Clinical Project Manager (with Senior CRA Responsibilities)

Çankaya, Turkey

Job Title  : Clinical Project Manager (with Senior CRA Responsibilities)

Location  : Turkey (Ankara/Istanbul preferred – hybrid/remote flexibility)

Company : Medex CRO

Industry   : Clinical Research

Job Type  : Full-Time



  What You’ll Do: (Responsibilities)   


   Act as the primary point of contact for assigned clinical trials, managing communication with sponsors, vendors, and internal teams.

  Oversee all phases of clinical trials (Phase I–IV) across multiple sites in Turkey and/or EMEA.

  Perform site selection, initiation, routine monitoring, and close-out visits, ensuring compliance with ICH-GCP and local regulatory requirements.

  Develop and review essential trial documentation (e.g., protocols, monitoring plans, regulatory submissions).

  Maintain up-to-date knowledge of regulatory requirements and ensure internal SOPs and practices remain compliant.

  Track site performance and enrollment metrics; proactively resolve operational issues.

  Mentor and support junior CRAs and project staff.

The Clinical Project Manager is responsible for the planning, execution, and oversight of clinical research projects. This role ensures coordination between sponsors, sites, and internal teams, while actively participating in monitoring activities and regulatory compliance. The manager ensures that project timelines, quality, and performance targets are successfully met.

  Clinical Project Manager – Job Description   

Nice to Have
  •  -  Experience working in a CRO environment with regional or global trial oversight.
  • -  PMP or equivalent project management certification.
  • -  Familiarity with clinical trial management systems (CTMS) and eTMF platform.
Must Have
  • - Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or related field.
  • - Demonstrated experience managing clinical sites and trial operations independently. 
  • - In-depth knowledge of ICH-GCP, Turkish MoH regulations, and global clinical trial processes
  • -  Strong experience with regulatory submissions, MoH processes, and Ethics Committee interactions in Turkey.
  • - Excellent communication skills in both Turkish and English.
  • - Strong organizational, time management, and problem-solving skills.
  • - Willingness to travel for monitoring visits and sponsor meetings, as required.

What's great in the job?


  • Competitive salary and performance-based incentives
  • Hybrid work model with flexible hours
  • Exposure to international clinical studies and global sponsors
  • A collaborative, transparent, and supportive team culture
  • Opportunities for long-term growth and career advancement
Our Services

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What We Offer


 

Employee Perks


A full-time position

Competitive salary

Seasonal gifts


Meal and Travel Allowence


Ticket 

Monetary support

Comprehensive Training and Development


Certification opportunities and workshops to grow your expertise in clinical research.