Senior Site Activation Coordinator - Patient Impact, Hybrid

IQVIA Inc; Fatih; Hybrid; TRY 550,000 - 850,000; Full time

Benefits offered by this job

Therapeutic exposure

Global team

New technologies

Career growth

Job summary

IQVIA is seeking a Senior Site Activation Coordinator (Maintenance Specialist) in Istanbul, Türkiye, operating in a hybrid setup. The role focuses on feasibility, site activation, and maintenance activities for clinical trial sites, ensuring regulatory and SOP compliance within budgetary guidelines.

Under supervision, you will prepare and track essential documents (CDA, ethics, ICF, Investigator Pack), collaborate with cross-functional teams, and maintain project plans and systems to support

Qualifications

• Bachelor’s Degree in Life Science or related field.
• Minimum 2 years’ work experience; 1+ years in healthcare or similar.
• Good interpersonal, communication and organisational skills to establish and maintain effective working relationships with co-workers, managers and sponsors.
• Ability to work on multiple projects.

Responsibilities

• Perform feasibility, site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs, and work instructions.
• Review documents for completeness, consistency, and accuracy, under guidance of senior staff.
• Prepare site documents, review, track and follow up the progress, the approval and execution of required documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Form, and Investigator Pack release documents.
• Support the updating and maintenance of internal systems, databases, tracking tools, timelines, and project plans with accurate and complete project specific information.

Skills

Interpersonal skills

Communication

Organizational skills

Education

Bachelor's Degree in Life Science

Job description

IQVIA is seeking a Senior Site Activation Coordinator (Maintenance Specialist) in Istanbul, Türkiye, operating in a hybrid setup. The role focuses on feasibility, site activation, and maintenance activities for clinical trial sites, ensuring regulatory and SOP compliance within budgetary guidelines.

Under supervision, you will prepare and track essential documents (CDA, ethics, ICF, Investigator Pack), collaborate with cross-functional teams, and maintain project plans and systems to support