Remote Clinical Trials Manager - Operations Lead (Phase I–III)

Bristol-Myers Squibb Company; United States; Remote; USD 135,000 - 163,000; Full time

Benefits offered by this job

Flexible Time Off

11 paid company holidays

Vacation for new hires

Job summary

RayzeBio, a Bristol Myers Squibb company, seeks a Clinical Trials Manager, Clinical Operations to oversee study planning and delivery across Phase I–III. You will manage CROs and vendors, ensuring adherence to SOPs, FDA regulations, and ICH/GCP guidelines, while coordinating with cross-functional teams to meet timelines and budgets.

The role is remote within the United States, with travel up to 20% as needed to support trial activities and site initiation.

Qualifications

• BA/BS in scientific or healthcare field.
• Minimum 5-7 years clinical operations experience.
• Experience managing CROs and vendors.
• Knowledge of GCP/ICH FDA regulations.
• Ability to work in cross-functional teams.

Responsibilities

• Lead the planning, execution, and closeout of clinical trials from Phase I–III.
• Oversee CROs and vendors to ensure on-time, on-budget delivery per SOPs and regulations.
• Lead cross-functional study execution teams and ensure timelines and deliverables.
• Plan and manage study timelines, milestones, and budgets.
• Monitor progress, enrollment, data quality, and risk indicators; escalate issues.
• Manage CRO/vendor budgets and invoicing; support feasibility and activation strategies.
• Summarize performance data and communicate risks to leadership.
• Up to 20% travel.

Skills

Independent communicator

Detail-oriented

Cross-functional

Flexible

Microsoft Project

Smartsheets

AI in Ops

Education

Bachelor's degree

Tools

Microsoft Project

Smartsheets

Job description

RayzeBio, a Bristol Myers Squibb company, seeks a Clinical Trials Manager, Clinical Operations to oversee study planning and delivery across Phase I–III. You will manage CROs and vendors, ensuring adherence to SOPs, FDA regulations, and ICH/GCP guidelines, while coordinating with cross-functional teams to meet timelines and budgets.

The role is remote within the United States, with travel up to 20% as needed to support trial activities and site initiation.