Local Trial Manager: Lead Fast-Track Clinical Trials

IQVIA; Durham (NC); On-site; USD 68,400 - 232,800; Full time

Job summary

IQVIA is seeking an Associate Project Lead (Local Trial Manager) to join our Durham, NC clinical delivery team. You will collaborate with clinical and functional teams to drive study execution under SOPs, delivering quality results and client satisfaction.

The role requires a Bachelor's in life sciences and at least 2 years of clinical trial management experience, with strong communication skills and proficiency in MS Office.

Qualifications

• Bachelors degree in life sciences or related field is required.
• Minimum 2 years clinical research experience in project or trial management.
• Solid understanding of clinical trials and ICH GCP guidelines.
• Strong written and verbal English communication and presentation skills.
• Good problem solving, planning and prioritization abilities.
• Experience coordinating with cross-functional teams and clients.
• Familiarity with study financials and change control processes.

Responsibilities

• Develop integrated study management plans with core project teams.
• Lead assigned portion of studies ensuring speed, quality and cost targets.
• Set objectives for sub-teams and monitor performance.
• Collaborate with other functions to meet milestones and resolve issues.
• Provide risk management input and support contingency planning.
• Ensure quality by addressing risks and implementing corrective actions.
• May serve as primary or backup contact for customers.
• Support project leader in vendor management and change control.
• Forecast opportunities to accelerate activities and revenue.

Skills

Project management

Communication skills

Problem solving

Organization

Time management

Collaboration

Cross-cultural awareness

Client focus

Education

Bachelor's Degree in life sciences

Tools

MS Office

Job description

IQVIA is seeking an Associate Project Lead (Local Trial Manager) to join our Durham, NC clinical delivery team. You will collaborate with clinical and functional teams to drive study execution under SOPs, delivering quality results and client satisfaction.

The role requires a Bachelor's in life sciences and at least 2 years of clinical trial management experience, with strong communication skills and proficiency in MS Office.