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Clinical Systems & Analytical Reporting, Senior Manager

US - California - Thousand Oaks - Field/Remote

Career Category

Research

Job Description

Join Amgen’s Mission of Serving Patients

At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.

Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

Clinical Systems & Analytical Reporting, Senior Manager

What you will do

Let’s do this. Let’s change the world. In this vital role you will be responsible for implementation of technical projects and management of day-to-day platform oversight and serve as the technical expert for one or more technologies. The successful candidate will have a strong technical background in clinical trial applications (e.g., eTMF, CTMS, EDC, site facing technologies) and be a leader with demonstrated ability to influence stakeholders, to engage cross-departmentally, and to partner with the application vendor(s) to ensure delivery of services. The candidate should be technologist with a desire to learn and adapt to a changing technology ecosystem.

Responsibilities include, but are not limited to, the following:

  • Drive innovation in the clinical trial technologies domain and be a change champion.
  • Lead technical, data-related, and automation initiatives.
  • Gather cross-functional input and drive implementation of technical solutions to meet regulatory and/or business requirements.
  • Provide oversight and implement configurations (including roles, permissions, and functionality settings).
  • Optimize the usage of the application (such as external tools, reports, and data repositories).
  • Advise on data integrations with 3rd party/internal applications and data lake implementation by providing expertise on data design and review of API and web-service calls.
  • Advise on validation scenario testing for configuration changes, defect fixes, and software enhancements.
  • Support vendor oversight.
  • Escalate technical issues that support critical business processes; Facilitate rapid issue resolution by working with the vendor and internally to resolve issues; provide technical troubleshooting expertise and …
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Job Profile

Regions

North America

Countries

United States

Restrictions

Field/Remote Hybrid

Benefits/Perks

Annual bonus program Career development Career development opportunities Career transformation Collaborative culture Competitive benefits Comprehensive employee benefits Comprehensive employee benefits package Discretionary annual bonus Financial plans Flexible Spending Accounts Flexible work models Hands-on experience Health and welfare plans Hybrid work Innovative environment Life and Disability insurance Mentorship Professional and personal growth Retirement and Savings Plan Stock-based long-term incentives Time-off plans Total Rewards Plan Welfare plans

Tasks
  • Communication
  • Data Management
  • Drive innovation
  • Issue resolution
  • Provide training and mentorship
  • Resolve issues
  • Study design
  • Training
Skills

Analytical Analytics API Automation Best Practices BioTech Biotechnology Business administration Business Requirements Change Management Clinical Research Clinical trials Coaching Communication Compliance Computer Science Cross-Department Collaboration CTMS Data Collection Data design Data Integration Data Management Data Sharing Development Documentation Drug Development EDC ETMF FDA FDA regulations GCP Good clinical practices Inflammation Innovation Insurance International regulatory requirements Issue Resolution Life sciences Management Matrix Environment Mentorship Negotiation Oncology Operations Organization Pharmaceutical Programming Project Management Quality Rare Disease Research Safety Sales Site Management Software Development SOPS Stakeholder engagement Statistical Programming Study Design Technical Troubleshooting Therapeutic Areas Training Troubleshooting Vendor oversight

Education

Associates Bachelor's Bachelor's degree Degree DO Doctorate Doctorate degree GED High School High school diploma High school diploma/GED Life Sciences Master's Master's degree MS

Timezones

America/Anchorage America/Chicago America/Denver America/Los_Angeles America/New_York Pacific/Honolulu UTC-10 UTC-5 UTC-6 UTC-7 UTC-8 UTC-9