161 Jobs für Clinical Investigator
Stellenangebote Clinical Investigator Jobs
Job vor 3 Tagen bei Jooble gefunden
Biontech
• Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz Mainz, DE
Führungs-/ Leitungspositionen
[. .. ] will directly contribute to advancing Bio NTechs mission by ensuring adherence to regulatory standards and fostering continuous improvement in clinical development activities. Your Contribution: Lead global audits [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with a focus on clinical investigator sites and vendor audits in the EU, UK, and surrounding regions Ensure audit objectives align with risk-based strategies to uphold quality standards Coordinate and oversee audits conducted by contracted auditors, including scheduling, resource selection, and report reviews Execute audits as the lead auditor for non-contracted audits (remote or [. .. ]
Job vor 4 Tagen bei Aktuelle TopJobs gefunden
Deutsche Rentenversicherung Baden- Württemberg
Sachbearbeiter/in Projektbüro (m/w/d)
• Karlsruhe oder Stuttgart
Sachbearbeiter/in Projektbüro (m/w/d) Deutsche Rentenversicherung Baden-Württemberg Karlsruhe oder Stuttgart Die Deutsche Rentenversicherung (DRV) Baden Württemberg ist einer der größten Regionalträger der gesetzlichen Rentenversicherung mit rund 3.600 Mitarbeitenden. Unsere Digitalisierungsabteilung stellt [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Anwenderinnen und Anwendern ein breit [. .. ]
Job vor 8 Tagen bei StepStone gefunden
Randstad Deutschland GmbH Co. KG
• Biberach an der Riß
Angebote von Zeitarbeitsunternehmen
30+ Urlaubstage
[. .. ] Meetings (Leitungsrunde etc. ) Unterstützung des COPI-Teams bei der Ausführung der Unternehmensvorschriften, z. B. Records Retention Interne und externe Korrespondenz sowie tägliche Koordination mit Kollegen weltweit/ übergreifender [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Regionen innerhalb Clinical Operations und anderen Funktionen Onboarding, Offboarding, Budget-Kontrolle und Rechnungsbearbeitung Übernahme der Funktion als Gleitzeitbeauftragter und Global Privacy Notice Manager Bearbeitung von Datenschutzanfragen zu Investigator-Daten für Clin Ops Global Abgeschlossene kaufmännische Ausbildung, z. B. als Kaufmann für Büromanagement, Industriekaufmann oder Management-Assistenz Erfahrung in einer ähnlichen Rolle in einem internationalen Arbeitsumfeld Sehr gute Kenntnisse in den gängigen MS-Office-Programmen (Word, Excel, Power Point, Outlook) Erfahrung mit Share Room, SAP, IDEA, BICTMS, Concur, My BI [. .. ]
Job am 25.04.2026 bei StepStone gefunden
Universität Bielefeld
Datenmanagerin (m/w/d) klinische Forschung
• Bielefeld
Homeoffice möglich
Flexible Arbeitszeiten 30+ Urlaubstage
[. .. ] für die translationale Forschung gehört. Diese in Entwicklung begriffene Struktur führt die bereits in Betrieb genommene Forschungsbiobank, das Datenintegrationszentrum für die medizinische Forschung sowie die Biometrie mit [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] der nun aufzubauenden Clinical Research Support Unit (CRSU) eng zusammen. Als zentrale Einrichtung der Universitätsmedizin OWL unterstützt die CRSU zukünftig Forschende bei der Antragstellung, Planung, Vorbereitung, Durchführung und den Abschluss von eigeninitiierten klinischen Studien (IITs) im gesamten Spektrum der patientenorientierten klinischen Forschung. Für das Angebot professioneller Datenmanagementleistungen sowie den Aufbau eines praxis- und prozessorientierten [. .. ] Das wünschen wir uns Kenntnisse in der Programmierung mit Java Kenntnisse der medizinischen Terminologie und Kodierung (Med DRA) Kenntnisse der CDISC Standards Erfahrung in der Planung und Umsetzung von Datenbanken bei Investigator Initiated Trials (IITs) Erfahrungen in der deskriptiven Datenauswertung Erfahrung in der regulativen Beratung bei studiesspezifischen Anfragen Vergütung nach E13 TV-L unbefristet Vollzeit interne und externe Fortbildungsmöglichkeiten Vielzahl von Gesundheits-, Beratungs- und Präventionsangeboten Vereinbarkeit von Familie und Beruf sicherer Arbeitsplatz fester Dienstort (Bielefeld) ohne Reisetätigkeit flexible Arbeitszeiten 30 Tage [. .. ]
Job am 01.04.2026 bei praktischArzt.de gefunden
Velocity Clinical Research
• 23, Lübeck, Deutschland
Führungs-/ Leitungspositionen
Leitende:r Prüfarzt/ Prüfärztin (w/m/d) (Principal
Investigator) Klinische Studien Leitende:r Prüfarzt/ Prüfärztin (w/m/d) (Principal Investigator) Klinische Studien Lübeck, Deutschland Velocity
Clinical Research ist eine international führende Organisation für klinische Forschungszentren und [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] steht für exzellente. . . . Leitende:r Prüfarzt/ Prüfärztin (w/m/d) (Principal Investigator) Klinische Studien Leitende:r Prüfarzt/ Prüfärztin (w/m/d) (Principal Investigator) Klinische Studien Lübeck, Deutschland Velocity Clinical Research ist eine international führende Organisation für klinische Forschungszentren und [. .. ]
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
Syneos Health, Inc.
On-site monitor open to diverse EMEA countries
• AT- 9 Wien
[. .. ] (SOPs) and Work Instructions (WIs) . Assure compliance with local regulations and appropriate guidance for assigned study design/ classification, including Good Pharmacoepidemiology Practices (GPP) and International Conference [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] on Harmonisation Good Clinical Practice (ICHGCP) . Conduct site management activities as per agreed Scope of Work (So W) , Site Management Plan (SMP) and relevant guidelines. Site identification contact sites to gauge interest, confirm contact details, and obtain relevant documents. Site qualification. Ensure selection of appropriate sites for assigned studies. Site startup with minimal supervision, working with study startup and regulatory teams. Conduct all remote and onsite monitoring activities through all study stages. Routinely review the Investigator Site File (ISF) for accuracy, timeliness and completeness; reconcile its contents with the Trial Master File (TMF) ; and ensure sites archive essential documents per local guidelines. Document activities via confirmation letters, followup letters, trip reports, communication logs, and other required project documents per SOPs and SMP; support subject recruitment, [. .. ]
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
IQVIA LLC
• AT- 9 Wien
Clinical Associate Regulatory Submissions, Austria, IQVIA Biotech page is loaded # # Clinical Associate Regulatory Submissions, Austria, IQVIA Biotechlocations: Vienna, Austriatime type: Full timeposted on: Posted Todayjob requisition id: R1522611 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Clinical Associate Submissions Regulatory Homebased Austria IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across [. .. ] and review for completeness and accuracy, along with reviewing, tracking, and following up the progress, the approval and execution of documents, questionnaires, CDA/ SIF, regulatory, ethics, Informed Consent Form, and Investigator Pack release documents, in line with project timelines. Coupled with informing team members of completion of feasibility, site ID, regulatory and contractual documents for individual sites, and providing local expertise to SAMs and project team during initial and on-going project timeline planning. Along with performing quality control of documents [. .. ]
Job vor 8 Tagen bei Mindmatch.ai gefunden
EM Tensor GmbH
Test Engineer Electromagnetic Tomography
• AT- 9 Wien
[. .. ] matter, ventricles, skull layers) , typical tissue geometry, and anatomical variation across patient populations. This knowledge directly informs phantom design choices, inclusionpositioning, and interpretation of anomalous scan [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] results. Familiarity with clinical investigation concepts: informed consent, inclusion/ exclusion criteria, adverse event reporting, source data, and the role of sponsor vs. investigator. The Test Engineer will interact with clinical data workflows and must understand the regulatory context of the measurements they produce. Key Responsibilities Daily Calibration and Environmental Monitoring Execute the daily system calibration before each scanning session: empty field scan, automated S-parameter comparison against reference values, and verification of dual [. .. ]
Job am 22.04.2026 bei Mindmatch.ai gefunden
Universität für Weiterbildung Krems
• AT- 3 Krems an der Donau
Homeoffice möglich Werkstudenten
[. .. ] Methods in Nutrition Research: Independently conduct scientific research aimed at advancing the methodologies used to conduct evidence synthesis in nutrition research and the development of evidence-based nutritional [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] guidelines. Co-Investigator Contribution: Actively contribute as a co-investigator to the BEETHOVEN project. Educational Contributions: Teach courses in clinical epidemiology and evidence-based medicine to undergraduate students, supervise bachelor theses. Research Dissemination: Publish research findings in international, peer-reviewed scientific journals. Conference Participation: Engage actively in both national and international conferences, presenting research findings and networking with peers in the scientific community. International Research Collaborations: Participate in global research [. .. ]
Job am 20.04.2026 bei Mindmatch.ai gefunden
Karlstad University
Early-Stage Researcher-PhD Student (m/f/d) , SB26-0059
• AT- 3 Krems an der Donau
Homeoffice möglich Werkstudenten
[. .. ] in Nutrition Research : Independently conduct scientific research aimed at advancing the methodologies used to conduct evidence synthesis in nutrition research and the development of evidence-based nutritional [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] guidelines. Co-Investigator Contribution : Actively contribute as a co-investigator to the BEETHOVEN project. Educational Contributions : Teach courses in clinical epidemiology and evidence-based medicine to undergraduate students, supervise bachelor theses. Research Dissemination : Publish research findings in international, peer-reviewed scientific journals. Conference Participation : Engage actively in both national and international conferences, presenting research findings and networking with peers in the scientific community. International Research Collaborations : Participate [. .. ]
Job am 12.04.2026 bei Mindmatch.ai gefunden
Medizinische Universität Wien
• AT- 9 Wien
[. .. ] consequential heart failure, as well as the evaluation and development of therapeutic strategies in structural heart interventions and heart valve medicine. We actively pursue and participate in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] pure academic studies, investigator initiated trials and industry-sposored studys. The research is embedded in a highly active academic and clinical environment with close interaction between clinical cardiology, cardiovascular imaging, heart failure, and interventional structural heart therapy. Participation in clinical research projects in the field of structural heart disease and valvular heart disease Scientific work on phenotyping of valve disease, in particular aortic valve disease and mitral and tricuspid valve disease [. .. ]
Job am 26.03.2026 bei Mindmatch.ai gefunden
Fortrea
FSP Start Up Contract Finance Specialist based in Vienna
• AT- 9 Wien
We are looking for a
Clinical Start Up Contract Finance Specialist to support clinical trial startup activities across Austria. This role is an excellent opportunity for professionals with experience [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in clinical startup operations, budget/ contract negotiations, and regulatory processes even if they have not previously worked in a Lead position. The successful candidate will receive development [. .. ] submissions and approvals for assigned protocols. Manage country-level deliverables, timelines, and outcomes to meet study commitments. Collaborate closely with sponsors, CROs, and site teams to streamline startup processes. Negotiate investigator budgets, manage financial forecasting, and track trialrelated expenses. Ensure timely delivery of clinical and financial contracts within fair market value through strong partnerships with local clinical teams. Oversee and track clinical researchrelated payments. Conduct payment reconciliation at study closeout. Qualifications University degree (life sciences preferred) or equivalent healthcarerelated certification. Fortrea [. .. ]
Job am 19.03.2026 bei Mindmatch.ai gefunden
Milestone One
• AT- 9 Wien
Milestone One is a Site Enabling Services organization with global headquarters in Zug, Switzerland. We understand what
clinical study sites need and our overall mission is to support sites [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in stronger study delivery. Job Description The Milestone One Site Coordinator role supports a Clinical Study Site in clinical trial related activities according to ICHGCP, protocol requirements within Study specific defined timelines and enrollment goals. The function of the [. .. ] reconciliation of investigational products and clinical supplies. Collect, handle and maintain all sitespecific regulatory documents as needed. Facilitate and support the contract and budget negotiations at the site level. Support Investigator and Site payments and processes as needed. Schedule and/or perform study procedures as per study requirements and delegation of responsibilities. Prepare for and participate in onsite study audits or regulatory agency inspections. Qualifications A university degree in Life Science, preferably in pharmacy, nursing or lab analytics. Minimum of 2 [. .. ]
Job am 11.03.2026 bei Mindmatch.ai gefunden
Teleflex
Clinical Research Associate
• AT- 9 Wien
Expected Travel: More than 50 Requisition ID: 13617 Position Summary The
Clinical Research Associate (CRA) is responsible for scheduling and conducting on-site and remote monitoring visits in compliance with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] applicable regulatory standards (MDR, ISO 14155, ICH/ GCP guidelines, Teleflex procedures and IRB/ EC policies) . The CRA conducts monitoring visits as identified by the monitoring plan, study team or department needs [. .. ] visit preparation. Conducts monitoring visits per the department SOP, WIs and monitoring plans. Applies MDR, ISO 14155, ICH/ GCP guidelines and Teleflex SOP and WIs to monitoring activities. Completes the Investigator Files with all appropriate documentation. Ensures all required documentation is completed prior to site initiation, during enrollment and followup, and at site close out. Provides findings to site staff, clear directions for resolution, appropriate retraining, and reviews data queries with site staff to ensure they are understood and can be [. .. ]
Job am 06.03.2026 bei Mindmatch.ai gefunden
Alimentiv
• AT- 9 Wien
[. .. ] quite matches what youre looking for, or not ready to make a move yet? Let us know We are proactively inviting qualified candidates to join our talent [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] pool for anticipated Clinical Research Associate needs (across multiple seniority levels) to support our Clinical Monitoring team. What the process looks like: A Talent Acquisition representative will contact selected candidates to schedule a qualifying call to learn more about your experience, and what your timeline looks like Well also share details about timelines on [. .. ] regulatory compliance. Assist/ lead (as appropriate) with query resolution, safety reviews, and adverse event follow-up throughout the study lifecycle. Support/ conduct (as appropriate) site startup and activation activities, including investigator coordination, trial material delivery, and recruitment support. Maintain accurate, timely, and complete TMF documentation, requesting updates as required. Provide day-to-day operational support to Senior CRA, and Lead CRAs. Participate in training, study meetings, and CRA development activities, building competencies required for role progression. Sr. Clinical Research Associate As [. .. ]
Job am 06.03.2026 bei Mindmatch.ai gefunden
PSI CRO
Site Identification Specialist
• AT- 9 Wien
[. .. ] committed to delivering high-quality, timely services across a wide range of therapeutic areas. Job Description We are in search of an experienced professional dedicated to developing strategic [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] relationships with clinical research sites, with the aim of optimizing and advancing the progress of clinical trials. Hybrid role in Vienna, Austria This is the main responsibility of a site ID specialist. Communicate and build relationship with clinical sites to identify potential centres for clinical trials. Maintain and refine internal site databases in [. .. ] recommended investigators or clinical sites. Support the project team throughout study startup and further on, whenever additional rounds of site identification are necessary, and/or additional information on the site/ investigator is needed. Qualifications University/ college degree (Md/Pharm D degree) , or an equivalent combination of education, training and experience. On-site monitoring experience is a plus. Understanding of Good Clinical Practice, local laws and applicable regulations in the region. Demonstrated ability to work in a dynamic environment, under compressed deadlines [. .. ]
Job am 02.03.2026 bei Mindmatch.ai gefunden
IQVIA
• AT- 9 Wien
A global provider of
clinical research services is seeking a Contract Specialist in Vienna. In this role, you will be responsible for developing contracts and coordinating
investigator grants [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to support clinical trials. You will need a Bachelors Degree or 5 years of relevant experience, along with strong negotiation and communication skills. Fluency in English and German is required. Join a leading firm dedicated to enhancing patient outcomes globally. J-18808-Ljbffr 82516537 [. .. ]
Job am 25.02.2026 bei Mindmatch.ai gefunden
IQVIA
Contract Negotiator 2-FSP-German speaker
• AT- 9 Wien
Essential Functions Develop coordinate the development of
investigator grants and estimates, contracting strategies and proposal text to support the proposal development process. Develop contract language, payment language and budget [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] templates as required as applicable to the position. Utilize and maintain contracting systems, tools, processes, and training materials for selected sponsors, studies or multi-protocol programs according to the [. .. ] RSU Management Plan. Provide specialist legal, operational and financial contracting support to the Study Teams, as applicable to site agreements to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements. Ensure overall contracting efficiency and adherence to project timelines and financial goals as applicable to site agreements. Report contracting performance metrics and out of scope contracting activities as required. Work with Quality Management to ensure appropriate contract management and quality standards. Mentor and [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Job Overview The Associate Medical Director/ Medical Director will provide medical,
clinical and scientific advisory expertise to all IQVIA divisions as requested. Participate in all aspects of Medical Science [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] involvement on assigned trials. Serve as a medical expert during project delivery lifecycle. Provide therapeutic and medical expertise to business development activities. Essential Functions The role includes predominantly Medical Monitoring responsibilities with Medical [. .. ] Brochure (IDB) , and/or Case Report Forms (CRFs) . # # Provides therapeutic area/ indication training for the project clinical team. # # Attends and presents at Investigator Meetings. # # Performs review and clarification of trial-related Adverse Events (AEs) . # # May perform medical case review of Serious Adverse Events (SAEs) , including review of case documentation and patient narrative, in collaboration with the Pharmacovigilance department. # # May provide medical support [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Sr Medical Director
• Bayern
Führungs-/ Leitungspositionen
Job Description Summary Strategic leadership and scientific oversight of a therapeutic area or disease domain across the
clinical development lifecycle. Responsibilities Define and drive the clinical strategy for the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] assigned care area (oncology) . Lead the development of Target Product Profiles (TPPs) , Integrated Evidence Generation Plans (IEGPs) , and clinical development plans. Represent the therapeutic area in governance forums and regulatory interactions. Engage with KOLs and external [. .. ] monitors working within the care area. Provide medical oversight for one or more clinical trials. Review safety data, assess adverse events, and support dose modifications or protocol amendments. Respond to investigator queries and support site engagement. Participate in Data Safety Monitoring Boards (DSMBs) and internal safety reviews. Contribute to clinical study reports (CSRs) , regulatory submissions, and medical writing. Collaborate with Clinical Operations and Pharmacovigilance teams. Qualifications MD or Ph D with deep expertise in the therapeutic area. Extensive experience in clinical [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Clinical Trials Lead Site Coordinator
• Zug
Führungs-/ Leitungspositionen
Overview Milestone One is a Site Enabling Services organization with global headquarters in Zug, Switzerland. We understand what
clinical study sites need and our overall mission is to support [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] sites in stronger study delivery. Job Description Milestone One Site Coordinator supports trial sites in all related activities according to ICH-GCP, protocol requirements within study-specific defined timelines and enrollment goals. Responsibilities Act as the main line of communication [. .. ] of investigational products and clinical supplies. Collect, handle and maintain all site-specific regulatory documents as needed. Facilitate and support the contract and budget negotiations at the site level. Support Investigator and Site payments and processes as needed. Schedule and/or perform study procedures as per study requirements and delegation of responsibilities. Prepare for and participate in onsite study audits or regulatory agency inspections. Build and sustain long-lasting relationships with existing and potential clients (sponsors, CROs, medical institutions) . Qualifications [. .. ]
Job vor 9 Tagen bei Jobleads gefunden
Medical Director-Psychiatry (m/w/d)
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Job Overview The Associate Medical Director/ Medical Director will provide medical,
clinical and scientific advisory expertise to all IQVIA divisions as requested. They will participate in all aspects of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] medical science involvement on assigned trials, serve as a medical expert during the project delivery lifecycle, and provide therapeutic and medical expertise to business development activities. Essential Functions Primarily responsible for medical monitoring [. .. ] review of the protocol, Investigative Drug Brochure (IDB) , and/or Case Report Forms (CRFs) . Provides therapeutic area/ indication training for the project clinical team. Attends and presents at Investigator Meetings. Performs review and clarification of trial-related Adverse Events (AEs) . May perform medical case review of Serious Adverse Events (SAEs) , including review of case documentation and patient narrative, in collaboration with the Pharmacovigilance department. May provide medical support for the Analysis of Similar Events (AOSE) , in [. .. ]
Job am 17.04.2026 bei Jobleads gefunden
Director, Medical Affairs (m/f/d)
• Eschborn, Hessen
Führungs-/ Leitungspositionen
[. .. ] Role Matters This is a highimpact position at the forefront of advancing innovative therapies for patients living with heart failure. The Director will play a key role [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in guiding the clinical and scientific strategy across a rapidly evolving portfolio, partnering closely with Clinical Affairs, R D, Market Access, Marketing, and Commercial teams. The role requires a significant global presence (approx. 60 travel) to engage with investigators, clinical sites, and internal stakeholders. This position will manage Clinical Research professionals to provide medical [. .. ] product safety processes and procedures for new products and technologies as clinical studies are implemented, worldwide regulatory approvals are obtained and new products are commercialized. Key responsibilities Regionally responsible for Investigator Initiated Study and Research Grant programs Develop the priorities for the Global Abbott HF ISS strategy Responsible for medical affairs contributions to physician level professional education on advanced HF, MCS and hemodynamic management Work with professional societies on increasing awareness and knowledge about advanced HF and hemodynamic management Assists the [. .. ]
Job am 17.04.2026 bei Jobleads gefunden
Medical Director
• Zürich
Führungs-/ Leitungspositionen
Discover Intenarnational is partnered with a Swiss Biotech in their search for an experienced Medical Director Oncology to provide medical and
clinical leadership across a portfolio of innovative oncology [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] assets within a fast-growing biotech group. This role will lead oncology clinical development strategy, provide medical oversight across studies, and work closely with R D and executive leadership to advance novel cancer therapies through clinical development. Key Responsibilities Lead medical strategy for [. .. ] focus on solid tumours and targeted therapies Provide oversight for oncology clinical trial design, protocols, and study execution Act as senior medical lead for safety review, clinical data interpretation, and investigator engagement Support regulatory submissions and health authority interactions Provide scientific leadership to internal teams, KOLs, and external partners Contribute to portfolio assessment and oncology asset strategy Requirements Md/MBBS with significant oncology drug development experience Strong background in clinical oncology trials (Phase IIII) Experience in biotech or pharma clinical development [. .. ]
Job am 08.04.2026 bei Jobleads gefunden
Sr. Medical Affairs Manager-DACH (w, m, d)
[. .. ] country launch plans for new products, and executes them with excellence. They will have and maintain an indepth understanding of diabetes, the current and future treatment landscape [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] along with ongoing clinical research with a focus on the diabetes device market. This individual has leadership responsibilities to ensure the execution of all above tasks. They will be responsible to lead a team in the development and successful execution of medical strategies and tactics that enhances regulatory approval, customer access and adoption of [. .. ] training with generation and delivery of medical content Inform strategize evidence generation plans, in answer to fulfil market access, regulatory and marketing needs Support the local execution of Insuletsponsored and Investigator Initiated trials Disseminate evidence within local markets Identify and engage with HCP to inform and seek advice on the companys solutions, through the execution of advisory boards, clinical activity, scientific Exchange and educational Events Establish and maintain credible peertopeer scientific relationships with national and regional KOLs Build confidence and advocacy [. .. ]
1 von 7Weiter » Weitere Suchergebnisse laden »
Häufig gestellte Fragen
Wieviel verdient man als Clinical Investigator pro Jahr?
Als Clinical Investigator verdient man zwischen EUR 60.000,- bis EUR 90.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Investigator Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 161 offene Stellenanzeigen für Clinical Investigator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Investigator Jobs?
Aktuell suchen 33 Unternehmen nach Bewerbern für Clinical Investigator Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Investigator Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Investigator Stellenangebote:
- Biontech (5 Jobs)
- Thermo Fisher Scientific (4 Jobs)
- IQVIA (2 Jobs)
- TFS Health Science (2 Jobs)
- ICON (2 Jobs)
In welchen Bundesländern werden die meisten Clinical Investigator Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Investigator Jobs werden derzeit in Bayern (42 Jobs), Niedersachsen (17 Jobs) und Nordrhein-Westfalen (15 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Investigator Jobs?
Clinical Investigator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
