Head of Central Quality Systems (all genders, full-/part-time) (Biologe/Biologin)

Entfalte das Besondere mit uns!

Sind Sie bereit, neue Wege zu gehen, Herausforderungen zu meistern und Neues zu entdecken? Wir wissen, dass Sie große Pläne haben – und die haben wir auch! Unsere Kolleg:innen auf der ganzen Welt lieben es, mit Wissenschaft und Technologie innovativ zu sein und das Leben der Menschen durch unsere Lösungen zu bereichern. Gemeinsam haben wir Großes im Sinn und engagieren uns mit Leidenschaft für Menschen, Kund:innen, Patient:innen und die Erde, auf der wir leben. Deshalb sind wir stets auf der Suche nach neugierigen Köpfen, die sich vorstellen können, mit uns Großartiges zu erreichen.

Ihre Aufgaben:
Unterstützung bei einfachen analytischen Aufgaben, insbesondere im Bereich ELISA (Enzyme-Linked Immunosorbent Assay) im Routinebetrieb.
Durchführung von Routine Zellkulturarbeiten innerhalb des Life Science und Healthcare Bereichs.
Dokumentation und Auswertung von Experimenten sowie Unterstützung bei der Erstellung von Berichten.
Mitarbeit in verschiedenen Projekten und Unterstützung des Teams bei der Erreichung der Projektziele.

Ihr Profil:

- Eingeschriebener Student (m/w/d) in einem relevanten Studiengang (z.B. Biologie, Biochemie, Lebenswissenschaften oder verwandte Fachrichtungen).
- Grundkenntnisse in analytischen Methoden, insbesondere ELISA und Zellkulturtechniken.
- Selbständige, strukturierte und sorgfältige Arbeitsweise.
- Teamfähigkeit und gute Kommunikationsfähigkeiten.
- Interesse an der Forschung im Bereich Life Science und Healthcare.
- Sehr gute (C1) Englisch- und Deutschkenntnisse in Wort und Schrift

Was können Sie bei uns erwarten?Wir sind neugierige Köpfe mit vielfältigen Hintergründen, Perspektiven, Beruf- und Lebenserfahrungen. Wir leben und schätzen die Vielfalt und sind überzeugt, dass sie Wissen und Innovation fördert und unsere Fähigkeit stärkt, in Wissenschaft und Technologie führend zu sein. Unser Ziel ist es, allen Mitarbeitenden die Möglichkeit zu geben, sich in ihrem eigenen Tempo zu entwickeln und zu wachsen. Unterstützen Sie uns, eine Kultur der Integration und Zugehörigkeit zu schaffen, die Millionen von Menschen beeinflusst und uns alle befähigt, sich für den menschlichen Fortschritt einzusetzen!

Bewerben Sie sich jetzt und werden Sie Teil unseres Teams!

Du möchtest deine Karriereentwicklung nicht dem Zufall überlassen? Dann gehe mit uns gezielt den nächsten Schritt. Dazu bringen wir bei FERCHAU als eine der führenden europäischen Plattformen für Technologie-Dienstleistungen die smartesten und innovativsten Köpfe mit Unternehmen verschiedenster Branchen zusammen. Wir suchen dich: als ambitionierte:r Biologin / Biologe mit dem Schwerpunkt Landschaftsökologie, der:die wie wir Technologien auf die nächste Stufe bringen möchte. Wir realisieren spannende Projekte für namhafte Kunden in allen Technologiebereichen und für alle Branchen und überzeugen täglich mit fundierter Expertise und fachlichem Know-how. Als Berufserfahrene:r unterstützt du deine Kolleg:innen mit deinem langjährigen Know-how und deiner Expertise. Als Berufseinsteiger:in unterstützt du deine Kolleg:innen mit neuen Ideen und festigst dein Wissen durch praktische Erfahrungen.

Biologe Landschaftsökologie (m/w/d)

Ihre Aufgaben:

Das ist zukünftig dein Job
*Überwachung und Einhaltung der naturschutzfachlichen Auflagen aus Genehmigungen
*Kommunikation mit beteiligten Personen, wie Fachfirmen oder Bauherren, direkt auf den Baustellen in der Region
*Teilnahme an Baubesprechungen
*Erstellung von Berichten und Dokumentationen
*Kartierung von Brutvögeln bei Bedarf

Deine Vorteile bei uns
*Hohe Planungssicherheit durch unbefristeten Arbeitsvertrag
*Attraktive, leistungsgerechte Vergütungsstrukturen
*Work-Life-Balance durch flexible Arbeitszeitmodelle sowie Sonderurlaub
*Weiterbildungsangebote unseres Inhouse-Instituts, der FERCHAU Academy (E-Learnings, Trainings, Seminare und LinkedIn-Learning)
*Satte Rabatte mit Einkaufsvergünstigungen, z. B. bei Reisen, Elektronik oder Autos

Ihre Qualifikationen:

Das bringst du mit
*Abgeschlossenes Studium der Biologie, Landschaftsökologie, Umweltwissenschaften oder einem ähnlichen Schwerpunkt
*Praktische Erfahrung in der ökologischen Baubegleitung
*Idealerweise ebenfalls Erfahrung im Bereich der Kartierung
*Kenntnisse in der Ornithologie
*Sicherer Umgang mit gängigen EDV-Anwendungen sowie GIS-Software (z.B. ArcGIS)
*Führerschein der Klasse B
*Fließende Deutschkenntnisse in Wort und Schrift (mindestens C1-Niveau)

Lust auf die nächste Herausforderung? Dann sollten wir uns unbedingt kennenlernen! Am schnellsten geht es, wenn du dich direkt bewirbst - gern unter der Kennziffer VA70-81432-DA bei Herrn B. Sc. Mark Haider. Lass uns gemeinsam das nächste Level nehmen und Technologie nach vorn bringen!

Work Your Magic with us!

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

Your Role:
Join our BioMonitoring Sales Team in Germany and take charge of driving sales for our microbiological portfolio, primarily focused on the pharma segment, QC, and contract labs. You’ll be the go-to person for your territory, actively engaging with customers, collaborating with various internal stakeholders to expand our customer base. This role requires a deep understanding of microbiological applications and the ability to communicate effectively with technical and non-technical stakeholders. Your structured yet analytical approach and excellent time management skills will help you follow up on customer projects effectively, while providing and demonstrating hands-on and top-notch technical information to meet their needs. Build long-term relationships with key clients and identify new business opportunities. The role offers great potential for growth and a clear career path within our dynamic organization.

Who You Are:

- Fluent in German and English (written and spoken)
- Responsible for postal code areas DE 40-42, 44-47, and 50-58; preference for candidates located within these regions. Valid driver's license and willingness to travel within the territory.
- Strong background in pharma QC, with knowledge of regulations and testing methods.
- 3+ years of sales experience in pharma QC or related sectors; knowledge of automation is a plus. Proven ability to manage territory, spending over 70% of time in the field, with a track record of meeting or exceeding sales targets.
- Strong interpersonal skills with the ability to build rapport and actively listen to client needs. Adaptable, resilient, and self-motivated, capable of working independently and collaboratively.
- Bachelor’s degree in microbiology, biology, or a related field.

What we offer:We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and become a part of our diverse team!

Über die TU DarmstadtDie TU Darmstadt steht für exzellente und relevante Wissenschaft. Die tiefgreifenden globalen Veränderungsprozesse – von Energiewende bis zu Künstlicher Intelligenz – gestalten wir durch herausragende Forschung und zukunftsweisende Studienangebote entscheidend mit. Zudem zählen wir zu den größten ausbildenden Institutionen in Südhessen; unser Angebot umfasst rund zwanzig Ausbildungsberufe und duale Studiengänge in mehreren Branchen. Als eine in der Metropolregion Frankfurt-Rhein-Main verankerte und sehr stark international geprägte Universität sehen wir uns den europäischen Werten und der europäischen Integration verpflichtet.
Über unseren BereichDie Universitäts- und Landesbibliothek (ULB) ist die zentrale Bibliothek der Technischen Universität Darmstadt. Als wissenschaftliche Universalbibliothek ist sie für die Informationsversorgung für die Bevölkerung Darmstadts und Südhessens sowie für die hier angesiedelten Ausbildungs- und Forschungseinrichtungen, Behörden, Kulturinstitutionen und Betriebe zuständig. Ihre Sammelschwerpunkte sind naturwissenschaftlich-technische Werke sowie geistes- und gesellschaftswissenschaftliche und landeskundliche Literatur. Sie entwickelt und betreibt verschiedene Dienste im Bereich der semantischen Dokumentation von Forschungsdaten und der Digitalisierung und betreut elektronische Publikationen im Open Access.

Ihre AufgabenWir suchen Nachwuchswissenschaftler:innen , die in Ihrem Studium Freude am Recherchieren von wissenschaftlicher Literatur und der Arbeit mit Daten gefunden haben, die teamorientiert denken und ihre Erfahrungen in diesen Feldern ausbauen möchten.

Wir machen Sie fit im Forschungsdatenmanagement, in rechtlichen und technischen Fragen der Bereitstellung von digitalen Medien und im digitalen Publizieren. Sie lernen neueste Techniken des Information Retrieval und der Literaturauswertung mit Methoden des Text- und Datamining kennen.

Eingebunden in verschiedene Arbeitsgruppen sammeln Sie eigene Erfahrungen im Anleiten und Führen von Menschen. Mit diesen Kenntnissen und Ihrem Fachstudium werden Sie eine kompetente Ansprechperson für Wissenschaft und Forschung mit Schnittstellenfunktion in Bibliotheken und Informationszentren.

Die Einstellung erfolgt im Rahmen des Vorbereitungsdienstes an wissenschaftlichen Bibliotheken des Landes Hessen ( Bibliotheksreferendariat ) und einem Beamtenverhältnis auf Widerruf für 2 Jahre. Sie endet mit einer Masterprüfung und der Laufbahnbefähigung für den Höheren Dienst. Diese ist Voraussetzung für Leitungs- und Führungsaufgaben in wissenschaftsnahen Informationseinrichtungen.
Das Referendariat umfasst neben dem Praxisanteil an der Ausbildungsbibliothek auch theoretische Ausbildungsanteile, die als Fernstudienmodule an der Humboldt Universität Berlin absolviert werden. Nähere Informationen hierzu finden Sie unter https://www.hebis.de/aus-und-fortbildung/ausbildung/.

Ihr ProfilBewerberinnen und Bewerber müssen ein Studium vorzugsweise der Biologie, Chemie, Geowissenschaften, Ökologie/Umwelttechnik oder Pharmazie an einer Universität durch Prüfung (Master oder gleichwertiger Abschluss) abgeschlossen haben.
Sie verfügen über diese aufgabenbezogenen Kompetenzen:
• Erste Erfahrungen im Umgang mit Forschungsdaten, Publikationen, Open Science
• Interdisziplinärer fachlicher Horizont
• Erfahrungen im Bibliotheks- und Informationswesen, im Bereich der Drittmittelakquise oder im Projektmanagement sind von Vorteil
• Sehr gute Englischkenntnisse in Wort und Schrift

Sie bringen diese persönlichen Kompetenzen mit:
• Soziale Kompetenzen (insbes. Teamfähigkeit und Kommunikationsfähigkeit)
• Organisationsgeschick
• Fähigkeit zu einem kollegialen Führungsstil
• Ausgeprägtes Servicedenken

Sie müssen darüber hinaus die Voraussetzung zur Einstellung als Beamtin/Beamter erfüllen und dürfen bei Einstellung höchstens 40 Jahre alt sein.

Wir bietenDie Technische Universität Darmstadt bietet
• Einen krisensicheren Ausbildungsplatz
• Eine Ausbildung im wissenschaftlichen Umfeld, mit Kontakt zu Wissenschaftler:innen, Studierenden und Kolleg:innen aus der ganzen Welt
• Einen Ausbildungsbetrieb, bei dem Themen, wie Nachhaltigkeit, Weltoffenheit und Respekt voreinander gelebt werden
• Vermögenswirksame Leistungen
• 30 Tage Erholungsurlaub im Jahr
• Flexible Arbeitszeit und mobiles Arbeiten möglich
• Freifahrtberechtigung im gesamten Regionalverkehr in Hessen durch das LandesTicket Hessen
• Kostengünstige Parkmöglichkeiten am Arbeitsort
• Ein umfassendes internes Weiterbildungsangebot
• Fit und Gesund - kostenlose medizinische Vorsorgeuntersuchungen und umfangreiches vergünstigtes Sportangebot
• Vielfältiges Essensangebot auf dem Campus der TU Darmstadt

Allgemeine Hinweise / DatenschutzDie Technische Universität Darmstadt strebt eine Erhöhung des Anteils der Frauen am Personal an und fordert deshalb besonders Frauen auf, sich zu bewerben. Bewerber:innen mit einem Grad der Behinderung von mindestens 50 oder diesen Gleichgestellte werden bei gleicher Eignung bevorzugt.
Mit dem Absenden Ihrer Bewerbung willigen Sie ein, dass Ihre Daten zum Zwecke des Stellenbesetzungsverfahrens gespeichert und verarbeitet werden. Sie finden unsere Datenschutzerklärung auf unserer Homepage.
AnsprechpersonFür Rückfragen stehen wir Ihnen unter [email protected] gerne zur Verfügung.
Bewerbungs- oder Reisekosten können nicht übernommen werden.

Work Your Magic with us!

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

A great opportunity has opened within the Data Monitoring, Management and Innovation department to further strengthen our Clinical Data Management team. As an Associate Director Clinical Data Manager, you will play a crucial role in managing and overseeing clinical data management activities within the organization. You will be responsible for ensuring the integrity, accuracy, and completeness of clinical trial data, while also coordinating a team of clinical data management professionals in a matrix setting.

Your role

- Accountable for all Clinical Data Management (CDM) related deliverables in assigned global (Phase I-IIIb) trials or programs of varying complexity
- Provide CDM leadership for assigned trial(s)/program(s), take global accountability and serve as the CDM representative at the study/program level
- Demonstrate project management and operational expertise in the strategic planning and delivery of CDM deliverables at study/program level, e.g. planning timelines and resources, risk identification and management, status tracking, internal and external stakeholder management etc
- Define and execute risk-based data collection, cleaning and quality assurance strategies for eCRF and external data (including coding)
- Ensure the accuracy, integrity, and completeness of clinical trial data through comprehensive data review and validation activities
- Ensure quality of clinical database/deliverables (incl. eCRF and external data) as well as submission readiness of the clinical data management deliverables and data packages (e.g. CDISC)
- Act as primary point of contact within CDM for any HA submission related activities (e.g. preparation of briefing books, attending HA meetings as requested)
- Manage and oversee CRO and vendor performance, including participation in selection/assessment and budget management as required, for assigned trial(s)
- Contribute to the development and maintenance of data management SOPs, work instructions, and best practices.
- Lead process improvement initiatives and drive innovation in the field of Clinical Data Management
- Additionally, if assigned to a program:
- Demonstrate good understanding of the compound profile to identify and assist in successful application of consistent CDM processes and documentation across assigned studies in an assigned program/indication e.g. ensuring consistency across data quality plans
- Utilise understanding of CDASH and SDTM, or other recognised industry standards, to ensure consistency of implementation across studies in assigned program/indication
- May act as a mentor for CDM colleagues within/beyond assigned program
- Demonstrate willingness to take on and lead any program level activity in support of study delivery

Who you are

- Bachelor's or Master's degree in a scientific or technical discipline, preferably in life sciences, data management, or a related field
- Minimum of 10 years of experience in clinical data management within the pharmaceutical, biotechnology, or healthcare industry
- Profound, long-standing experience in leading clinical data management activities in complex Oncology development projects (including large phase III trials) both on trial and program level
- Experience in working in different sourcing models with a focus on in-house models
- Committed to continuous personal and professional development, and bringing external insights to the role to drive innovation and process improvement
- Proficient in contributing to non-study related initiatives e.g. process improvements, in addition to study assignm ents
- Strong project management, analytical, communication, collaboration, and problem-solving skills
- Ability to work proactively and independently on assigned tasks or projects of varying complexity; prioritising and managing multiple activities simultaneously
- Demonstrated ability to lead and oversee end-to-end data management activities within a clinical trial, as well as leading and coordinating global teams in a matrix organization
- Familiar with autonomously providing reports to senior management, including updates on financials, forecasts and timelines
- Proficiency in data management systems and tools, including strong knowledge of regulatory requirements, industry standards, and best practices related to clinical data management
- Experience in Risk Based Data Monitoring/Management, and with clinical trial data standards, such as CDISC, is preferred

What we offer:We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and become a part of our diverse team!

Work Your Magic with us!

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

Your role

In Healthcare Research & Development Quality and Risk Management (RDQRM), we are looking for a dynamic and experienced Senior Project Manager. This role supports the RDQRM Leadership Team (LT) in driving strategic initiatives, managing key projects, and enhancing operational efficiency across the organization. This role requires a proactive leader with exceptional organizational, communication, prioritization and problem-solving skills, as well as excellent stakeholder management capabilities. Your key responsibilities would be to assist the RDQRM Head and executive team in developing and implementing strategic plans and initiatives; manage and prioritize the LT’s schedule, ensuring effective time management and alignment with organizational goals; lead and oversee the RDQRM organizational changes; be responsible for RDQRM communication strategy and related execution; prepare and analyze reports, presentations, and communications for internal and external stakeholders; act as a liaison between the RDQRM LT and various departments, ensuring alignment and effective execution of strategies; oversee special projects and initiatives as directed by the RDQRM Head or LT; foster a positive organizational culture and support employee engagement initiatives; provide leadership and guidance to staff members on various operational and strategic matters.

Who you are

- Ideally, a degree in Life Sciences (Biology, Chemistry, Pharmacy, etc.), equivalent related professional experience may be considered.
- 8+ years in project management within pharmaceutical industry or CROs, with 5+ years of experience leading cross-functional projects with proven implementation skills.
- Project Management Certification, an MBA, Six Sigma Certification is a plus.
- Deep understanding of drug development process and pharmaceutical industry and demonstrated success in working in a global and multi-cultural environment.
- Knowledge of global regulatory GXP requirements with focus on GLP, GCP, GVP.
- Strong understanding of Operational Excellence principles.
- Demonstrated leadership in change management.
- Able to successfully navigate within varying degrees of ambiguity in a fast-paced environment.
- Strong mature leadership, negotiation and influencing skills.
- Fluent in English with excellent writing skills.

What we offer:We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and become a part of our diverse team!

Work Your Magic with us!

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

Your role:
As the Head of Central Quality Systems, you will play a pivotal role in shaping the strategic direction of global quality systems within our organization. Your leadership will ensure compliance, efficiency, and continuous improvement of regulated GxP processes. You will establish and nurture strategic partnerships with key business leaders to align quality systems with overarching business objectives. Driving process standardization and regulatory compliance will be at the forefront of your responsibilities. You will lead a dedicated team of quality experts, guiding them in the development and implementation of comprehensive strategies for global regulated processes. Your data-driven decision-making will facilitate the identification of opportunities for quality enhancements. Additionally, you will oversee complex RDQRM projects and manage a comprehensive communication strategy. By ensuring the integrity and effectiveness of our global quality systems, you will reinforce operational excellence and foster a robust culture of compliance. This is an exceptional opportunity to make a significant impact on our organization’s quality landscape.

Who you are:

- You hold an advanced degree (PhD or MSc) in Life Sciences (e.g., Biology, Chemistry, Pharmacy) or possess equivalent professional experience.
- You have over 10 years of experience as a strategic leader in the international Pharmaceutical/Biopharmaceutical sector, focusing on quality management systems and processes.
- You possess in-depth knowledge of GxP areas, particularly GCP, GVP, and GLP, along with a comprehensive understanding of global regulatory requirements like ICH.
- You have demonstrated success in managing complex projects and leading change management initiatives in a global, multicultural environment.
- You are fluent in English and possess strong communication skills, both written and verbal.
- You have proven people leadership skills, with the ability to engage and influence stakeholders at all organizational levels.
- You are experienced in regulatory inspections and audits, and you understand the nuances of pharmaceutical drug development.
- You are equipped with continuous improvement knowledge and familiarity with tools such as Lean, Six Sigma, and Business Process Management.

What we offer:We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and become a part of our diverse team!

Work Your Magic with us!

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

Your role:

Join our team and take part in delivering cutting-edge statistical input and Real World Data (RWD) analyses essential for driving clinical development, regulatory compliance, and pharmacovigilance initiatives. Your role will involve architecting, designing, and scaling data analytics solutions, predictive modeling, data science, mining, visualization, and implementing algorithms.

You will be instrumental in writing statistical sections of study protocols, collaborating closely with study teams, and effectively communicating results to relevant stakeholders. Your expertise will also extend to articulating, refining, and defending data analytics standards while applying advanced analytics techniques. This may entail processing large datasets, scaling algorithms, or creating user-friendly application interfaces.

In addition to meeting timelines and maintaining high-quality deliverables in line with company and international standards, you will provide invaluable RWD/RWE advice to both internal and external stakeholders.

If you're passionate about RWD/RWE and novel methods to drive informed decision-making and thrive in a dynamic, collaborative environment, we invite you to join us in shaping the future of healthcare.

Who you are:

- Background in health and life sciences (biostatistics, epidemiology), or quantitative data sciences
- Doctoral and/or master’s degree (e.g., PhD, MSc) in Biostatistics, Epidemiology, Mathematics or related field
- Extensive prior experience with RWD/RWE required  - Prior experience in the pharmaceutical industry required (4-8 years)
- Demonstrable experience in writing and implementing statistical analysis plans for studies required
- Demonstrable experience in processing large real-world datasets for analyses and studies required
- Experience in predictive modeling, machine learning and artifical intelligence methodology a plus
- Experience in coding (r) a plus
- Excellent oral and written communication skills and demonstrated ability to engage and communicate scientific evidence to peers
- Collaborative, proactive working style, with ability to work independently.

What we offer:We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and become a part of our diverse team!