- Partner with global and local country teams to provide high level country strategy and actively drive study progress and local/country level study delivery
- Planning, management and oversight of clinical study execution in accordance with the global program strategy, through leadership with engagement of the cross-functional Local Study Team
- Communicate country status (including timelines and deliverables) to key partners including updates to relevant systems for transparency
- Provides country level input into the Country Operational Plan and partners with the Development Feasibility Manager through feasibility and with the Global Clinical Managers to ensure local delivery of the study
- Support internal audit and inspection activities and contribute to CAPAs, including leading resolution of issues when appropriate e.g., vendor management
- Assign and lead all aspects of deliverables of study support staff and continually review country level risk mitigation to ensure study delivers to plan
- Doctorate degree OR
- Master's degree & 3 years of directly related experience OR
- Bachelor's degree & 5 years of directly related experience OR
- Associate's degree & 10 years of directly related experience OR
- High school diploma / GED & 12 years of directly related experience
- Advanced knowledge of global clinical trial management
- Fluency in Spanish language and business English
- BA/BS/BSc
- Minimum 2-3 years' experience of leading local/regional or global teams
- Minimum 2-3 years' clinical trial project management experience
- 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 management and oversight of external vendors (e.g., CROs, central labs, imaging vendors, etc.)
- Must be a local/country expert with proven project management experience locally
- Must be able to build strong site relationships as well as other local relationships to ensure end to end study delivery is met
- Full support and career-development resources to expand your skills, enhance your expertise, and maximize your potential along your career journey
- A diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
- Generous Total Rewards Plan—comprising health, finance and wealth, work/life balance, and career benefits
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Local Trial Manager - España - Amgen Inc. (IR)
Descripción
Local Trial Manager - Multiple openings page is loaded
Local Trial Manager - Multiple openings
Apply remote type Remote locations Spain - Remote time type Full time posted on Posted Today job requisition id RCareer Category
ClinicalJob Description
If you feel like you're part of something bigger, it's because you are. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to becoming one of the world's leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It's time for a career you can be proud of. Join us as:
LOCAL TRIAL MANAGER - REMOTE POSITION
LIVE What you will do
Let's do this. Let's 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 start-up to close out (CSR/Archival) at a country level in accordance with ICH-GCP and other applicable local regulations. You will maintain the quality and scientific integrity of clinical trials at a local/country level and actively collaborate with cross functional internal and external partners to ensure timely delivery, budget execution of clinical trial results within the local country.
Key Activities:
WIN
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The qualified professional we seek is a Trial Manager with these qualifications.
Minimum Requirements
Preferred Requirements
THRIVE
Some of the vast rewards of working here
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 is committed to equal treatment, diversity and the inclusion of employees with disabilities, and is open to all. If you have a disability, do not hesitate to inform your Human Resources contact of any adaptations or tools required for the recruitment process to run smoothly. If you have any specific questions relating to your disability, please do not hesitate to ask them in confidentiality.
.About Us
Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology.
Amgen focuses on areas of high unmet medical need and leverages its biologics manufacturing expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential.
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