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Clinical research associate Jobs in Gie%C3%9Fen

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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
In House Clinical Research Associate - CRA

In House Clinical Research Associate - CRA

AvaniaHesse, DE
Vollzeit
In House Clinical Research Associate - IHCRA .The In-house CRA is an entry level CRA who will be trained on all basics in regards to the execution of a clinical research project.In-house...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
  • Gesponsert
Clinical Research Associate

Clinical Research Associate

TFS HealthScienceBerlin, DE
TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) dedicated to partnering with biotechnology and pharmaceutical companies throughout their entire clinical developm...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Clinical Research Associate II

Clinical Research Associate II

ErgomedAny location, Germany
Performs on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visit activities to ensure that facilities and staff at the investigational site continue to be adequate for the ...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Senior Clinical Research Associate - Germany

Senior Clinical Research Associate - Germany

Rocket PharmaceuticalsDE
Work at ROCKET PHARMA and help cure rare diseases!.Rocket Pharma is a fully integrated, clinical-stage company advancing gene therapies with curative potential for multiple rare childhood diseases....Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
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Clinical Research Coordinator / / Berlin

Clinical Research Coordinator / / Berlin

Hobson PriorBerlin, Berlin, Germany
Hobson Prior is seeking a Clinical Research Coordinator for a part-time contract role in Berlin.This position focuses on supporting oncology research studies and requires immediate attention to key...Mehr anzeigenZuletzt aktualisiert: vor 1 Tag
  • Gesponsert
Senior Clinical Research Associate fmd

Senior Clinical Research Associate fmd

EurofinsHamburg, Hamburg, Germany
We are looking for an experienced Clinical Research Associate (CRA) / Lead CRA for our CRA team at Eurofins bioskin in Hamburg. The senior CRA will manage all aspects of clinical monitoring to ensure...Mehr anzeigenZuletzt aktualisiert: vor 5 Tagen
Clinical Research Associate / Senior CRA

Clinical Research Associate / Senior CRA

PSI CROMunich, Bavaria, Germany
Homeoffice
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 ...Mehr anzeigenZuletzt aktualisiert: vor 18 Tagen
Senior Clinical Research Associate - Germany - Home based

Senior Clinical Research Associate - Germany - Home based

Worldwide Clinical TrialsHamburg, 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
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(All levels) Clinical Research Associate / CRA (m / f / d)

(All levels) Clinical Research Associate / CRA (m / f / d)

MeetCologne Bonn Region, Germany
Are you 120% sure you are having your dream job ?.By simply clicking "apply" or contacting me, you wil enjoy the following benefits : . Customized consultative assistance in Job search.Assistance thro...Mehr anzeigenZuletzt aktualisiert: vor 11 Tagen
Clinical Research Nurse

Clinical Research Nurse

ParexelBerlin, Germany
When our values align, there's no limit to what we can achieve.Lust auf einen Job, der wirklich was bewirkt?.Wie? Indem wir brandneue Medikamente testen - und dafür brauchen wir dich! .Anspruchsvol...Mehr anzeigenZuletzt aktualisiert: vor 25 Tagen
Clinical Research Associate (CRA) (m / w / d)

Clinical Research Associate (CRA) (m / w / d)

Universitätsklinikum Schleswig-HolsteinLübeck, Schleswig-Holstein, DE
Das Zentrum für klinische Studien (ZKS) Lübeck bietet umfassende Beratung und Unterstützung bei der Planung, Durchführung und Auswertung klinischer Forschungsprojekte. Damit tragen wir zur Verbesser...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Research Associate

Research Associate

Deutsches Krebsforschungszentrum (DKFZ)Heidelberg
Research for a life without cancer“ is our mission at the German Cancer Research Center.We investigate how cancer develops, identify cancer risk factors and look for new cancer prevention str...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Clinical Research Associate (m / w / d) - Talent Pipeline

Clinical Research Associate (m / w / d) - Talent Pipeline

Novo NordiskMainz, Rheinland-Pfalz, Germany
Leben ist Veränderung – Leben verbessern ist unsere Motivation.Mitarbeiter : innen setzen wir als globales Life Science Unternehmen alles daran, schwere chronische Krankheiten zu besiegen.Mit unseren...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
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Experienced Clinical Research Associate

Experienced Clinical Research Associate

MedpaceCologne , DE
Medpace is a full-service clinical contract research organization (CRO).We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries.Our mi...Mehr anzeigenZuletzt aktualisiert: vor 1 Tag
  • Gesponsert
Experienced Clinical Research Associate

Experienced Clinical Research Associate

PharmiwebCologne, DE
Our clinical activities are growing rapidly, and we are currently seeking an.Experienced Clinical Research Associate.Clinical Operations team in Munich. This position will work on a team to accompli...Mehr anzeigenZuletzt aktualisiert: vor 3 Tagen
  • Gesponsert
Senior Clinical Research Associate

Senior Clinical Research Associate

Advanced Resource ManagersDüsseldorf, DE
Our client, a leading player in the clinical research market, is currently seeking SCRAs to support long term sponsors across Germany. As a Senior Clinical Research Associate, you will have the oppo...Mehr anzeigenZuletzt aktualisiert: vor 11 Tagen
Clinical Research Associate

Clinical Research Associate

Edwards LifesciencesGermany,
Vollzeit
Mainly responsible for the northern or western part of Germany.Responsible for remotely supporting field clinical research associate / site activities to ensure the overall integrity of study implem...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Clinical Research Associate (m / w / d), Single Sponsor

Clinical Research Associate (m / w / d), Single Sponsor

IQVIAFrankfurt, Hesse, Germany
Vollzeit
Clinical Research Associate / CRA (m / w / d) home-based throughout Germany.Whether you're just starting out or looking to deepen your expertise, this role promises to offer intentional career growth a...Mehr anzeigenZuletzt aktualisiert: vor über 30 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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