Freelance Clinical Trial Site Coordinator

Milestone One; Konak; On-site; EUR 30,000 - 60,000; Full time

Job summary

Ein aufstrebendes Unternehmen sucht einen Site Coordinator, der klinische Studien unterstützt und als Hauptkommunikationslink zwischen Sponsoren und Studienorten fungiert. In dieser Rolle sind Sie für die Einhaltung der Studienprotokolle verantwortlich, helfen bei der Planung und Durchführung von Monitoring-Besuchen und stellen sicher, dass alle Dokumente ordnungsgemäß verwaltet werden. Wenn Sie in einem dynamischen Umfeld arbeiten möchten, das Wert auf die Entwicklung seiner Mitarbeiter legt, könnte dies die perfekte Gelegenheit für Sie sein.

Qualifications

• Abschluss in Lebenswissenschaften, vorzugsweise Pharmazie oder Pflege.
• Erfahrung in der Koordination klinischer Studien vor Ort.

Responsibilities

• Hauptkommunikationslink zwischen Sponsor und Studienort.
• Verfolgen der Patientenrekrutierung und Unterstützung der Projektziele.

Skills

Koordination klinischer Studien

Kommunikationsfähigkeiten

Problemlösungsfähigkeiten

Flexibilität

Education

Abschluss in Lebenswissenschaften

Erfahrung in der klinischen Forschung

Job description

Milestone One is a Site Enabling Services organization with global headquarters in Zug, Switzerland. We understand what clinical study sites need, and our overall mission is to support sites in delivering stronger study results.

Job Description

Milestone One Site Coordinator supports trial sites in all related activities according to ICH-GCP, protocol requirements, within study-specific timelines and enrollment goals.

In this role, you will:

1. Act as the main communication link between the Sponsor or CRO and the site.
2. Ensure responses to feasibility questions are provided promptly.
3. Assist in scheduling and preparing for monitoring visits at the medical institution/research center.
4. Be present and available during monitoring visits to respond to monitors.
5. Track patient enrollment and support the site and CRO/Sponsor team in meeting project timelines and goals.
6. Maintain study-specific and general document tracking at the site.
7. Enter data accurately and timely into study-specific EDC systems and resolve data queries.
8. Report and follow up on adverse events and protocol deviations promptly.
9. Handle, account for, and reconcile investigational products and supplies.
10. Maintain all site-specific regulatory documents.
11. Support contract and budget negotiations at the site.
12. Assist with investigator and site payments and processes.
13. Schedule and perform study procedures as required.
14. Prepare for and participate in site audits or inspections.

Qualifications

1. College or university degree in Life Sciences, preferably pharmacy, nursing, or lab analytics.
2. Experience in coordinating clinical trials on-site.
3. Ability to work in a fast-paced environment with tight timelines and multiple tasks.
4. Effective communication skills, especially under stress, and problem-solving abilities.
5. Flexibility in working hours depending on study schedules.

Additional Information

If you are ready to showcase your skills and knowledge within a growing company that values its people, Milestone One is the right place for you.