Site Activation Lead – Clinical Trials

IQVIA; Indianapolis (IN); On-site; USD 60,000 - 157,000; Full time

Job summary

IQVIA, a global leader in clinical research, seeks a Site Activation Lead in Indianapolis area to direct strategic, operational and financial delivery of site activation for assigned studies across regions. Responsibilities include coordinating site ID/selection, ethics and regulatory processes, and site contracting while ensuring ICH-GCP compliance and timelines.

You will collaborate with internal and external stakeholders, drive risk mitigation, and maintain project plans.

Qualifications

• Bachelor's degree in Life Science or related field required.
• At least 3 years relevant experience in a scientific or clinical environment.
• Demonstrable experience in an international role; or equivalent combination of education, training and experience.
• In-depth knowledge of clinical systems, procedures, and corporate standards.
• Strong knowledge of medical terminology and regulations.
• Broad knowledge of clinical research.
• Strong knowledge of Microsoft Office and e-mail applications.
• Effective communication, organizational, and interpersonal skills.
• Ability to work independently and to effectively prioritize tasks.
• Ability to delegate effectively.
• Ability to manage multiple projects.
• Attention to detail.
• Ability to establish and maintain effective working relationships with coworkers, managers and clients.

Responsibilities

• Direct and manage the execution of the strategic, operational and financial delivery of Site Activation activities across regions.
• Provide strategic planning and project oversight to accelerate site activation and patient enrollment.
• Oversee Start Up and Lifecycle Maintenance for assigned projects in compliance with timelines and regulatory requirements.
• Collaborate with stakeholders across regions and countries to deliver project scope.
• Develop and maintain the Site Activation Management Plan within the agreed project strategy.
• Communicate updates to study teams and senior leaders as required.
• Ensure completion and maintenance of internal systems, databases and timelines.
• Review and create documentation to support business development and study initiation.

Skills

Project management

Regulatory understanding

Cross-functional collaboration

ICH-GCP knowledge

Microsoft Office

Education

Bachelor's Degree Life Science or related field

Job description

IQVIA, a global leader in clinical research, seeks a Site Activation Lead in Indianapolis area to direct strategic, operational and financial delivery of site activation for assigned studies across regions. Responsibilities include coordinating site ID/selection, ethics and regulatory processes, and site contracting while ensuring ICH-GCP compliance and timelines.

You will collaborate with internal and external stakeholders, drive risk mitigation, and maintain project plans.