20 beste Stellen als regulatory specialist in frankfurt am main, he – aktuell auf Personalsuche

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(Sr.) Site Activation Specialist (m/w/d), office-based in Frankfurt, Germany
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Site Activation Specialist - Germany

IQVIA -
Frankfurt am Main

Jetzt bewerben

Details zur Stelle

Vollzeit
vor 14 Tagen

Qualifikationen

Bachelor

Vollständige Stellenbeschreibung

Frankfurt/Main, Germany | Full time | Home-based | R1547830

Freelance Site Activation Specialist – Germany (Home-Based)

Location: Germany (home-based)
Contract type: Freelance

FTE: 1.0 - full time
Start: immediately
Duration: around 4 month

About the Role

We are looking for a Freelance Site Activation Specialist based in Germany to support country-level clinical trial start-up and site management activities.

This role focuses on feasibility, site identification, regulatory submissions, and activation, with some involvement in maintenance activities. Candidates with experience in Switzerland or exposure to the DACH region are highly preferred.

Key Responsibilities

Act as the primary point of contact for assigned investigative sites
Execute feasibility, site identification, and site activation activities in line with SOPs, regulations, and project timelines
Prepare, review, and manage essential site and regulatory documents, ensuring completeness and accuracy
Support contract and budget processes in collaboration with internal stakeholders
Maintain and update tracking tools, timelines, and internal systems with accurate project data
Monitor and report on site activation progress and performance metrics
Ensure compliance with ICH-GCP, local regulations (Germany and ideally Switzerland), and study requirements
Collaborate closely with Site Activation Managers, Project Management, and cross-functional teams

Requirements

Based in Germany with strong understanding of the local regulatory environment
2–3+ years of experience in site activation, study start-up, or clinical research
Bachelor’s degree in Life Sciences or related field
Solid knowledge of clinical trial start-up processes and regulatory requirements
Experience managing site documentation and submission processes
Strong attention to detail and ability to manage multiple sites and timelines
Fluent in German and English (written and spoken)
Experience working on clinical studies in Switzerland or familiarity with Swiss regulatory requirements an advantage
Exposure to cross-border (DACH) studies an advantage

If this role sounds of interest, please apply today!

#LI-DNP

#LI-CES

#LI-HCPN

#LI-NS1

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.

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Erweiterte Suche

regulatory specialist Jobs in frankfurt am main, he

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(Sr.) Site Activation Specialist (m/w/d), office-based in Frankfurt, Germany

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HRBP & Talent Reward Partner

Ich möchte aktuelle Job-E-Mails für Stellen als regulatory specialist in frankfurt am main, he erhalten

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Freelance Site Activation Specialist – Germany (Home-Based)

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