Local Trial Manager - Brazil

Amgen SA; São Paulo; Presencial; BRL 20.000 - 80.000; Tempo integral

Resumo da oferta

Amgen is seeking a Local Trial Manager to lead clinical trials in São Paulo, Brazil. This role involves managing study implementation, ensuring compliance with regulations, and collaborating with global teams. The ideal candidate will possess a strong educational background in life sciences and extensive experience in project management within clinical settings. If you are passionate about advancing health and making a difference, we invite you to apply.

Serviços

Competitive and comprehensive Total Rewards Plans

Qualificações

• Doctorate degree or related qualification.
• 2-10 years of Clinical Trials experience required depending on degree.

Responsabilidades

• Lead and coordinate clinical trials from startup to close out.
• Collaborate with cross-functional teams for study delivery.
• Manage external vendors and site relationships.

Conhecimentos

Project Management

Vendor Management

Clinical Trial Management

Communication

Team Leadership

Fluency in Portuguese

Business English

Formação académica

Doctorate degree

Master’s degree

Bachelor’s degree

Associate’s degree

High school diploma / GED

Descrição da oferta de emprego

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. 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.

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 conformity with ICH-GCP and other applicable local regulations. You will maintain the quality and scientific integrity of clinical trials and actively collaborate with cross functional internal and external partners to ensure timely delivery, budget implementation of clinical trial results within the local country.

Key Activities:

• You will 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 implementation in accordance with the global program strategy, through leadership with engagement of the cross-functional Local Study Team
• Communicate country status (including timelines and results) 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 deliver all study support staff and continually review country level risk mitigation to ensure study delivers to plan
• You will build strong site relationships as well as other local relationships to ensure end to end study delivery is met.

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 Local Trial Manager with the following qualifications.

Basic Qualifications:

Doctorate degree

OR

Master’s degree & 2 years of Clinical Trials experience

OR

Bachelor’s degree & 4 years of Clinical Trials experience

OR

Associate’s degree & 8 years of Clinical Trials experience

Or

High school diploma / GED & 10 years of Clinical Trials experience

Preferred Qualifications:

• Educational Background in Life Science
• Work experience in life sciences or medical related field, including biopharmaceutical clinical research experience acquired working on clinical trials in a biotech, pharmaceutical or CRO company
• Minimum 2 years leading local/regional or global teams experience
• Minimum 2 years Clinical Trial Project Management experience
• Proficiency in Portuguese and business English
• Experience in management and oversight of external vendors (e.g., CROs, central labs, imaging vendors, etc.)
• Must be a local/country expert with identifiable project management experience

Please upload your resume in English

Thrive

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.

In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.

Apply now for a career that defies imagination

Objects in your future are closer than they appear. Join us. careers.amgen.com

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.

Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.

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.