26 Jobs für Clinical Coding Manager
Stellenangebote Clinical Coding Manager Jobs
Neu Job vor 4 Std. bei Jobleads gefunden
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Senior
Clinical Data Team Lead (Senior DTL) - FSP Be among the first 25 applicants. The Sr. CDM will lead and contribute to data management activities in support of Clients [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] studies across all stages of clinical drug development. Summary of Key Responsibilities Contribute to data management activities as a lead study data manager in support of Clients clinical studies. Lead database build activities including leading crossfunctional review of e CRF content, review of edit check specifications, and perform user acceptance testing. Monitor data collection, coding, and cleaning by vendors through tracking of study metrics and targeted data reviews. Oversight of database lock activities and ultimate archiving of study data. Collaborate with internal and external partners, including Biostatistics, Statistical Programming, Clinical Operations, Medical, Quality Assurance, Global Patient Safety and Risk Management, Regulatory Affairs, CROs, central and [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Business Analytics Consultant, Senior Manager
Beratungs-/ Consultingtätigkeiten
[. .. ] 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. Position [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Summary The Senior Manager Analytic Consultant is an experienced customerfacing analyst who supports the Account Teams ability to craft a compelling story and become trusted advisors by way of turning a customers data into meaningful and actionable information. This role is responsible for medical claims and economics reporting and analytics for a book of [. .. ] directly with customer in a strategic advisory role. Work closely with Plan Sponsor reporting routine reporting partners to advise on the most recent trends and necessary updates. Work closely with Clinical Program Consultants to provide fluid, combined financial and clinical, reporting, and trusted advising. Required Qualifications Business/ Industry Knowledge: Minimum of 5-8 years of industry experience interpreting/ analyzing all aspects of a customers experience (financial results, medical management results, population health, effectiveness of incentive/ wellness strategies, etc. ) . Experience [. .. ] business results, issues, and strategies in a clear, concise, and confident manner to all levels and positions of an organization (internal and external) . Must have strong knowledge of claim coding (CPT/ DRG, etc. ) , provider networks, benefit designs, healthcare products/ funding, medical management programs and financial acumen. Education Bachelors degree/ specialized training/ relevant professional qualification Pay Range The typical pay range for this role is: 67, 900.00-199, 144.00 This pay range represents the base hourly rate [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
• Frankfurt, Hesse
Manager Clinical Safety (1-year maternity leave cover) Join to apply for the Manager Clinical Safety (1-year maternity leave cover) role at Bio NTech SE Mainz, Germany; London, United Kingdom; Munich, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Germany full time Job ID: 10511 About The Role As a Clinical Safety Manager, you will play a key role in [. .. ] as the primary safety contact for assigned trials, ensuring timely execution of safety deliverables and oversight of IMP-related activities. Supervise end-to-end ICSR processes, including case triage, Med DRA coding, causality assessments, and vendor oversight. Coordinate SUSAR reporting to regulatory authorities and Ethics Committees, ensuring compliance with global timelines. Support Safety Physicians in medical review, safety data interpretation, and trial-specific documentation. Develop and review safety documents (e. g. , Safety Management Plans, DSURs) and contribute to process improvements. Ensure [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Clinical Scientist-Manager/ Senior Manager (m/f/d)
• München, Bayern
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 lifecycle 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 trial [. .. ] 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 vor 10 Tagen bei Jobleads gefunden
• Köln, Nordrhein- Westfalen
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 [. .. ]
Job am 30.11.2025 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
• 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 21.11.2025 bei Jobleads gefunden
Clinical Scientist-Manager/ Senior Manager (m/f/d)
• 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 [...]
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 23.10.2025 bei Jobleads gefunden
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 22.10.2025 bei Jobleads gefunden
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 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 [. .. ]
Neu Job vor 4 Std. bei Neuvoo gefunden
NVision Imaging Technologies
• Ulm, Baden- Württemberg
[. .. ] Development: You assemble and modify test setups involving pneumatic and fluidic components (e. g. valves, tubing, fittings) . You execute experiments in the lab and support troubleshooting [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] across disciplines. Automation Coding: You write scripts (e. g. in Python) to automate processes and support prototype operation. System Testing : You define and execute parameter tuning, calibrations, and exploratory testing to optimize system performance. Data Documentation Analysis : Document test plans and results, analyze findings, and contribute to design decisions and process improvements. [. .. ] Wellpass Relocation support contact information Join us in making a difference Submit your application to be considered for this exciting opportunity. Any questions? Please contact: Emilija Stojanovska Sr. Talent Acquisition Manager mail: About us NVision is a quantum biotech startup based in Ulm, Germany, with Tier 1 investors from the USA and Europe. We are just leaving stealth mode, moving from local R D to global commercialization and expansion. We are developing a technology that will enable MRI-based imaging of [. .. ] York, MD Anderson in Texas, Technical University of Munich, Cambridge University in the UK and more. NVision is developing fast, robust and easy-to-use hyperpolarization technology for preclinical and clinical research in our POLARIS product line. Those devices are placed close to an MRI scanner in a research or clinical environment to produce hyperpolarized contrast agents on demand in a fast, fully-automated, multi-step chemical process. Key steps of the process contain fluidic transport across multiple vessels and chemical [. .. ]
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 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 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)
• 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 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)
• 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)
• 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)
• Munich
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 [. .. ]
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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 26 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 (3 Jobs) und Hamburg (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Coding Manager Jobs?
Clinical Coding Manager Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
