Submission Specialist

LocationChennai
Work modehybrid
Typefull-time
SenioritySenior
Experience5+ yrs
Company size10,000+ people
PostedApr 30, 2026 · 5mo ago
Verified live13h ago
At a glanceSummarised by Seekless from the posting.
5+ years' experience in pharma advertising with knowledge of regulatory review process
Strong planning and organization skills with extraordinary attention to detail
Excellent verbal and written communication skills
Basic comprehension of scientific content
Proficient with MLR Submission Platforms
Proficient with Microsoft Office
Proficient with Adobe Acrobat
Efficient, self-starter, quick study, flexible
Bachelor's Degree or equivalent experience required
Background in account management/project management ideal
Skills
Microsoft Office
Adobe Acrobat
Veeva
Zinc
MAP
Agency :
Havas Creative
Job Description :
Prose on Pixels is looking for a full-time Submission Specialist to play a key role in supporting the operations team. The candidate will partner with project management, account, editorial, copy to ensure flawless project submissions in client platforms like Veeva, Zinc, MAP. We offer a positive, team-oriented environment and are looking for an experienced candidate that will be trained in our process. The Submission Specialist will be responsible for working with the extended teams on the coordination and preparation of documents for submission to our client’s medical, legal, and regulatory review panels. This
role will serve as the go-to expert on the client regulatory submission process and the systems/tools used for the submission. S/he will also be responsible for staying abreast of updates, creating/maintaining the regulatory process binders and working with PMs to communicate updates to project teams.
Responsibilities
You will work across several clients and brands and be responsible for supporting the project teams on ancillary activities as needed.
Works closely with project management, account, editorial, copy and junior submission specialists, to ensure all components of submission meet platform requirements.
• Become the expert on system requirements
• Be the primary point of contact for all submission needs and guidance
• Become the internal gatekeeper/QA for submission packages
Requirements:
•
5± years’ experience in pharma advertising with knowledge of regulatory review process. Strong planning and organization skills with extraordinary attention to detail.
•
Excellent verbal and written communication skills and a basic comprehension of scientific content.
•
Background in account management/project management ideal, but candidates with copy or editorial background could also be trained.
•
Proficient with MLR Submission Platforms, Microsoft Office and Adobe Acrobat.
•
Efficient, self- starter, quick study, flexible. Bachelor’s Degree or equivalent experience required.
Contract Type :
Permanent
Here at Havas across the group we pride ourselves on being committed to offering equal opportunities to all potential employees and have zero tolerance for discrimination. We are an equal opportunity employer and welcome applicants irrespective of age, sex, race, ethnicity, disability and other factors that have no bearing on an individual’s ability to perform their job.
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