Junior Regulatory Affairs Associate

Junior Regulatory Affairs Associate

Parexel International (India) Pvt. Ltd.
Not Specified
Not Specified

Job Description


Project Administration
. Under supervision provide basic paper and electronic publishing services including document preparation, legacy conversion, scanning, rendering,
bookmarking, compilation, table of contents creation, pagination, and formatting of reports and simple submissions.
. Provide basic regulatory affairs services including preparing submission packages Capitalizes on opportunities to improve project efficiency, results
or team performance and proactively takes action
Document Management
. Under supervision perform basic document management tasks including file transfer, storage, tracking, and archival.
Regulatory Guidelines
. Develop a familiarity with current global regulatory submission standards.
Standard Operating Procedures
. Develop a familiarity with departmental standard operating procedures and work instructions.
Product Support
. Under supervision provide support to regulatory activities related to marketed/investigational products.Qualifications
[Skills]
. Project management knowledge
. Client-focused approach to work
. Results orientation
. Teamwork and collaboration skills
. Communication skills
. Excellent interpersonal and intercultural communication skills, both written and verbal
. Critical thinking and problem-solving skills
. Proficiency in local language and extensive working knowledge of the English language
[Knowledge and Experience]
. Initial years of experience in an industry-related environment
[Education]
Minimum of a Bachelor's Degree in a Scientific or Technical Discipline(pharmacy background is preferred)

Job Details

Employment Types:

Industry:

Function:

IT

As part of Parexel Consulting, you will create and maximize value for clients throughout the product lifecycle. You will be a strategic guide in getting products to market faster, smarter - and keeping them there -your scientific, technical, regulatory, and/or commercial expertise will put best practice standards to work for biopharmaceutical and medical device companies large and small. In return, you will be provided with interesting opportunities for growth and development and exposed to a variety of challenging assignments, product types, geographic regions, and therapeutic areas. Plus, as member of Parexel Consulting, you will enjoy all the advantages of working remotely, combined with access to the mentorship from a team of highly experienced regulatory professionals at the height of their careers. Join our team, and you will design solutions for the complexities of an ever-changing global marketplace.

Job Source : jobs.parexel.com

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