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Research librarian • feldkirchen

Zuletzt aktualisiert: vor 11 Tagen
Clinical Research Associate II (Germany)

Clinical Research Associate II (Germany)

AllucentMunich, BY, DE
Quick Apply
At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need acr...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
  • Gesponsert
Tenure-track positions at Lise Meitner Research Group

Tenure-track positions at Lise Meitner Research Group

Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V.München, Deutschland
Free science is as natural as free breathing.Lise MeitnerFurthermore, the MPG is committed to increasing the number of individuals with disabilities in its workforce and therefore encourages applic...Mehr anzeigenZuletzt aktualisiert: vor 11 Tagen
Director UX Research (m / w / d)

Director UX Research (m / w / d)

Verivox GmbHMünchen
Als Director UX Research liegt deine Mission darin, die strategische Bedeutung von Research im Unternehmen zu etablieren und das Research-Team in seiner disziplinarischen Führung und fachlichen Ent...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
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Research Engineer (m / f / d)

Research Engineer (m / f / d)

MED-ELMünchen, Bayern, Germany
MED-EL is a leading manufacturer of innovative medical devices for the treatment of various types and degrees of hearing loss. Our unique portfolio of implantable hearing solutions benefits thousand...Mehr anzeigenZuletzt aktualisiert: vor 20 Tagen
(Junior) Research Analyst (w|m|d)

(Junior) Research Analyst (w|m|d)

zebMünchen
Beratungserfolg basiert auf Fakten.Diese stellst du durch deine Arbeit unseren Consultants zur Verfügung und bist somit ein wesentlicher Teil unseres Wertschöpfungsprozesses.Als fachliche Ansprechp...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Research Analyst (m / w / d)

Research Analyst (m / w / d)

TREUGAST Solutions GroupMünchen, DE
Sprachliche und rhetorische Versiertheit, Fähigkeit, sich präzise auszudrücken.Erfahrung mit Recherchetätigkeiten.Interesse an der Hotellerie und bestenfalls erste Arbeitserfahrung.Verantwortungsvo...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Junior Research Scientist Trustworthy Digital Health

Junior Research Scientist Trustworthy Digital Health

Fraunhofer-GesellschaftMunich
Safe Intelligence - this forms the core brand of the.Fraunhofer Institute for Cognitive Systems IKS.Connected cognitive systems drive innovationin many sectors, including mobility, healthcare, and ...Mehr anzeigenZuletzt aktualisiert: vor 13 Tagen
Clinical Research Associates (all levels) - Germany

Clinical Research Associates (all levels) - Germany

Thermo Fisher ScientificMunich, Germany
Vollzeit
At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale.Join our colleagues in bringing our Mission to life - enabling our customers to make the ...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Research Analyst

Research Analyst

ParticulaMunich, Bavaria, Germany
Homeoffice
Quick Apply
Hi, we are Particula, the leading rating and monitoring platform for digital assets! Our mission? To make the market for digital assets more accessible, secure and transparent for institutional inv...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Senior Clinical Research Associate I

Senior Clinical Research Associate I

PSI CROMunich, Bavaria, Germany
Homeoffice
As a Senior Clinical Research Associate I at PSI you will be involved in improving patients' lives while enjoying a variety of monitoring tasks and working on clinical studies in different therapeu...Mehr anzeigenZuletzt aktualisiert: vor 18 Tagen
Principal AI Datacenter Research Engineer

Principal AI Datacenter Research Engineer

Huawei Research Center Germany & AustriaMünchen, Bayern, DE
Huawei's vision is to enrich life through communication.We are a fast growing and leading global information and communications technology (ICT) solutions provider. Driven by a commitment to operati...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Werkstudent •in User Research (all genders)

Werkstudent •in User Research (all genders)

reevMünchen, DE
Unser Ziel bei reev ist es, E-Mobilität für alle zugänglich zu machen.Die reev Software hilft Unternehmen, Ladesäulen effektiv und effizient einzusetzen und damit Fahrer •innen von Elektrofahrzeugen...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Open position as research / teaching assistant

Open position as research / teaching assistant

Technical University of MunichMunich, DE
Open position as research / teaching assistant.Studentische Hilfskräfte, Praktikantenstellen, Studienarbeiten.Die Professur für Wissenschafts- und Technologiepolitik am Department für STS (Department...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Praktikant (w / m / d) Research

Praktikant (w / m / d) Research

HorváthMünchen
Der Bereich Research verantwortet als interner Business Partner Recherchen und Analysen für alle Horváth Mitarbeiterinnen und Mitarbeiter, insbesondere aus der Managementberatung, dem Partner- und ...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Working Student - Market Research (all genders)

Working Student - Market Research (all genders)

zooplus SEMunich, Germany
We are looking for a passionate and results orientated .Central Sales Operations & Project Management Team with Market Research Analytics. Do you want to gain valuable work experience ...Mehr anzeigenZuletzt aktualisiert: vor 21 Tagen
Senior Tax Research Analyst (mw / d)

Senior Tax Research Analyst (mw / d)

Corporate Business SolutionsMünchen
Recherche, Tracking, Interpretation und Validierung legaler Anforderungen im Bereich E-Invoicing und E-Reporting mit dem Schwerpunkt Steuern und Steuerrecht. Know-How-Aufbau und -Pflege zu Legalen A...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
  • Gesponsert
Clinical Research Coordinator- Clinical Research Associate Home-Based

Clinical Research Coordinator- Clinical Research Associate Home-Based

PharmiwebMunich, DE
Clinical Research Coordinators wanted at Medpace! Become a CRA and join our growing team!.This is an exciting opportunity for clinical research professionals with at least one year of Clinical Rese...Mehr anzeigenZuletzt aktualisiert: vor 24 Tagen
Research Assistants - Munich

Research Assistants - Munich

Clyde & CoMunich
Job Title Research Assistants - Munich Job Location Munich Job Type Fee earners Country / Territory Germany Region UK & Europe Description. If you're looking for the perfect environment to learn, deve...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Content Creator : Schwerpunkt Research Reports

Content Creator : Schwerpunkt Research Reports

Julian HospMunich, Bavaria, Germany
Homeoffice
Quick Apply
I-UNLIMITED steht für wegweisende Finanzbildung, innovative Ansätze im Bereich nachhaltiger Investmentstrategien sowie Unternehmertum. Zur Verstärkung unseres dynamischen Teams suchen wir einen erfa...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Intern UniCredit Research (m / f / d)

Intern UniCredit Research (m / f / d)

UniCreditMunich, Germany
Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
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Clinical Research Associate II (Germany)

Clinical Research Associate II (Germany)

AllucentMunich, BY, DE
Vor 30+ Tagen
Anstellungsart
  • Quick Apply
Stellenbeschreibung

At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.

We are looking for a Clinical Research Associate II (CRAII) to join our A-team (hybrid

  • remote). As a CRAII at Allucent, you will independently control and monitor investigation sites, pro-actively detect issues, provide solutions to ensure clinical studies are performed according to the trial protocol and in compliance with SOPs, applicable regulations, and the principles of Good Clinical Practice.

In this role your key tasks will include :

  • Governs quality standards for trial monitoring activities.
  • Performs Selection, Initiation, Monitoring and Closure Visits at Investigator Sites according to project schedule. Adheres to project guidelines and Allucent SOPs for monitoring requirements.
  • Monitors activities at clinical study sites to assure adherence to GCP, ICH, SOPs, and study protocols.
  • Tracks and supervises collection of ongoing study data for purpose of regular project status reporting.
  • Collects and reviews regulatory documents as required.
  • Prepares site visit reports and telephone contact reports.
  • Maintains and updates CTMS in compliance with SOPs and study-specific directives.
  • Acts as Document Owner for collected documents.
  • May participate in the start-up process including preparing Informed Consent forms, developing study documents, EC / CA submissions, and / or site contract management
  • Aims to pro-actively prevent and / or mitigate issues. Resolves site issues, including site recruitment challenges, and determines status for IP shipment.
  • Acts as the main line of communication between the project team and the site staff.
  • Works in collaboration with Allucent Centralized Monitoring Team to evaluate risk-based monitoring activities to facilitate oversight of the study conduct at the sites and prevent issues. Activities are related to but not limited to : Investigational Product supplies, non-IP study supplies, subject eligibility, protocol compliance, facilities, and PI oversight.
  • Identifies potential logistical / practical problems and support Project team to create solutions / contingency plans, with timeframes for resolution.
  • Ensures the continuous maintenance of the Trial Master File and Investigator Site File.
  • Assists the Project Manager (PM) and Clinical Team Leader (CTL) with generation of study specific forms for completion by CRA and Investigators and follow up with the teams to ensure timely completion and submission.
  • Works with Project Manager (PM); Clinical Team Leader (CTL), SSU (Study Start Up) team members or sponsor to ensure authorization of regulatory documents and site contracts.
  • Attends Investigator Meetings (IM) to include organizing and presenting at investigator meetings. and study specific training meetings.
  • May translate, coordinate translations or review completed translations of the essential documents as required.
  • May participates in feasibility and / or site identification activities. Contacts local opinion leaders, medical consultants or specified investigators and identifies sites with the potential for participation. May follow feasibility procedures for documentation of feasibilities performed in collaboration with the Study Start Up Department.
  • Where applicable, identifies the documentation required for review by Regulatory Authorities and Ethical Committees. May prepare Regulatory and Ethics Committee submissions working in conjunction with Study Start Up Department. Ensure written approvals are obtained and distributed appropriately prior to Site Initiation.
  • Prepares and attends an Assessment Visit with a more senior CRA, CTL or Clinical Research Manager as required.
  • May process interim and final payments to Investigators, including preliminary calculations, review and approval from Project Management, liaison with finance, logging trial expenditure, receipts, invoices, and income.
  • Assists the Project Team with the day-to-day management of critical studies as required, including attendance at team meetings.
  • Provides secondary in-house review of CRFs (if required).
  • Support site staff in preparation for study related site audits and inspections.
  • Where applicable, reports Quality Issues and supports the root cause analysis, writing of and resolution of the Corrective and Preventative Actions.
  • May be assigned other tasks / activities / responsibilities related to the study execution in the country.
  • May support initiatives in the country, GCO, and / or CTO to contribute to improvements and quality.
  • Must work both independently and in a team environment.

    • Requirements

    To be successful you will possess :

  • At least three years clinical monitoring experience and / or relevant clinical trial experience.
  • Relevant life science degree / health care / nursing background and / or related degree.
  • Sound knowledge of medical terminology and clinical monitoring process.
  • Strong communication in Local and English language in both written and verbal skills.
  • Strong interpersonal and organizational skills.
  • Ability to translate guidelines, rules and regulations in clear and usable recommendations
  • Representative, outgoing and client focused
  • Ability to work in a fast-paced challenging environment of a growing company
  • In-depth therapeutic and protocol knowledge
  • Ability to travel for up to 8 days on site per month, depending on the project needs.
  • In-depth therapeutic and protocol knowledge as provided in previous, or company provided training.
  • Attention to detail.
  • Ability to work independently and to effectively prioritize tasks, establish, and maintain strong working relationships with co-workers, managers, investigators, site personnel and clients.
  • Demonstrated ability to manage multiple projects.
  • Administrative excellence
  • Proficiency with various computer applications such as Word, Excel, and PowerPoint required
  • Demonstrated ability to develop, organize and manage new skills and tasks and mentor colleagues.
  • Ability to manage multiple projects

    • To be successful you will possess :

  • At least three years clinical monitoring experience and / or relevant clinical trial experience.
  • Relevant life science degree / health care / nursing background and / or related degree.
  • Sound knowledge of medical terminology and clinical monitoring process.
  • Strong communication in Local and English language in both written and verbal skills.
  • Strong interpersonal and organizational skills.
  • Ability to translate guidelines, rules and regulations in clear and usable recommendations
  • Representative, outgoing and client focused.
  • Ability to work in a fast-paced challenging environment of a growing company.
  • In-depth therapeutic and protocol knowledge.
  • Ability to travel for up to 8 days on site per month, depending on the project needs.
  • In-depth therapeutic and protocol knowledge as provided in previous, or company provided training.
  • Attention to detail.
  • Ability to work independently and to effectively prioritize tasks, establish, and maintain strong working relationships with co-workers, managers, investigators, site personnel and clients.
  • Demonstrated ability to manage multiple projects.
  • Administrative excellence.
  • Proficiency with various computer applications such as Word, Excel, and PowerPoint required.
  • Demonstrated ability to develop, organize and manage new skills and tasks and mentor colleagues.
  • Ability to manage multiple projects.

    • Benefits

    Benefits of working at Allucent include :

  • Comprehensive benefits package per location
  • Competitive salaries per location
  • Departmental Study / Training Budget for furthering professional development
  • Flexible Working hours (within reason)
  • Opportunity for remote / hybrid
  • working depending on location
  • Leadership and mentoring opportunities
  • Participation in our Buddy Program as a new or existing employee
  • Internal growth opportunities and career progression
  • Financially rewarding internal employee referral program
  • Access to online soft-skills and technical training via GoodHabitz and internal platforms
  • Eligibility for our Spot Bonus Award Program in recognition of going above and beyond on projects
  • Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employees

    • Disclaimers :

  • Our hybrid work policy encourages a dynamic work environment, prescribing 2 days in office per week for employees within reasonable distance from one of our global offices .

    • The Allucent Talent Acquisition team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively “Allucent”). Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third-party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources.”

    LI-BL1