Global Medical Indication Lead – Rheumatology (US)

Planet Pharma

Boston (MA)

On-site

USD 180,000 - 240,000

Full time

14 days+
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Job summary

Planet Pharma in Boston seeks a Global Medical Indication Lead (Rheumatology) to lead the clinical team and translate the asset strategy into a Clinical Development Plan, ensuring time, quality, and budget.

You will oversee cross-functional collaboration, manage a team of Global Clinical Trial Physicians, provide strategic medical insight, ensure compliant studies, and drive harmonization across trials while engaging with IRBs, investigators, and management.

Qualifications

  • MD with relevant specialty education, preferred in rheumatology, immunology or related fields.
  • Experience leading cross-functional medical teams in pharma/biotech.
  • Excellent English written and spoken; ability to travel.

Responsibilities

  • Provide strategic medical insight and planning for the indication across development stages.
  • Own the Clinical Development Plan and participate in long-range strategic planning.
  • Line management of Global Clinical Trial Physicians; coach and set example for high-quality medical support.
  • Oversee medical aspects of studies in real time and communicate with management and study teams.
  • Ensure harmonization of communications to external stakeholders (IRBs, regulatory authorities) and maintain efficiency.
  • Lead indication medical advisory boards as appropriate.
  • Build and maintain a high-caliber team of development medical doctors.
  • Ensure compliance of all studies in the indication.

Skills

Leadership
Clinical trial design
Strategic thinking
Communication
Travel readiness

Education

MD with relevant specialty

Job description

Global Medical Indication Lead (Rheumatology)


The Global Medical Indication Lead will lead the clinical team for an indication, translating the TPP as set by the Asset Strategy Team into a Clinical Development Plan that answers the relevant questions safeguarding time, quality, and budget. The Global Medical Indication Lead will work in close collaboration with the other members of the cross functional team, in order to maximize the potential of the asset for a given indication.


Roles And Responsibilities


  • Provide continuous strategic medical insight and planning for the indication during all the stages of development

  • Own the Clinical development plan and participate in long range strategic planning as data emerges in the indication

  • Line management of the Global Clinical Trial Physicians working on the indication. Provide coaching and set example for team ensuring high quality medical support for the study teams

  • Real time oversight of the medical aspects of studies in the indication, including the relevant communication to management as well as the different study teams

  • Safeguard harmonization across the studies so that communications to external stakeholders ( e.g. questions of IRBs, RAs) are consistent and company efficiency is maintained in close collaboration with peers as well as management of the different functional groups

  • Lead indication medical ad boards as appropriate

  • Help build and maintain a “best in class” group of development medical doctors

  • Ensure compliance of all studies in the indication


Education, Experience And Qualifications


  • Medical Doctor with relevant specialty education preferred ( e.g. neurology, hematology, dermatology , immunology, rheumatology, internal medicine, pediatric)

  • At least 3-5 years in the pharma/biotech industry, having acquired an in-depth understanding of end to end ( phase I to registration) drug development

  • Excellent English, both written and spoken is a must, as well as ability to travel

  • Proven leadership, motivational and interpersonal skills in a global and intercultural environment, including leading through influence

  • Pro-active problem solver with negotiation skills

  • Must provide clear vision, direction, and purpose to the different study teams

  • Demonstrated expertise in clinical trial design, conduct and interpretation of clinical data

  • Strong communication skills to ensure that study plans and status are transparent, and that risks, issues, and results are clear to all involved parties.

  • Additional skills in gathering decision information, negotiation and communicating decisions and action

  • Executes responsibilities with knowledge, accuracy, persistence, resilience and creativity, being an accomplished team player whilst maintaining medical integrity

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