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Clinical Implementation Manager Jobs in Springfield, PA

Erickson

Clinical Manager, RN

Warminster, PA · On-site

The Clinical Manager is an active member of the clinical leadership team who is responsible for the assessment, coordination, implementation, and evaluation of the delivery of safe and effective ...

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Clinical Trial Manager

Blue Bell, PA

As a Senior Clinical Trial Manager at ICON, you will manage clinical trial operations activities ... Improving Study Integrity Review trip reports and implement corrective and preventative action ...

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ICON

Clinical Project Manager

Blue Bell, PA · On-site

Clinical Project Manager, Immunology - Remote, US ICON is a global healthcare intelligence and ... Monitoring project progress, identifying potential risks and issues, and implementing strategies to ...

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Clinical Project Manager

Blue Bell, PA · Remote

Clinical Project Manager, Immunology - Remote, US ICON is a global healthcare intelligence and ... Monitoring project progress, identifying potential risks and issues, and implementing strategies to ...

Erickson

Clinical Manager, RN

Glen Mills, PA · On-site

$115K/yr

The Clinical Manager will also facilitate, precept, and mentor staff to grow professionally and ... Coordinating, implementing, and overseeing the clinical care of guests/residents in skilled nursing ...

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Clinical Implementation Manager information

See Springfield, PA salary details

$36.8K

$97.7K

$158.5K

How much do clinical implementation manager jobs pay per year?

As of Jun 10, 2026, the average yearly pay for clinical implementation manager in Springfield, PA is $97,654.00, according to ZipRecruiter salary data. Most workers in this role earn between $71,200.00 and $114,100.00 per year, depending on experience, location, and employer.

What is the difference between Clinical Implementation Manager vs Clinical Project Coordinator?

AspectClinical Implementation ManagerClinical Project Coordinator
CredentialsTypically requires a healthcare-related degree and experience in clinical settingsOften requires a bachelor's degree, with some roles preferring healthcare or project management background
Work EnvironmentLeads clinical implementation projects, collaborates with healthcare providers and vendorsSupports project activities, coordinates schedules, and assists project teams
Employer & Industry UsageUsed in hospitals, healthcare companies, and medical device firmsCommon in healthcare organizations, research institutions, and pharmaceutical companies

The Clinical Implementation Manager focuses on leading and executing clinical implementation strategies, ensuring successful deployment of new systems or protocols. In contrast, the Clinical Project Coordinator provides support and coordination for clinical projects, assisting with scheduling, documentation, and communication. Both roles are essential in healthcare settings but differ in scope and responsibilities.

How does a Clinical Implementation Manager typically collaborate with clinical staff and technology teams during new system rollouts?

Clinical Implementation Managers play a crucial role in bridging the gap between clinical staff and technology teams. They coordinate with clinicians to gather workflow requirements and ensure that new systems align with patient care needs. Simultaneously, they work closely with IT professionals to translate clinical requirements into technical specifications, facilitate troubleshooting, and manage timelines. Effective communication and the ability to tailor training sessions for various user groups are key to successful collaboration and system adoption.

What are the key skills and qualifications needed to thrive as a Clinical Implementation Manager, and why are they important?

To thrive as a Clinical Implementation Manager, you need a background in healthcare or life sciences, strong project management skills, and experience with clinical workflows or health IT systems. Familiarity with electronic health record (EHR) platforms, implementation methodologies, and relevant certifications like PMP or Lean Six Sigma is often required. Outstanding interpersonal communication, problem-solving, and change management abilities help you gain stakeholder buy-in and drive successful adoption. These skills are crucial for ensuring smooth integration of clinical solutions, optimizing workflow efficiency, and achieving desired healthcare outcomes.

What does a Clinical Implementation Manager do?

A Clinical Implementation Manager oversees the deployment and integration of healthcare technologies, systems, or processes within clinical settings. Their responsibilities include coordinating with healthcare staff, training users, ensuring compliance with regulations, and troubleshooting any issues during the implementation phase. They act as a liaison between technical teams and clinical staff to ensure smooth transitions and adoption of new tools or procedures. This role is crucial for improving patient care and operational efficiency when adopting new clinical solutions.
What cities near Springfield, PA are hiring for Clinical Implementation Manager jobs? Cities near Springfield, PA with the most Clinical Implementation Manager job openings:
Clinical Implementation Manager jobs near you
Director / Associate Director Companion Diagnostics Lead, Translational Sciences

Director / Associate Director Companion Diagnostics Lead, Translational Sciences

Incyte Corporation

Wilmington, DE • On-site

Full-time

Posted 6 days ago

Job description

Overview
A global biopharmaceutical company on a mission to Solve On, Incyte follows science to find solutions for patients with unmet medical needs. Through the discovery, development, and commercialization of proprietary therapeutics, Incyte has established a portfolio of first-in-class medicines for patients and a strong pipeline of products in Hematology, Oncology and Inflammation and Autoimmunity. Headquartered in Wilmington, Delaware, Incyte has operations in North America, Europe, and Asia.
Job Summary (Primary function)
Associate Director, Companion Diagnostics Lead is a leadership role responsible for the development and implementation of clinical diagnostic plans including companion diagnostics (CDx) requirements within drug development programs. This involves active participation in CDx strategy setup and deployment, managing logistics, vendor selection and relationships, and ensuring timely CDx delivery.
Key duties include:
  • Serve as subject matter expert in CDx development process (from concept to commercialization)
  • Lead selection and management of diagnostic partners
  • Monitor assay analytical and clinical performance evaluation activities
  • Author CDx related parts across documents
  • Ensure CDx representation in cross-functional teams

  • Serve as alliance and project manager between Incyte and key diagnostic partners
  • Generate and review new project agreements as needed
  • Manage and maintain CDx budget for projects
  • Track and approve milestones for each project
  • Lead Joint project team (JPT) meetings with alliance partner

  • Supervise validation and implementation of clinical trial assay (CTA) at testing laboratory
  • Maintain alignment between diagnostics partner and testing laboratory
  • Ensure timelines are met
  • Oversee operational aspects of clinical implementation

  • Ensure compliance with regulatory and ethical guidelines
  • Develop and apply expertise in regulatory requirements for CDx across regions (US FDA, EU IVDR etc)
  • Supervise Incyte review of CDx documentation such as clinical study performance plans (CPSP), Instructions for Use etc
  • Ensure creation and review of informed consent, CPSP and country submissions/responses are timely and compliant
  • Develop and Maintain Expertise in Delivery of Companion Diagnostics
  • Maintain relationships with key stakeholders

Qualifications (Minimal acceptable level of education, work experience, and competency)
  • Minimum BS Degree in a scientific discipline with 7+ years of experience in the diagnostic and/or pharmaceutical industry (clinical studies).
  • Understanding of Good Clinical Practices (GCP) and relevant regulatory requirements. Ability to manage external research activities through CROs and collaborators.
  • Ability to balance execution of multiple tasks to accomplish program goals.
  • A high level of emotional intelligence and willing to work closely and collaboratively with other functional groups internal and external to the company.
  • Exceptional verbal and written communication skills.

Preferred Qualifications:
  • Advanced degree in a scientific discipline with extensive experience in CDx development, registration and commercialization and IVD clinical studies.
  • Extensive knowledge of assay development using Next Generation Sequencing, PCR and Immunohistochemistry.
  • Experience in CDx and/or precision medicine including IVDR.

Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.
Incyte Corporation is committed to creating a diverse environment and is proud to be an equal opportunity employer.
We Respect Your Privacy
Learn more at: http://www.incyte.com/privacy-policy
The Incyte hiring organization processes your personal data to manage your job application in order to enter into an employment relationship with you if you are the successful candidate.
During the process, you may be asked to respond to questions that will screen out your application if you do not meet certain objective criteria required by the job. You can learn more about this process here.
You may have the right to access, delete, restrict, edit, move, or object to the use of your personal data. You may also have a right to report concerns to the authority responsible for data privacy in the country where the position is based or where you live or work.
You can learn more about Incyte's data protection practices here. By accessing this link you can learn about the types of personal data we collect, how we use it, whether collection and processing is optional, sources of the personal data we process, how it is shared, where it is stored or transferred to, how long we keep it, and contact information for Incyte, Incyte's data protection officer, and your supervisory authority (if applicable).
Please contact privacy@incyte.com if you have any questions or concerns or would like to exercise your rights.

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