Clinical Research Manager (CRM)
Location: Client Office (as assigned)
Travel: Up to 25%, domestic and international
About the Role
As a Clinical Research Manager, you’ll lead and oversee local clinical trial operations, ensuring regulatory and financial compliance while driving performance across protocols. You’ll be the key point of contact for investigators and external partners, representing the client and building strong relationships that support trial success.
This role combines strategic oversight with hands-on execution, requiring strong leadership, scientific knowledge, and the ability to manage multiple priorities in a dynamic environment.
Key Responsibilities
- Trial Oversight: Ensure protocol compliance and performance across assigned studies.
- Stakeholder Management: Serve as the primary contact for investigators, vendors, and internal teams.
- Quality & Compliance: Monitor site activities, review reports, and address training needs.
- Operational Leadership: Oversight of budgets, contracts, and resource forecasting.
- Cross-Functional Collaboration: Align with regulatory, PV, medical affairs, and global teams.
What You Bring
- Master’s degree in life sciences or related field (or equivalent experience).
- 6–8 years of clinical research experience in pharma, CRO, or healthcare.
- Previous monitoring experience is needed.
- Strong knowledge of ICH-GCP, local regulations, and clinical trial processes.
- Excellent communication, organizational, and leadership skills.
- Ability to manage multiple protocols and lead cross-functional teams.
- Fluent in English and Polish (written and spoken).
Preferred Skills
- Experience with site selection, start-up, and vendor management.
- Proven ability to mentor junior staff and foster team performance.
- Comfortable working independently and in virtual environments.
Learn more about our EEO & Accommodations request here.
Skills Required
- Master's degree in life sciences or a related field, or equivalent experience
- 6-8 years of clinical research experience in pharma, CRO, or healthcare
- Previous clinical trial monitoring experience
- Strong knowledge of ICH-GCP, local regulations, and clinical trial processes
- Excellent communication, organizational, and leadership skills
- Ability to manage multiple protocols and lead cross-functional teams
- Fluency in written and spoken English and Polish
- Experience with site selection, study start-up, and vendor management
- Ability to mentor junior staff and foster team performance
- Comfort working independently and in virtual environments
What We Do
Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development and patient access solutions to the life sciences industry. We partner with emerging and large biopharmaceutical, medical device and diagnostic companies to drive healthcare innovation that accelerates life changing therapies to patients in need. Fortrea provides phase I-IV clinical trial management, clinical pharmacology, differentiated technology-enabled trial solutions and post-approval services. Fortrea’s solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network. Our talented and diverse team working in more than 90 countries is scaled to deliver focused and agile solutions to customers globally. Learn more about how Fortrea is becoming a transformative force from pipeline to patient at Fortrea.com.
