Senior Clinical Trial Manager

Vera Therapeutics, Inc.

WorldwideFully remoteFull TimeSeniorHealthcare & Telemedicine
USD 130,000–190,000 a yearPosted 5h ago

Why we think you can apply

Hiring model
Open worldwide · the employer states no country restriction
Work from
Anywhere, the UAE included

Posted 5 hours ago · apply link checked 4 hours ago

About the role

Responsibilities

  • Manage all clinical operational aspects of a global clinical trial from start-up to close-out
  • Monitor trial adherence to GCP, protocol, SOPs and key performance indicators
  • Oversee CRO and sites, serving as primary CRO/vendor contact
  • Identify study risks and implement solutions
  • Manage study timelines aligned with corporate goals
  • Contribute to protocols and clinical study reports
  • Lead clinical operational and study team meetings
  • May travel up to 30% to support clinical programs

Requirements

  • BS or higher in life sciences or health-related field
  • 5+ years clinical development experience
  • Progressive clinical research experience in pharma or biotech
  • Working proficiency in GCP, ICH guidelines and FDA regulations
  • Experience managing and mentoring junior staff
  • Proficiency with MS Office
  • Strong interpersonal and written communication skills

Preferred Qualifications

  • Rare disease or inflammatory disease study experience
  • Regulatory filing and inspection readiness experience

Benefits

  • Annual performance incentive bonus and equity
  • Medical, dental and vision insurance, 401k match, flexible time off, paid holidays

About the Company

Vera Therapeutics is a commercial-stage biotechnology company focused on autoimmune disease, starting with the kidney.

What we look for

  • BS or higher in life sciences or health-related field
  • 5+ years clinical development experience
  • Progressive clinical research experience in pharma or biotech
  • Working proficiency in GCP, ICH guidelines and FDA regulations
  • Experience managing and mentoring junior staff
  • Proficiency with MS Office
  • Strong interpersonal and written communication skills
  • Rare disease or inflammatory disease study experience
  • Regulatory filing and inspection readiness experience
MS OfficeGCPClinical ResearchCRO ManagementICHRegulatory Filing
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