ED/VP – Medical Science & Strategy – Oncology, Mandarin Proficiency

Thermo Fisher Scientific

. Drive strategic and measurable business outcomes for Oncology medical science and strategy .

Posted 10/19/2026full-timeRemote • Oregon • United States, CanadaLead💰 $200,000 - $400,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Oncology clinical development, including strategic planning, regulatory compliance, and protocol design. Proficient in client engagement and mentorship within multidisciplinary teams, with strong communication skills in English and Mandarin.

Highest-signal resume keywords

MD Or EquivalentCertified OncologistClinical Development LeadershipRegulatory Briefing Document AuthoringBilingual Proficiency In English And Mandarin

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial Protocol DesignInvestigator Brochure AuthoringNDA/MAA Clinical Package PreparationFeasibility Study DesignDrug Class Issues Analysis

Soft Skills

Strong Presentation SkillsEffective CommunicationMentoring And SupervisingInfluencing And Motivating StaffDealing With Sensitive Issues

Certifications & Qualifications

Active Medical License Preferred

Industry Keywords

OncologyClinical ResearchPharmaceutical IndustryStrategic Alliance DevelopmentClient Governance

About the role

Key responsibilities & impact

Drive strategic and measurable business outcomes for Oncology medical science and strategy
Provide high-quality input into significant requests for proposals, including development strategy, regulatory issues, drug class issues, protocol and indication considerations, safety, and team education
Engage with client physicians and indication leaders before and during bid defenses
Identify business opportunities for the PPD clinical research business
Conduct proactive peer-to-peer client engagement with therapeutic area leaders and senior company directors
Support strategic alliance development, client governance, and advisory boards
Provide product development plans and clinical trial protocol designs through PPD’s consulting practice
Provide indication-specific training and guidance during clinical trial execution
Author and review Investigator Brochures, clinical study reports, NDA/MAA clinical packages, and regulatory briefing documents
Contribute to feasibility study design and reporting
Liaise with investigators and key opinion leaders
Mentor and supervise clinical scientists
Participate in multidisciplinary teams and working groups supporting innovative initiatives

Requirements

What you’ll need

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
Must be legally authorized to work in the United States or Canada without sponsorship
Must be able to pass a comprehensive background check, including drug screening where applicable
Must be able to work with some overlap to support China working hours
Active medical license preferred but not required
Able to work in a matrix organization
Able to lead, influence and motivate staff within and across departments
Strong presentation and communication of complex information
Able to deal with sensitive and confidential issues
Capable of implementing and following through on activities and projects
Flexibility to travel domestically and internationally

Benefits

Comp & perks

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