20 beste Stellen als clinical trial in frankfurt am main, he – aktuell auf Personalsuche

Clinical Trial Transparency Associate
ICON Plc —Frankfurt am Main
- Vollzeit
- Microsoft Excel
- Projektmanagement
- Bachelor
Clinical Trials Assistant 2 (m/w/d), based in the Düsseldorf area
IQVIA —Frankfurt am Main
- Vollzeit
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
12 Tage
Senior Clinical Research Associate II/III (m/w/d), Multi-Sponsor, Germany
IQVIA —Frankfurt am Main
- Forschungserfahrung
- Mit Reiseanteil
11 Tage
Senior Clinical Project Support Specialist - Sponsor dedicated (m/w/d)
IQVIA —Frankfurt am Main
- Ab 58.500 € pro Jahr
- Forschungserfahrung
- Microsoft Office
Clinical Trialist in der Krebsforschung
füreinanderdasein GmbH —Frankfurt am Main
- Teilzeit
- Krankenhaus
4 Tage
Clinical Lead, Early Clinical and Experimental Therapeutics
Sanofi —Frankfurt am Main
- 101.040 € – 134.720 € pro Jahr
- Doktorat
- Schreibfähigkeiten
- Forschungserfahrung
4 Tage
Senior Clinical Site Associate
ICON Plc —Frankfurt am Main
- Vollzeit
- Forschungserfahrung
- Bachelor
- Mit Reiseanteil
12 Tage
Senior Scientific / Medical Expert (m/f/d), Post-Market & Life Cycle Management, R&D Clinical Development
Merz Aesthetics GmbH —Frankfurt am Main
- Vollzeit
- Doktorat
- Schreibfähigkeiten
- Master
- Gleitzeit
Direkt bewerben
Senior Manager Clinical Operations (m/f/d)
Fresenius Kabi —Bad Homburg vor der Höhe
- Vollzeit
- Doktorat
- Englisch
- Microsoft Office
Clinical Quality Manager (m/f/d)
Merz Aesthetics GmbH —Frankfurt am Main
- Vollzeit
- Microsoft Office
- Master
- Gleitzeit
Direkt bewerben
Clinical Trialist in der Krebsforschung
Universitätsmedizin Frankfurt —Frankfurt am Main
- Teilzeit
- Krankenhaus
Direkt bewerben
Principal CRA
ICON Plc —Frankfurt am Main
- Vollzeit
- Forschungserfahrung
- Bachelor
- Mit Reiseanteil
Clinical Research Associate (m/w/d)
GBG Forschungs GmbH —Neu-Isenburg
- Vollzeit
- Englisch
- Forschungserfahrung
- Mit Reiseanteil
- Employee Assistance Program
- Flexible Arbeitszeiten
11 Tage
Site Contract Negotiator
ICON Plc —Frankfurt am Main
- Vollzeit
- Forschungserfahrung
- Bachelor
- Wirtschaft
12 Tage
Therapeutic Strategy Lead - Internal Medicine/Immunology , Home-Based (m/w/d)
IQVIA —Frankfurt am Main
- Homeoffice
- Vertrieb
- Englisch
- Forschungserfahrung
11 Tage
Senior Clinical Project Manager Medical Devices (m/f/d)
Merz Aesthetics GmbH —Frankfurt am Main
- Vollzeit
- Forschungserfahrung
- Microsoft Office
- Projektmanagement
- Gleitzeit
Direkt bewerben
6 Tage
Associate Project Manager - Cell and Gene Therapies m/w/d
UPS —Frankfurt am Main
- Vollzeit
- Projektmanagement
- Kommunikationsfähigkeit
Regulatory Affairs Assistant (m/w/d)
GBG Forschungs GmbH —Neu-Isenburg
- Vollzeit
- Medizin
- Englisch
- Forschungserfahrung
- Employee Assistance Program
- Flexible Arbeitszeiten
11 Tage
Director, Medical Safety Physician Product Lead (m/f/d)
Otsuka Pharma GmbH —Frankfurt am Main
- Vollzeit
- Hybrides Arbeiten
- Mit Reiseanteil
- Führungserfahrung
Director, Medical Safety Physician Product Lead (m/f/d)
Otsuka Pharma —Frankfurt am Main
- Mit Reiseanteil
- Führungserfahrung

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Clinical Trial Transparency Associate

ICON Plc -
Frankfurt am Main

Jetzt bewerben

Details zur Stelle

Vollzeit

Qualifikationen

Microsoft Excel
Projektmanagement
Bachelor
SharePoint
Dokumentenmanagementsysteme
Zeitmanagement

Vollständige Stellenbeschreibung

Clinical Trial Transparency Associate

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

As a Clinical Trial Transparency Associate at ICON, you will be responsible for processing the anonymization of clinical trial documents and datasets required for public disclosure. The Anonymization Specialist will partner with internal and external collaborators on the planning, initiation, and delivery of anonymized documents and datasets in support of the EU Clinical Trial Regulation (EU CTR), ClinicalTrials.gov, and Publications and Regulatory Authority Transparency Submissions (e.g., EMA Policy 0070, Health Canada PRCI), manuscript publications, and data sharing.

What You Will Do:

Manage and facilitate anonymization of datasets and documents against planned timelines, in accordance with Incyte SOPs and regulatory requirements.
Assess documents in-scope for public disclosure according to EMA Policy 0070 and Health Canada PRCI.
Work closely with Biostatistics and Programing groups and Medical Writing teams to identify and assimilate the required documents and datasets.
Develop anonymization plans based on direct and indirect identifiers by measuring and mitigating re-identification risk according to GDPR guidance.
Process datasets and documents and apply required transformations.
Contribute to Anonymization Reports to support anonymization packages for policies of Health Canada and EMA.
Ensure accurate and consistent redaction of clinical trial documents to support EU CTR, ClinicalTrials.gov, and Publications.
Quality check of documents redacted/anonymized by other team members.
Collaborate with Regulatory Operations to ensure the publishing of redacted documents in the Regulatory Document Management System.
Experience with the use of Technology Tools for delivery of Anonymized Clinical Documents.

Your Profile:

Bachelor’s degree in a scientific or technical field.
Experience with documents anonymization and clinical trial transparency
Minimum 3 years of work experience in either the health sciences or related industries (pharmaceutical, CRO, etc.).
Working knowledge of the global regulatory guidelines pertaining to clinical trial disclosure and transparency.
Demonstrated experience in global clinical trial disclosure and transparency processes and systems.
Demonstrated Excel and analytical skills, working knowledge of SharePoint and/or document management systems.
Strong communication, organizational, time management, and project management skills.
Knowledge of ICH-GCP, awareness of clinical publication practices and standards (ie, ICMJE).

#LI-Remote

#LI-NR1

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Jetzt bewerben

Erweiterte Suche

clinical trial Jobs in frankfurt am main, he

Clinical Trial Transparency Associate

Clinical Trials Assistant 2 (m/w/d), based in the Düsseldorf area

Senior Clinical Research Associate II/III (m/w/d), Multi-Sponsor, Germany

Senior Clinical Project Support Specialist - Sponsor dedicated (m/w/d)

Clinical Trialist in der Krebsforschung

Clinical Lead, Early Clinical and Experimental Therapeutics

Senior Clinical Site Associate

Senior Scientific / Medical Expert (m/f/d), Post-Market & Life Cycle Management, R&D Clinical Development

Senior Manager Clinical Operations (m/f/d)

Clinical Quality Manager (m/f/d)

Clinical Trialist in der Krebsforschung

Principal CRA

Clinical Research Associate (m/w/d)

Site Contract Negotiator

Therapeutic Strategy Lead - Internal Medicine/Immunology , Home-Based (m/w/d)

Senior Clinical Project Manager Medical Devices (m/f/d)

Associate Project Manager - Cell and Gene Therapies m/w/d

Regulatory Affairs Assistant (m/w/d)

Director, Medical Safety Physician Product Lead (m/f/d)

Director, Medical Safety Physician Product Lead (m/f/d)

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

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