Overview

As a Clinical Scientist Director in Early Development Oncology, you translate scientific strategy into actionable clinical execution in early-phase trials. You provide hands-on oversight of protocol execution, data quality, and medical data review to enable decision-ready data. You collaborate across cross-functional teams to align trials with protocol intent, regulatory expectations, and Amgen standards. You contribute medical monitoring, data interpretation, and governance with CROs and external partners. This role offers the chance to shape oncology development and impact patient outcomes within a collaborative, science-driven culture.

Compensaciones / Beneficios

- Retirement and savings plan
- group medical, dental and vision coverage
- life and disability insurance
- discretionary annual bonus program
- stock-based long-term incentives
- adaptable work models (remote and hybrid)

Responsabilidades

- Oversee protocol execution and data quality in early-phase oncology trials
- Contribute to medical monitoring and assessment of subject-level data to identify risks and issues
- Collaborate across cross-functional teams to translate clinical strategy into study concepts and documents
- Provide guidance in managing collaborators, consultants, and CROs for key projects
- Ensure protocol integrity and governance for clinical plans and final deliverables




- Review and analyze trial data for accuracy, regulatory compliance, and completeness
- Conduct data quality assessments within a data monitoring plan across the trial lifecycle
- Support regulatory submissions and high-level clinical regulatory responses
- Draft and contribute as an author to publications and conference presentations
- Utilize data analysis tools (e.g., Spotfire) for clinical data interpretation

Requisitos principales

- Doctorate, 4+ years in life sciences/healthcare OR Master’s, 7 years OR Bachelor’s, 9 years (substantial clinical drug development experience)
- Experience in pharmaceutical early-phase oncology development
- Strong communication and presentation skills for leadership audiences
- Experience designing, monitoring, and implementing oncology clinical trials under GCP
- Ability to perform data readouts, data cleaning, and outputs for regulatory or internal use
- Experience drafting regulatory submission materials and responses
- Contributing author experience for scientific publications and conferences
- Familiarity with Spotfire or similar data analysis tools

- clear communicator
- cross-functional collaboration
- problem solving
- clinical trial design and execution
- data interpretation and statistics basics
- GCP regulatory knowledge

📌 Clinical Scientist Director, Early Development Oncology (Marbella)
🏢 Amgen
📍 Marbella