Associate Director Study Start-up
Career Category
Join Amgen’s Mission of Serving Patients
What you will do
Let's do this. Let's change the world . In this vital role you will drive world-class study start-up planning and execution across a global portfolio, ensuring clinical trials launch with quality, efficiency, and speed .
- Lead and manage a team of Study Start-up Managers, ensuring high-quality, compliant study start-up delivery across multiple programs and therapeutic areas.
- Drive end-to-end study start-up planning and execution from global to local, delivering milestones on time, within budget, and in line with ICH-GCP and regulatory requirements.
- Provide portfolio-level oversight of study start-up performance, resourcing, and delivery metrics, escalating risks with solution-focused recommendations.
- Build team capability through coaching, mentoring, performance management, and role modelling of best practices in study start-up delivery.
- Partner with functional and hub leaders to strengthen study start-up capabilities, ways of working, and operational readiness across the organisation.
- Own and embed study start-up business processes, ensuring consistent application through training, knowledge sharing, and continuous improvement.
- Foster a collaborative, high-engagement culture that encourages innovation, learning, and the sharing of knowledge and best practice.
- Contribute to the evolution of the Study Start-up Hub model, shaping future ways of working through feedback, insights, and continuous improvement initiatives.
What we expect of you
About the role
Basic Qualifications
Pharma Expertise
Management Experience
Tech Skills
No prior Veeva experience required
- Doctorate degree and 3 years of clinical execution experience OR
- Master's degree and 7 years of clinical execution experience OR
- Bachelor's degree and 9 years of clinical execution experience OR
- Associate's degree and 12 years of clinical execution experience OR
- High school diploma / GED and 14 years of clinical execution experience
- In addition to meeting at least one of the above requirements, you must have a minimum of 3 years' experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation of resources. Your managerial experience may run concurrently with the required technical experience referenced above .
Preferred Qualifications
- 7 years work experience in life sciences industry, particularly focusing on clinical trial work, including 5 years of biopharmaceutical clinical research experience obtained at a biotech or pharmaceutical company
- Experience managing multiple teams / direct reports across multiple clinical functions
What you can expect of us
The annual base salary range for this opportunity in the U.S. is $182,145 - $212,860.
In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of 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 that may include:
- 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
for a career that defies imagination
careers.amgen.com
Salary Range
Not included in the source posting: benefits.
Skills
Who can apply
The employer didn't state any visa, work authorization, citizenship or clearance requirements in this posting. Confirm with the employer before applying.
Read automatically from the employer's posting text. Always confirm with the employer — requirements can change after a job is published.