20 beste Stellen als sr. quality control in eschborn – aktuell auf Personalsuche

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

IQVIA -
Frankfurt am Main

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Details zur Stelle

Vollzeit

Leistungen

Homeoffice-Möglichkeit

Vollständige Stellenbeschreibung

Frankfurt am Main, Germany | Full time | Home-based | R1547606

IQVIA currently offers the exciting opportunity for a (Sr.) Site Activation Specialist (m/w/d) to work in the Country Site Activation Department home-based within Germany.

In this role you will perform tasks at a country level associated with clinical research site activation activities in accordance with applicable local and/or international regulations, standard operating procedures, project requirements and contractual/budgetary guidelines.

Your responsibilities might include:

Serve as Single Point of Contact in assigned studies for investigative sites, RSU Team Lead, Clinical Operations, Feasibility, Site Identification, Project Management and the client.
Ensure adherence to standard operating procedures (SOPs), work instructions, quality of designated deliverables and to project timelines.
Perform Regulatory, Start-up and Maintenance activities according to applicable regulations, SOPs and work instructions.
Review, prepare and negotiate site contracts and budgets with sites. Prepare site regulatory documents, reviewing for completeness and accuracy. Perform quality control of documents provided by sites.
Complete and submit approval request documents to Local Regulatory and Ethical Committees. Ensure regulatory documents and approvals are granted, IP Release authorized and specific project deliverables are completed.
Review, track and follow up the progress, the approval and execution of documents, including contracts, regulatory, ethics ICF and IP Release documents, in line with project timelines.
Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.
Review, establish and agree on project planning and project timelines. Ensure overall project efficiency and adherence to project timelines. Ensure monitoring measures are in place and implement contingency plan as needed.
Review and provide feedback to management on site performance metrics.

Qualifications:

University Degree in life science or other scientific discipline or apprenticeship in health care or as legal secretary / paralegal.
Clinical research experience, preferable in study start-up, alternatively an equivalent combination of education, training and experience.
Knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Fluent language skills in German (on at least C1 level) and a good command of English.
Strong written and verbal communication skills.
Attention to detail and ability to work on multiple tasks and prioritize.

What you can expect:

Supportive leaders, mentors and teams.
Resources that promote your career growth.
Dynamic work environments that expose you to new experiences.
Flexible working schedule and home-office.
Competitive salary, bonus system, pension and more.

Whatever your career goals, we are here to ensure you get there!

Please apply with your English CV and motivation letter.

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.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

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Erweiterte Suche

sr. quality control Jobs in eschborn

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

Sr. Quality Control Engineer

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EMEA Event Manager (m/w/d)

Head of Real Estate Management and Office Services (f/m/d)

Head of Regulatory Relationship Management, Managing Director

Senior Specialist: IT Audit & Cyber Risk (2nd Line) (f/m/d)

Senior Director Global Quality Supply

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(Senior) Project Manager – Data Centers (f/m/d)

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Director - Health, Safety & Environment

Senior Project Manager Office & Workplace (m/f/d) / Real Estate Management

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Senior Compliance Officer – Global Markets Advisory (m/f/d)

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Senior Contract Manager (m/f/d) – Hydropower & Water Infrastructure

Ich möchte aktuelle Job-E-Mails für Stellen als sr. quality control in eschborn erhalten

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