Azenta Life Sciences

Clinical Project Manager II

Azenta Life Sciences$74K — $93K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in science or related field with 2+ years of project management experience, or a High School Diploma with 5+ years of experience.
  • Experience in FDA and GXP regulated environments.
  • Preferred master's degree in science or related field.
  • Preferred CSPO, CSM, or PMP certification.
  • Strong organizational skills and attention to detail.
  • Excellent verbal and written communication skills, including the ability to engage in effective problem-solving conversations.
  • Demonstrated ability to collaborate and prioritize work.

Responsibilities

  • Serve as the primary client contact for assigned projects, ensuring client satisfaction.
  • Document customer expectations and ensure compliance with regulatory requirements.
  • Act efficiently with changing timelines and priorities.
  • Monitor and report performance metrics for project accountability.
  • Create and implement project plans, revising them as necessary.
  • Monitor project schedule and scope to ensure they remain on track.
  • Engage in quality assurance and risk management activities to meet project deliverables.

Benefits

  • Work in a collaborative, growth-oriented environment.
  • Opportunity for mentorship and professional development.
  • Involvement in continuous improvement initiatives and development of new processes.
  • A clean and safe working environment with adherence to health protocols.
  • Potential for partial remote work with occasional travel.
Full Job Description
Job Title
Clinical Project Manager II

Job Description

Azenta Life Sciences is a global leader in the life sciences space with headquarters with offices and operations worldwide. We are a market leader in automated bio sample management solutions and genomic services across areas such as drug development, clinical and advanced cell therapies for the industry's top pharmaceutical, biotech, academic and healthcare institutions globally. We provide unparalleled capabilities with our lab analysis, sample management and storage services, informatics software, and consumables, with the largest installed base managing over 1 billion samples globally.

How You'll Add Value:

The Clinical Project Manager within the Program Management Organization (PMO) is expected to provide project management support to internal team members, as well as customers, to deliver Azenta Life Sciences solutions (Long Term Sample Management, Active Clinical Trial Sample Management, Regulated Products (GMP/GTP) Management) to clients, partners, and alliances. Under guidance from the Director, Clinical Program Management or Program Manager, 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'll Do:
  • Serve as the primary client contact for assigned projects 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 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 Life Sciences and client requirements
  • Participate in pre-sale discussions and client meetings as required
  • Actively participate in Azenta Life Sciences development through continuous improvement initiatives, contributing to Azenta's culture of quality and productivity initiatives including the development of new processes and SOPs, and the maintenance of SOPs to maintain audit-ready alignment with the Azenta Business Systems
  • Mentor Client Coordinator as needed
  • Managing queries and resolutions


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


Join us and help enable life-changing discoveries by keeping critical life science systems running reliably-every day.

#IND123

United States Base Compensation: $74,000.00 - $93,000.00

The posted pay range for this position is an estimate based on current market data and internal pay structure. Final compensation may vary above or below this range depending on factors such as experience, education (including licensure and certifications), qualifications, performance, and geographic location, among other relevant business or organizational needs.

About Azenta Life Sciences

Azenta Life Sciences is a pharmaceutical company that specializes in developing and commercializing innovative therapies for the treatment of cancer. The company's lead product candidate is a novel small molecule inhibitor of the Wnt signaling pathway, which is being developed for the treatment of various types of cancer. Azenta Life Sciences was founded in 2018 and is headquartered in Oakbrook Terrace, Illinois.
Learn more about Azenta Life Sciences
Size
10 employees
Industry
Founded
2018

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