As part of PAREXEL Consulting, you will create and maximize value for clients throughout the product lifecycle. You will be a strategic guide in getting products to market faster, smarter – and keeping them there –your scientific, technical, regulatory, and/or commercial expertise will put best practice standards to work for biopharmaceutical and medical device companies large and small.
In return, you will be provided with interesting opportunities for growth and development and exposed to a variety of challenging assignments, product types, geographic regions, and therapeutic areas. Plus, as member of PAREXEL Consulting, you will enjoy all the advantages of working remotely, combined with access to the mentorship from a team of highly experienced regulatory professionals at the height of their careers. Join our team, and you will design solutions for the complexities of an ever-changing global marketplace.
What makes a successful Consultant at PAREXEL? Check out the top traits we're looking for and see if you have the right mix.
"They say if you are passionate about what you do, you will never work a day in your life. I can honestly say that this applies to me. I love what I do."Jasen - Consultant
"My experience so far with PAREXEL has been great! I had initially started at PAREXEL as an Independent Consultant but was then presented with a full time job opportunity to really become a part of this fascinating company. I have enjoyed the flexibility to be able to orchestrate a good work/life balance, as well as learn from so many experts in consulting arena and really have a hands-on role with every day bringing a new but exciting challenge."Aqip – Consultant
"I was offered an incredible opportunity to continue my career in regulatory affairs without relocating 1,000 miles away and making major life changes. PAREXEL is an innovative, growing company which offers much needed flexibility and opportunities for professional growth."Blaine – Consultant
"PAREXEL is a very large organization and holds a top position amongst the different companies engaged in the Consulting business. It can offer many opportunities for development and career progression. Also the diversity of projects can offer a great expansion of knowledge in many areas of the Regulatory Affairs arena. Last (but not least), PAREXEL offers a variety of rewards to the employees (bonus scheme, benefits etc)."Giannis – Consultant
"PAREXEL is a CRO that I had always inspired to join because of the variety of knowledge, experts, culture, flexibility and exposure to be client facing as well as to use my technical knowledge all under a professional and diligent environment. I believe it has provided me the right platform to grow both professionally and individually with the opportunities to present my views and to dialogue with colleagues and clients with all but positive outcomes."Aqip – Consultant
We are one truly global team working together to propel each client´s journey ahead faster.
We value work-life balance. We try and keep regular hours and an emphasis on life outside the office.
Work with industry leaders and subject matter experts.
The ability to innovate, ask “what if” and try new solutions without fear of failure.
Opportunities to work on multiple accounts – never boring!
Strong management with depth of experience working for global health authorities.
Ein Consultant sollte ein gutes Verständnis der durch PAREXEL angebotenen Dienstleistungen besitzen. Ein Consultant sollte darüber hinaus über solide fachliche Expertise verfügen und in der Lage sein, sich weitergehendes Expertenwissen anzueignen.
Ein Consultant sorgt für die zeitgerechte Ausführung der zugewiesenen Aufgaben innerhalb der vorgegeben Projektparameter und entsprechend den Qualitätsanforderungen des Kunden und PAREXELs.
- Das Erstellen klinischer Zulassungsdokumente (MAA, IMPD, IND, NDA, BLA), Dokumente zur Arzneimittelsicherheit (PSUR, DSUR, RMP), Orphan Drug Applications, Paediatric Investigational Plans etc.
- Teilnahme an Diskussionen bezüglich regulatorischer Strategien mit allen beteiligten Interessengruppen, mit Unterstützung erfahrener Kollegen
- Vertrautheit mit Zulassungsverfahren in Deutschland, idealerweise inklusive nationaler Zulassungen, Zulassungspflege, Labelling und Behördenkontakt
- Entsprechende Expertise in Bezug auf die Schweiz und Österreich von Vorteil
- Fortgeschrittene Deutschkenntnisse in Wort und Schrift
- Erfahrung mit der Erstellung von klinischen CTD Dokumenten (Modul 2.5/2.7)
- Kritisches Denken
- 5 Jahre Erfahrung im regulatorischen Umfeld
- Gute Projektmanagement Fähigkeiten
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