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Clinical Trial Manager (CTM)

1 hour, 38 minutes ago
United States
Full-time
Senior
Program Manager
Project and Program Management
GCP
Apply Now
bridgebiowp

bridgebiowp

bridgebiowp is a biotechnology firm focused on designing transformative medicines specifically for patients suffering from genetic diseases and cancers that have identifiable genetic drivers.

Pharmaceuticals
251-1K
Founded 2014
$2300M raised
View All Jobs 38

Description

  • Coordinate and drive operational activities across assigned study workstreams, including study start-up, enrollment, monitoring, database lock, and close-out.
  • Maintain study trackers, timelines, and deliverable logs, and escalate schedule risks with mitigation plans.
  • Manage CROs and external vendors throughout study start-up, conduct, and close-out to ensure on-time, on-budget, and compliant delivery.
  • Oversee clinical monitoring activities, including review of monitoring visit reports and monitoring oversight visits.
  • Participate in cross-functional and vendor meetings and document decisions and action items.
  • Oversee site-level operational activities such as specimen management, subject visit tracking, and timely data review.
  • Support site feasibility, selection, and initiation, and help develop and approve key study documents such as monitoring plans, ICFs, CRFs, pharmacy manuals, and laboratory manuals.
  • Oversee study supply management, review budgets, and evaluate CRO/vendor invoices.
  • Maintain the Trial Master File so it remains current, accurate, and inspection-ready.
  • Support protocol development, study report development, and investigator meetings.

Requirements

  • BA/BS in life sciences, nursing, or a related field, or equivalent work experience.
  • At least 5 years of progressive experience in clinical operations, clinical research, or a CRO/pharma environment.
  • Direct experience with site management, monitoring, or clinical operations, including site visit experience.
  • Hands-on experience with eTMF systems and clinical data systems (EDC).
  • Proficiency with common study tracking tools such as Excel and Smartsheet.
  • Working knowledge of ICH-GCP and applicable regulatory requirements, including FDA and EMA standards.
  • Strong organizational skills, attention to detail, and the ability to manage competing priorities.
  • Excellent interpersonal and written/verbal communication skills and comfort coordinating across functional teams.

Benefits

  • Salary range of $145,000 to $177,000 USD for California-based candidates.
  • Market-leading compensation, including base pay and an annual performance bonus.
  • Company equity, including participation in an Employee Stock Purchase Program (ESPP).
  • 401(k) with employer match.
  • 100% employer-paid medical, dental, and vision premiums for employees and dependents.
  • Health Savings Account (HSA) with annual employer contributions and Flexible Spending Accounts (FSA).
  • Flexible, hybrid work model with remote flexibility and quarterly or as-needed travel to San Francisco.
  • Flexible “take-what-you-need” paid time off plus company-paid holidays.
  • Comprehensive paid medical and parental leave.
  • Fertility and family-forming benefits.
  • Expanded mental health support, including therapy and coaching resources.
  • Subsidized lunch and parking on in-office days.
  • Referral bonus for hired candidates.
  • Professional development and career pathing through LinkedIn Learning, LifeLabs, and BetterUp Coaching.

Interested in this position?

Apply directly on the company website

Apply Now

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