Clinical Project Manager

Position
:
Clinical Project Manager

Salary Range: $80K-$135K

Location: Baltimore, MD

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

Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 locations in the US, UK, China, and Singapore, we support drug discovery through to manufacturing with fully integrated high-quality services. We’re proud of the impact we make and just last year, we supported 887 discovery projects, 1,100+ CMC programs, and 1,397 clinical trials across all phases.

Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,300 global customers. To learn more, visit

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.

• 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

• 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.

Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery,…