Senior Oncology Project Lead — Global Clinical Trials

NCBioImpact; Durham (NC); On-site; USD 129,000 - 255,000; Full time

Benefits offered by this job

Competitive benefits package

Job summary

Worldwide Clinical Trials is seeking a Senior Project Manager to lead clinical trials in oncology from start-up to closeout. You will direct technical, financial, and operational aspects and coordinate with functional leads to ensure on-time, on-budget study delivery.

Ideal candidates have 6–7 years in CRO clinical PM, oncology experience, a Life Science degree, and willingness to travel. The role includes comprehensive benefits and transparent compensation.

Qualifications

• 6-7 years of industry experience in a Clinical Project Management role within a CRO setting.
• Oncology experience in a PM role is required.
• Ability to travel when needed.

Responsibilities

• Senior Project Manager (SPM) is responsible for the overall coordination and management of clinical trials from start-up through closeout activities.
• Directs the technical, financial and operational aspects of the projects—thus securing the successful completion of clinical trials.
• Works with major functional area leads to identify and evaluate fundamental issues on the project, interpret data on complex issues, make good business decisions and ensure solutions are implemented.
• Works to ensure that all project deliverables meet the customer’s time/quality/cost expectations.
• The SPM, with support from the Project Management Directors, working in collaboration with other functional area leads, is accountable for ensuring that all project deliverables meet the customer/contract expectations.

Skills

Clinical project management

Oncology experience

Team leadership

Budget management

Travel willingness

Education

Life Science degree

Job description

Worldwide Clinical Trials is seeking a Senior Project Manager to lead clinical trials in oncology from start-up to closeout. You will direct technical, financial, and operational aspects and coordinate with functional leads to ensure on-time, on-budget study delivery.

Ideal candidates have 6–7 years in CRO clinical PM, oncology experience, a Life Science degree, and willingness to travel. The role includes comprehensive benefits and transparent compensation.