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Grad Co-op - R&D (Discovery Research Operations) - United States  

Company managed [?] Still accepting applications

Posted on : 22 October 2017

Project Description

The Co-op (Research Operations) will primarily support regulatory activities related to scientific study report writing and contributions to regulatory submissions from Discovery Research. He/she will ensure consistency and compliance with report writing procedures, and provide technical support to researchers during the process of report writing. The Co-op will be responsible for editing draft reports for content and format, coordinating internal and external reviews, and finalizing reports for electronic signature and regulatory submission. He/she will also be involved in the quality control (QC) of regulatory submissions from Discovery Research functions to ensure consistency with supporting regulatory documentation. The Co-op will assist in defining and monitoring timelines for the Discovery Research contributions to regulatory submissions, and will be responsible for ensuring timely compliance. The role will support seamless communication flow between diverse groups across sites and functional areas and assist with timely issue resolution and escalation. This role will also require manual entry and verification of information onto a web-based document-management platform, and execution of reports/dashboards for regulatory related activities. The position may also include additional activities to support Discovery Research business operations, such as database entry or other small projects.

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 with a 3.0 minimum GPA or equivalent

Completion as a first year graduate student before internship starts and currently enrolled in a MBA program for a MBA internship OR a Master’s program for a Masters internship OR a PharmD program for a PharmD internship OR PhD for a PhD internship from an accredited college or university

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

Basic Qualifications
Pursuing a Master’s degree in Regulatory Science
Ability to be proactive and independently understand, follow, and implement instructions
Strong attention to detail, including the ability to verify data/information, proofread and reformat documents
Able to manage multiple tasks at once and to work effectively with teams using strong interpersonal skills
Excellent verbal and written communication expertise
Scientific writing or technical writing experience
Fluent in MS Windows 7, MS Office, and Adobe.
Familiarity with working in data management systems
Writing sample and/or assessment of editing skills may be requested


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, or disability status.

Only candidates who apply via www.careers.amgen.com will be considered. Please search the Keyword section for 46093.

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, or disability status.