Clinical Affairs Manager (m/w/x)

TN Germany; Berlin; Vor Ort; EUR 40.000 - 60.000; Vollzeit

Zusammenfassung

Ein innovatives Unternehmen sucht einen Clinical Affairs Manager, der die Verantwortung für die klinische Strategie und Dokumentation übernimmt. In dieser spannenden Rolle arbeiten Sie an der Entwicklung von Produkten, analysieren klinische Daten und unterstützen internationale Teams bei der Registrierung von Medizinprodukten. Ihre Expertise in klinischen Angelegenheiten und regulatorischen Anforderungen wird entscheidend sein, um sicherzustellen, dass Produkte den höchsten Standards entsprechen. Wenn Sie eine Leidenschaft für medizinische Innovationen haben und in einem dynamischen Umfeld arbeiten möchten, könnte dies die perfekte Gelegenheit für Sie sein.

Qualifikationen

• Mindestens 5 Jahre Erfahrung in klinischen Angelegenheiten in der Medizintechnik.
• Gute Kenntnisse der relevanten regulatorischen Anforderungen für klinische Studien.

Aufgaben

• Teilnahme an komplexen Produktentwicklungsprojekten und Planung der klinischen Strategie.
• Erstellung und Pflege klinischer Dokumentation für regulatorische Zwecke.

Kenntnisse

Projektmanagement

Analytische Fähigkeiten

Medizinisches Schreiben

Kommunikationsfähigkeiten

Kreativität

Ausbildung

Vierjährige Hochschulausbildung in Optometrie, Medizin, Medizintechnik oder Naturwissenschaften

Jobbeschreibung

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Clinical Affairs Manager (m/w/x), Berlin

Client:

ZEISS Group

Location:

Berlin, Germany

Job Category:

Other

EU work permit required:

Yes

Job Reference:

ef2384e7f23a

Job Views:

2

Posted:

25.04.2025

Expiry Date:

09.06.2025

Job Description:

Your role

1. Participate in complex project product development with R&D and PM, identify potential clinically relevant issues emerging from (absence of) features and their clinical consequences, define and implement the appropriate clinical evaluation strategy and necessary clinical studies for the product.
2. Responsibility for budget and time planning for the entire clinical strategy and for compliance with this, taking into account economic aspects and project risks as well as defining minimization measures.
3. Independently plan, generate and maintain clinical documentation for regulatory purposes (e.g. Clinical Evaluation Plan and Report, clinical content for regulatory submissions), including continuous gap analysis and conclusion on sufficiency of clinical evidence, adapt clinical strategy when necessary.
4. Planning and execution of CA tasks of post-market surveillance incl. database analysis and literature search, regular update of clinical assessments.
5. If necessary, selection and coordination of external service providers for the aforementioned activities.
6. Create and/or review manuscript for scientific publications.
7. Review and approval of product specific marketing materials and publications.
8. Support clinical/regulatory affairs teams worldwide in product registrations.
9. Report on project progress.
10. Act as an internal consultant/subject-matter expert adaptation and improvement of Clinical Affairs processes.

Your profile

1. Education: Minimum four-year college degree in optometry, medicine, medical technology/engineering, or natural sciences.
2. At least 5 years of experience in Clinical Affairs/Clinical evaluation in the medical device industry or with contract research organizations.
3. Good knowledge of relevant regulatory requirements for clinical trials for medical devices (ICH-GCP, ISO 14155).
4. In-depth knowledge of relevant regulatory requirements in clinical evaluations for medical devices (MDR, MPDG, MDCG, MEDDEV, IMDRF guidelines).
5. Good knowledge in biostatistics, data interpretation, and critical reading of publications.
6. Good knowledge of regulatory requirements for CE, FDA, NMPA, Health Canada, etc.
7. Demonstrated qualities in project management and medical writing.
8. Strong analytical skills coupled with creativity and intuition.
9. Commitment and creative drive as well as strong communication and organizational skills in an international environment.
10. Very good oral and written communication in English.