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Regulatory Affairs Associate - I //Seattle, WA
Ref No.: 18-31615
Location: Seattle, Washington
Position Type:Contract
Start Date / End Date: 07/02/2018 to 03/01/2019
Job Title: Regulatory Affairs Associate - I
Work Location: Seattle, WA
Length of Assignment: 6 Months
Position Type: Contract Full Time
Client:  A Big Pharmaceutical Company


Regulatory Operations Associate - Document Processing

Specific Responsibilities: Will interact with management and team members to perform document formatting and compilation activities associated with preparing documents for submissions in accordance with global regulatory guidelines.

The ideal candidate will possess experience working in the life sciences. Including work with electronic document management systems, document control, regulatory submissions, work with clinical or quality documentation, or other experience directly related to Regulatory Operations. Expertise in the use of document management and complex Word formatting experience is highly desired.

Entry level candidates will be considered but must have a strong working knowledge of MS Word, Word templates, Adobe Acrobat and standard Office tools.

Essential Duties and Job Functions: As a member of the Regulatory Operations team, this position prepares and completes a variety of document formatting and compilation activities.
* Works closely with authors in Medical Writing, Clinical and Regulatory Affairs to perform routine general formatting, template adherence, ToC generation, version control and non-routine document processing activities associated with the preparation of submission-standard regulatory documents for both hard copy and electronic submissions.
* Coordinates the endnote referencing process in terms of managing entries into the endnote database, generating within-document bibliographies and providing individual assistance to document authors.
* Obtains cited references and ensures entry into the Reference Repository in submission acceptable format.
* Assists with the compilation of routine documents such as clinical study reports.
* Participates in supporting and promoting current electronic initiatives in moving the company forward with electronic submissions and electronic archives.
* Participates in the development or upgrading of templates as well as guidance documents and SOPs that relate to document standards, content and processes.
* Will interface with project managers, regulatory product managers, and or content authors to provide guidance on submission preparation and content.
* In addition to document formatting activities, and may assist with the development and management of projects as applicable in support of the Regulatory Operations department.
* Maintains constructive and positive interactions with colleagues.
Knowledge, Experience and Skills: Typically requires a BA/BS with 2+ years of relevant experience or an MS with 1+ years of relevant experience.

+ Experience in document management and complex document formatting as applicable is a plus.
+ Familiarity with pharmaceutical development and regulatory submissions is a plus.
+ Must have excellent verbal and written skills, strong organizational and time management skills and strong attention to detail.
+ Must be able to balance multiple tasks simultaneously to achieve goals and satisfy customers.
+ Works under limited direction and may independently determine and develop approaches to non-routine problems.
+ Must possess flexibility to work effectively within an environment that has quickly changing processes, priorities and deadlines.

If you are interested in this job than please send me your most updated resume on reena.sangwan@artechinfo.com or you can reach me at #973-507-7579