57 Jobs für Medical Records
Stellenangebote Medical Records Jobs
Job vor 4 Tagen bei StepStone gefunden
International SOS GmbH
• Großpolen
Homeoffice möglich
[. .. ] with patients to obtain detailed clinical information including past medical history to allow for accurate on-going case management Support the medical collection team in obtaining the discharge [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] summary and medical records from the care provider Profil Registered General Nurse or equivalent with minimum 3 years of experience with registration to practice in Poland Recognized qualification to minimum diploma level or equivalence in practice demonstrated through portfolio/ CV A demonstrable commitment to professional development Able to communicate Polish and proficiently in English [. .. ]
Job vor 10 Tagen bei StepStone gefunden
International SOS GmbH
Client Relationship Lead
• Frankfurt am Main
Führungs-/ Leitungspositionen Homeoffice möglich
[. .. ] overall contractual KPI deliverables for Military Treatment Facilities (MTF) , engagement, coordination of collaboration across all client and TOP stakeholders, securing access to care, contractual provider availability [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and network services, medical records collections, claims handling, beneficiary services. Oversight and support in the coordination of execution of all tasks that impact the MTF through in-country personnel (clinical/ non-clinical) in the Area of Responsibility (AOR) . Maintain and strengthen relationships with stakeholders by means of identifying and communicating client needs in a [. .. ]
Job am 23.07.2026 bei StepStone gefunden
SUTER DENTAL LABOR GmbH
• Bremervörde
Teilzeit Abgeschlossene Ausbildung
[. .. ] abgeschlossene Ausbildung im Bereich Zahntechnik mit Abrechnungserfahrung. Fundierte Kenntnisse in der medizinischen Terminologie sowie im Bereich der zahnärztlichen Abrechnung Erfahrung mit medizinischer Dokumentation, medizinischer Kodierung (Medical coding) [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] und medizinischer Aktenführung (Medical records) Umgang mit gängiger Bürosoftware. Ausgeprägte analytische Fähigkeiten sowie Genauigkeit bei der Bearbeitung komplexer Sachverhalte Gute Kommunikationsfähigkeit im Umgang mit Kolleg:innen und Praxisteams Organisationstalent und selbstständige Arbeitsweise Wir bieten JBRT1DE. SUTER DENTAL LABOR Gmb H sucht in Bremervörde eine/n Zahnmedizinische Fachangestellte (m/w/d) , Abrechnungsfachkraft im Dentallabor, ZFA, ZMF, ZMV, [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
Abbott Laboratories
Manager, Intl Health Systems Integrations
• AT- 2 Schweiz
[. .. ] timeposted on: Posted Todayjob requisition id: 35000065 # # JOB DESCRIPTION: Position Overview The Manager, Intl Health Systems Integrations supports O-US healthcare organizations in integrating their electronic [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] health and medical records (EMR/ HER) systems with Abbott Cancer Diagnostics platforms and workflows. Working directly with hospitals, laboratories, and healthcare IT teams, this role helps establish clinical workflows, streamline data exchange, and support operational goals. The holder of the role as a key liaison between external healthcare partners and internal Abbott Cancer Diagnostics [. .. ]
Job am 05.04.2026 bei Job-Consult gefunden
Recruiter Vitaly Pryadka
• Schweden/ sonstiges/ Europa
[. .. ] rear guard schedule stabilisation of trauma emergency surgery and paediatric patients for further treatment responsibility for anaesthesia pain relief life saving intervention and advanced medical treatment preoperative [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] assessments according to medical records and patient interviews qualifications approved anaesthesiologist in an eu country certified supervisor personal characteristics independent and curious by nature good communication skills both written and orally positive and flexible positive attitude and good cooperation skills why choose our client join the team of experienced and talented colleagues at an elevated [. .. ]
Job am 05.04.2026 bei Job-Consult gefunden
Recruiter Vitaly Pryadka
General Practitioner
• Irland/ (England/ UK/ Irland)
[. .. ] participate in the provision of repeat prescriptions attend to house calls when required provision of reports as required by insurance companies or solicitors issuing of medical certificates [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] when requested maintaining medical records in a professional manner maintaining practice documentation as per practice protocols you are required to keep abreast of professional improvements in the role of gp and in your fields of speciality in addition to the above the post holder will strive to maintain quality within the practice whilst supporting the [. .. ]
Job am 05.04.2026 bei Job-Consult gefunden
Herman Medical Staffing GmbH
• UAE/ sonstiges/ weltweit
Führungs-/ Leitungspositionen
[. .. ] safety champion strategic planner thinker passionate mentor leader role model to inspire lead and motivate some duties and responsibilities leadership and managerial clinical operational strategic financial budget [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] planning research education medical records clinical collaboration and management change management management reporting strategic development and implementation of policies systems processes and procedures essential requirements western educated trained and experienced addiction psychiatrist board certified in psychiatry or equivalent sub specialist board certification fellowship training or specialist training in addiction psychiatry specialist training in addiction treatment [. .. ]
Job gestern bei StepStone gefunden
European Semiconductor Manufacturing Company
Senior Learning Development Specialist (m/f/d)
• Dresden
[. .. ] Operations Qualification Management: Build and maintain qualification frameworks and learning processes for a highly regulated manufacturing environment. Implement and manage Learning Management System (LMS) structures and training [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] documentation. Ensure training records, qualification matrices and learning documentation are complete, transparent and audit-ready. Define sustainable governance for learning administration and reporting. Ensure Compliance Quality: Develop processes supporting ISO-compliant qualification and training management. Prepare learning documentation for internal and external audits. Ensure compliance with local regulations, internal policies and global quality standards. [. .. ] professional experience in Learning Development, Learning Operations, Training Management or a related discipline Experience building or significantly developing Learning Development structures, processes or governance Experience in manufacturing, semiconductor, automotive, pharmaceutical, medical device or another regulated industry is highly desirable Knowledge of Learning Management Systems and learning administration Experience with qualification management, quality systems or ISO-related training processes is an advantage Strong project management and stakeholder management skills Excellent communication skills in German and English High intercultural competence and enthusiasm for [. .. ]
Job vor 4 Tagen bei StepStone gefunden
International SOS GmbH
• Amberg, Weiden Weiden;Kreisfreie Stadt Weiden
Homeoffice möglich
International SOS is the worlds leading
medical and security services company with over 12, 000 employees working in 1, 000 locations in 90 countries. International SOS Government Services administers the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] TRICARE Overseas Program providing high-quality, accessible health care services for U. S. Military service members, family members, retirees, and other eligible beneficiaries overseas. We are looking [. .. ] Identify and onboard new providers where there are gaps in coverage Keep provider information accurate and up to date across systems Support providers with medical record submissions, including Electronic Health Records transfers Identify recurring provider or client issues and coordinate solutions (e. g. claims, credentialing, site assessments) Profil Proven service delivery experience in a professional services B2B environment or senior account management experience or program management experience Bachelors degree, equivalent or qualification by experience Highly proficient in English (written and verbal) [. .. ]
Job vor 11 Tagen bei StepStone gefunden
European Southern Observatory (ESO)
Head of Internal Audit Office
• Garching
Führungs-/ Leitungspositionen Homeoffice möglich
Work-Life-Balance
[. .. ] and overseeing the internal audit function, ensuring its independence, effectiveness, and alignment with organisational objectives. The role encompasses the full spectrum of internal audit activities, including the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] review of accounting records, assessment of procedural compliance, and evaluation of the efficiency and effectiveness of operations. The Head of Internal Audit will engage with personnel and management at all levels across the organisation, providing strategic guidance and assurance. The position involves ensuring the reliability and integrity of financial and operational information, evaluating the [. .. ] Wir bieten Remuneration and Contract: We offer an attractive remuneration package including a competitive salary (free of income tax for applicants from ESO member states) , comprehensive pension scheme and medical, educational and other social benefits, as well as financial help in relocating your family and support to place your child/children in daycare. Our Salary Structure ESOs salary structure is based upon a range of career paths which reflect the nature and level of our jobs. Each career path is [. .. ]
Job vor 11 Tagen bei StepStone gefunden
ZEISS
• Oberkochen (Baden- Württemberg) Oberkochen (Baden- Württemberg)
[. .. ] regardless of gender, nationality, ethnic and social origin, religion, philosophy of life, disability, age, sexual orientation or identity. Apply now It takes less than 10 minutes. Seeing [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] beyond-future of medical technology For more than 100 years, ZEISS medical technology has been driving progress in ophthalmology and microsurgery. In ophthalmology, our solutions help to maintain and improve peoples vision at every stage of their lives. In microsurgery, our solutions enable targeted interventions on diseased tissue so that small and sensitive organs [. .. ] English; German language skills are an advantage Sounds exciting? Then become part of #team ZEISS and help us shape the future Please provide your complete application documents (CV, transcript of records ) . Wir bieten JBRT1DE. ZEISS sucht in Oberkochen (Baden-Württemberg) eine/n Internship Post-sales digital customer interactions (f/m/x) (ID-Nummer: 14092750) 99871042 [. .. ]
Job vor 4 Tagen bei Mindmatch.ai gefunden
TÜV SÜD Produkt Service GmbH
Product Reviewer (IVD Clinical Review/E-ICR) (w/m/d)
• München Muenchen
Flexible Arbeitszeiten Betriebliche Altersvorsorge
[. .. ] class D, etc. ) Evaluate clinical evidence and performance evaluation documentation, including scientific validity, analytical performance, and clinical performance Review planning, conduct, monitoring, and results of performance [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] studies for IVD medical devices Assess the state-of-the Art, clinical relevance and medical plausibility of intended purpose, claims, target population, and benefit-risk considerations Identify deficiencies, prepare structured review comments, and participate in iterative review cycles with manufacturers and internal stakeholders (e. g. product reviewer) . Prepare clear and well-structured assessment [. .. ] reviewers, QMS auditors, software experts, and other technical specialists in multidisciplinary assessment teams Internal Support in product classification Oversight and assessment of various European national databases for Field Safety Notice Records Qualification: The role requirements are based on IVDR expectations for notified body personnel and the internal qualification framework for E-ICR (Expert for IVD Clinical Review) : University degree in medicine, pharmacy, biochemistry, genetics, biology, biomedical science, biotechnology, laboratory medicine, or another relevant scientific discipline Minimum of 4 years of [. .. ]
Job vor 14 Tagen bei XING gefunden
Inter Systems GmbH
• 64293 Darmstadt
Homeoffice möglich
[. .. ] first data platforms solve interoperability, speed, and scalability problems for organizations around the globe. Inter Systems also develops and supports data management in hospitals through the worlds [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] most proven electronic medical record, as well as unified care records for health systems and governments through a powerful suite of healthcare data integration solutions. The company is committed to excellence through its award-winning, 247 support for customers and partners in more than 80 countries. Privately held and headquartered in Cambridge, Massachusetts, Inter Systems has 25 offices worldwide. Tasks Identify [. .. ]
Job vor 3 Tagen bei JobMESH gefunden
Inter Systems GmbH
Bid Coordinator-1 year Contract
• Hesse 64293 Darmstadt
Homeoffice möglich
[. .. ] first data platforms solve interoperability, speed, and scalability problems for organizations around the globe. Inter Systems also develops and supports data management in hospitals through the worlds [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] most proven electronic medical record, as well as unified care records for health systems and governments through a powerful suite of healthcare data integration solutions. The company is committed to excellence through its award-winning, 247 support for customers and partners in more than 80 countries. Privately held and headquartered in Cambridge, Massachusetts, Inter Systems has 25 offices worldwide. Tasks Identify [. .. ]
Job vor 3 Tagen bei JobMESH gefunden
Inter Systems GmbH
Bid Coordinator-1 year Contract
• Hesse 64293 Darmstadt
Homeoffice möglich
[. .. ] first data platforms solve interoperability, speed, and scalability problems for organizations around the globe. Inter Systems also develops and supports data management in hospitals through the worlds [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] most proven electronic medical record, as well as unified care records for health systems and governments through a powerful suite of healthcare data integration solutions. The company is committed to excellence through its award-winning, 247 support for customers and partners in more than 80 countries. Privately held and headquartered in Cambridge, Massachusetts, Inter Systems has 25 offices worldwide. Bitte lesen [. .. ]
Job vor 14 Tagen bei JobMESH gefunden
TÜV SÜD Produkt Service GmbH
Product Reviewer (IVD Clinical Review/E-ICR) (w/m/d)
• Bavaria Munich
Flexible Arbeitszeiten Betriebliche Altersvorsorge
[. .. ] class D, etc. ) Evaluate clinical evidence and performance evaluation documentation, including scientific validity, analytical performance, and clinical performance Review planning, conduct, monitoring, and results of performance [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] studies for IVD medical devices Assess the state-of-the Art, clinical relevance and medical plausibility of intended purpose, claims, target population, and benefit-risk considerations Identify deficiencies, prepare structured review comments, and participate in iterative review cycles with manufacturers and internal stakeholders (e. g. product reviewer) . Prepare clear and well-structured assessment [. .. ] reviewers, QMS auditors, software experts, and other technical specialists in multidisciplinary assessment teams Internal Support in product classification Oversight and assessment of various European national databases for Field Safety Notice Records Qualification: The role requirements are based on IVDR expectations for notified body personnel and the internal qualification framework for E-ICR (Expert for IVD Clinical Review) : University degree in medicine, pharmacy, biochemistry, genetics, biology, biomedical science, biotechnology, laboratory medicine, or another relevant scientific discipline Minimum of 4 years of [. .. ]
Job am 25.07.2026 bei Mindmatch.ai gefunden
TÜV SÜD Produkt Service GmbH
• Munich, BY
Flexible Arbeitszeiten Betriebliche Altersvorsorge
[. .. ] class D, etc. ) Evaluate clinical evidence and performance evaluation documentation, including scientific validity, analytical performance, and clinical performance Review planning, conduct, monitoring, and results of performance [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] studies for IVD medical devices Assess the state-of-the Art, clinical relevance and medical plausibility of intended purpose, claims, target population, and benefit-risk considerations Identify deficiencies, prepare structured review comments, and participate in iterative review cycles with manufacturers and internal stakeholders (e. g. product reviewer) . Prepare clear and well-structured assessment [. .. ] reviewers, QMS auditors, software experts, and other technical specialists in multidisciplinary assessment teams Internal Support in product classification Oversight and assessment of various European national databases for Field Safety Notice Records Qualification: The role requirements are based on IVDR expectations for notified body personnel and the internal qualification framework for E-ICR (Expert for IVD Clinical Review) : University degree in medicine, pharmacy, biochemistry, genetics, biology, biomedical science, biotechnology, laboratory medicine, or another relevant scientific discipline Minimum of 4 years of [. .. ]
Job am 22.07.2026 bei Neuvoo.com gefunden
TÜV SÜD Produkt Service GmbH
Product Reviewer (IVD Clinical Review/E-ICR) (w/m/d)
• Bavaria Munich
Flexible Arbeitszeiten Betriebliche Altersvorsorge
[. .. ] class D, etc. ) Evaluate clinical evidence and performance evaluation documentation, including scientific validity, analytical performance, and clinical performance Review planning, conduct, monitoring, and results of performance [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] studies for IVD medical devices Assess the state-of-the Art, clinical relevance and medical plausibility of intended purpose, claims, target population, and benefit-risk considerations Identify deficiencies, prepare structured review comments, and participate in iterative review cycles with manufacturers and internal stakeholders (e. g. product reviewer) . Prepare clear and well-structured assessment [. .. ] reviewers, QMS auditors, software experts, and other technical specialists in multidisciplinary assessment teams Internal Support in product classification Oversight and assessment of various European national databases for Field Safety Notice Records Qualification: The role requirements are based on IVDR expectations for notified body personnel and the internal qualification framework for E-ICR (Expert for IVD Clinical Review) : University degree in medicine, pharmacy, biochemistry, genetics, biology, biomedical science, biotechnology, laboratory medicine, or another relevant scientific discipline Minimum of 4 years of [. .. ]
Job vor 4 Tagen bei JobMESH gefunden
TÜV SÜD Produkt Service GmbH
Product Reviewer (IVD Clinical Review/E-ICR) (w/m/d)
• Bayern
Flexible Arbeitszeiten Betriebliche Altersvorsorge
[. .. ] class D, etc. ) Evaluate clinical evidence and performance evaluation documentation, including scientific validity, analytical performance, and clinical performance Review planning, conduct, monitoring, and results of performance [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] studies for IVD medical devices Assess the state-of-the Art, clinical relevance and medical plausibility of intended purpose, claims, target population, and benefit-risk considerations Identify deficiencies, prepare structured review comments, and participate in iterative review cycles with manufacturers and internal stakeholders (e. g. product reviewer) . Prepare clear and well-structured assessment [. .. ] reviewers, QMS auditors, software experts, and other technical specialists in multidisciplinary assessment teams Internal Support in product classification Oversight and assessment of various European national databases for Field Safety Notice Records Qualification: The role requirements are based on IVDR expectations for notified body personnel and the internal qualification framework for E-ICR (Expert for IVD Clinical Review) : University degree in medicine, pharmacy, biochemistry, genetics, biology, biomedical science, biotechnology, laboratory medicine, or another relevant scientific discipline Minimum of 4 years of [. .. ]
Job vor 4 Tagen bei Stellen-Online.de gefunden
TÜV SÜD Produkt Service GmbH
Product Reviewer (IVD Clinical Review/E-ICR) (w/m/d) - Vollzeit
• Deutschland, 99986 Oppershausen
Flexible Arbeitszeiten Betriebliche Altersvorsorge
[. .. ] class D, etc. ) Evaluate clinical evidence and performance evaluation documentation, including scientific validity, analytical performance, and clinical performance Review planning, conduct, monitoring, and results of performance [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] studies for IVD medical devices Assess the state-of-the Art, clinical relevance and medical plausibility of intended purpose, claims, target population, and benefit-risk considerations Identify deficiencies, prepare structured review comments, and participate in iterative review cycles with manufacturers and internal stakeholders (e. g. product reviewer) . Prepare clear and well-structured assessment [. .. ] reviewers, QMS auditors, software experts, and other technical specialists in multidisciplinary assessment teams Internal Support in product classification Oversight and assessment of various European national databases for Field Safety Notice Records Qualification:The role requirements are based on IVDR expectations for notified body personnel and the internal qualification framework for E-ICR (Expert for IVD Clinical Review) :University degree in medicine, pharmacy, biochemistry, genetics, biology, biomedical science, biotechnology, laboratory medicine, or another relevant scientific discipline Minimum of 4 years of professional experience [. .. ]
Job vor 14 Tagen bei Stellen-Online.de gefunden
TÜV SÜD Produkt Service GmbH
Product Reviewer (IVD Clinical Review/E-ICR) (w/m/d) - Vollzeit
• München, 80333
Flexible Arbeitszeiten Betriebliche Altersvorsorge
[. .. ] class D, etc. ) Evaluate clinical evidence and performance evaluation documentation, including scientific validity, analytical performance, and clinical performance Review planning, conduct, monitoring, and results of performance [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] studies for IVD medical devices Assess the state-of-the Art, clinical relevance and medical plausibility of intended purpose, claims, target population, and benefit-risk considerations Identify deficiencies, prepare structured review comments, and participate in iterative review cycles with manufacturers and internal stakeholders (e. g. product reviewer) . Prepare clear and well-structured assessment [. .. ] reviewers, QMS auditors, software experts, and other technical specialists in multidisciplinary assessment teams Internal Support in product classification Oversight and assessment of various European national databases for Field Safety Notice Records Qualification: The role requirements are based on IVDR expectations for notified body personnel and the internal qualification framework for E-ICR (Expert for IVD Clinical Review) : University degree in medicine, pharmacy, biochemistry, genetics, biology, biomedical science, biotechnology, laboratory medicine, or another relevant scientific discipline Minimum of 4 years of [. .. ]
Neu Job vor 2 Std. bei Mindmatch.ai gefunden
Healthcare Businesswomens Association
Qualified Person (QP/ Sachkundige Person) (m/w/d)
• AT- 7 Schaftenau
[. .. ] with AMBO 2009 and EU GMP Annex 16, covering medicinal products for human and veterinary use where applicable. Review and approve key GMP documentation, including bills of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] materials, master batch records, stability protocols and reports, APQRs, CAPAs, quarantine shipment requests, and re-packaging requests. Review and approve quality control documentation, including specifications, sampling instructions, test methods, and other QC procedures. Assess and approve deviations, OOX investigations, and quality events, ensuring robust rootcause analysis, appropriate corrective actions, and timely closure. Contribute to [. .. ] and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Accessibility and Accommodation: If because of a medical condition, physical disability or a neurodiverse condition you require an adjustment during the recruitment process, please reach out to and let us know the nature of your request as well as your contact information. The support which we can provide will include advice on suitable positions as well as guidance [. .. ]
Neu Job vor 2 Std. bei Mindmatch.ai gefunden
100283 Johnson Electric International AG Operation
Supervisor, Quality System
• AT- 2 Lavamünd
Führungs-/ Leitungspositionen
[. .. ] improvement. Collaborate with cross-functional teams, including production, engineering, and supply chain, to integrate quality requirements throughout the product lifecycle. Manage and maintain quality documentation, including procedures, work [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] instructions, and records, ensuring they are current and accessible. Participate in new product introduction (NPI) processes, ensuring quality gates are met and potential risks are mitigated. Drive continuous improvement initiatives using lean manufacturing and Six Sigma methodologies. Represent the company during customer and third-party quality audits. Job Qualifications Bachelors degree in Engineering, [. .. ] Group The Johnson Electric Group is a global leader in electric motors, actuators, motion subsystems and related electromechanical components. It serves a broad range of industries including Automotive, Smart Metering, Medical Devices, Business Equipment, Home Automation, Ventilation, White Goods, Power Tools, Lawn Garden Equipment, Warehouse Automation, Liquid Cooling and Robotic joints. The Group is headquartered in Hong Kong and employs over 30, 000 individuals in over 20 countries worldwide. Johnson Electric Holdings Limited is listed on The Stock Exchange of Hong [. .. ]
Job vor 3 Tagen bei Mindmatch.ai gefunden
Anteris Technologies
Principal Regulatory Affairs Specialist
• AT- 2 Schweiz
[. .. ] of a healthy heart valve. We are seeking a Principal Regulatory Affairs Specialist to lead and execute regulatory activities supporting the development, clinical investigation, approval, and lifecycle [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] management of Anteris medical device products across Europe. This individual will serve as a senior regulatory subject matter expert, with primary responsibility for EU regulatory strategy and submissions for Class III cardiovascular devices. The Principal Regulatory Affairs Specialist will work closely with Clinical Affairs, Quality, R D, Medical Affairs, and other cross-functional partners [. .. ] requirements and approved product claims. Support product registrations, certificate renewals, licenses, and regulatory maintenance activities across European and other international markets. Maintain complete, accurate, and audit-ready regulatory documentation, including records required for Notified Body assessments and regulatory inspections. Author, review, and approve regulatory procedures, work instructions, and other controlled documents. Monitor changes in European regulations, guidance, standards, and regulatory practices; assess potential business impact and communicate requirements to appropriate stakeholders. Provide regulatory leadership, mentorship, and strategic guidance to colleagues and [. .. ]
Job vor 8 Tagen bei Mindmatch.ai gefunden
International Atomic Energy Agency
Research Contracts Officer (P3)
• AT- 9 Wien
[. .. ] , with particular focus on complex, non-routine and exceptional cases. Prepares working papers for the Committees for Coordinated Research Activities (CCRAs) , maintains accurate and up-to-date CRP [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] records, and provides technical guidance to Project Officers on procedures across the full CRP life cycle. Coordinates and oversees the review and approval of research proposals, progress and final reports, and amendment requests, ensuring compliance with established policies, financial regulations, and availability of funds. Analyses the financial aspects of Coordinated Research [. .. ] based interview. Candidates under serious consideration for selection may be subject to reference and background checks as part of the recruitment process. Appointment information Appointment is subject to a satisfactory medical report. Staff members may be assigned to any location. Candidates appointed to posts in the Professional and higher categories are subject to IAEA rotation policy and their maximum tour of service shall normally be seven years. The IAEA retains the discretion not to make any appointment to this vacancy, to [. .. ]
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Häufig gestellte Fragen
Wieviele offene Stellenangebote gibt es für Medical Records Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 57 offene Stellenanzeigen für Medical Records Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Medical Records Jobs?
Aktuell suchen 31 Unternehmen nach Bewerbern für Medical Records Jobs.
Welche Unternehmen suchen nach Bewerbern für Medical Records Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Medical Records Stellenangebote:
- Eumetsat (8 Jobs)
- Stryker (4 Jobs)
- International SOS GmbH (3 Jobs)
- Inter Systems GmbH (3 Jobs)
- International Atomic Energy Agency (3 Jobs)
- Bristol- Myers Squibb (3 Jobs)
In welchen Bundesländern werden die meisten Medical Records Jobs angeboten?
Die meisten Stellenanzeigen für Medical Records Jobs werden derzeit in Bayern (4 Jobs), Baden-Württemberg (1 Jobs) und Sachsen (1 Jobs) angeboten.
