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Cro Clinical Project Manager Jobs (NOW HIRING)

PharmaOut

Clinical Project Manager

Gaithersburg, MD · On-site

Manages CRO and vendor activities to ensure adherence to deliverables and timelines. Provides updates on project status and deliverables to Clinical Project Management leads (deliverables may include ...

Biolinq Incorporated

Clinical Project Manager

San Diego, CA · On-site

$75K - $90K/yr

The Clinical Project Manager should be able to create and maintain a good and effective working ... Support selection, qualification, and day-to-day oversight of clinical sites and vendors (e.g., CRO ...

Biolinq Incorporated

Clinical Project Manager

San Diego, CA · On-site

$75K - $90K/yr

The Clinical Project Manager should be able to create and maintain a good and effective working ... Support selection, qualification, and day-to-day oversight of clinical sites and vendors (e.g., CRO ...

Alto Neuroscience, Inc.

Clinical Project Manager

$125K - $170K/yr

Provide CRO and vendor oversight, including review and execution of vendor oversight plans and ... clinical project management experience * Demonstrated knowledge of multiple aspects of clinical ...

Bioclinica

Clinical Project Manager

Franklin, TN · On-site

Company Description Bioclinica is one of the leading global CRO company which focuses on bringing ... Clinical Project Manager will focus on study start up through close out activities and perform ...

Bioclinica

Clinical Project Manager

Princeton, NJ · On-site

Company Description Bioclinica is one of the leading global CRO company which focuses on bringing ... Clinical Project Manager will focus on study start up through close out activities and perform ...

Pharmaron

Clinical Project Manager

Baltimore, MD · On-site

$80K - $135K/yr

Clinical Project Manager Salary Range: $80K-$135K Location: Baltimore, MD Unfortunately, we cannot ... CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 ...

EDETEK

Senior Clinical Project Manager

The ideal candidate will bring solid experience in a CRO environment and hands-on experience ... Minimum of 7 years of clinical project management experience in the pharmaceutical, biotechnology ...

Laborie

Clinical Project Manager

Minnetonka, MN · On-site

$130K - $135K/yr

Minimum 2 years of clinical project management experience at a sponsor or CRO company is preferred. * Therapeutic/intervention experience in urogynecology, gastroenterology, and/or OB/GYN. * ...

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

As of Sep 11, 2026, the average hourly pay for cro 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 Cro Clinical Project Manager job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 80% Physical, 2% Hybrid, and 18% 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)