Senior Clinical Trial Associate

Scorpion Therapeutics

United States

Remote

USD 65,000 - 95,000

Full time

13 days ago
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Job summary

Scorpion Therapeutics is seeking a Clinical Trial Associate to support ophthalmology trials under supervision. You will assist planning, protocol development, IRB submissions, site communication, monitoring support, and TMF maintenance.

The role requires strong knowledge of GCP and FDA regulations, plus excellent medical terminology, communication, and computer skills. Remote US work with minimal travel is expected.

Qualifications

  • Bachelor's degree in health or science field.
  • At least 3 years of clinical trial experience.
  • Strong knowledge of GCP and FDA regulations.
  • Proficient in medical terminology, communication, and computer skills.

Responsibilities

  • Assist study planning, protocol and documentation development.
  • IRB submissions, site communication, monitoring support, and TMF maintenance.
  • Ensure compliance with GCP, FDA, and international regulations across clinical investigations.
  • Collaborate with cross-functional teams such as R&D, Regulatory, Safety, and Quality.

Skills

GCP knowledge
FDA regulations
Medical terminology
Communication skills
Computer skills

Education

Bachelor's in health or science field
Advanced degree preferred

Job description

Role: Clinical Trial Associate supporting the execution and management of ophthalmology clinical studies, under supervision.

Responsibilities
  • Assisting with study planning, protocol and documentation development, IRB submissions, site communication, monitoring support, and TMF maintenance.
  • Ensures compliance with GCP, FDA, and international regulations across clinical investigations.
  • Collaborates with cross-functional teams such as R&D, Regulatory, Safety, and Quality.
  • Provides operational support, tracks study payments, and aids in study start-up activities.
Qualifications
  • Bachelor’s in health or science field
  • minimum 3 years of clinical trial experience
  • strong knowledge of GCP and FDA regulations
  • proficient in medical terminology, communication, and computer skills
  • Preferred: advanced degree

Work setup is remote in the US, with minimal travel expected.

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