Site Activation Partner – Global Trials & Compliance

Parexel; Turkey; On-site; TRY 180,000 - 240,000; Full time

Job summary

Parexel in Turkey is seeking a Site Activation Specialist to coordinate activation activities and regulatory submissions for clinical trials. You will assist with site initiation, ethics approvals, and TMF maintenance while collaborating with cross-functional teams in a fast-paced environment.

The role requires Turkish and English fluency, knowledge of GCP, and experience in clinical research and regulatory processes. Travel to investigator sites is expected as needed.

Qualifications

• Bachelor's degree or equivalent; life sciences background preferred.
• Fluency in Turkish and English is required for communication with site teams.
• Experience in clinical research, site activation, and regulatory processes.

Responsibilities

• Initiate and coordinate site activation activities and essential documents.
• Manage regulatory submissions and keep trial master files up to date.
• Support site ethics approvals and local country requirements.
• Communicate with study teams and investigators to ensure timely study startup.
• Assist with audits/inspections and ensure compliance with GCP and SOPs.

Skills

Clinical research

Site activation

Regulatory knowledge

GCP compliance

Documentation management

Travel willingness

Turkish language

English language

Education

Bachelor’s degree or equivalent

Life sciences background preferred

Tools

CTMS

eTMF/Florence

Shared Investigator Platform

Job description

Parexel in Turkey is seeking a Site Activation Specialist to coordinate activation activities and regulatory submissions for clinical trials. You will assist with site initiation, ethics approvals, and TMF maintenance while collaborating with cross-functional teams in a fast-paced environment.

The role requires Turkish and English fluency, knowledge of GCP, and experience in clinical research and regulatory processes. Travel to investigator sites is expected as needed.