Clinical Project Lead, Life Sciences Programs

Azenta Life Sciences; Plainfield (IN); On-site; USD 74,000 - 93,000; Full time

Job summary

Azenta Life Sciences is seeking a Clinical Project Manager II to lead and deliver complex clinical projects in a regulated environment.

You will act as the primary client contact, manage project plans, timelines, and scope, and collaborate with internal teams to ensure successful delivery and compliance. Strong communication and problem‑solving skills are essential for this role in a dynamic office setting.

Qualifications

• Bachelor's degree in science or related field with 2+ years of project management experience, or High School Diploma with 5+ years of PM experience.
• Experience in FDA and GXP regulated environments is required.
• Preferred Master’s degree in science or related field; CSPO/CSM/PMP certifications are a plus.

Responsibilities

• Serve as the primary client contact for assigned projects and develop strong client relationships for satisfaction and repeat business.
• Ensure all customer expectations are documented and comply with regulatory requirements.
• Create, monitor, and adjust project plans and schedules; manage scope and timelines.
• Coordinate logistics and trial support activities across Azenta Life Sciences services.
• Mentor junior team members and support continuous improvement initiatives.

Skills

Project management

Regulatory experience

Communication

Education

Bachelor's degree in science or related field

High School Diploma with 5 years PM experience

Master's degree (preferred)

Tools

CSPO

CSM

PMP

Job description

Azenta Life Sciences is seeking a Clinical Project Manager II to lead and deliver complex clinical projects in a regulated environment.

You will act as the primary client contact, manage project plans, timelines, and scope, and collaborate with internal teams to ensure successful delivery and compliance. Strong communication and problem‑solving skills are essential for this role in a dynamic office setting.