IQVIA

Site Enablement Lead & Site Facing Line Manager

Türkiye · Work style not stated · Full time

Apply on the employer’s site ↗See how well you match this job

You apply directly with the employer. ROLIVA does not submit applications from this page and is not the employer.

About the role

Description from the employer’s posting. Check the employer’s page for the current version.

  • EmployerIQVIA
  • LocationTürkiye
  • Work styleWork style not stated
  • Employment typeFull time
  • Employer posted

At IQVIA, we are transforming clinical research by helping sites operate more efficiently and enabling faster access to innovative treatments for patients. We are looking for a Site Enablement Lead & Site-Facing Line Manager (SEL/SFLM) to support the successful implementation and delivery of Site Enablement Solutions across clinical research sites in Turkey.

In this unique role, you will act as the primary point of contact for assigned sites while also providing leadership and support to site-based clinical research staff. You will work closely with investigators, study teams, and internal partners to ensure high-quality service delivery, strong site engagement, and operational excellence throughout the clinical trial lifecycle.

What You'll Do

  • Lead the implementation and ongoing delivery of Site Enablement Solutions at clinical research sites.
  • Build strong relationships with investigators, site personnel, and study teams to support successful study execution.
  • Support the onboarding, development, performance, and engagement of site-based clinical research staff.
  • Monitor service delivery, identify risks, and drive solutions that improve site performance and study outcomes.
  • Provide training and operational support for site enablement tools and services.
  • Collaborate with cross-functional stakeholders to ensure quality, compliance, and operational efficiency.
  • Support patient recruitment and site engagement initiatives, including innovative site solutions where applicable.
  • Contribute to continuous process improvement and the growth of IQVIA's Site Enablement capabilities in Turkey.
Show full description

What We're Looking For

  • Bachelor's degree in Life Sciences, Healthcare, Clinical Research, Business, or a related field.
  • Experience within clinical research, site operations, patient recruitment, site management, or a similar environment.
  • Previous experience working directly with clinical research sites, investigators, or site staff.
  • Experience leading, coaching, mentoring, or managing personnel.
  • Good understanding of clinical trial processes and ICH-GCP requirements.
  • Strong stakeholder management, communication, and problem-solving skills.
  • Fluency in Turkish and English, both written and spoken.
  • Ability to manage multiple priorities in a dynamic, matrixed environment.
  • Willingness to travel within Turkey as required.

Preferred Experience

  • Clinical Research Coordinator (CRC), Clinical Research Associate (CRA), Site Manager, Study Coordinator, or similar background.
  • Experience supporting patient recruitment or site support services.
  • Experience working across multiple studies or sites.
  • Clinical research certification (e.g., CCRC, CCRP).

Why Join IQVIA?

You'll have the opportunity to make a meaningful impact on clinical research delivery while working with industry-leading teams, innovative technologies, and a global network of healthcare and research professionals. Join us in helping accelerate the development of life-changing treatments for patients worldwide.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Staying safe while you apply

  • Never pay to apply, interview or accept an offer. ROLIVA never asks you for payment to apply to a job.
  • Apply only through the official “Apply on the employer’s site” button, on the employer’s own site, and check that a recruiter’s email uses that employer’s own domain rather than a free email address.
  • Be cautious of an offer made with no real interview, or pressure to decide quickly or share financial details early.

Does something look wrong with this listing? Use “Report broken link” in the role details, or read ROLIVA’s full job-safety guidance ↗.

Preparing for this role with ROLIVA

  • Check the fit.

    Compare the requirements with the experience you have confirmed, including gaps.

  • Prepare honestly.

    Build interview stories and application drafts from your own evidence.

  • Keep track.

    Save the role and record your own application status and follow-ups.

Create a free workspace or log in.

At a glance

  • Employment typeFull time
  • SeniorityLead / Principal
  • Employer posted
  • Added to ROLIVA
  • Last checked

Skills in this posting

Skills ROLIVA found in the employer’s own description above. A mention is not a requirement.

GCP Stakeholder management

Explore similar roles

Similar jobs