Clinical Project Manager

Pharmaron

$80K — $135K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Associate's degree/60 college credit hours in a related field plus 2 years as a Project Manager; OR Bachelor of Science in a related field plus 1 year as a Project Manager; OR 3 years of Project Management experience in a Clinical Research environment may substitute educational requirements.
  • Bachelor of Science in a related field with 2 years of Project Management experience in a Clinical Research environment preferred.

Responsibilities

  • Partner with Business Development for feasibility assessments and site qualification.
  • Collaborate with regulatory teams for accurate feasibility documentation.
  • Build strong sponsor relationships by understanding client needs.
  • Contribute to proposal development including cost estimations.
  • Lead project kick-off meetings and align cross-functional teams.
  • Coordinate with vendors to define scope, timelines, and deliverables.
  • Develop and manage project timelines, identifying risks and implementing strategies.
  • Serve as primary contact for sponsors, ensuring clear communication.

Benefits

  • Comprehensive Medical, Dental & Vision Insurance with employer contributions.
  • 401(k) Retirement Plan with generous employer matching.
  • Paid Time Off (PTO), Paid Sick Leave, and Company Holidays.
  • Employer-funded Health Savings Account (HSA) contributions and Flexible Spending Accounts.
  • 100% Employer-paid Employee Life, AD&D, and Disability Insurance.
  • Employee Assistance Program (EAP) and wellness programs.
  • Family-friendly benefits including fertility support and maternity resources.
  • Professional development and career growth opportunities within a leading global CRO/CDMO.
Full Job Description
Position: Clinical Project Manager

Salary Range: $80K-$135K

Location: Baltimore, MD

Unfortunately, we cannot support work visa permit applications for this role

Job Overview:

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 plans and guiding cross-functional teams from study initiation and first-subject-in through CSR submission and TMF delivery. Acting as the primary interface for Sponsors, investigators, vendors, and senior leadership, the CPM governs study scope, timelines, budgets, and risk, ensuring ICH-GCP and global regulatory compliance while protecting project margin through rigorous change-order and vendor oversight. Leveraging real-time dashboards and eClinical systems, the CPM drives proactive issue resolution, produces executive-level status reports, and maintains inspection-ready documentation. Success is defined by on-time, on-budget delivery of high-quality data, exemplary Sponsor satisfaction, and continuous process improvement that elevates PM Department and clinical unit performance.

Key Responsibilities:
  • Partner with Business Development to support feasibility assessments and site qualification activities
  • Collaborate with regulatory teams to ensure accurate and complete feasibility documentation
  • Build strong sponsor relationships by understanding client needs and ensuring confidence in study execution
  • Contribute to proposal development, including cost estimation and preparation of sponsor-ready submissions
  • Lead project kick-off meetings and align cross-functional teams and external stakeholders
  • Coordinate with vendors and consultants to define scope, timelines, and deliverables
  • Develop and manage project timelines, proactively identifying risks and implementing mitigation strategies
  • Serve as the primary point of contact for sponsors, ensuring clear communication and on-time delivery
  • Monitor project progress, budgets, and performance metrics; analyze trends and address issues proactively
  • Review financials, approve vendor expenses, and partner with Project Finance on scope and budget changes
  • Ensure high-quality study closeout deliverables, respond to sponsor inquiries, and lead lessons learned for continuous improvement

What We're looking for Clinical Project Manager:
  • CPM: Associates / equivalency (60 or more college credit hours) in related field + 2 years as a Project Manager; OR Bachelor of Science in related field + 1 year as a Project Manager. 3 years of Project Management experience in a Clinical Research environment may be substituted for educational requirements.
  • CPM: Bachelor of Science in related field + 2 year as a Project Manager Clinical Research environment preferred.

Benefits:

As part of our commitment to your well-being, we offer a comprehensive benefits package:
  • Comprehensive Medical, Dental & Vision Insurance with significant employer contributions
  • 401(k) Retirement Plan with generous employer matching
  • Generous Paid Time Off (PTO), Paid Sick Leave & Company Holidays to support work-life balance
  • Employer-funded Health Savings Account (HSA) contributions (for eligible plans), plus Healthcare & Dependent Care Flexible Spending Accounts
  • 100% Employer-paid Employee Life Insurance, AD&D, Short- and Long-Term Disability Insurance
  • Employee Assistance Program (EAP), mental health resources, and wellness programs
  • Family-friendly benefits, including fertility support and maternity resources
  • Professional development and career growth opportunities within a leading global CRO/CDMO

How to Apply:

Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!

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