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Research associate Jobs in Feldkirchen

Zuletzt aktualisiert: vor 23 Stunden
Sr. Clinical Research Associate (Germany)

Sr. Clinical Research Associate (Germany)

AllucentMunich, BY, DE
Vollzeit
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
Clinical Research Associate Senior CRA

Clinical Research Associate Senior CRA

PSI CROMunich, Germany
As a CRA at PSI you will be involved in improving patients lives while enjoying a variety of monitoring tasks and working on clinical studies in different therapeutic indications maintaining the hi...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
  • Gesponsert
Senior Clinical Research Associate mfd

Senior Clinical Research Associate mfd

TFS HealthScienceMunich, Germany
TFS HealthScience is a leading global midsize Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journe...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Research Analyst

Research Analyst

ParticulaMunich, Bavaria, Germany
Homeoffice
Quick Apply
Hi! Wir sind Particula, die führende Rating- und Analyseplattform für digitale Vermögenswerte! Unsere Mission? Den Markt für digitale Assets für institutionelle Investoren zugänglicher, sicherer un...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
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Research Working Student

Research Working Student

Kickbase GmbHMunich, Germany
At Kickbase were on a mission to revolutionize the way fans experience football.Our vision is to push the boundaries in the football industry creating immersive and exciting experiences for fans to...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
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Research Scientist fmx

Research Scientist fmx

ExoMatterMunich, Germany
50,00 € stündlich
We are looking for an exceptional theoretical materials scientist to join ExoMatter as a Research Scientist.In this role you will be researching methods for the calculation of materials properties ...Mehr anzeigenZuletzt aktualisiert: vor 24 Tagen
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Praktikant Economics and Research all genders

Praktikant Economics and Research all genders

Roland BergerMunich, Germany
Unsere Consultants verlassen sich auf kompetente Analysen die aussagekrftige Informationen fr Projekte Ausschreibungen und Studien liefern. Darber hinaus entwickeln wir eigene Studien und erstellen ...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
  • Gesponsert
Clinical Research Specialist (m / w / d)

Clinical Research Specialist (m / w / d)

MED-ELMünchen, DE
MED-EL ist ein führender Hersteller von innovativen medizinischen Geräten zur Behandlung verschiedener Arten von Hörverlust. Als international tätiges Unternehmen mit Hauptsitz in Innsbruck beschäft...Mehr anzeigenZuletzt aktualisiert: vor 23 Stunden
Research Associate for Design of Security Chips 1

Research Associate for Design of Security Chips 1

Fraunhofer-GesellschaftGarching (Munich)
The Fraunhofer Institute for Applied and Integrated Security AISEC with its main site in Munich and offices in Berlin and Weiden supports the digital transformation in key application domains such ...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
  • Gesponsert
Market Research Officer (m / w / d)

Market Research Officer (m / w / d)

Servier Deutschland GmbHMünchen, DE
Wir suchen zum nächstmöglichen Termin in München einen.Market Research Officer (m / w / d).Servier ist ein global agierendes wie auch forschendes Pharmaunternehmen mit Hauptsitz in Frankreich und deuts...Mehr anzeigenZuletzt aktualisiert: vor 4 Tagen
Research Associate (Doctoral Student) (m / f / x) in Entrepreneurship and Family Enterprise

Research Associate (Doctoral Student) (m / f / x) in Entrepreneurship and Family Enterprise

Technical University of MunichMunich, DE
Research Associate (Doctoral Student) (m / f / x) in Entrepreneurship and Family Enterprise.TUM School of Management at TUM Campus Heilbronn invites applications for a Research Associate (m / f / x) at the...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Senior Clinical Research Associate - Germany - Home based

Senior Clinical Research Associate - Germany - Home based

Worldwide Clinical TrialsMunich, Germany
Requisition Number8065Employment Type : Regular.Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutica...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
  • Gesponsert
Sensory Research Manager

Sensory Research Manager

EurofinsMunich, Germany
Supporting and consulting of our clients in all aspects of sensory and consumer research.Preparation of proposals (test design price calculation). Project management and coordination.Supervision of ...Mehr anzeigenZuletzt aktualisiert: vor über 30 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
  • Gesponsert
Klinischer Monitor / Clinical Research Associate (m / w / d) - Münchner Studienzentrum

Klinischer Monitor / Clinical Research Associate (m / w / d) - Münchner Studienzentrum

Klinikum rechts der Isar der Technischen Universität MünchenMünchen, Bayern, Germany
Ihr Universitätsklinikum im Herzen Münchens.Klinikum rechts der Isar (MRI) der Technischen Universität München (TUM).Als Uniklinikum widmen wir uns neben der Krankenversorgung auch der Forschung un...Mehr anzeigenZuletzt aktualisiert: vor 2 Tagen
Clinical Research Associate II, Dermatology & Rheumatology, Germany

Clinical Research Associate II, Dermatology & Rheumatology, Germany

Innovaderm ResearchMunich, BY, DE
Homeoffice
Unbefristet
Clinical Research Associate II, Dermatology & Rheumatology, Germany.The Clinical Research Associate II (CRA II) will monitor the progress of clinical studies at investigative sites or remotely,...Mehr anzeigenZuletzt aktualisiert: vor 10 Tagen
  • Gesponsert
Clinical Research Associate

Clinical Research Associate

PharmiwebMunich, DE
ICON plc is a world-leading healthcare intelligence and clinical research organization.We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join u...Mehr anzeigenZuletzt aktualisiert: vor 11 Tagen
Senior Hardware Research Engineer - CPU (RISCV)

Senior Hardware Research Engineer - CPU (RISCV)

CodasipMunich, BY, DE
Vollzeit
Quick Apply
We believe Codasip is the most innovative processor solutions company.We take pride in designing and developing cutting-edge, high-performance, and energy-efficient RISC-V CPU cores from scratch, a...Mehr anzeigenZuletzt aktualisiert: vor 5 Tagen
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Sr. Clinical Research Associate (Germany)

Sr. Clinical Research Associate (Germany)

AllucentMunich, BY, DE
Vor 30+ Tagen
Anstellungsart
  • Vollzeit
  • 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 Sr. Clinical Research Associate (Sr. CRA) to join our A-team (hybrid

  • remote). As a Sr. CRA at Allucent, you will independently control and monitor investigational 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.

    • Requirements

    To be successful you will possess :

  • At least 5 years clinical monitoring experience.
  • Relevant life science degree / health care / nursing background and / or related degree.
  • Sound knowledge of medical terminology and clinical monitoring process.
  • Ability to travel for up to 8 days on site per month, depending on the project needs.
  • 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.
  • Attention to detail.
  • Ability to manage multiple projects.
  • Ability to work in a fast-paced challenging environment of a growing company.
  • In-depth therapeutic and protocol knowledge.
  • 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.
  • Proficiency with various computer applications such as Word, Excel, and PowerPoint required

    • 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.”

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