Aktuelle Jobs im Zusammenhang mit Cra Ii - Berlin - KCR

  • Cra Ii

    vor 3 Monaten


    Berlin, Deutschland Warman O'Brien Vollzeit

    A global CRO is looking to hire experienced CRAs (CRA II or Senior CRAs) to join them on a permanent basis in Germany. These roles will be sponsor dedicated, you will work exclusively on one sponsors trials and SOPs; you will work for a client that values their staff and puts an emphasis on career development. Working across therapeutic areas, the CRA will...


  • Berlin, Berlin, Deutschland Meet Vollzeit

    Clinical Research Associate/CRA II Job Description **Job Summary:** We are seeking a highly skilled Clinical Research Associate/CRA II to join our team. As a CRA II, you will be responsible for performing clinical study site management/monitoring activities in compliance with ICH-GCP and Sponsor SOPs. **Key Responsibilities:** * Perform clinical study...


  • Berlin, Berlin, Deutschland Meet Vollzeit

    Clinical Research Associate/CRA II Job Description **Job Summary:** We are seeking a highly skilled Clinical Research Associate/CRA II to join our team. As a CRA II, you will be responsible for performing clinical study site management/monitoring activities in compliance with ICH-GCP and Sponsor SOPs. **Key Responsibilities:** * Perform clinical study...


  • Berlin, Berlin, Deutschland Meet Vollzeit

    Clinical Research Associate/CRA II Job Description **Job Summary:** We are seeking a highly skilled Clinical Research Associate/CRA II to join our team in a homebased role. As a CRA II, you will be responsible for performing clinical study site management/monitoring activities in compliance with ICH-GCP and Sponsor SOPs. **Key Responsibilities:** *...


  • Berlin, Berlin, Deutschland Meet Vollzeit

    Clinical Research Associate/CRA II Job Description **Job Summary:** We are seeking a highly skilled Clinical Research Associate/CRA II to join our team in a homebased role. As a CRA II, you will be responsible for performing clinical study site management/monitoring activities in compliance with ICH-GCP and Sponsor SOPs. **Key Responsibilities:** *...


  • Berlin, Berlin, Deutschland Meet Vollzeit

    About the RoleWe are seeking a highly skilled Clinical Research Associate/CRA II to join our team in a homebased opportunity with one of our well-regarded CRO clients.Key ResponsibilitiesPerform clinical study site management/monitoring activities in compliance with ICH-GCP and Sponsor SOPs.Develop a strong understanding of regulatory documentation for study...


  • Berlin, Berlin, Deutschland Meet Vollzeit

    About the RoleWe are seeking a highly skilled Clinical Research Associate/CRA II to join our team in a homebased opportunity with one of our well-regarded CRO clients.Key ResponsibilitiesPerform clinical study site management/monitoring activities in compliance with ICH-GCP and Sponsor SOPs.Develop a strong understanding of regulatory documentation for study...


  • Berlin, Berlin, Deutschland Meet Vollzeit

    Job Summary:Meet is seeking a highly skilled Clinical Research Associate/CRA II to join our team in a homebased opportunity. As a CRA II, you will be responsible for performing clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs.Key Responsibilities:Perform site initiation, monitoring, and close-out visits in...


  • Berlin, Berlin, Deutschland Meet Vollzeit

    Job Summary:Meet is seeking a highly skilled Clinical Research Associate/CRA II to join our team in a homebased opportunity. As a CRA, you will be responsible for performing clinical study site management/monitoring activities in compliance with ICH-GCP and Sponsor SOPs.Key Responsibilities:Perform site initiation, monitoring, and close-out activities in...


  • Berlin, Berlin, Deutschland Meet Vollzeit

    Job Summary:Meet is seeking a highly skilled Clinical Research Associate/CRA II to join our team in a homebased opportunity. As a CRA II, you will be responsible for performing clinical study site management/monitoring activities in compliance with ICH-GCP and Sponsor SOPs.Key Responsibilities:Perform site initiation, monitoring, and close-out visits in...


  • Berlin, Berlin, Deutschland Parexel Vollzeit

    {"title": "Clinical Site Monitor/CRA II", "description": "Join Our Team of VisionariesParexel FSP is a global leader in clinical research and development, and we're seeking a highly skilled Clinical Site Monitor/CRA II to join our team.As a Clinical Site Monitor/CRA II, you will be responsible for ensuring the integrity and quality of clinical trial data,...


  • Berlin, Berlin, Deutschland Parexel Vollzeit

    {"title": "Clinical Site Monitor/CRA II", "description": "Join Our Team of VisionariesParexel FSP is a global leader in clinical research and development, and we're seeking a highly skilled Clinical Site Monitor/CRA II to join our team.As a Clinical Site Monitor/CRA II, you will be responsible for ensuring the integrity and quality of clinical trial data,...

  • CRA II

    vor 2 Monaten


    Berlin, Deutschland Proclinical Staffing Vollzeit

    Proclinical is seeking multiple CRAs to join a reputable Clinical Research Organisation in Germany. The successful candidate will work as part of a vast team and a fast-paced environment alongside a dedicated team to select, initiate and close-out investigational sites for clinical studies in phases I - IV, ensuring adherence to applicable regulations and...


  • Berlin, Deutschland Sitero LLC Vollzeit

    Sitero is an emerging leader in Clinical services and software solutions for the life sciences industry. We have experience and expertise in a diverse range of therapeutic areas and focus on innovative, technology-enabled solutions that allow our clients to focus on their core strengths. For early phase studies through Phase III clinical trials, our...


  • Berlin, Berlin, Deutschland Parexel Vollzeit

    {"title": "Clinical Site Monitor/CRA II", "description": "Transforming Patients' Lives through InnovationParexel FSP is seeking a dedicated Clinical Site Monitor (CRA) I or II to join our team.As a single sponsor dedicated to a worldwide biopharmaceutical company, we're committed to pushing the boundaries of medical innovation. Our daily efforts contribute...


  • Berlin, Berlin, Deutschland Parexel Vollzeit

    {"title": "Clinical Site Monitor/CRA II", "description": "Transforming Patients' Lives through InnovationParexel FSP is seeking a dedicated Clinical Site Monitor (CRA) I or II to join our team.As a single sponsor dedicated to a worldwide biopharmaceutical company, we're committed to pushing the boundaries of medical innovation. Our daily efforts contribute...


  • Berlin, Berlin, Deutschland Parexel Vollzeit

    About the Role:Parexel FSP is seeking a highly skilled Clinical Site Monitor (CRA) I or II to join our team. As a Clinical Site Monitor, you will play a critical role in ensuring the integrity and quality of clinical data, while ensuring compliance with ICH GCP and local regulations.Key Responsibilities:Conduct site monitoring activities in accordance with...


  • Berlin, Berlin, Deutschland Parexel Vollzeit

    About the Role:Parexel FSP is seeking a highly skilled Clinical Site Monitor (CRA) I or II to join our team. As a Clinical Site Monitor, you will play a critical role in ensuring the integrity and quality of clinical data, while ensuring compliance with ICH GCP and local regulations.Key Responsibilities:Conduct site monitoring activities in accordance with...


  • Berlin, Deutschland Pharmiweb Vollzeit

    CRA II - Germany, Berlin 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 us on our mission to shape the future of clinical development. We are hiring for all levels of CRA in Germany  ICON plc is a...


  • Berlin, Deutschland Parexel Vollzeit

    When our values align, there's no limit to what we can achieve.   Parexel FSP is hiring for a home-based Clinical Site Monitor ( CRA) I or II. Single sponsor dedicated to a worldwide biopharmaceutical company that relentlessly seeks breakthroughs to improve patients’ lives. Their daily innovation contributes to a healthier global community....

Cra Ii

vor 4 Monaten


Berlin, Deutschland KCR Vollzeit

**Clinical Research Associate II/Senior Clinical Research Associate** - **_Oncology Preferred_**

**Location: home-based, up to 7 DOS**

Our Clinical Monitoring team is growing in Germany and we are looking for a CRO experienced Clinical Research Associate to be involved in challenging projects across the country and to shape the future of pharmaceutical therapies.

**Your responsibilities will include**:

- Performing site visits and monitoring activities in accordance with protocol, GCP/ICH Guidelines and other applicable requirements,
- Ensuring overall integrity of study and adherence to guidelines, protocol and regulations,
- Taking an active role in the project team by providing feedback and suggestions for successful completion of the project,
- Leading, coaching and mentoring CRAs team to assist in their development and training,
- Responsible for execution of KPI's for assigned staff and for all site deliverables within required time and budget,
- Providing leadership for the development and implementation of new training programs and improvement of current programs for assigned staff.

**Requirements**:

- University degree in life sciences/pharmacy/biotechnology
- At least 2 years of independent monitoring experience (including pre-study, initiation, routine monitoring and close-out visits) according to protocol monitoring guidelines, SOPs, GCP/ICH Guidelines.
- Oncology study monitoring experience will be an asset
- Computer literate, and adaptable to new technologies
- Fluent English, written and spoken.
- Ability to complete tasks in an accurate and timely manner.
- Flexibility to travel c7 visits per month

At **KCR** we put our mission**:WE SEE HUMAN BEHIND EVERY NUMBER** into our actions, therefore we offer our Employees benefits that comply with national regulations and provide the coverage that best meets employee needs.

Joining KCR, you will be able to benefit from:

- Onboarding process and induction training to develop deep sector knowledge and complex skills.
- Latest technology and the most advanced equipment and working tools.
- An open culture based on slim processes, in an agile structure with a flat hierarchy and direct access to the Management to share ideas and implement change and continuous improvement.
- Mentoring and training programs related to clinical trials, therapeutic areas, hard and soft skills
- An extra day off for your birthday

KCR is a clinical development solutions provider creating value for biotechnology and pharmaceutical organizations. Founded in 1997, our expert teams support clients with full-service clinical development capabilities across three main areas: Trial Execution, Consulting and Placement. KCR operates across North America, Europe, and Australia, with main office locations in Boston US, Berlin Germany, and Warsaw Poland. Our geographical coverage across 25+ countries, cutting-edge technical capabilities and tailored offerings allow for the optimized delivery of solutions to develop life-changing therapies. KCR offers access to an estimated population of 1.1 billion people.

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KCR is an equal opportunity employer providing its staff with excellent opportunities to build dynamic, long-term careers.