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Ai Clinical Project Manager Jobs (NOW HIRING)

Pharmaron

Clinical Project Manager

Baltimore, MD · On-site

$80K - $135K/yr

Clinical Project Manager Salary Range: $80K-$135K Location: Baltimore, MD Unfortunately, we cannot support work visa permit applications for this role About Pharmaron Pharmaron is a global contract ...

Pharmaron

Clinical Project Manager

Baltimore, MD · On-site

$80K - $135K/yr

Clinical Project Manager Salary Range: $80K-$135K Location: Baltimore, MD Unfortunately, we cannot support work visa permit applications for this role About Pharmaron Pharmaron is a global contract ...

Pharmaron

Clinical Project Manager

Baltimore, MD · On-site

$80K - $135K/yr

The Clinical Project Manager (CPM) is the single, accountable leader for early-phase (FIH, SAD/MAD, food-effect, DDI, 14C etc.) clinical trials, translating Sponsor protocols into integrated project ...

Buck Institute

Clinical Project Manager

Novato, CA · On-site

$90K - $100K/yr

The Clinical Project Manager will oversee study operations, staff, regulatory compliance, data and biospecimen quality, timelines, budgets, and coordination with internal and external stakeholders.

Clario

As a Clinical Project Manager, you will play a critical role in leading cross-functional clinical projects, driving operational excellence, and ensuring successful study execution from start-up ...

PSI CRO

Clinical Project Manager

Take your career to the next level and lead challenging full-service clinical research projects in phase II and III, managing the full scope of responsibilities and getting hands-on involvement in ...

PSI CRO

Clinical Project Manager

Take your career to the next level and lead challenging full-service clinical research projects in phase II and III, managing the full scope of responsibilities and getting hands-on involvement in ...

Bioclinica

Clinical Project Manager

As a Clinical Project Manager, you will play a critical role in leading cross-functional clinical projects, driving operational excellence, and ensuring successful study execution from start-up ...

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How much do ai clinical project manager jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for ai clinical project manager in the United States is $60.70, according to ZipRecruiter salary data. Most workers in this role earn between $42.31 and $71.15 per hour, depending on experience, location, and employer.

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Infographic showing various Ai Clinical Project Manager job openings in the United States as of June 2026, with employment types broken down into 92% Full Time, 7% Part Time, and 1% Contract. Highlights an 70% Physical, 3% Hybrid, and 27% Remote job distribution, with an average salary of $126,262 per year, or $60.7 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)