Business Development Manager (US-Based)
Fire&Spark
Boston, MA (Remote)
$88K/yr - $124K/yr (Est.)AgencyFull-timeMid level
3 hrs ago
Marketing Coordinator
New Jersey, USA (On-site)
$75K/yr – $98K/yrEntry Level2+ years expFull time
Posted 3 months ago
Top 1% of applicants do these two things.
The other 99% submit and hope. You're about to do something different.
Job Summary
Drive end-to-end promotional materials operations for CorMedix, owning PRC submissions, version control, and vendor coordination to ensure compliant, on-brand assets.
- Must-have: 1–2 years in regulated life sciences with structured approval workflows.
- Standout: Familiarity with Veeva PromoMats or PRC coordination across clinical, legal, and regulatory reviews.
- Ownership of vendor coordination, budgeting, and on-time deliverables.
Job Description
Responsibilities
- Promotional Material Management: Manage the promotional review process, updates, and lifecycle of promotional materials (sales aids, brochures, digital assets).
- Maintain version control and document tracking.
- Ensure all materials are on-brand and aligned to current label and strategy.
- Product Review Committee Coordination: Own the PRC submission process including the preparation of submission packages, routing of materials through review systems (e.g., Veeva PromoMats).
- Track review timelines and comments/revisions.
- Coordinate feedback consolidation across clinical, legal and regulatory reviewers.
- Ensure all materials are approved, compliant, and audit-ready including annotations and anchored references.
- Agency and Vendor Coordination: Coordinate creative updates, copy revisions, and production timelines.
- Ensure deliverables meet deadlines, budget constraints and quality standards.
- Budget Tracking: Reviews SOWs with Brand leads to ensure costs align.
Requirements
- Bachelor’s degree (preferably in Marketing, Business, Communications, Life Sciences, or Healthcare Administration)
- 1-2 years of relevant experience (ideally in pharmaceutical, biotech, or medical device industries, OR regulated industries with structured approval workflows)
- Familiarity with the Microsoft Office Suite
Preferred
- Experience in pharmaceutical, biotech, or medical device industries (or regulated industries with structured approval workflows).
- Familiarity with PRC processes and Veeva PromoMats (or similar systems) is a plus.
Melinta Therapeutics LLC
High touch and big impact are trademarks of Melinta. We are nimble and agile without sacrificing our dedication to adding value everywhere we go.You see, the people of Melinta are believers. Woven into the fiber of our culture is tenacity, brilliance, resilience, excellence and courage. Nothing can weaken our resolve. We take each responsibility seriously, because when we make a move, it matters.Watch us as we grow. We are the company of the moment and the enterprise of the future. We’re unparalleled in our ability to meet the unmet needs of our patients, and we do so collaboratively. Because we believe the most diverse teams produce the most meaningful impact.We can’t wait to make legendary strides. Every step counts.
