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Project Coordinator (MLRPRC promotional review coordinator) US Based (remote)


Job Location:

Princeton, NJ - USA

Yearly Salary: USD 75000 - 75000
Posted: 24 September 2026 (Yesterday)
Application Deadline: 22 December 2026
Vacancies: 1 Vacancy

Job Summary

We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations be future ready. We offer accelerated global growth opportunities for talent thats bold industrious and nimble. With Indegene you gain a unique career experience that celebrates entrepreneurship and is guided by passion innovation collaboration and empathy. To explore exciting opportunities at the convergence of healthcare and technology check out


What if we told you that you can move to an exciting role in an entrepreneurial organization without the usual risks associated with it We understand that you are looking for growth and variety in your career at this point and we would love for you to join us in our journey and grow with us. At Indegene our roles come with the excitement you require at this stage of your career with the reliability you seek. We hire the best and trust them from day 1 to deliver global impact handle teams and be responsible for the outcomes while our leaders support and mentor you.


We are a profitable rapidly growing global organization and are scouting for the best talent for this phase of growth. With us you are at the intersection of two of the most exciting industries of healthcare and technology. We offer global opportunities with fast-track careers while you work with a team that is fueled by purpose. The combination of this will lead to



PROJECT COORDINATOR (MLR/PRC Promotional Review Coordinator)

You will be responsible for:

Workflow Management:

  • Manage MLR/PRC workflows end-to-endfrom concept review through final approval including resubmissions and re-reviews
  • Assign and route reviewers based on content type and regulatory requirements
  • Proactively manage the material pipeline including active workflows and offline activities

Quality Control (First-Time-Right):

  • Perform readiness assessments at each stage using pre-submission checklists to ensure SOP compliance before review initiation
  • Flag non-compliant or incomplete submissions; partner with originators to resolveescalate where necessary
  • Manage material expiry tracking and timely re-review/retirement

MLR/PRC Meeting Facilitation:

  • Chair PRC/MLR meetingslead discussions capture decisions and log action items in the review systemPrepare and distribute meeting agendas; update based on reviewer feedback and workflow status
  • Attend brand therapy area and business-unit-specific prioritization meetings

Stakeholder & Agency Management:

  • Serve as the primary coordination interface between reviewers project owners agencies and material owners
  • Drive agency accountability for submission quality and process adherence
  • Share job aids and policy guidance; identify training gaps and escalate

Reporting & Analytics:

  • Generate compliance reports on submission review approval expiry and usage status
  • Extract and analyze process metrics; provide actionable recommendations
  • Maintain therapeutic area trackers and planning & prioritization forecasts
  • Run periodic reports (90-day re-review Open Jobs Status) to monitor job progression

Process Improvement:

  • Proactively identify optimization opportunities aligned with business objectives
  • Co-create actionable strategies with stakeholders to enhance efficiency and measurable impact
  • Support process documentation training materials and refresher sessions

Must Have:

  • Bachelors degree
  • 5 years in MLR/PRC (promotional review coordination workflow management and reporting support) within the biopharma industry; experience working in a pharma or healthcare advertising environment
  • Excellent interpersonal and collaboration skills
  • Project management skills and experience preferred
  • Strong presentation and meeting facilitation skills
  • Experience with electronic review systems (e.g. Veeva Vault PromoMats) submission routing metadata management approval tracking
  • Cross-functionalstakeholder management across Medical Legal Regulatory Marketing and Agency partners
  • Proficiency in reporting and dashboarding (system-native reports PowerBI SmartSheet)
  • Attention to detail high-volume multitasking analytical mindset
  • Remote in US but availability to work Eastern Time Zone hours


Compensation: $75000USD


EQUAL OPPORTUNITY

Indegene is proud to be an Equal Employment Employer and is committed to the culture of Inclusion and Diversity. We do not discriminate on the basis of race religion sex color age national origin pregnancy sexual orientation physical ability or any other characteristics. All employment decisions from hiring to separation will be based on business requirements candidates merit and qualification.


Required Experience:

Manager


About Company

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Partners for Medical Writing - Trilogy Writing & Consulting GmbH - providing all necessary regulatory documentation in support of your clinical development.

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