Sr. Manager, Clinical Program Management, Clinical Operations

Working with Us
Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.

Job Title: Sr. Manager, Clinical Program Management -Clinical Operations

Department: Clinical

Location: Remote

Summary:

The Sr. Manager, Clinical Program Management is responsible for the oversight, planning and delivery of assigned global clinical study(ies) within the RayzeBio programs, including oversight and management of the study Clinical Research Organization (CRO) and Vendors according to and in compliance with corporate and program Standard Operating Procedures (SOPs), Good Clinical Practice (GCP)/International Conference on Harmonization (ICH) guidelines and other applicable federal (FDA) and state regulations, in order to achieve established study goals within timelines and budget and of the highest quality.

Please review the must-have experience for this role before applying.

Job Responsibilities:

Essential duties and responsibilities include the following.  Other duties may be assigned.

• Manage global clinical study teams, CROs and vendors to ensure that the study(ies) are completed

on time, within budget, and in compliance with RayzeBio SOPs, FDA regulations and ICH/GCP guidelines

• Leads the cross-functional study execution team in achieving the study goals and deliverables

• Plan and execute study timelines

• Develop and manage risk mitigation strategies for clinical studies

• Tracks, monitors and reports on study progress and proactively escalates issues to key internal stakeholders to ensure timely resolution of issues

• Manage study CRO and vendor budgets and invoicing procedures according to study contract

• Perform oversight review and quality control of CRO and vendor scope of activities, ensuring compliance to key performance metrics and overall inspection readiness

• Active participant in CRO and vendor meetings, responsible to review key CRO and vendor study operational plans and provides input to operational strategy, including country and site feasibility and start-up

• Summarizes CRO and vendor performance data and escalates study risks to the Head of Clinical Operations

• Performs other related duties as assigned

• Up to 20% travel required

Education and Experience:

·Minimum 5-7 years clinical operations experience within biotech, pharma or CRO industry

·Must have experience directly managing global Phase III studies

·Must have some experience at small/mid-sized biotech in Clinical Operations

·BA/BS degree, scientific or healthcare discipline preferred

Skills and Qualifications:

• Independent professional who proactively communicates frequently and effectively.

• Detail and action-oriented, organized and committed to quality and consistency.

• Ability to work successfully in cross-functional teams.

• Ability to work in a dynamic environment with a high degree of flexibility.

• Expertise in Microsoft Project and Smartsheets desired.

Work Environment:

The noise level in the work environment is usually moderate.

The starting compensation for this job is a range from $142,000-$193,000.00 plus incentive cash and stock opportunities (based on eligibility). The sta