Clinical Study Program Lead

Integrated Resources Inc.; New Haven (CT); On-site; USD 90,000 - 150,000; Full time

Job summary

A leading company specializing in strategic workforce solutions seeks a Clinical Study Manager to oversee the execution and integrity of clinical studies. The ideal candidate will have a strong background in clinical research and project management, ensuring data quality and adherence to regulatory standards. This role demands effective collaboration with various teams to achieve operational excellence and safeguard volunteer safety throughout the clinical trials.

Qualifications

• Minimum of BA/BS in a biomedical discipline required.
• Relevant experience in clinical research and drug development with clinical operations experience required.
• Experience in Project Management and leadership of matrix teams is essential.

Responsibilities

• Leads the cross-functional execution of clinical studies.
• Coordinates and reviews all study activities.
• Ensures compliance with GCP and regulatory requirements.

Skills

Project Management

Data management

Clinical study management

Regulatory processes

Problem Solving

Education

BA/BS in a biomedical discipline

Advanced training/education preferred

Tools

MS Office tools

Job description

A leading company specializing in strategic workforce solutions seeks a Clinical Study Manager to oversee the execution and integrity of clinical studies. The ideal candidate will have a strong background in clinical research and project management, ensuring data quality and adherence to regulatory standards. This role demands effective collaboration with various teams to achieve operational excellence and safeguard volunteer safety throughout the clinical trials.