Global Pain Clinical Strategy Lead

Scorpion Therapeutics

Indianapolis (IN)

On-site

USD 140,000 - 200,000

Full time

5 days ago
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Job summary

Scorpion Therapeutics seeks a Global Pain Clinical Research Scientist to provide scientific and clinical expertise across drug development, from trial design to regulatory submission and post-launch support.

You will develop global medical and clinical strategies, lead trial design, oversee trial conduct, ensure regulatory compliance with FDA/ICH/GCP, support regulatory submissions, and collaborate with Medical Affairs, Regulatory, and Business units while engaging with external experts and

Qualifications

  • Advanced degree (PharmD, PhD, DVM, MSN/NP) with 5+ years of clinical or pharmaceutical experience, or BS/MS with 7–10 years in clinical trials, drug development, or related fields.
  • Must demonstrate scientific expertise in Pain and Neuroscience, clinical trial methodology, and regulatory processes.
  • Strong communication, influence, and collaboration skills are essential; willingness to travel domestically/internationally.

Responsibilities

  • Develop global medical and clinical strategies for pain therapeutics.
  • Contribute to trial design and oversee trial conduct.
  • Ensure compliance with FDA, ICH, and GCP regulations.
  • Support regulatory submissions and communications with regulators.
  • Collaborate with cross-functional teams including Clinical Ops, Medical Affairs, Regulatory, and Marketing.
  • Engage with external investigators, regulators, and professional societies.
  • Mentor teams and support scientific publications and educational activities.

Skills

Clinical trial design
Pain and Neuroscience expertise
Regulatory knowledge (FDA/ICH/GCP)
Scientific communication
Cross-functional collaboration

Education

PharmD
PhD in Neuroscience/Pharmacology
DVM
MSN/NP
BS/MS with 7–10 years in trials

Job description

Scorpion Therapeutics seeks a Global Pain Clinical Research Scientist to provide scientific and clinical expertise across drug development, from trial design to regulatory submission and post-launch support.

You will develop global medical and clinical strategies, lead trial design, oversee trial conduct, ensure regulatory compliance with FDA/ICH/GCP, support regulatory submissions, and collaborate with Medical Affairs, Regulatory, and Business units while engaging with external experts and

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