Clinical Scientist Associate Director, Late Development Oncology

🕒 June 19

🇺🇸 United States – Remote

💵 $169.8k - $229.7k / year

⏰ Full Time

🟠 Senior

🧪 Clinical Research

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 40%

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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Amgen

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1980

🏥 Healthcare

🧬 Biotechnology

💊 Pharmaceuticals

💰 $28.5G Post-IPO Debt on 2022-12

Healthcare • Biotechnology • Pharmaceuticals

Amgen is a global leader in biotechnology, focusing on the development and commercialization of innovative medicines made from living cells. The company aims to treat serious illnesses, often targeting diseases with limited therapeutic options. Amgen emphasizes scientific innovation and is committed to ethical research, patient safety, and environmental sustainability. It actively engages in clinical trials and is known for its contributions to the fields of cancer treatment and obesity management among others.

📋 Description

• Support setup and execution of late-phase oncology clinical trials with a focus on data quality • Assist in authoring clinical protocols, Investigator Brochures, and other regulatory documents • Provide input into and implement data management plans and CRF design • Oversee clinical trial data review, analysis, and presentation preparation • Support internal decision-making, external interactions, and regulatory submissions • Assist with management of collaborators, consultants, and Clinical Research Organizations • Anticipate and actively manage problems across cross-functional teams • Translate clinical strategy into study concept documents, protocols, and related documents • Support training, recruitment, and development requirements for matrix team resources

🎯 Requirements

• Doctorate degree and 3 years of clinical development experience, or Master’s degree and 5 years, or Bachelor’s degree and 7 years, or Associate’s degree and 12 years, or high school diploma/GED and 14 years • 3 years of pharmaceutical industry experience preferred, including at least 1 year supporting early- or late-phase clinical development in a relevant therapeutic area or disease indication • Oncology experience preferred • Experience contributing to clinical trial process improvements • Strong written and oral communication and presentation skills • Experience supporting clinical trial design, monitoring, and implementation in compliance with Good Clinical Practice and regulatory requirements • Working knowledge of data cleaning, database lock, data extraction, and clinical data outputs • Experience contributing to regulatory submission documents and clinical regulatory responses • Experience as a contributing author on scientific publications or data presentations • Experience with clinical data analysis tools such as Spotfire or similar tools • Sponsorship for this role is not guaranteed

🏖️ Benefits

• A comprehensive employee benefits package • Retirement and Savings Plan with generous company contributions • Group medical, dental and vision coverage • Life and disability insurance • Flexible spending accounts • Discretionary annual bonus program • Stock-based long-term incentives • Award-winning time-off plans • Flexible work models where possible • Career development opportunities • Financial plans with opportunities to save towards retirement or other goals • Work/life balance support