Senior Clinical Trial Manager Decentralized Neurology Trials

Neurocentria, Inc.

Walnut Creek (CA)

On-site

USD 160,000 - 190,000

Full time

7 days ago
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Benefits offered by this job

401(k) with above-market company match
Comprehensive medical, dental, vision,
Life insurance

Job summary

Neurocentria, Inc. is seeking a Senior Clinical Trial Manager to lead two concurrent fully decentralized Phase 2 trials in neurology and cognitive health. You will own day-to-day CRO performance, budgets, timelines, and regulatory compliance from startup through database lock.

This senior individual contributor role collaborates directly with the Principal Investigator and Head of Clinical Operations in a lean team to ensure trials advance on time and within scope.

Qualifications

  • Bachelor’s degree in life sciences or clinical research required.
  • Advanced degree preferred (MS/MPH/PharmD).
  • Minimum 8 years of clinical trial operations experience.
  • Minimum 3 years of sponsor-side CRO oversight.
  • Experience with decentralized or hybrid trials.

Responsibilities

  • Sponsor-side lead for two decentralized Phase 2 trials; oversee CRO performance.
  • Identify operational risks and mitigation strategies.
  • Lead study startup, CRO RFPs, and contract reviews.
  • Maintain Trial Master File and SAEs reporting timelines.
  • Manage budgets and CRO invoicing; approve change orders.
  • Support IND amendments, IRB submissions, and regulatory interactions.

Skills

CRO oversight
DCT experience
IND regulatory knowledge
EDC systems
GCP knowledge
Budget management

Education

Bachelor’s degree in life sciences, clinical research, nursing, or related field
MS / MPH / PharmD preferred

Tools

REDCap / Medidata Rave

Job description

Neurocentria, Inc. is seeking a Senior Clinical Trial Manager to lead two concurrent fully decentralized Phase 2 trials in neurology and cognitive health. You will own day-to-day CRO performance, budgets, timelines, and regulatory compliance from startup through database lock.

This senior individual contributor role collaborates directly with the Principal Investigator and Head of Clinical Operations in a lean team to ensure trials advance on time and within scope.

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