- Location
- India - Hyderabad
- Workplace
- Onsite
- Type
- Full-time
- Seniority
- Entry
- Source
- Workday
Description
Career Category
ResearchJob 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. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, obesity and obesity-related conditions. 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.
What you will do:
Project management support - initiate program meetings, update trackers, monitor milestones
Responsible for managing day-to-day activities related to assigned biobank tasks and responsibilities
Responsible for representation on study startup meetings to discuss protocol, ICF, and assent language requirements
Participate in study planning discussions with applicable stakeholders
Support process improvement projects
Support revision of controlled documents
Responsible for supporting sample, data and consent transfers from various vendors
Basic Qualifications:
Master’s degree & 5 years of related experience OR
Bachelor’s degree & 7 years of related experience
Preferred Qualifications:
Experience using electronic document management systems and principles
Outstanding attention to detail, including the ability to verify data/information, proofread, and reformat documents
Strong team player working across multiple sites and R&D functions
Proficient in Microsoft office and online collaboration tools
Sharp learning agility, problem solving, and multi-tasking skills
Reliable contributor with the ability to work independently
Core Competencies:
Understanding and application of principles, concepts, theories and standards of professional field
Specialized knowledge within the informed consent field, biobank operations, and basic knowledge about laboratory information management systems
Drafting and interpreting clinical protocol and ICF language
Knowledge of related regulatory/industry considerations and compliance issues
What you can expect of us
As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.
As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.
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