Robert Half

Robert Half

Account Manager, Pharma Agency

New Jersey, USFull-time$80k - $110k/YEAR2 days agovia LinkedIn

Job description

Location: 2 days onsite in Hunterdon County, NJ

Salary: $80-110K

Account Manager, Pharma Market Access

Account & Client Management
• Serve as day-to-day client lead for major pharmaceutical accounts, ensuring exceptional service and long-term relationship development.
• Lead and facilitate weekly status meetings, capturing actions, aligning stakeholders, and driving deliverables forward.
• Act as a strategic partner, proactively identifying client needs and offering solutions that align with business goals.

Project & Workflow Management
• Oversee projects from intake to delivery—ensuring scope clarity, milestone tracking, and flawless execution.
• Manage timelines, budgets, resource allocation, and delivery expectations.
• Ensure all content and materials move through appropriate review and approval workflows within Veeva Vault.

Cross-Functional Collaboration
• Partner with creative, medical, strategy, and production teams to ensure integrated delivery.
• Communicate priorities clearly and ensure consistent alignment across all workstreams.
• Support quality control across all assets and deliverables.

Business Growth & Opportunity Development
• Identify and activate new opportunities within existing accounts (expanded scopes, new initiatives, or service offerings).
• Support proposal development, SOW creation, and forecasting.
• Contribute to account planning and client roadmap development.

Regulatory & Submission
• Manage workflows for regulatory submission materials, including FDA/OPDP and internal MLR review processes.
• Partner closely with cross-functional regulatory, medical, and legal teams to ensure timely review cycles.
• Guide clients and internal teams on submission strategy, timelines, and requirements.

Required Skills & Experience
• 5–7+ years of account management experience within a life sciences/healthcare communications agency.
• Proven ability to run client status meetings, maintain project momentum, and manage multiple concurrent initiatives.
• Exceptional written and verbal communication skills; comfortable interacting with senior client stakeholders.
• Strong project management skills: timeline development, scope management, and problem-solving.
• Experience supporting or growing existing client business.
• Understanding of regulatory submissions, MLR processes, and medical/regulatory content requirements.
• Hands-on experience working within Veeva Vault

Preferred Qualifications
• Experience in patient support and/or market access or advocacy experience.

Responsibilities

  • Account & Client Management
  • Serve as day-to-day client lead for major pharmaceutical accounts, ensuring exceptional service and long-term relationship development
  • Lead and facilitate weekly status meetings, capturing actions, aligning stakeholders, and driving deliverables forward
  • Act as a strategic partner, proactively identifying client needs and offering solutions that align with business goals
  • Project & Workflow Management
  • Oversee projects from intake to delivery—ensuring scope clarity, milestone tracking, and flawless execution
  • Manage timelines, budgets, resource allocation, and delivery expectations
  • Ensure all content and materials move through appropriate review and approval workflows within Veeva Vault
  • Cross-Functional Collaboration
  • Partner with creative, medical, strategy, and production teams to ensure integrated delivery
  • Communicate priorities clearly and ensure consistent alignment across all workstreams
  • Support quality control across all assets and deliverables
  • Business Growth & Opportunity Development
  • Identify and activate new opportunities within existing accounts (expanded scopes, new initiatives, or service offerings)
  • Support proposal development, SOW creation, and forecasting
  • Contribute to account planning and client roadmap development
  • Regulatory & Submission
  • Manage workflows for regulatory submission materials, including FDA/OPDP and internal MLR review processes
  • Partner closely with cross-functional regulatory, medical, and legal teams to ensure timely review cycles
  • Guide clients and internal teams on submission strategy, timelines, and requirements

Qualifications

  • 5–7+ years of account management experience within a life sciences/healthcare communications agency
  • Proven ability to run client status meetings, maintain project momentum, and manage multiple concurrent initiatives
  • Exceptional written and verbal communication skills; comfortable interacting with senior client stakeholders
  • Strong project management skills: timeline development, scope management, and problem-solving
  • Experience supporting or growing existing client business
  • Understanding of regulatory submissions, MLR processes, and medical/regulatory content requirements
  • Hands-on experience working within Veeva Vault

Benefits

  • Salary: $80-110K

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