ED/VP, Medical Science & Strategy – Oncology

🕒 August 24

🇬🇧 United Kingdom – Remote

⏰ Full Time

🔴 Lead

👔 Vice President

👻 Ghost score 19%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1956

🏥 Healthcare

📦 Logistics

🏭 Manufacturing

Healthcare • Logistics • Manufacturing

Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.

📋 Description

• Ensure the highest possible quality of input into significant requests for proposals, including development strategy and regulatory issues, drug class issues, protocol and indication considerations including safety, team education, client physician interactions, and identifying business opportunities • Support proactive client engagement with therapeutic area leaders and senior directors • Develop and support strategic alliances • Participate in client governance and advisory boards • Provide industry-standard product development plans and top-level clinical trial protocol designs through PPD’s consulting practice • Provide therapeutic and developmental expertise to internal teams • Deliver indication-specific training for clinical teams • Guide clinical trial execution • Author and review Investigator Brochures, clinical study reports, NDA/MAA clinical packages, and other regulatory briefing documents • Contribute to feasibility study design and reporting • Liaise with investigators and KOLs • Mentor and supervise clinical scientists • Participate in multidisciplinary teams and working groups contributing to innovative initiatives • Travel to China, with relocation potentially considered

🎯 Requirements

• MD or equivalent required • Certified Oncologist with at least 5+ years’ experience in pharmaceutical industry leading clinical development of at least one asset from discovery through registration • Proficient in spoken and written English and Mandarin • Active medical license preferred but not required • Able to work in a matrix organization • Able to demonstrate decisive, customer driven, flexible thinking, smart-risk taking and continuous improvement behaviors • Leads, influences and motivates staff within and across departments • Strong in presenting and communicating complex information clearly • Able to deal with sensitive and confidential issues • Possesses a “can do” attitude and is capable of implementing and following through on activities / projects • Flexibility to travel domestically and internationally

🏖️ Benefits

• Competitive salary and benefits • Mentorship and training • Work diversity, exposure to several assets in different stages of clinical development from several clients • Exciting work environment • Full time position