Clinical Trial Start-Up Specialist (Contractor)

Tigermed; Turkey; On-site; TRY 60,000 - 110,000; Full time

Job summary

Tigermed is seeking to strengthen its RSU regulatory and start-up capabilities to ensure compliant site activation for global clinical trials. The role focuses on coordinating feasibility, CDAs, regulatory submissions, and cross-functional collaboration to streamline start-up timelines.

Responsibilities include liaising with cross-functional teams, managing feasibility questionnaires, negotiating CDAs, and maintaining regulatory submissions while supporting process improvements across the

Responsibilities

• Liaise with Clinical Monitoring, Site Contracts, Regulatory Affairs, other interdepartmental team members and sponsors to enable rapid clinical trial start-up.
• Coordinate development of feasibility questionnaire for a study; obtain client approval of the study-specific feasibility questionnaire.
• Support PM/Legal in working with client to obtain/agree to CDA templates and feasibility questionnaire; distribute to sites.
• Review and negotiate CDAs per country requirements; seek legal/management review when required.
• Send regulatory packages to selected sites and follow up on start-up process.
• Lead or review strategy, content and costing of proposals with BD, PM, and other functions.
• Provide cross-functional input to improve service quality; participate in bid defense meetings as needed.

Job description

Tigermed is seeking to strengthen its RSU regulatory and start-up capabilities to ensure compliant site activation for global clinical trials. The role focuses on coordinating feasibility, CDAs, regulatory submissions, and cross-functional collaboration to streamline start-up timelines.

Responsibilities include liaising with cross-functional teams, managing feasibility questionnaires, negotiating CDAs, and maintaining regulatory submissions while supporting process improvements across the