NEW ROLE ** Asia Pacific Regulatory Liaisons ** Expanding ONCOLOGY Pipeline ** China Or Japan ** Gain More RA Strategy And Liaison For China And Japan!

Hiring By - Biostaffic



Job Highlights

Not Disclosed

Posted 4 months ago
Job details
Job Description
My client, a SME (Small to Medium Sized) Bio-Pharmaceutical organization, is enjoying a BIG growth period and expansion due to a significant number of Regulatory approvals in their nascent Oncology pipeline specifically in rarer Oncology Indications (Solid Tumor and Haemo). As part of this, my client is #hiring for 2 new Asia Pac Key Country Partners to focus on Japan, China and HK.
What I like about these roles are:-
  • Growing Oncology Portfolio & Pipeline: our client is hitting double digit growth consistently and has over achieved its product targets early in advance by 2 years with a recent string of Regulatory approvals to their credit and many Line Extension New Indications pending (with a near 100% success rate so far)
  • Variety: you will support LEs and INDs for Bridging and Registration studies as well as Phase 1/2 INDs for NMEs – you will collaborate with the countries local teams to validate and shape clinical phase submissions not just MAAs and LEs
  • Support & Visibility: coached and led in matrix to the GRL and Global Regulatory subteam, acting as the bridge between global, the regulatory and global project team and the local affiliates’ teams
  • Focus: it is only working on international Majors not ASEAN or smaller countries so you can build up a strong working relationship with your chosen country (China or Japan), working across multiple LE New Indication filings and supporting CTAs for early stage assets (variety)
About You …
  • Prior experience in International which could be LATAM, ASEAN, ME or CE and E in Rx drug registrations; prior experience in co-developing local clinical phase OR filing strategies; prior experience means as a guide 6.5-10 plus years (we have bandwidth on package)
  • The line manager values the experience in working with challenging international Regulators as more important per se than working just one of these countries - if you have worked with Australia TGA, China FDA, SK FDA, PMDA or Health Canada or ANVISA or similar, this is sufficient!
  • Mentoring & Coaching: you will start your journey in growing with the company with the support of the team and a ‘buddy’, and the role comes with fully expenses international relocation to a central European city in a French speaking part of the world (core dossier and project team meetings are in English)
  • An interest in Oncology: you might have now or want to gain Oncology experience and be scientifically curious, and know you to use both liaison and regulatory intelligence skills to help shape more effective strategies in the region
  • You will want to develop either into strategy or eventually people management (you will coach Trainees and Industrial Rotations from the start)
About Me – How to apply!
I am retained by and working directly with the client and will help you every step of the way. To apply please contact me, Christian, at +44.207.801.3382, or send a full CV to – I look forward to hearing from you!

Benefits Offered?

  • No

Bonus Offered?

  • No

Travel Required?

  • No


  • France

Global Experience Needed?

  • No

Specialized Experience Needed?

  • No

Apply before:

  • Apr 18, 2024
Company Overview
ADV Talent Partners
ADV Talent Partners

Current Openings: 0

Advanced Regulatory, Advanced Search & Selection and our sister company ADV Talent Partners, have been operating since 2004. We recruit in the USA, UK, Europe, Switzerland and Asia Pacific - we have offices or partners in 3 different countries. We are first and foremost known for regulatory hiring and expanded on this several years ago to include physicians and experts involved in translational medicines, clinical development, commercialization and lifecycle strategies. We also cover Legal and Public Affairs. We hire for major biopharmaceutical companies and healthcare organizations in clinical, medical, drug safety, regulatory affairs and regulatory CMC, in the USA, UK, Europe and Switzerland as well as other major markets. Please contact us if you would like to talk to us about your career options on +44(0)207 801 3380 or in the US +1.855.505.1382 or alternatively, you can send an enquiry and we will respond by return to For companies wanting to see how we can enable their business to grow in new markets or therapeutic areas, especially in immuno-oncology, inflammation, or neurology and internal medicine please contact us, asking for Theo Moore or Matt Greig on US +1.855.505.1382 or +442078013382 or alternatively please contact us by email, to
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