Clinical Project Manager

Description:

The Clinical Project Manager within the Project Management Organization (PMO) is expected to provide project management support to internal team members, as well as customers, to deliver Azenta Life Sciences solutions to clients, partners, and alliances. Under guidance from the Director, Clinical Program Management, the Clinical Project Manager is expected to gain an in-depth understanding of the key clients and become an expert in Azenta Life Sciences services.

What You Will Do

Serve as the primary client contact for assigned project and establish working relationships with client project teams which result in client satisfaction, operational excellence and thereby increase potential for repeat business. Ensure that all customer expectations are documented and acted upon in compliance with regulatory requirements. Able to act efficiently in an environment with dynamic timelines and priorities. Accountable for the implementation, monitoring, and reporting of performance metrics. Create required project plans. Implement and monitor progress against project plans and revise as necessary. Monitor project schedule and scope to ensure both remain on track. Project support may include kit provision and logistics, sample management, lab services support, relocation services, training, management, or support of alliances/ partnerships. Proactively engage in both quality assurance and risk management activities to ensure project deliverables are met according to both Azenta and client requirements. Actively participate in Azenta development through continuous process improvement, quality, and productivity. Participate in pre-sale discussion and client meetings as required. Participate and/ or present sponsor investigator meeting and/or on site visit as requested by the sponsor. Mentor and support other PMO team members.

What You Will Bring
 

• Bachelor's degree in science or related field with a minimum of 2 years of project management experience.
• OR High School Diploma or its equivalent and a minimum experience of 5 years of project management experience.
• Experience working in an FDA and GXP regulated environments.
• Preferred master’s degree in science or related field.
• Preferred CSPO, CSM, PMP
• Strong organizational skills and attention to detail.
• Excellent verbal and written communication skills; presentation skills, ability to engage in effective problem-solving conversations.
• Demonstrated ability to collaborate and gain commitment from others.
• Demonstrated ability to prioritize work, customers, internal and external demands.
• Demonstrated ability to complete long-range projects as assigned.
  
   

Your Working Conditions:
 

• General office setting.
• The Employee may occasionally travel, up to 10% of working time.
• The Employee may occasionally work in an area with potentially infectious materials.
• The Employee will be responsible for maintaining a clean work environment and enforcing and following Universal Precautions for bloodborne pathogens when working in an area considered to be potentially contaminated.