Associate Clinical Research Manager

FTPOL Fortrea Poland Sp z o.o.

Apply to this job
Bucharest Until 9/28/2026 6+ years exp First posted July 30, 2026 Last posted July 30, 2026
Job description

The Clinical Research Manager (CRM) leads the execution and oversight of clinical trial activities within an assigned country, ensuring compliance with ICH-GCP, local regulations, and company quality standards. Acting as the primary country-level contact for assigned studies, the CRM drives study performance, operational delivery, regulatory compliance, and stakeholder engagement while partnering with internal teams, investigators, and external vendors.

Key Responsibilities

  • Lead country-level delivery of assigned clinical trials, ensuring timelines, quality standards, and regulatory requirements are met.
  • Serve as the primary point of contact for assigned studies and oversee study execution, budgets, contracts, and resource planning.
  • Provide quality oversight of CRAs, CTCs, vendors, and study activities, including monitoring compliance and training requirements.
  • Support site identification, feasibility, selection, activation, recruitment, and investigator engagement.
  • Build and maintain strong relationships with investigators, sites, vendors, and key external stakeholders.
  • Collaborate cross-functionally with Regulatory Affairs, Pharmacovigilance, Medical Affairs, and Regional Operations to support study delivery and country strategy.
  • Mentor junior team members and contribute to continuous improvement initiatives.

Qualifications & Experience

  • Degree in Life Sciences, Nursing, Pharmacy, Medical Technology, or a related field; equivalent clinical research experience will also be considered.
  • 6–8 years of clinical research experience within a pharmaceutical company or a CRO
  • Strong knowledge of ICH-GCP, clinical trial regulations, drug development processes, and local regulatory requirements.
  • Experience managing clinical studies and coordinating cross-functional stakeholders.
  • Excellent communication, organisational, and stakeholder management skills.
  • Proven ability to work independently, manage multiple priorities, and lead in a matrix environment.
  • Fluent in English and Romanian.

    Learn more about our EEO & Accommodations request here.

    About this role

    Summary

    Lead and oversee clinical trials ensuring compliance, quality, and stakeholder engagement.

    Job title

    Associate Clinical Research Manager

    Experience level

    6-8 years

    Minimum experience

    6+ years exp

    Industry

    pharmaceuticals

    Location requirements

    Bucharest, on-site work, no remote work allowed

    Salary

    Not specified

    Management role

    Yes

    Skills & keywords

    Required skills

    ICH-GCPclinical trialregulationsdrug developmentstakeholder management

    Preferred skills

    None specified

    Specializations

    clinical trialsregulatory compliancestakeholder management
    Locations

    Structured locations inferred from the posting.

    Bucharest, Romania

    On-site City