Clinical Research Manager (Sponsor-dedicated)

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.

Responsibilities

• 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.
• Ensure protocol compliance and performance across assigned studies.
• Serve as the primary contact for investigators, vendors, and internal teams.
• Monitor site activities, review reports, and address training needs.
• Oversight of budgets, contracts, and resource forecasting .
• Align with regulatory, PV, medical affairs, and global teams.

Requirements

• 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.

Preferred

Learn more about our EEO & Accommodations request here .