Position: 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 research and…
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$80k–$135k/yr
Full-time
associate degree, bachelor degree
Comprehensive Medical Insurance, Dental Insurance, Vision Insurance, 401(k) Retirement Plan, Paid Time Off, Paid Sick Leave
Posted 7d ago
~40 hrs/week
Responsibilities
The Clinical Project Manager leads early-phase clinical trials by translating protocols into project plans and managing cross-functional teams from initiation to study closeout. They serve as the primary point of contact for sponsors and vendors, ensuring projects remain on-time, on-budget, and compliant with regulatory standards.
Requirements
Candidates must have an Associate degree with 2 years of project management experience or a Bachelor of Science with 1 year of project management experience. Alternatively, 3 years of project management experience in a clinical research environment may be substituted for educational requirements.
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
About Pharmaron
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 www.pharmaron.com.
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.
Why Pharmaron?
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, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 21,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.
Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.
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!
As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.
Pharmaron: Global Life Sciences Services Provider
Stock Code: 300759.SZ/3759.HK
Founded in 2004, Pharmaron is a premier life sciences service provider that offers a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products.
Pharmaron’s Comprehensive CRO & CDMO Services
• Synthetic, Medicinal, and Analytical Chemistry Services
• Biology Services (e.g., in vitro screening, structural biology, biomarkers)
• DMPK Services (e.g., in vitro ADME, in vivo PK, PKPD, mass balance)
• Pharmacology Services (e.g., in vivo pharmacology, animal disease models, immunotoxicity)
• Drug Safety Assessment Services (e.g., toxicology, safety pharmacology, genetic toxicology)
• Radiochemistry and Isotopically Labelled Metabolism Services (e.g., 14C/Carbon-14 radiosynthesis, 3H/tritium radiosynthesis, QWBA, mARG)
• CMC Services (e.g., API manufacturing, process chemistry, formulation development)
• Clinical Development Services (e.g., First-in-Human [FIH], ethnobridging, microdosing Phase 0, absolute bioavailability)
Commitment to Excellence and Innovation
With a proven track record of success, Pharmaron continually invests in its people, facilities, and technologies to meet evolving scientific and regulatory demands. The company prides itself on enabling scientific breakthroughs and supporting its partners in advancing human health.
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Learn More: Explore Pharmaron’s services to discover how to accelerate your R&D programs. www.pharmaron.com.
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Keywords: CRO, CDMO, synthetic chemistry, medicinal chemistry, biology, radiochemistry, toxicology, First-in-Human, API manufacturing, PKPD, 14C radiosynthesis, discovery biologics, clinical development, small molecules, biologics, cell and gene therapy (CGT) products
Offices: 6 Taihe Road, BDA, Beijing, 100176, CN · 201 East Jefferson Street, Louisville, KY 40202, US · 404 Wyman St, Suite 365, Waltham, Massachusetts 02451, US · 800 West Baltimore St, Baltimore, MD 21201, US · 20340 Seneca Meadows Pkwy, Germantown, Maryland 20876, US
How many Science & Research jobs are open in Baltimore, MD right now?
There are currently 886 open science & research positions in Baltimore, MD listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Science & Research roles in Baltimore, MD?
Companies currently hiring include John Hopkins University, University System of Maryland, Northrop Grumman, Northrop Grumman Mission Systems, Inc., University of Maryland Medical System, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Science & Research jobs in Baltimore, MD?
Yes — 227 of the 886 open science & research positions offer remote or hybrid work (55 remote, 172 hybrid).
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