Clinical Associate Regulatory Submissions - Vienna

As Regulatory & Start-Up Specialist, you will work and lead complex projects under general supervision, serve as Single Point of Contact in assigned studies for investigative sites, Site Activation Manager, Project Management team, and other departments as necessary. · ...

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. · ...

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 ...

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 ...

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. · ...

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 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 ...

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 ...

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. · This role is an excellent opportunity for professionals with experience in clinical start-up operations, budget/contract negotiations, and regulato ...

We are hiring a Business Development Lead, European Public Sector to support and contribute to our EU/EEA growth function. This senior individual contributor role supports end-to-end capture for non-dilutive funding and partnerships across key European agencies. · ...

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 ...

The Regulatory Affairs Lead Austria is responsible for leading the local CHC Regulatory team in Austria, · ensuring compliance of the existing CHC portfolio, effective and timely approval of all marketing authorizations, · maintenance, provide appropriate input on the development ...

Your role at Dynatrace · Dynatrace seeks a knowledgeable and globally experienced Strategic Lead for HR Compliance, Reporting and Mobility. You will lead on defining the strategy, developing and execute our global compliance reporting and global mobility programs. · This role is ...

We are seeking highly qualified candidates to fill the position of Clinical Scientist (CS) responsible for executing and overseeing observational, epidemiological, non-interventional, pragmatic, and low-interventional studies. · ...

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. · ...

This role promises to offer intentional career growth and professional development. You'll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas and in covering projects. · ...