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Medical Sciences Director – Late Development, Blincyto

None years
$211,263 – $251,166 USD
10 Sept. 2, 2025
Job Description
Job Type: Remote Education: None Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Medical Sciences Director – Late Development, Blincyto

Location: United States – Remote
Job ID: R-219207
Date Posted: August 19, 2025
Work Type: Remote
Category: Clinical Development
Salary Range: $211,263 – $251,166 USD
(Actual salary depends on experience, skills, and qualifications.)


About Amgen

Since 1980, Amgen has been at the forefront of biotechnology, serving patients living with serious illnesses. Focused on four core therapeutic areas—Oncology, Inflammation, General Medicine, and Rare Disease—Amgen reaches millions of patients globally each year.

Our culture is science-driven, innovative, collaborative, and grounded in a shared mission: to serve patients.


Position Overview: Medical Sciences Director – Blincyto (Late Development)

As a Medical Sciences Director for Blincyto in Late Phase Clinical Development, you will provide clinical and translational science leadership to support the continued development of this oncology asset. This high-impact role offers the opportunity to shape clinical trial strategy, design, execution, and data analysis within a cross-functional, innovative, and science-led environment.


Key Responsibilities

Clinical & Scientific Expertise

  • Serve as a clinical and translational subject matter expert in oncology.

  • Support medical monitoring in ongoing clinical trials; assist in issue resolution.

  • Provide scientific leadership in the interpretation of trial data and overall clinical strategy.

Trial Design & Strategy

  • Contribute to study concept development, clinical protocol design, and related documentation.

  • Ensure integrity and scientific validity in protocol development and trial execution.

  • Support study implementation, including data review, interpretation, and reporting.

Data & Analytics

  • Lead data quality assessments and ensure adherence to regulatory and scientific standards.

  • Review trial data and support data cleaning, database lock, and statistical output review.

  • Interpret and summarize clinical findings for publications and regulatory submissions.

Collaboration & Communication

  • Work cross-functionally with translational scientists, regulatory teams, CROs, and external collaborators.

  • Represent clinical science at internal/external meetings, conferences, and leadership presentations.

  • Participate in the selection and oversight of key external partners including CROs and academic collaborators.


Basic Qualifications

One of the following combinations is required:

  • Doctorate degree (PhD, MD, PharmD) + 4 years of life sciences/healthcare experience

  • Master’s degree + 7 years of life sciences/healthcare experience

  • Bachelor’s degree + 9 years of life sciences/healthcare experience


Preferred Qualifications

  • 5+ years in pharmaceutical clinical drug development

  • Late-phase oncology trial experience, especially in hematologic malignancies

  • Demonstrated experience in clinical trial process improvement

  • Track record in:

    • Designing, monitoring, and implementing oncology clinical trials

    • Regulatory submissions and writing clinical response documents

    • Data analysis using tools like Spotfire

    • Authorship of publications and presentations at scientific conferences

  • Strong understanding of GCP and global regulatory standards

  • Excellent written and verbal communication skills, including ability to simplify complex data

  • Ability to collaborate in a matrixed, cross-functional environment


What Amgen Offers

Amgen is committed to supporting your well-being, career development, and financial security. Our Total Rewards Plan includes:

Compensation & Benefits

  • Competitive base salary + annual discretionary bonus

  • Stock-based long-term incentives

  • Comprehensive benefits:

    • Medical, dental, and vision coverage

    • Life and disability insurance

    • Flexible spending accounts (FSAs)

    • Retirement and Savings Plan with company contributions

Work-Life Balance

  • Flexible remote work arrangements (where possible)

  • Award-winning time-off policies

  • Bi-annual company-wide shutdowns

Professional Growth

  • Career development and leadership opportunities

  • Access to training, learning programs, and scientific communities


Application Details

Deadline:
There is no application deadline. Applications are accepted until the position is filled.

Equal Opportunity Employer:
Amgen is an Equal Opportunity Employer, committed to a diverse and inclusive workforce. We welcome applications from all qualified individuals, regardless of race, gender, age, disability, or background.

Accommodation:
Amgen provides reasonable accommodations to individuals with disabilities during the application and hiring process. Please contact us if you need assistance.


Ready to Make an Impact?

Apply now and become part of a team that is transforming science and transforming lives.
🔗 Apply at: careers.amgen.com