What you will do
Let’s do this. Let’s change the world. In this vital role you will do to author and gain approval of scientific and regulatory submission documents that comply with global regulatory standards. To maintain key business relationships with appropriate cross-functional product team members. As requested, this role may serve as functional area lead on product teams, manage (with supervision) writing activities for product submissions, train and mentor more junior writers, and assist with departmental activities
Author regulatory submission documents, as assigned, including Clinical Study Reports, Investigator Brochures, Responses to Questions, Protocols, Protocol Amendments, Informed Consent Forms, Table of All Studies, Clinical Overview Addenda, eCTD Module 2 Clinical Summary Documents, Briefing Documents, Pediatric Investigation Plans, and other regulatory documents;
Conduct the formal review and approval of authored documents, following applicable standard operating procedures;
With considerable supervision, manage regulatory writing activities for product submissions, including new and supplemental drug applications/biologics license applications;
Serve as functional area lead on product teams (e.g., Global Regulatory Team, Evidence Generation Team, Global Safety Team, Label Working Group)
May provide functional area input for Global Regulatory Plan and team goals
May work with contract and freelance writers
May participate in training and mentoring of junior medical writers
May participate in departmental and cross-departmental initiatives, as appropriate.
Generate document timelines, with team input
Keep abreast of relevant professional information and technology
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The [vital attribute] professional we seek is a [type of person] with these qualifications.
Basic Qualifications:
Doctorate degree OR
Master’s degree and 3 years of directly related experience OR
Bachelor’s degree and 5 years of directly related experience OR
Associate’s degree and 10 years of directly related experience OR
High school diploma / GED and 12 years of directly related experience
Preferred Qualifications:
Proficiency with word processing and other Microsoft Office Programs
Significant knowledge of scientific/technical writing and editing, and of overall clinical development process for new compounds;
Ability to understand and follow complex standard operating procedures (SOP’s), guidance documents, and work instructions;
Understanding and application of principles, concepts, theories and standards of scientific/technical field.
Substantial knowledge and understanding of International Council on Harmonization (ICH) and Good Clinical Practice (GCP) guidance’s and requirements.
Soft Skills:
Excellent written/oral communication skills and attention to detail
Ability to effectively demonstrate leadership in a team environment which requires negotiation, persuasion, collaboration, and analytical judgment;
Proficient time and project management skills.
Self-starter with a drive and perseverance to achieve results
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.
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