LOCAL TRIAL MANAGER - MEXICO

Career Category Clinical Job Description 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.
We have proudly achieve certifications as Great Place to Work and Equidad MX.
It’s time for a career you can be proud of.
Join us.
Local Trial Manager (LTM) 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 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.
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 such as, European Union Clinical Trials Regulation (EU CTR), In Vitro Diagnostic Medical Devices Regulation (IVDR) directives etc.
Accountable for study results and drives key decisions within country 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 (LST) Contribute and develop program/study-specific materials – e.
., monitoring plan, study specific training documents.
Support and contribute to Clinical Study Teams (CSTs) / Trial Management Teams (TMTs) as applicable, agenda driven, present at meetings when needed 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) Manage, oversee and supervise applicable vendor activities e.
., laboratories and equipment provisioning Utilize local/country regulatory knowledge to contribute to NAMP provisioning and import/export license processes Actively engage and lead local cluster team with LOC from a study perspective (e.
., Local Medical, DOM).
Manage, supervise, and review country and study trends Identify and facilitate resolution of cross-functional study-specific issues Provide updates regarding the study budget and obtain approval for budget deviations for clinical sites (outside of range) Effectively own and bring up any issues related to delivery, timelines, or budget to study team as required Conduct on-site quality visits with CRAs where/when appropriate and supports the maintenance of Amgen investigator site relationships Implement regulatory agency inspection readiness activities (e.
., TMF review, story board generation) Support internal audit and inspection activities and contribute to CAPAs, including leading resolution of issues when appropriate e.
., vendor management Participate in cross-functional task forces/process improvement groups Assign and lead all aspects of deliverables of study support staff e.
., Study Management Associate, SASM (Snr.
Assc.
Study management) Coordinate site contracting, budgeting, insurance and payment process by supervising local support roles Lead and continually review country level risk mitigation activities to ensure study delivers to plan Maintain relevant therapeutic knowledge Triage / tailor communication from study / local team to sites to ensure efficient and effective communication flow Provide input into potential site list as part of FIRE process 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 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 Preferred Requirements 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.
., 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.
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—with compensation and benefits rated above 4 stars (out of 5) on Glassdoor Apply now for a career that defies imagination Objects in your future are closer than they appear.
Join us.
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om 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.
Amgen requires all staff in the United States and Puerto Rico to be vaccinated from COVID 19 as a condition of employment.
In accordance with applicable law, Amgen will provide reasonable accommodations to staff members who qualify based on a medical reason or a sincerely held religious belief, practice, or observance.
Such accommodation may not pose an undue hardship to Amgen, its operations, or its staff..
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 , 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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