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Cta • Switzerland

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Expert Clinical Trial Documentation - Clinical Trial Associate (CTA)

Octapharma AGLachen SZ, CH

Become part of a vital chain and contribute to our common goal of making people’s lives better.Headquartered in Lachen, Switzerland, Octapharma is one of the largest human protein manufacturers in ... Mostra di più

Leiter Beschaffung w/m/d

Logjob AG - For Supply Chain ExpertsMünsingen (BE), CH

Unsere Kundin, die CTA AG, ist ein erfolgreiches international tätiges Industrieunternehmen mit Hauptsitz in Münsingen BE und zählt zu den führenden Anbietern von Wärmepumpen- und Klimasystemen.Mit... Mostra di più

Mitarbeiter/in Quality Control 80-100%

CelerionFehraltorf, Zürich, Switzerland, 8320

Mitarbeiter/in Quality Control 80-100%.Celerion ist eines der weltweit führenden Unternehmen der bioanalytischen Auftragsforschung und unterstützt seit mehr als 40 Jahren Pharma- und Biotechfirmen ... Mostra di più

Medical Director Endocrinology Europe, MD

Neurocrine BiosciencesCH Allschwil

Neurocrine Biosciences is a leading biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs.We are dedicated to discovering, developing and commercializing... Mostra di più

Laboratory Technician - Release Testing (80-100%)

Ophtapharm AGHettlingen, CH

Die Ophtapharm AG ist eine FDA/EU-GMP zertifizierte Produzentin im Pharmabereich (Ophthalmika).An unserem Produktionsstandort in Hettlingen bei Winterthur werden für internationale Märkte qualitati... Mostra di più

Group Consolidation Analyst

Michael Page SuisseLausanne Region, Genève, CH

Our client is a privately held international trading group, headquartered in the Lake Geneva region.With a long-standing track record across global markets and operations spanning multiple continen... Mostra di più

Associate Director, Analytical Strategy (m/w/x)

CSLBern, Berne, Switzerland

Associate Director, Analytical Strategy (m/f/x).The Associate Director, Analytical Strategy will lead the development and execution of analytical strategies to support biopharmaceutical development... Mostra di più

 • In evidenza

Senior Clinical Trial Assistant (m/f/x) - 12 months

Randstad (Schweiz) AGLausanne, Vaud

Vers-chez-les-Blanc, Switzerland.Clinical Research Unit, Nestlé Research.The Senior Clinical Trial Assistant (Sr.CTA) provides high-quality operational and administrative support to clinical trial ... Mostra di più

Webdesigner/in

Spaeth-Wiesner GmbHAugst, Basel-Landschaft, Switzerland
Quick Apply

Du hast ein Auge für gutes Design, denkst aber nicht nur kreativ, sondern auch strukturiert und lösungsorientiert? Du willst nicht einfach nur schöne Websites gestalten, sondern Webauftritte entwic... Mostra di più

Leiter*in Programm und Teilprojekte SmartMove@CTA

CTA AGMünsingen, CH

Wir sorgen dafür, dass Temperatur und Klima stimmen – für Mensch und Natur.Als unabhängiges, familiengeführtes Schweizer Unternehmen mit über 300 Mitarbeitenden setzen wir uns seit 1981 für erneuer... Mostra di più

Chemielaborant/in

Drossapharm AGArlesheim, CH

Analytik trifft Validierung – Qualität beginnt mit verlässlichen Methoden!.Sie begeistern sich für die Entwicklung und Validierung analytischer Methoden und lösen analytische Fragestellungen mit Pr... Mostra di più

Expert Clinical Trial Documentation - Clinical Trial Associate (CTA)

OctapharmaLachen, CH

Expert Clinical Trial Documentation - Clinical Trial Associate (CTA).Job Level: Professionals Job Category: Research and Development Employment Type: Permanent position Career Level:.Become part of... Mostra di più

Berufsschullehrer/-in oder Erwachsenenbildner/-in HLKE

Engineering Management Selection E.M.S. AGMünsingen, CH

Gestalten Sie den Campus bei der CTA in Münsingen.Unsere Auftraggeberin, die CTA AG in Münsingen, entwickelt, produziert und vertreibt mit über 300 Mitarbeitenden Wärmepumpen, Klimageräte und Kälte... Mostra di più

Lab Technician HPLC und CE (m/w/d)

unisite agKaiseraugst, Schweiz

Lab Technician HPLC und CE (m/w/d).Arbeitsort: Kaiseraugst | Pensum: 100% | Vertragsdauer: Temporär – langfristige Temporäranstellung mit Option auf eine Festanstellung.Solvias ist ... Mostra di più

Senior Clinical Trial Assistant (m/f/x) - 12 months

RandstadLausanne

Vers-chez-les-Blanc, Switzerland.Clinical Research Unit, Nestlé Research.The Senior Clinical Trial Assistant (Sr.CTA) provides high-quality operational and administrative support to clinical trial ... Mostra di più

Associate Director / Senior Regulatory Affairs CMC

gloor&lang AGBasel, Basel City, Switzerland
Quick Apply

Innovative Biopharmaceutical Company | Northwestern Switzerland.Shape the Global Regulatory Strategy for Innovative Small Molecule Therapies.Our client is an innovative, research-driven biotechnolo... Mostra di più

Sachbearbeiter Rohstoffbewirtschaftung für die API-Produktion (m/w/d)

Dottikon Exclusive Synthesis AGDottikon, CH

Bewirtschaftung der Lagerbestände (Rohstoffe, Freigabeanalytik, Reststoffverwertung etc.Beauftragung der Produktionsanlagen nach entsprechender Freigabe.Berufserfahrung in der chemisch- pharmazeuti... Mostra di più

Mitarbeiter/in Quality Control 80-100%

Celerion Switzerland AGFehraltorf, CH

Celerion ist eines der weltweit führenden Unternehmen der bioanalytischen Auftragsforschung und unterstützt seit mehr als 40 Jahren Pharma- und Biotechfirmen auf der ganzen Welt.Celerion bietet Die... Mostra di più

Production Technician (m/w/d)

CARBOGEN AMCIS AGAarau, CH

Gerätereinigungen im GMP-regulierten Umfeld.Wenn Sie nach einer abwechslungsreichen und spannenden neuen beruflichen Herausforderung suchen, sind Sie bei uns genau richtig.Selbstständige Durchführu... Mostra di più

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Expert Clinical Trial Documentation - Clinical Trial Associate (CTA)

Expert Clinical Trial Documentation - Clinical Trial Associate (CTA)

Octapharma AGLachen SZ, CH
7 giorni fa
Descrizione dell’offerta di lavoro

Become part of a vital chain and contribute to our common goal of making people’s lives better. Headquartered in Lachen, Switzerland, Octapharma is one of the largest human protein manufacturers in the world, developing and producing medicines sourced from human plasma and human cell lines. We are a privately-owned company, where the warmth of family meets the scale of a global organisation.

Join us in shaping our vision to provide new health solutions advancing human life.

Expert Clinical Trial Documentation - Clinical Trial Associate (CTA)Your main tasks and responsibilities
  • Set up and maintain Trial Master Files (TMFs) and lnvestigator Site Files (ISFs) according to Octapharma SOPs
  • Support the Clinical Team in preparing clinical trial documents and documentation for regulatory submissions
  • Track clinical trial documents such as insurance certificates, confidentiality agreements and study contracts throughout the trial lifecycle
  • Maintain audit and inspection readiness through periodic review of TMF accuracy and completeness, quality control checks, and a unified TMF management approach. Support audits and inspection preparation and execution with regards to the TMF
  • Act as a central contact for trial documentation, designated project communications, support ad hoc tasks
  • Manage returning/archiving of TMF documents
  • Assist in the organization of lnvestigator Meetings
  • Perform various administrative tasks to support team members with clinical trial execution, as required ( literature search or document formatting review for regulatory submissions)
  • In addition, for the senior position:
    • Assume Data Protection / Information Security Champion responsibilities
    • Assists in development of SOPs
    • Perform vendor evaluation and oversight for selected vendors
Your expertise and ideal skill set
  • A minimum of 1 year of experience as a CTA/documentation expert in international clinical trials or similar (3 years for the senior position)
  • Fluent in both written and spoken English; preferably also in German
  • Experience with various CTMS and TMF systems
  • Excellent command of Microsoft Office applications and Adobe Acrobat DC
  • Able to prioritize workload with attention to details and within timelines
  • Able to learn on the job and apply new knowledge to future challenges
  • Able to manage multiple and various tasks with a positive and flexible attitude
  • Strong operational, organizational, documentation, communication, and interpersonal skills, able to work in a team and independently
Your department - where you make an impact
  • The Clinical Research and Development (CR&D) team in Lachen develops medicines that target complex and life-threatening conditions in Haematology and Critical Care
  • We specialize in clinical development of new as well as already marketed products
  • The successful candidate will work closely with CPMs, CTMs, and colleagues across CR&D in Lachen to support a wide variety of clinical trials
  • This position reports to the Global Senior Director CR&D in Lachen and is a permanent role within the team.
“Join an international environment with exciting projects and responsibilities — be proactive, contribute, and grow together with a great team”
- Dr. Cristina Solomon, Global Vice President CRD Lachen
Thrive with us
  • You help save lives - Every day is meaningful as we produce life-saving medicines
  • Family values - Long-term perspective for employees and relationships
  • Be rewarded with market-related salary and benefits package
  • You will have a high level of influence where you can make a difference and leave your footprint
  • Work with skilled and fun colleagues in a relatively informal organization
  • Skills development - We offer various internal and external employee and leadership trainings, trainee programs and digital solutions
It´s in our blood

We live diversity and stand for equal opportunities as an employer! We therefore look forward to receiving your application - regardless of age, gender, origin, sexual orientation, and religion.
Please apply in English.

Do you have any questions? Then get in touch with your contact person.

Claudia Vignau
Senior Expert Talent & Acquisition

Octapharma AG

Seidenstrasse 2, 8853 Lachen

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