Clinical Trial Jobs
- ICON PlcWien, W
- You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.
- Life assurance and disability coverage.
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- Gehalt-Suche: Clinical Research Associate Gehälter
Clinical Site Coordinator
Antwortet häufig innerhalb von 1 TagMilestone OneWien, W- The Milestone One Site Coordinator role supports a Clinical Study Site in clinical trial related activities according to ICH-GCP, protocol requirements within…
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- Gehalt-Suche: Clinical Site Coordinator Gehälter
- GlaxoSmithKlineWien, W
- Experience in clinical research, clinical trial management, clinical operations, Medical Affairs or a related pharmaceutical industry function.
- Alle GlaxoSmithKline Jobs anzeigen – Jobs in Wien – Clinical Trial Manager Jobs - Wien, W
- Gehalt-Suche: Clinical Trial Operational Manager(m/f/d) Gehälter
- GlaxoSmithKlineWien, W
- Experience in clinical research, clinical trial management, clinical operations, Medical Affairs or a related pharmaceutical industry function.
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- Gehalt-Suche: Clinical Trial Operational Manager(m/f/d) Gehälter
- サイネオス・ヘルスHome Office
- This includes conducting remote monitoring of trial sites to verify compliance with regulatory requirements and clinical protocols.
- Alle サイネオス・ヘルス Jobs anzeigen – Jobs in Home Office – Clinical Research Associate Jobs - Home Office
- Gehalt-Suche: CRA Austria Gehälter in Home Office
- The Clinical Specialist plays a key role in ensuring the integrity and reliability of clinical trial data.
- Minimum 3 years administering psychiatric assessments…
- Alle IQVIA Jobs anzeigen – Jobs in Wien – Clinical Trial Administrator Jobs - Wien, W
- Gehalt-Suche: Job Posting Title Clinical Trial Psych Rater - German Speaking Gehälter
- Takeda PharmaceuticalWien, W
- Oversee medical affairs activities, including budget management, internal knowledge transfer, and support for clinical trials and regulatory functions.
- Alle Takeda Pharmaceutical Jobs anzeigen – Jobs in Wien – Neurologist Jobs - Wien, W
- Gehalt-Suche: Medical Scientific Liaison - Neurology Gehälter
- Lesen Sie sich häufig gestellte Fragen & Antworten zu Takeda Pharmaceutical durch
- Takeda PharmaceuticalWien, W
- Oversee medical affairs activities, including budget management, internal knowledge transfer, and support for clinical trials and regulatory functions.
- Alle Takeda Pharmaceutical Jobs anzeigen – Jobs in Wien – Liaison Jobs - Wien, W
- Gehalt-Suche: Medical Scientific Liaison - PDT Gehälter in Wien, W
- Lesen Sie sich häufig gestellte Fragen & Antworten zu Takeda Pharmaceutical durch
- Otto Bock HealthCare Deutschland GmbHHome Office
- Assist customers (both virtually and onsite) in the clinical environment by educating patients and clinicians, directing care, and conducting trials to support…
- Syneos - Clinical and Corporate - ProdHome Office
- Participates in global clinical monitoring/project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions…
- Takeda PharmaceuticalWien, W
- Oversee medical affairs activities, including budget management, internal knowledge transfer, and support for clinical trials and regulatory functions.
- Alle Takeda Pharmaceutical Jobs anzeigen – Jobs in Wien – Liaison Jobs - Wien, W
- Gehalt-Suche: Medical Scientific Liaison - Oncology Gehälter in Wien, W
- Lesen Sie sich häufig gestellte Fragen & Antworten zu Takeda Pharmaceutical durch
- Scantox A/SGrambach, ST
- Accurate documentation of experimental procedures.
- Review and quality control of data and analyses.
- Participation in laboratory organization and management.
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- Gehalt-Suche: Lab Technician – Cell Culture (m/f/d) Gehälter
Global Expert Clinical Strategy (m/f/d) - Clinical R&D
Antwortet häufig innerhalb von 3 TagenOctapharmaWien, W- Strong expertise in protocol development, clinical study design, clinical study reports and clinical development planning.
- Alle Octapharma Jobs anzeigen – Jobs in Wien – R&D Engineer Jobs - Wien, W
- Gehalt-Suche: Global Expert Clinical Strategy (m/f/d) - Clinical R&D Gehälter in Wien, W
- Takeda PharmaceuticalWien, W
- Serves as an advisor to assoc. med directors and clinical scientists.
- Of clinical development plans for potential alliances and or in-licensing opportunities…
- Alle Takeda Pharmaceutical Jobs anzeigen – Jobs in Wien – Director of Science Jobs - Wien, W
- Gehalt-Suche: Medical Director, Global Clinical Science, Immunodeficiency (f/m/d), Hybrid Gehälter
- Lesen Sie sich häufig gestellte Fragen & Antworten zu Takeda Pharmaceutical durch
- Thermo Fisher ScientificHome Office
- With approximately 20 years of experience, our highly trained staff provide medical writing services for all phases of the product lifecycle, helping to create…
- Alle Thermo Fisher Scientific Jobs anzeigen – Jobs in Home Office – Medical Writer Jobs - Home Office
- Gehalt-Suche: Principal Medical Writer (Publications) Gehälter
- Lesen Sie sich häufig gestellte Fragen & Antworten zu Thermo Fisher Scientific durch
- IQVIAWien, W
- Understanding of regulated clinical trial environment and knowledge of drug development process.
- In-depth knowledge of clinical systems, procedures, and…
- Alle IQVIA Jobs anzeigen – Jobs in Wien – Regulatory Specialist Jobs - Wien, W
- Gehalt-Suche: Regulatory and Start Up Specialist - Austria Gehälter
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Job Post Details
Clinical Research Associate - job post
Stellenbeschreibung
Anstellungsart
- Vollzeit
Arbeitsort
Vollständige Stellenbeschreibung
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 CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
What You Will Do:
You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include:
- Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
- Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
- Collaborating with investigators and site staff to facilitate smooth study conduct.
- Performing data review and resolution of queries to maintain high-quality clinical data.
- Contributing to the preparation and review of study documentation, including protocols and clinical study reports
Your Profile:
You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.
Required qualifications and experience:
- Bachelor's degree in a scientific or healthcare-related field.
- Minimum of 2 years of experience as a Clinical Research Associate.
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
- Fluent German and English
- Strong organizational and communication skills, with attention to detail.
- Ability to work independently and collaboratively in a fast-paced environment.
- Willingness to travel as required (approximately 60%)
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 .
Are you a current ICON Employee?