Global Trial Manager
2 months ago
HOW MIGHT YOU DEFY IMAGINATION?
Youve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared missionto serve patientsdrives all that we do. It is key to our becoming one of the worlds leading biotechnology companies, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role.
Global Trial Manager (GTM)
Live
What you will do
Lets do this. Lets change the world. In this vital role you will be the primary point of contact to lead, manage and co-ordinate the conduct of clinical trials from study design to close out at a global level in accordance with ICH-GCP.
Responsibilities:
Oversee the quality and scientific integrity of clinical operations for studies at a global level Line Management of Local Trial Managers Collaborate with cross functional stakeholders to ensure timely and on budget execution of clinical trial deliverables Lead the Clinical Study Team to drive effective decision making Plan and manage the reporting of clinical studies conducted by Global Development through oversight of cross-functional study activities, identification and resolution of issues, and communication of study timelines/deliverables Ensure implementation and conduct of study(ies) in accordance with SOPs and ICH-GCP guidelines Management of study budget and timelines Management of vendors to the required standards 5% travel to support the execution of clinical studiesWin
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The Clinical professional we seek is an emerging leader with these qualifications.
Basic Qualifications:
Doctorate degree or Masters degree and 3 years of clinical trial project management experience or Bachelors degree and 5 years of clinical trial project management experience or Associates degree and 10 years of clinical trial project management experience or High school diploma / GED and 12 years of clinical trial project management experiencePreferred Qualifications:
Bachelors degree 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 Experience in oversight of external vendors (e.g. CROs, central labs, imaging vendors, etc.) Experience of collaborating and leading cross-functional teams in a matrix environment Experience of working internationally Experience of managing complex projects across multiple countries and time zones Experience of anticipating and resolving problems Evidence of excellent interpersonal skillsThrive
What you can expect of us
As we work to develop treatments that take care of others, we also work to care for our teammates professional and personal growth and well-being.
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 possibleApply now
for a career that defies imagination
Objects in your future are closer than they appear. Join us.
careers.amgen.com
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.
Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
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