Research Associate

Sotalent; Fatih; On-site; TRY 240,000 - 420,000; Full time

Job summary

Sotalent in Istanbul is seeking an experienced Clinical Research Site Monitor to manage site activities through the full trial lifecycle, ensuring adherence to protocols and ICH-GCP guidelines. The role focuses on on-site monitoring, site selection, initiation, routine monitoring, and close-out, acting as the main liaison between sponsor and site to uphold trial quality.

Candidates should hold a life sciences degree, have at least one year of on-site monitoring experience, be fluent in English,

Qualifications

• A university degree in a life sciences or healthcare related field.
• At least one year of direct experience performing on site monitoring visits.
• Thorough understanding of GCP and ICH frameworks and clinical trial methodology.
• Professional fluency in English with strong written and verbal communication skills.
• Strong technical proficiency in Microsoft Office and clinical trial management software.
• Proven ability to manage multiple priorities and meet tight deadlines.
• Strong interpersonal skills with the ability to build rapport with site staff and internal teams.

Responsibilities

• Conduct all phases of site visits to verify data integrity and protocol compliance.
• Collaborate with sites to establish and maintain effective patient recruitment strategies.
• Deliver study specific training to investigators and site personnel.
• Monitor site performance and elevate any quality or safety concerns promptly.
• Oversee the maintenance of the Trial Master File and Investigator Site Files.
• Manage data flow by tracking enrollment, CRF completion, and query resolution.
• Produce detailed monitoring reports and follow up correspondence within required timelines.
• Support site financial management and local regulatory submission processes as needed.

Skills

GCP knowledge

Site monitoring

ICH guidelines

Data management

English proficiency

Education

Bachelor's degree in life sciences

Tools

CTMS

eTMF

Excel

Job description

I am currently recruiting for a global leader in healthcare intelligence and clinical development who is seeking an experienced professional to join their monitoring team in Istanbul. This is an excellent opportunity for a clinical research professional to take ownership of site management activities and ensure the highest standards of trial execution.

In this role, you will be responsible for the full lifecycle of site activities, including selection, initiation, routine monitoring, and close out procedures. You will serve as the primary link between the sponsor and the clinical site, ensuring that all operations adhere strictly to study protocols, ICH GCP guidelines, and local regulatory requirements.

Key Responsibilities

Conduct all phases of site visits to verify data integrity and protocol compliance.

Collaborate with sites to establish and maintain effective patient recruitment strategies.

Deliver study specific training to investigators and site personnel.

Monitor site performance and elevate any quality or safety concerns promptly.

Oversee the maintenance of the Trial Master File and Investigator Site Files.

Manage data flow by tracking enrollment, CRF completion, and query resolution.

Produce detailed monitoring reports and follow up correspondence within required timelines.

Support site financial management and local regulatory submission processes as needed.

Candidate Requirements

A university degree in a life sciences or healthcare related field.

At least one year of direct experience performing on site monitoring visits.

Thorough understanding of GCP and ICH frameworks and clinical trial methodology.

Professional fluency in English with strong written and verbal communication skills.

Strong technical proficiency in Microsoft Office and clinical trial management software.

Proven ability to manage multiple priorities and meet tight deadlines.

Strong interpersonal skills with the ability to build rapport with site staff and internal teams.

This organization is dedicated to accelerating medical innovation and improving patient health outcomes worldwide. If you are a motivated professional looking to advance your career with a premier clinical research provider, I would like to hear from you.