IMAGING SPECIALIST MANAGER
LIVE
What you will do
In this vital role you will plan and execute the operational aspects of clinical trials globally. You will manage and coordinate the operational imaging strategy, plan, risk assessment, mitigation, and execution for oncology and non-oncology clinical trials across all phases from study start-up to close-out.
Responsibilities:
Maintain the quality and scientific integrity of imaging-related elements in clinical trials
Working with the Imaging Scientist Team within Clinical Biomarkers & Diagnostics to enable E2E Imaging specialist support throughout the portfolio
Serve as an internal subject matter expert, advising Clinical Program Operations (CPO), and other Global Development Operations (GDO) functions, on best practices, ensuring consistent standards and key lessons learned are applied across the portfolio for continuous improvement and maximum impact of the solutions
Build global cross-functional relationships and collaborate with clinical teams to integrate imaging into trials and update senior management
WinWhat we expect of you
We are all different, yet we all use our unique contributions to serve patients. The professional we seek has these qualifications.
Basic Qualifications:Doctorate degree Or
Master's degree and 2 years experience Or
Bachelor's Degree and 4 years experience Or
Associate’s degree and 8 years experience Or
High school diploma / GED & 10 years experience
Preferred Qualifications:- BA/BS/BSc
- 7 years work experience in life sciences or medically related field, including 4 years of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company
- Minimum 5 years experience in leading global teams
- Experience with operationalizing clinical studies with imaging elements and Imaging vendor management
Knowledge
- Strong understanding of drug development process, clinical trial conduct, ICH-GCP and local regulations, requirements, and guidelines
- Strong knowledge of the clinical trial process, including regulations, patient recruitment, feasibility, business operation and the associated supportive vendors and technologies preferred.
- Good understanding of quality oversight and process improvement
- Project and Program management including oversight of quality, study deliverables and timelines
- Ability to network and build relationships cross-functionally
- Various therapeutic area knowledge
Thrive
What you can expect of us
As we work to develop treatments that take care of others, we also work to care for our teammates92 professional and personal growth and well-being.
The expected annual salary range for this role in the U.S. (excluding Puerto Rico) $98,125-132,757.
Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.
Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:
- Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.
- A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
- Stock-based long-term incentives
- Award-winning time-off plans and bi-annual company-wide shutdowns
- Flexible work models, including remote work arrangements, where possible
Apply now and make a lasting impact with the Amgen team.
careers.amgen.com
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Application deadline
Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.
Sponsorship
Sponsorship for this role is not guaranteed.
