Job Information
Amgen Grad Intern - Regulatory Writing in Washington D.C., District Of Columbia
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.
Grad Intern - Regulatory Writing
What You Will Do
Let’s do this. Let’s change the world. During this program, you will help prepare scientific and regulatory submission documents that comply with global regulatory standards.
Understands and complies with SOPs, templates, best practices, policies, regulatory writing style guides
Writes and edits sections of non-complex regulatory documents (eg, simple clinical study report, investigator brochure) and simple standalone documents with mentor oversight as defined by the organization
Reviews their own draft document content with mentor for feedback
Participates in collaborative team activities for non-complex documents, including support to collect input from authors/reviewers
Participates in the cross-functional document review process, comment triage, meeting attendance, and incorporation of feedback for development of subsequent drafts or for finalization
Participates (under close supervision) in project management activities ie, timeline tracking and scheduling meetings with team members
Generates appropriate in-text tables and figures
Performs document-level QC (including abbreviations, references to sources, data in text versus data in tables, figures, or graphs, etc)
Learns and uses organizationally required authoring tools and technology platforms
Attends cross-functional meetings with other writers and departments, as appropriate, to share and gather information relevant for successful completion of their own and inter-dependent projects
Documents in scope include: clinical study reports/observational research study reports, plain language summaries, investigator brochures, risk management plans, informed consent forms, nonstrategic regulatory documents, original protocols/amendments/country-specific supplements
What We Expect of You
We are all different, yet we all use our unique contributions to serve patients. The innovative, proactive individual we seek is a problem solver with these qualifications:
Basic Qualifications:
Amgen requires that all individuals applying for a grad internship or a co-op assignment at Amgen must meet the following criteria:
18 years or older
Graduated with a bachelor’s degree from an accredited college or university
Currently enrolled in an MBA program for an MBA internship OR a Master’s program for a Master’s internship OR a PharmD program for a PharmD internship OR Ph.D. for a PhD internship from an accredited college or university and completion of the first year of MBA OR Master’s OR Pharm D OR Ph.D. program before the internship starts
Enrolled in an accredited college or university following the potential internship or co-op assignment
Must not be employed at the time the internship starts
Student must be located in the United States for the duration of the internship OR co-op
Preferred Qualifications:
Degree concentration in Life Sciences, Pharmacy, Medicine, Business or Related Field
Experience in interpretation of scientific data
Scientific or medical knowledge
Exposure to or working knowledge of basic statistical and medical communication principles
Demonstrated passion for writing and engagement in writing activities (extra-curricular, scientific, etc.)
Strong oral and written communication skills, including ability to write scientific documents and summarize scientific data
Able to collaborate with others, and to build solid and positive relationships with cross‐functional team members
Able to work independently and to resolve basic problems on their own and more complicated problems under supervision
Attention to detail and accuracy
Organizational skills in time management and in project management; ability to manage more than one project simultaneously
Working knowledge of typical office applications (e.g., Microsoft Office, SharePoint)
What You Can Expect of Us
As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.
The base pay range for this opportunity in the U.S. is $30 - $40 per hour.
Build a network of colleagues that will endure and grow throughout your time with us and beyond.
Bring your authentic self to the table and become the professional you’re inspired to be through accepting a culture that values the diversity of thought and experience and will flex to your strengths and possibilities.
Participate in executive and social networking events, as well as community volunteer projects.
Apply now
for an internship/co-op that defies imagination
Objects in your future are closer than they appear. Join us.
careers.amgen.com Please search for Keyword R-198654
In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.
Application deadline
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.
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.
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