Clinical Trials Activation Lead

Dartmouth-Hitchcock Medical Center; Lebanon (NH); On-site; USD 65,000 - 85,000; Full time

Job summary

Dartmouth-Hitchcock Medical Center is seeking a start-up specialist to manage clinical trial activation activities from feasibility to site activation. You will collaborate with internal and external stakeholders to ensure timely study startup and regulatory compliance.

The role emphasizes site selection, activation tracking, and coordination with Regulatory teams and clinical units to streamline processes and meet sponsor expectations.

Qualifications

• Bachelor’s degree with 5 years of clinical research experience.
• Excellent organizational, writing, and office software skills.
• Excellent oral communication and interpersonal skills.
• Knowledge of FDA/ICH regulations and human subjects protections.

Responsibilities

• Organizes and manages implementation of activities required for the study activation process, including feasibility, committee approvals, and regulatory information.
• Leads study site selection and start-up activities.
• Responsible for tracking progress of all studies in the department activation pipeline and reviews progress with research teams.
• Coordinates and attends Resource Meetings with the Clinical Trials Office and study team members; ensures follow-up items progress.

Skills

Organizational skills

Writing skills

Oral communication

Scheduling coordination

Education

Bachelor’s degree

Tools

Clinical trials management system

Job description

Dartmouth-Hitchcock Medical Center is seeking a start-up specialist to manage clinical trial activation activities from feasibility to site activation. You will collaborate with internal and external stakeholders to ensure timely study startup and regulatory compliance.

The role emphasizes site selection, activation tracking, and coordination with Regulatory teams and clinical units to streamline processes and meet sponsor expectations.