Clinical Project Lead - GMP/GxP Trials

Azenta US, Inc.; Plainfield (IN); On-site; USD 74,000 - 93,000; Full time

Job summary

Azenta Inc. is seeking a Clinical Project Manager II to join Azenta Life Sciences. You will serve as the primary client contact on assigned projects, ensuring regulatory compliance and successful delivery of long-term sample management and other clinical services.

The role requires a science degree and project management experience in FDA/GXP environments, with opportunities to mentor others and contribute to process improvements across global programs.

Qualifications

• Bachelor's degree in science or related field with a minimum of 2 years of project management experience.
• High School Diploma or its equivalent with a minimum of 5 years of project management experience.
• Experience working in an FDA and GXP regulated environments.

Responsibilities

• Serve as the primary client contact for assigned projects and establish working relationships with client project teams.
• Ensure that all customer expectations are documented and acted upon in compliance with regulatory requirements.
• Create required project plans and monitor progress against them.
• Mentor Client Coordinator as needed.
• Participate in pre-sale discussions and client meetings.

Skills

Project management

Regulatory compliance

Communication

Organizational skills

Mentoring

Education

Bachelor's degree in science or related field

Master's degree in science or related field

CSPO/CSM/PMP certification

Tools

Regulatory systems

Job description

Azenta Inc. is seeking a Clinical Project Manager II to join Azenta Life Sciences. You will serve as the primary client contact on assigned projects, ensuring regulatory compliance and successful delivery of long-term sample management and other clinical services.

The role requires a science degree and project management experience in FDA/GXP environments, with opportunities to mentor others and contribute to process improvements across global programs.