Global Regulatory Writing Manager

 

Career Category:Regulatory  
 

About The Role : 
Let’s do this. Let’s change the world. In this vital role you will 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.

  
 

Roles & Responsibilities: 

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 4 to 6 years of directly related experience OR

Bachelor’s degree and 6 to 8 years of directly related experience OR

Diploma and 10 to 12 years of directly related experience

Preferred Qualifications:

 

Functional Skills: 

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