20 Jobs für Clinical Coding Manager
Stellenangebote Clinical Coding Manager Jobs
Neu Job vor 4 Std. bei Jobleads gefunden
• Köln, Nordrhein- Westfalen Koeln
Führungs-/ Leitungspositionen
[. .. ] established itself as a trusted leader in medical software and data analytics, impacting millions of lives globally. As they continue to develop innovative platforms that enhance patient [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] care and streamline clinical workflows, they are now seeking an experienced Head of Development C #. NET to lead their software teams in building transformative healthcare solutions. This role is based in Dresden, one of Germanys most vibrant tech hubs. Responsibilities as Head of Development: Lead, mentor, and develop a high-performing software team [. .. ] ensuring top standards in security, reliability, and scalability. Oversee the entire software development lifecycle from concept and architecture through to deployment and continuous optimisation. Promote and enforce best practices in coding, testing, and documentation, with adherence to healthcare regulations and standards. Drive the adoption of new technologies and methodologies, using the latest in C #. NET and cloud-based architectures to improve development efficiency and patient impact. Requirements for the Head of Development position: A Bachelors degree in Computer Science, Software [. .. ] Germany 2 weeks ago Bonn, North Rhine-Westphalia, Germany 1 week ago Bonn, North Rhine-Westphalia, Germany 4 days ago Bonn, North Rhine-Westphalia, Germany 3 weeks ago Senior Project Manager (f/m/d) Main Ground Combat System (MGCS) Cologne, North Rhine-Westphalia, Germany 2 weeks ago Lead Developer Software Architect (m/w/d) Cologne, North Rhine-Westphalia, Germany 2 months ago Cologne, North Rhine-Westphalia, Germany 2 weeks ago Cologne, North Rhine-Westphalia, Germany 5 days ago Working Student Leadership [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Junior Full Stack Engineer
• Berlin
Absolventen, Einsteiger, Trainees
[. .. ] in : AI agents multistep reasoning systems LLM application architectures Toolcalling, retrieval, orchestration, and evaluation Modern AI toolchains and best practices You will work closely with engineering, [...]
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[...] data, product, and clinical teams to build our AI features endtoend and help shape the future of our platform. This is a role with massive influence were early enough that your architectural choices, code, and AI expertise will have a lasting impact. Our stack (You dont need all of this, but strong React/ Type [. .. ] Open AI function calling Agent frameworks (custom, or e. g. Lang Graphstyle) Evaluation suites, guardrails, prompt tooling Monitoring + model observability What Youll do AI Architecture Agentic Systems Design and implement coding agents, taskspecific AI agents, and multistep workflows that power userfacing features. Build and refine retrieval pipelines, embeddings flows, and hybrid RAG/ logic systems. Architect robust prompting, functioncalling, and tool orchestration systems. Full Stack Product Development Own features across backend services, and mobile/ web. Translate product and clinical requirements into AIpowered [. .. ] Autonomy, ownership, and a chance to shape foundational AI systems from the ground up. Interview Process CV Check Get to know Kyan, Girish (30 minutes Call) Get to know your manager, Nacho (45 minutes Call) Team Interview (s) , Hans Victoria (30 minutes each call) Onsite Live Coding Exercise (Nacho/ Hans/ Victoria, 120 minutes) Offer Stage: Meet the founder (s) (30 minutes) / Reference check/ Offer Please note we only accept applications submitted through our official Careers Page. Applications submitted via [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
[. .. ] how they choose in a way that is uniquely more connected, more convenient and more compassionate. And we do it all with heart, each and every day. [...]
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[...] Position Summary The Clinical Operations Advisor is a clientfacing role that collaborates with Health Plan Clinical Advisor to understand the clients clinical strategy and roadmap to create a clinical operations plan. The Clinical Operations Advisor works with the Benefit Relationship Manager and client to facilitate gathering formulary and utilization management requirements and designs the druglevel setup for projects on the operations plan while ensuring compliance to internal best practice and federal and state guidelines. The Clinical Operations Advisor designs the clinical setups using Caremark technology solutions and supports the coding teams in the loading of clinical data into the adjudication system. The Clinical Operations Advisor partners with account team members to document clinical design best practices, provide input to streamline processes, and identify opportunities to improve the efficiency and accuracy of clinical setups. The Clinical Operations Advisor supports internal and [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Clinical Scientist-Manager/ Senior Manager (m/f/d)
Clinical Scientist-
Manager/ Senior Manager (m/f/d) Direct message the job poster from Tubulis Gmb H Be part of our team As a Clinical Scientist (m/f/d) and member of our Clinical Development [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] team, you will support the planning and execution of full life-cycle development of our antibody-drug conjugates (ADCs) [. .. ] of responses to regulatory interactions. Play a key role in the review of study data to ensure timely and highquality data entry, including review of case report forms, assist in coding, analysis, and proper and complete documentation of clinical data. Participate in investigator meetings, investigator engagement, including assisting in the preparation of Advisory Board meetings. Support the Medical Director in managing sites to ensure study treatment discontinuation or other safety decisions are made per protocol and align with stakeholders within the [. .. ]
Job am 21.11.2025 bei Jobleads gefunden
• Köln, Nordrhein- Westfalen
Be part of our team As a
Clinical Scientist (m/f/d) and member of our Clinical Development team, you will support the planning and execution of full life-cycle development of our [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] antibodydrug conjugates (ADCs) global clinical trials. You will support the review, analysis, and interpretation of clinical trial data, contribute to the development of critical clinical [. .. ] of responses to regulatory interactions. Play a key role in the review of study data to ensure timely and highquality data entry, including review of case report forms, assists in coding, analysis, and proper and complete documentation of clinical data. Participate in investigator meetings, investigator engagement, including assisting in the preparation of Advisory Board meetings. Support the Medical Director in managing sites to ensure study treatment discontinuation or other safety decisions are made per protocol and align with stakeholders within the [. .. ]
Job am 21.11.2025 bei Jobleads gefunden
Clinical Scientist-Manager/ Senior Manager (m/f/d)
• Düsseldorf, Nordrhein- Westfalen
Be part of our team As a
Clinical Scientist (m/f/d) and member of our Clinical Development team, you will support the planning and execution of full life-cycle development of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] our antibodydrug conjugates (ADCs) global clinical trials. You will support the review, analysis, and interpretation of clinical trial data, contribute to the development of critical clinical [. .. ] of responses to regulatory interactions. Play a key role in the review of study data to ensure timely and highquality data entry, including review of case report forms, assists in coding, analysis, and proper and complete documentation of clinical data. Participate in investigator meetings, investigator engagement, including assisting in the preparation of Advisory Board meetings. Support the Medical Director in managing sites to ensure study treatment discontinuation or other safety decisions are made per protocol and align with stakeholders within the [. .. ]
Job am 09.11.2025 bei Jobleads gefunden
• München, Bayern
[. .. ] design and set-up Creation of Data Management Plan and Data Validation Plan User acceptance testing (including creating testing scenarios) e CRF completion guideline Data cleaning, SAE reconciliation, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] query management Medical coding (e. g. , Med DRA, WHO-DD) Programming of plausibility checks User Access Management Creation of SDTMs, define. xml and c SDRG is an advantage Your profile University degree in data science, statistics, computer science, or comparable studies At least two years of professional experience as a data manager with responsibility for clinical studies Ability to understand and follow SOPs, working instructions and relevant guidelines Knowledge of CDISC standards (CDASH, SDTM, define. xml, c SDRG) Knowledge of relevant terminology in clinical and non-clinical research Knowledge of relevant guidelines GCP, ICH Quick comprehension and analytical thinking Team player with high degree of initiative Good [. .. ]
Job am 19.10.2025 bei Jobleads gefunden
Clinical Scientist-Manager/ Senior Manager (m/f/d)
• Dortmund, Nordrhein- Westfalen
Be part of our team As a
Clinical Scientist (m/f/d) and member of our Clinical Development team, you will support the planning and execution of full life-cycle development of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] our antibody-drug conjugates (ADCs) global clinical trials. You will support the review, analysis, and interpretation of clinical trial data, contribute to the development of critical [. .. ] responses to regulatory interactions. Play a key role in the review of study data to ensure timely and high-quality data entry, including review of case report forms, assists in coding, analysis, and proper and complete documentation of clinical data. Participate in investigator meetings, investigator engagement, including assisting in the preparation of Advisory Board meetings. Support the Medical Director in managing sites to ensure study treatment discontinuation or other safety decisions are made per protocol and align with stakeholders within the [. .. ]
Job am 05.10.2025 bei Jobleads gefunden
Clinical Scientist-Manager/ Senior Manager (m/f/d)
• Essen, Nordrhein- Westfalen
Overview Be part of our team As a
Clinical Scientist (m/f/d) and member of our Clinical Development team, you will support the planning and execution of full life-cycle development [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of our antibody-drug conjugates (ADCs) global clinical trials. You will support the review, analysis, and interpretation of clinical trial data, contribute to the development of critical [. .. ] responses to regulatory interactions. Play a key role in the review of study data to ensure timely and high-quality data entry, including review of case report forms, assists in coding, analysis, and proper and complete documentation of clinical data. Participate in investigator meetings, investigator engagement, including assisting in the preparation of Advisory Board meetings. Support the Medical Director in managing sites to ensure study treatment discontinuation or other safety decisions are made per protocol and align with stakeholders within the [. .. ]
Job am 22.09.2025 bei Jobleads gefunden
Clinical Scientist-Manager/ Senior Manager (m/f/d)
• Planegg, München, Bayern
Clinical Scientist-
Manager/ Senior Manager (m/f/d) Permanent employee, Full-time Planegg (Germany) , Remote (Germany) Be part of our team As a Clinical Scientist (m/f/d) and member of our Clinical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Development team, you will support the planning and execution of full life-cycle development of our antibody-drug conjugates [. .. ] responses to regulatory interactions. Play a key role in the review of study data to ensure timely and high-quality data entry, including review of case report forms, assists in coding, analysis, and proper and complete documentation of clinical data. Participate in investigator meetings, investigator engagement, including assisting in the preparation of Advisory Board meetings. Support the Medical Director in managing sites to ensure study treatment discontinuation or other safety decisions are made per protocol and align with stakeholders within the [. .. ]
Job am 11.11.2025 bei Neuvoo.com gefunden
Tubulis GmbH
Clinical Scientist-Manager/ Senior Manager (m/f/d)
• Essen
Be part of our team As a
Clinical Scientist (m/f/d) and member of our Clinical Development team, you will support the planning and execution of full life-cycle development of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] our antibody-drug conjugates (ADCs) global clinical trials. You will support the review, analysis, and interpretation of clinical trial data, contribute to the development of critical [. .. ] responses to regulatory interactions. Play a key role in the review of study data to ensure timely and high-quality data entry, including review of case report forms, assists in coding, analysis, and proper and complete documentation of clinical data. Participate in investigator meetings, investigator engagement, including assisting in the preparation of Advisory Board meetings. Support the Medical Director in managing sites to ensure study treatment discontinuation or other safety decisions are made per protocol and align with stakeholders within the [. .. ]
Job am 11.11.2025 bei Neuvoo.com gefunden
Tubulis GmbH
Clinical Scientist-Manager/ Senior Manager (m/f/d)
• Cologne
Be part of our team As a
Clinical Scientist (m/f/d) and member of our Clinical Development team, you will support the planning and execution of full life-cycle development of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] our antibody-drug conjugates (ADCs) global clinical trials. You will support the review, analysis, and interpretation of clinical trial data, contribute to the development of critical [. .. ] responses to regulatory interactions. Play a key role in the review of study data to ensure timely and high-quality data entry, including review of case report forms, assists in coding, analysis, and proper and complete documentation of clinical data. Participate in investigator meetings, investigator engagement, including assisting in the preparation of Advisory Board meetings. Support the Medical Director in managing sites to ensure study treatment discontinuation or other safety decisions are made per protocol and align with stakeholders within the [. .. ]
Job am 11.11.2025 bei Neuvoo.com gefunden
Tubulis GmbH
Clinical Scientist-Manager/ Senior Manager (m/f/d)
Be part of our team As a
Clinical Scientist (m/f/d) and member of our Clinical Development team, you will support the planning and execution of full life-cycle development of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] our antibody-drug conjugates (ADCs) global clinical trials. You will support the review, analysis, and interpretation of clinical trial data, contribute to the development of critical [. .. ] responses to regulatory interactions. Play a key role in the review of study data to ensure timely and high-quality data entry, including review of case report forms, assists in coding, analysis, and proper and complete documentation of clinical data. Participate in investigator meetings, investigator engagement, including assisting in the preparation of Advisory Board meetings. Support the Medical Director in managing sites to ensure study treatment discontinuation or other safety decisions are made per protocol and align with stakeholders within the [. .. ]
Job am 11.11.2025 bei Neuvoo.com gefunden
Tubulis GmbH
Clinical Scientist-Manager/ Senior Manager (m/f/d)
• Stuttgart
Be part of our team As a
Clinical Scientist (m/f/d) and member of our Clinical Development team, you will support the planning and execution of full life-cycle development of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] our antibody-drug conjugates (ADCs) global clinical trials. You will support the review, analysis, and interpretation of clinical trial data, contribute to the development of critical [. .. ] responses to regulatory interactions. Play a key role in the review of study data to ensure timely and high-quality data entry, including review of case report forms, assists in coding, analysis, and proper and complete documentation of clinical data. Participate in investigator meetings, investigator engagement, including assisting in the preparation of Advisory Board meetings. Support the Medical Director in managing sites to ensure study treatment discontinuation or other safety decisions are made per protocol and align with stakeholders within the [. .. ]
Job am 14.10.2025 bei Neuvoo.com gefunden
Tubulis GmbH
Clinical Scientist-Manager/ Senior Manager (m/f/d)
• Düsseldorf
Be part of our team As a
Clinical Scientist (m/f/d) and member of our Clinical Development team, you will support the planning and execution of full life-cycle development of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] our antibody-drug conjugates (ADCs) global clinical trials. You will support the review, analysis, and interpretation of clinical trial data, contribute to the development of critical [. .. ] responses to regulatory interactions. Play a key role in the review of study data to ensure timely and high-quality data entry, including review of case report forms, assists in coding, analysis, and proper and complete documentation of clinical data. Participate in investigator meetings, investigator engagement, including assisting in the preparation of Advisory Board meetings. Support the Medical Director in managing sites to ensure study treatment discontinuation or other safety decisions are made per protocol and align with stakeholders within the [. .. ]
Job am 14.10.2025 bei Neuvoo.com gefunden
Tubulis GmbH
Clinical Scientist-Manager/ Senior Manager (m/f/d)
• Berlin
Be part of our team As a
Clinical Scientist (m/f/d) and member of our Clinical Development team, you will support the planning and execution of full life-cycle development of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] our antibody-drug conjugates (ADCs) global clinical trials. You will support the review, analysis, and interpretation of clinical trial data, contribute to the development of critical [. .. ] responses to regulatory interactions. Play a key role in the review of study data to ensure timely and high-quality data entry, including review of case report forms, assists in coding, analysis, and proper and complete documentation of clinical data. Participate in investigator meetings, investigator engagement, including assisting in the preparation of Advisory Board meetings. Support the Medical Director in managing sites to ensure study treatment discontinuation or other safety decisions are made per protocol and align with stakeholders within the [. .. ]
Job am 14.10.2025 bei Neuvoo.com gefunden
Tubulis GmbH
Clinical Scientist-Manager/ Senior Manager (m/f/d)
• Frankfurt
Be part of our team As a
Clinical Scientist (m/f/d) and member of our Clinical Development team, you will support the planning and execution of full life-cycle development of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] our antibody-drug conjugates (ADCs) global clinical trials. You will support the review, analysis, and interpretation of clinical trial data, contribute to the development of critical [. .. ] responses to regulatory interactions. Play a key role in the review of study data to ensure timely and high-quality data entry, including review of case report forms, assists in coding, analysis, and proper and complete documentation of clinical data. Participate in investigator meetings, investigator engagement, including assisting in the preparation of Advisory Board meetings. Support the Medical Director in managing sites to ensure study treatment discontinuation or other safety decisions are made per protocol and align with stakeholders within the [. .. ]
Job am 14.10.2025 bei Neuvoo.com gefunden
Tubulis GmbH
Clinical Scientist-Manager/ Senior Manager (m/f/d)
• Hamburg
Be part of our team As a
Clinical Scientist (m/f/d) and member of our Clinical Development team, you will support the planning and execution of full life-cycle development of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] our antibody-drug conjugates (ADCs) global clinical trials. You will support the review, analysis, and interpretation of clinical trial data, contribute to the development of critical [. .. ] responses to regulatory interactions. Play a key role in the review of study data to ensure timely and high-quality data entry, including review of case report forms, assists in coding, analysis, and proper and complete documentation of clinical data. Participate in investigator meetings, investigator engagement, including assisting in the preparation of Advisory Board meetings. Support the Medical Director in managing sites to ensure study treatment discontinuation or other safety decisions are made per protocol and align with stakeholders within the [. .. ]
Job am 14.10.2025 bei Neuvoo.com gefunden
Tubulis GmbH
Clinical Scientist-Manager/ Senior Manager (m/f/d)
• Dortmund
Be part of our team As a
Clinical Scientist (m/f/d) and member of our Clinical Development team, you will support the planning and execution of full life-cycle development of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] our antibody-drug conjugates (ADCs) global clinical trials. You will support the review, analysis, and interpretation of clinical trial data, contribute to the development of critical [. .. ] responses to regulatory interactions. Play a key role in the review of study data to ensure timely and high-quality data entry, including review of case report forms, assists in coding, analysis, and proper and complete documentation of clinical data. Participate in investigator meetings, investigator engagement, including assisting in the preparation of Advisory Board meetings. Support the Medical Director in managing sites to ensure study treatment discontinuation or other safety decisions are made per protocol and align with stakeholders within the [. .. ]
Job am 06.10.2025 bei Neuvoo.com gefunden
Tubulis GmbH
Clinical Scientist-Manager/ Senior Manager (m/f/d)
• Leipzig
Be part of our team As a
Clinical Scientist (m/f/d) and member of our Clinical Development team, you will support the planning and execution of full life-cycle development of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] our antibody-drug conjugates (ADCs) global clinical trials. You will support the review, analysis, and interpretation of clinical trial data, contribute to the development of critical [. .. ] responses to regulatory interactions. Play a key role in the review of study data to ensure timely and high-quality data entry, including review of case report forms, assists in coding, analysis, and proper and complete documentation of clinical data. Participate in investigator meetings, investigator engagement, including assisting in the preparation of Advisory Board meetings. Support the Medical Director in managing sites to ensure study treatment discontinuation or other safety decisions are made per protocol and align with stakeholders within the [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Clinical coding manager pro Jahr?
Als Clinical coding manager verdient man zwischen EUR 60.000,- bis EUR 90.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Coding Manager Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 20 offene Stellenanzeigen für Clinical Coding Manager Jobs.
In welchen Bundesländern werden die meisten Clinical Coding Manager Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Coding Manager Jobs werden derzeit in Nordrhein-Westfalen (8 Jobs), Bayern (2 Jobs) und Niedersachsen (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Coding Manager Jobs?
Clinical Coding Manager Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
