across clinical development and pharmacovigilance, contribute to innovative clinical programs, and play a key role in ensuring the safe use of medicines.
- Work Location: Allschwil, Switzerland
- Business Area: Global Business Development, Drug Safety
Questions about this listing
What salary does Idorsia Pharmaceuticals offer for this role?
Idorsia Pharmaceuticals lists CHF 85'500 - 129'500 gross per year for this position in Allschwil. This is the salary published in the original listing (or, when the employer omits a figure, a realistic estimate for the role and sector) — the calculator on this site converts it to your actual net take-home once cross-border tax and social contributions are applied.
Is this a full-time role, and what type of contract does Idorsia Pharmaceuticals offer?
This listing is a full-time position. The contract type shown here comes directly from the employer's original posting; always confirm exact hours, notice period and probation length with Idorsia Pharmaceuticals during the application process, since these details can vary by role even within the same contract category.
Do I need a cross-border work permit for a role in Basel?
EU/EFTA residents living in the border zone of the country adjoining Canton Basel can apply for a G permit; the Swiss employer files it with that canton's migration office after the contract is signed. Border-zone rules and processing times vary by neighbouring country and canton, so confirm the specifics with Basel's cantonal migration office or with HR during the application.
How do I apply for this position at Idorsia Pharmaceuticals?
Use the "Apply now" button on this page — it links directly to Idorsia Pharmaceuticals's original listing at careers.idorsia.com, so your application goes straight to the employer's own applicant-tracking system. Frontaliere Ticino does not collect or forward applications itself.
