HOW MIGHT YOU DEFY IMAGINATION?
You’ve earned your degree. How will you use that achievement to reach your goals? Do more with the knowledge you’ve worked hard to acquire and the passion you already have. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies, reaching over 10 million patients worldwide. Become the professional you are meant to be in this meaningful role.
Local Trial Manager (LTM)

Live

What you will do
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 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.
You will be working closely with the Nordic & Baltic Global Study Organization based in Stockholm and also with the local medical affairs teams in the Nordic & Baltic countries.
The position is based in Solna in Stockholm with flexibility to work remotely on a part time basis.

Key Activities:

• Partner with global and local country teams to provide high level country strategy and actively drive study progress and local/country level study delivery
• Responsible for compiling and submitting submissions to ethics committees/councils within the country/ies as well as submissions relating to other aspects country needs
• Planning, management, and oversight of clinical study execution in accordance with the global program strategy
• Communicate country status (including timelines and deliverables) to key partners including updates to relevant systems for transparency
• Accountable for site-level goal setting and study-specific deliverables for clinical sites within their country(ies)
• Implement regulatory agency inspection readiness activities
• Support internal audit and inspection activities and contribute to CAPAs, including leading resolution of issues when appropriate e.g., vendor management
• Lead and continually review country level risk mitigation activities to ensure study delivers to plan
• Maintain relevant therapeutic knowledge
• Drive site evaluation and selection process within country

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

• Life Science degree & directly related work experience
• Knowledge of global clinical trial management
• Fluency in a Scandinavia language both in speaking and writing
• Fluency in business English in both speaking and writing

Preferred Requirements

• Experience of leading local/regional or global teams
• Clinical trial project management experience
• Previous work experience in life sciences or medically related field, 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.)
• Local/country knowledge with proven project management experience locally
• Knowledge of other Nordic and Baltic languages

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.

• 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

Apply now

for a career that defies imagination
Objects in your future are closer than they appear. Join us.

careers.amgen.com

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.
For more information about the position, please contact Eleonore Hassila, Human Resources Lead Sweden: +46 76 109 9428

For union related questions, please contact Daniel Erlandsson: derlands@amgen.com