Clinical Associate Regulatory Submissions - Vienna

Clinical Associate Submissions – Regulatory · Austria, SwitzerlandIQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. · agile structure, collaborative culture, and deep therapeut ...

Shape the future of regulatory excellence at IQVIA. As a Regulatory Affairs Specialist, you will play a key role in ensuring compliance and supporting successful product lifecycle management across Germany, Switzerland, and Austria. · ...

Position: Regulatory Affairs Manager – Medical Devices · Level: Mid-Level or Senior · Type: Internal, Full-time · Location: Kufstein or Vienna, Austria (work permit provided for non-EU employees, must be willing to relocate) · Job description: This is a full-time role for a Regul ...

At IQVIA we advance healthcare by helping clients bring safe medicines to patients As a Regulatory Affairs Specialist you will play a key role in ensuring compliance and supporting successful product lifecycle management across Germany Switzerland and Austria You ll collaborate w ...

Role Overview · The Regulatory Compliance Lead is responsible for overseeing and strengthening the firm's regulatory compliance framework across applicable jurisdictions. This role plays a critical part in supporting global expansion, ensuring regulatory compliance, and enabling ...

Job Title: QA/RA Lead · Employment Status: Full-time · Office Hours: Mon, Wed, Fri with WFH option on Tue & Thu · Location: Vienna, Austria · Compensation: Starting from 90,000 EUR gross base salary + performance-based bonus and equity options. Compensation may be negotiated base ...

We are looking for a Clinical Start‑Up Contract & Finance Specialist to support clinical trial start‑up activities across Austria. This role is an excellent opportunity for professionals with experience in clinical start‑up operations, budget/contract negotiations, and regulatory ...

We are looking for a Clinical Start-Up Contract & Finance Specialist to support clinical trial start-up activities across Austria. · Drive and oversee clinical trial country submissions and approvals for assigned protocols. · Negotiate investigator budgets, manage financial forec ...

Job Title: QA/RA Lead · Employment Status: Full-time · Office Hours: Mon, Wed, Fri with WFH option on Tue & Thu · Location: Vienna, Austria · Compensation: Starting from 90,000 EUR gross base salary + performance-based bonus and equity options. Compensation may be negotiated base ...

This is an exciting opportunity to join our Research & Development team as a Regulatory Information Management Specialist. · Delivering high-quality regulatory information management services for Grünenthal. · ...

Job Title: QA/RA Lead · Employment Status: Full-time · Office Hours: Mon, Wed, Fri with WFH option on Tue & Thu · Location: Vienna, Austria · Compensation: Starting from 90,000 EUR gross base salary + performance-based bonus and equity options. · Final compensation is negotiable ...

We're continuously exploring innovative new treatment options to make a stronger impact on patients' lives in Research & Development. · You'll work with talented colleagues in R&D environment developing medicines that change lives. · ...

Job summaryProject Manager Tech Transfer & Operational Excellence in Pharma/Biopharma Europe Hybrid · Degree in Life Sciences Pharmacy Chemistry Engineering or related discipline · ...

· This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Senior Legal Counsel - Regulatory in Austria. · Join a dynamic legal team at the forefront of global workforce innovation. In this role, you will provide strategic regulatory gu ...

This is a full-time role for a Regulatory Affairs Manager with flexible location based in Austria. · The position will offer the opportunity to work with a global cross-functional team, supporting medical device design stage initiatives while gaining exposure to various technolog ...

Role Overview · The Regulatory Compliance Lead is responsible for overseeing and strengthening the firm's regulatory compliance framework across applicable jurisdictions. This role plays a critical part in supporting global expansion, ensuring regulatory compliance, and enabling ...

We are looking for a Platform Compliance Manager with a strong focus on audits. In this role, you drive the planning, execution, and successful closure of platform, security, and regulatory audits across multiple markets. You'll interpret compliance requirements, translate them i ...

We are leveraging the human immune system to unlock safer, more effective drugs.We believe immunotherapies are the future of medicine, but their discovery is hindered by outdated models that fail to capture the complexity of the human immune system. · ...

Join IQVIA Biotech as a Clinical Research Associate 2 / CRA 2 to work home-based throughout Germany and preferably in the Munich or Hamburg area. You will enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with ou ...

Join us as our Global Manufacturing Sciences CMC Lead and drive high-impact, · high-visibility CMC projects for innovative biologics in a dynamic global environment. · Advanced degree (Master's or higher preferred) in engineering or life sciences. · At least 10 years of experienc ...