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Ecg Project Manager Jobs (NOW HIRING)

Medpace, Inc.

Oncology Project Manager

Cincinnati, OH · On-site

The primary role of the Project Manager is to provide tactical management, administration, and ... central imaging, ECG, and/or remote biosensing technology data management; * Utilize study ...

Medpace

Neuroimaging Project Manager

Cincinnati, OH · On-site

The primary role of the Project Manager is to provide tactical management, administration, and ... central imaging, ECG, and/or remote biosensing technology data management; * Utilize study ...

Medpace, Inc.

Oncology Project Manager

Cincinnati, OH · On-site +1

The primary role of the Project Manager is to provide tactical management, administration, and ... central imaging, ECG, and/or remote biosensing technology data management; * Utilize study ...

Medpace, Inc.

Oncology Project Manager

Denver, CO · On-site

$80K - $120K/yr

The primary role of the Project Manager is to provide tactical management, administration, and ... central imaging, ECG, and/or remote biosensing technology data management; * Utilize study ...

Medpace, Inc.

Oncology Project Manager

Denver, CO · On-site +1

$80K - $120K/yr

The primary role of the Project Manager is to provide tactical management, administration, and ... central imaging, ECG, and/or remote biosensing technology data management; * Utilize study ...

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Ecg Project Manager information

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How much do ecg project manager jobs pay per year?

As of Sep 11, 2026, the average yearly pay for ecg project manager in the United States is $102,682.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,500.00 and $123,000.00 per year, depending on experience, location, and employer.

What does an ECG project manager do?

An ECG Project Manager oversees projects related to electrocardiogram (ECG) technology, ensuring that tasks are completed on time and within budget. They coordinate between different teams, manage resources, and monitor project progress, often within healthcare or clinical research settings. Their responsibilities may include planning project timelines, managing regulatory compliance, and facilitating communication between stakeholders such as clinicians, engineers, and sponsors. The role requires strong organizational, leadership, and communication skills, as well as a good understanding of ECG technology and medical regulations.

What are the key skills and qualifications needed to thrive as an ECG project manager?

To thrive as an ECG Project Manager, you need expertise in clinical research, project management, and a background in life sciences or healthcare, often supported by a relevant degree. Familiarity with ECG acquisition and analysis systems, project management tools (like MS Project), and regulatory compliance standards such as GCP is typically required. Strong organizational, leadership, and communication skills help coordinate teams and stakeholders across complex projects. These skills ensure accurate data collection, adherence to timelines, and successful delivery of ECG-related clinical study objectives.

How does an ECG project manager coordinate with clinical teams and technical staff during a project?

An ECG Project Manager regularly acts as a liaison between clinical teams, such as cardiologists and research coordinators, and technical staff, including data analysts and device engineers. They facilitate clear communication to ensure project requirements are understood and met, manage timelines for data collection and analysis, and troubleshoot any operational challenges. This collaborative approach helps maintain regulatory compliance and ensures high-quality results, making strong interpersonal and organizational skills essential for success in this role.

What is the difference between Ecg Project Manager vs Ecg Technician?

AspectEcg Project ManagerEcg Technician
CredentialsBachelor's degree in healthcare or related field, project management certification often preferredCertification as an ECG Technician or similar, with specialized training
Work EnvironmentOversees multiple projects, coordinates teams, manages budgets in healthcare settingsPerforms ECG tests directly on patients in clinics or hospitals
ResponsibilitiesPlanning, executing, and closing ECG-related projects; team leadershipConducting ECG procedures, maintaining equipment, recording data

The Ecg Project Manager focuses on overseeing ECG projects, coordinating teams, and managing resources, while the Ecg Technician performs the actual ECG tests and handles patient procedures. Both roles require specialized knowledge, but differ in scope and responsibilities.

What are popular job titles related to Ecg Project Manager jobs?

For Ecg Project Manager jobs, the most frequently searched job titles are:

Infographic showing various Ecg Project Manager job openings in the United States as of September 2026, with employment types broken down into 74% Full Time, 13% Contract, and 13% Nights. Highlights an 87% In-person, and 13% Hybrid job distribution, with an average salary of $102,682 per year, or $49.4 per hour.

Clinical Project Manager

Skaneateles, NY • On-site

Stark Pharma Solutions Inc
See more jobs at Stark Pharma Solutions Incexternal

Contractor

Re-posted 15 days ago

Job description

Hi,

My name is Karthik Mutyala and I’m a Recruitment Manager with Stark Pharma Solutions Inc, specializing in pharmaceutical, biotechnology, and medical device roles. I came across your profile and wanted to see if you are open to new opportunities.

If interested, please send me your updated resume along with the best number and time to reach you.

Job title: Clinical Project Manager

Location: Skaneateles, NY

Duration: 4 Months

Summary:

Responsible for managing the organization and conduct of clinical studies in compliance with Clinical Operations policies and procedures, Regulatory (Health) Authority requirements and guidelines, and International Conference on Harmonization (ICH) Guidelines in support of global business objectives.

Reports directly to Sr. Director of Medical Affairs. The Clinical Project Manager plans for and executes the required global or domestic clinical development plan of drugs and devices to generate data to support the launch and expansion of critical treatments for patients. This data serves to globally support regulatory submissions, post-marketing complaint handling and promotional claims for marketing strategies.

This role also partners cross-functionally with regulatory, engineering, marketing, sales, and research teams to support problem-solving and decision-making efforts.

Top skills needed:

  • 4–5 years of clinical research experience, including 1–2+ years as a Clinical Project Manager
  • Proactive, collaborative, and self-driven with a take-charge attitude
  • End-to-end clinical study experience (site selection, contracting, execution, and closeout)

Essential Duties and Responsibilities:

  • Partner with relevant Baxter functions to develop clinical study plan for each project including timelines and budgets for the clinical program.
  • Prepare directly or facilitate preparation of study documentation including protocols, case report forms, informed consent, enrolment feasibility evaluations and all relevant internal plans required for study conduct.
  • CRO management (when applicable): Lead the day-to-day oversight of the CRO personnel plus the project budget, deliverables and timeline/milestones.
  • Site activities (either directly or managing others): Identify and assess study sites, conduct investigator meetings and site training, prepare and execute research agreements and negotiate study budgets.
  • Study monitoring (either directly or managing others): Formulate clinical monitoring plan, perform study initiation visits, manage clinical study monitoring resources, oversee standard interim monitoring visits and closeout activities
  • Perform study closeout procedures, directly or through other resources, including accurate completion of critical documents, disposition of study product and preparation of study sites for regulatory authority audits.
  • Develop and maintain tracking systems as needed for study management, e.g. screening, enrolment, study completion, (serious) adverse events, budgets and forecasts, milestones.

Qualifications, Education, and Experience

  • Bachelor's degree in a scientific field
  • Minimum 5 years of clinical operations experience (pharma, biotech, or medical device)
  • 1–2+ years of direct Clinical Project Manager experience preferred
  • Knowledge of FDA, ICH/GCP, and global regulatory requirements
  • Understanding of clinical trial phases (Phase 1–4)
  • Experience with clinical systems (EDC, CTMS, eTMF)
  • Strong project management skills
  • Knowledge of arrhythmias, ECG interpretation, or ambulatory cardiac monitoring systems
  • Ability to interpret diagnostic performance metrics (e.g., sensitivity, specificity, PPV/NPV) and translate findings into clinical insights
  • Experience assessing risk/benefit and clinical implications of algorithm performance differences
  • Familiarity with algorithm-based diagnostics or AI/ML-driven medical devices
  • Understanding of validation requirements for medical devices (e.g., EU MDR, FDA expectations)