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  4. Click Websites.
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Jobs or company...

Veeva Medical Regulatory Compliance Lead (REMOTE)

Salary undisclosed
Checking job availability...
Original
Simplified

Please note that this is a 10-month contract position.

Top Skills:

Veeva

Medical, legal, and regulatory (MLR) experience.

Regulatory process and deliverables, project management.

Medical/Pharmaceutical industry experience.

3-5 years experience.
Job Description:

Operates as primary content approval contact for Global Sales Education/ Professional Education/ US Marketing.

Prepares documents for VEEVA submissions; annotating and cross checking references, tagging/linking/loading all related documents into the system.

Serve as the liaison between the reviewers and content developers/SMEs to reach editorial solutions

Immersion in relevant project claims matrices and references to become a Subject Matter Expert (SME) to proficiently and proactively navigate reviewer comments and make content recommendations that remedy compliance issues, if and when possible

Ensures that all submissions accurately and consistently capture MLR comments and follow submissions through to approval.

Create an internal tracking process that captures the current status of all projects routing for compliance review.

Troubleshoots and guides submission workflow in challenging situations, supporting submission approval.

Meets with reviewers to develop relationships, build rapport, and influence without authority.

Develops best practices for content submission within Global Sales Education/ Professional Education/ US Marketing.

Applicants must provide their phone number. Reference job number A4559.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
Report this job

Please note that this is a 10-month contract position.

Top Skills:

Veeva

Medical, legal, and regulatory (MLR) experience.

Regulatory process and deliverables, project management.

Medical/Pharmaceutical industry experience.

3-5 years experience.
Job Description:

Operates as primary content approval contact for Global Sales Education/ Professional Education/ US Marketing.

Prepares documents for VEEVA submissions; annotating and cross checking references, tagging/linking/loading all related documents into the system.

Serve as the liaison between the reviewers and content developers/SMEs to reach editorial solutions

Immersion in relevant project claims matrices and references to become a Subject Matter Expert (SME) to proficiently and proactively navigate reviewer comments and make content recommendations that remedy compliance issues, if and when possible

Ensures that all submissions accurately and consistently capture MLR comments and follow submissions through to approval.

Create an internal tracking process that captures the current status of all projects routing for compliance review.

Troubleshoots and guides submission workflow in challenging situations, supporting submission approval.

Meets with reviewers to develop relationships, build rapport, and influence without authority.

Develops best practices for content submission within Global Sales Education/ Professional Education/ US Marketing.

Applicants must provide their phone number. Reference job number A4559.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
Report this job