143 Jobs für Medical Investigator
Stellenangebote Medical Investigator Jobs
Job vor 3 Tagen bei Aktuelle TopJobs gefunden
Buspaket Derenbach GmbH Co.KG
Bürohilfe (m/w/d)
• 10405 Berlin
Bürohilfe (m/w/d) Buspaket Derenbach Gmb H Co. KG 10405 Unternehmensprofil Die Buspaket Derenbach Gmb H ist Ihr zuverlässiger Partner für nachhaltige Busreisen und individuelle Mobilitätslösungen. Unser Unternehmen setzt auf Umweltschutz [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] und Zukunftsfähigkeit, weshalb wir ausschließlich mit modernen Elektrobusen unterwegs sind. Damit leisten wir ein [. .. ]
Job am 25.04.2026 bei StepStone gefunden
Universität Bielefeld
Datenmanagerin (m/w/d) klinische Forschung
• Bielefeld
Homeoffice möglich
Flexible Arbeitszeiten 30+ Urlaubstage
[. .. ] eine Datenmanagerin gesucht. Als Datenmanagerin arbeiten Sie eng mit den Kolleginnen der weiteren unterstützenden Einheiten für klinische Studien zusammen, insbesondere der Arbeitsgruppe Biostatistik und Medizinische Biometrie und [...]
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[...] dem Servicezentrum für Medical Data Science. An der Schnittstelle zwischen Medizinischer Fakultät und den Krankenhausträgern des UK OWL (Webseite des Universitätsklinikums OWL ) sowie dem Herz- und Diabeteszentrum NRW (HDZ) erwartet Sie eine herausfordernde und spannende Tätigkeit. Die junge Fakultät ist von kurzen Abstimmungswegen und einer offenen und wertschätzenden Gesprächskultur geprägt. In der Medizinischen [. .. ] 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 [. .. ]
Neu Job vor 3 Std. bei Mindmatch.ai gefunden
Syneos Health, Inc.
• AT- 9 Wien
[. .. ] 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. [...]
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[...] 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, [. .. ] and project levels and support audit preparation and followup actions. Prepare for, attend, and participate in Investigator Meetings and/or sponsor facetoface meetings. Collaborate and build relationships with Sponsor affiliates, medical science liaisons, and local country sponsor staff as required. For assigned activities, understand project scope, budgets, and timelines; manage sitelevel activities and communications to meet project objectives, deliverables, and timelines; and adapt quickly to changing priorities under the oversight of the Clinical Operations Lead or designee. Identify and communicate outofscope [. .. ]
Neu Job vor 3 Std. bei Mindmatch.ai gefunden
IQVIA LLC
Clinical Associate Regulatory Submissions, Austria, IQVIA Biotech
• AT- 9 Wien
[. .. ] 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 [...]
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[...] 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 [. .. ] experience, specifically in submissions. Experience in EUCTR and CTIS submission procedures, feasibility and Country Inform Consent adaptation for DACH regions. Experience in Site Contract negotiations with DACH sites. Experience in medical device submissions is beneficial. In-depth knowledge of clinical systems, procedures, and corporate standards. Skills Good negotiating and communication skills in local language. Effective communication, organizational, and interpersonal skills. Ability to work independently and to effectively prioritize tasks. Ability to manage multiple projects. Knowledge and ability to apply GCP/ ICH [. .. ]
Job vor 8 Tagen bei Mindmatch.ai gefunden
EM Tensor GmbH
• AT- 9 Wien
[. .. ] the highest standards of accuracy and reliability. You will not just run tests you will design them, analyze the data, and provide critical feedback that shapes the [...]
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[...] future of our medical technology. You will work directly with our electromagnetic brain imaging prototype, executing calibration procedures, phantom-based validation studies, and RF characterization workflows that feed directly into our regulatory documentation package (EU MDR) . Your Profile Education Bachelors degree or higher (University, FH) in Medical Engineering, Electrical Engineering, Physics, or a [. .. ] design choices, inclusionpositioning, and interpretation of anomalous scan 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 01.04.2026 bei Mindmatch.ai gefunden
Abb Vie
Affiliate Medical Operations Advisor (1 year contract, m/w/d)
• AT- 9 Wien
Overview About Abb Vie. Abb Vies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the
medical challenges of tomorrow. We [...]
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[...] strive to have a remarkable impact on peoples lives across several key therapeutic areas including immunology, oncology and neuroscience-and products and services in our Allergan Aesthetics portfolio. For more information about Abb Vie, please visit us at Follow abbvie on Linked In, Facebook, Instagram, X [. .. ] level project management to medical activities, that include evidence generation, planning processes, and management of Quality System documentation. Participates and supports in medical operations responsibilities related to non-interventional studies, investigator-initiated-studies, collaborative research studies ensuring compliance with local laws, guidelines and Abb Vies internal requirements, interacts with Global, Area and local medical team regarding issues, timelines, resources and general activities. Builds up competence and support for medical affairs teams in strategic and innovative primary secondary evidence generation (RWE) studies [. .. ]
Job am 30.03.2026 bei Mindmatch.ai gefunden
Allergan
• AT- 9 Wien
Company Description About Abb Vie Abb Vies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the
medical challenges of [...]
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[...] tomorrow. We strive to have a remarkable impact on peoples lives across several key therapeutic areas including immunology, oncology and neuroscience-and products and services in our Allergan Aesthetics portfolio. For more information about Abb Vie, please visit us at Follow abbvie on Linked In, Facebook, Instagram, X [. .. ] to medical activities, that include evidence generation, planning processes, and management of Quality System documentation. Core Job Responsibilities Participates and supports in medical operations responsibilities related to non-interventional studies, investigator-initiated-studies, collaborative research studies ensuring compliance with local laws, guidelines and Abb Vies internal requirements, interacts with Global, Area and local medical team regarding issues, timelines, resources and general activities. Builds up competence and support for medical affairs teams in strategic and innovative primary secondary evidence generation (RWE) studies [. .. ]
Job am 23.03.2026 bei Mindmatch.ai gefunden
Planet
Senior Software Engineer, Geometry
• AT- 3 St. Pölten
Homeoffice möglich
[. .. ] error budgets, and calibration concepts for our highresolution and nextgeneration monitoring programs, ensuring spatial integrity across diverse fleets. Additionally, you will drive ongoing performance characterization and serve [...]
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[...] as a lead investigator for complex image quality issuestroubleshooting sensor models and geometric anomalies to architect the longterm fixes that maintain Planets high standard of spatial data. This is a fulltime, remote position based in Austria. If located near an office, you are expected to work from that office 3 days per week. Impact [. .. ] from all backgrounds to apply. Planet is an equal opportunity employer, and committed to providing employment opportunities regardless of race, religious creed, color, national origin, ancestry, physical disability, mental disability, medical condition, genetic information, marital status, sex, gender, gender identity, gender expression, pregnancy, childbirth and breastfeeding, age, sexual orientation, military or veteran status, or any other protected classification, in accordance with applicable federal, state, and local laws. Know Your Rights. Accommodations Planet is an inclusive community and we know that everyone [. .. ]
Job am 19.03.2026 bei Mindmatch.ai gefunden
Milestone One
• AT- 9 Wien
[. .. ] the Sponsor or CRO and the site. Ensure response to feasibility questions are provided in due time. Assist in scheduling and preparation for all types of monitoring [...]
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[...] visits at the medical institution/ research center. Be present and available to respond to monitors during all types of monitoring visits conducted at the medical institution. Track patient enrollment and actively support the medical site and CRO/ Sponsor team in meeting project timelines and enrollment goals. Maintain study specific and general tracking of documents [. .. ] 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
[. .. ] . The CRA conducts monitoring visits as identified by the monitoring plan, study team or department needs to evaluate data accuracy and subject safety required by review [...]
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[...] of regulatory documents, medical records, reported data and device storage, if applicable. The CRA must be able to identify issues, present findings to the site staff, provide retraining if needed, provide problemsolving strategies and communicate findings to the study team and department management via escalation of issues and/or within the monitoring visit report. [. .. ] 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 25.02.2026 bei Mindmatch.ai gefunden
IQVIA
• 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 [...]
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[...] 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 [. .. ] global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https:/ / jobs. iqvia. com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any [. .. ]
Job vor 2 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. Participate in all aspects of Medical Science [...]
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[...] 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 [. .. ] 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
• Bayern
Führungs-/ Leitungspositionen
[. .. ] and clinical development plans. Represent the therapeutic area in governance forums and regulatory interactions. Engage with KOLs and external experts to shape development strategy. Oversee cross-functional alignment [...]
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[...] across Regulatory, Medical Affairs, Commercial, and Clinical Operations. Mentor and guide clinical scientists and medical 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
[. .. ] the Sponsor or CRO and the site. Ensure response to feasibility questions are provided in due time. Assist in scheduling and preparation for all types of monitoring [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] visits at the medical institution/ research center. Be present and available to respond to monitors during all types of monitoring visits conducted at the medical institution. Track patient enrollment and actively support the medical site and CRO/ Sponsor team in meeting project timelines and enrollment goals. Maintain study specific and general tracking of documents [. .. ] 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
• 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 [...]
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[...] 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. [. .. ] 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
Director,
Medical Affairs page is loaded # # Director, Medical Affairslocations: Germany-Hesse-Eschborntime type: Full timeposted on: Posted Todayjob requisition id: 31144421 # # JOB DESCRIPTION:Director Global Medical Affairs-Heart Failure [...]
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[...] Abbott Heart Failure Division Abbotts Heart Failure business is expanding its Global Medical Affairs organization, and we are seeking an [. .. ] 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
• 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 [...]
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[...] 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 [. .. ] 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)
Position Overview The
Medical Affairs Lead for DACH is accountable for developing and executing the Medical Affairs strategy for the 3 countries. They lead the creation and execution of [...]
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[...] the country medical plans in alignment with the business objectives of the Insulets affiliate. The medical plans encompass value-generating activities on medical education, evidence [. .. ] 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 [. .. ]
Job am 08.04.2026 bei Jobleads gefunden
• Berlin
Jobticket
Munich, Germany full time Job ID: 10560 About the Role: As a Manager
Medical Science Liaison Oncology, your main role is to establish collaborations with external healthcare professionals/ experts, [...]
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[...] scientific opinion leaders and institutions to share and discuss evidencebased medical and scientific information about our oncology portfolio. You act as the field subject matter expert in oncology, while planning and executing stakeholder engagement and [. .. ] or lung cancer. Support clinical trials by identifying study sites, participating in SIVs (Site Initiation Visits) , assisting with patient enrollment, and ensuring smooth information exchange. Identify research opportunities, including Investigator Initiated Trials, Real World Evidence, and other evidencegeneration studies. Represent the organization at scientific conferences, advisory boards, and educational events, sharing insights and preparing reports for internal stakeholders. Ensure timely documentation of HCP interactions, compliance with local policies, and accurate reporting of insights and safety information. A Good Match: Advanced [. .. ]
Job am 06.04.2026 bei Jobleads gefunden
Medical Affairs Director Kardiologie (m/w/d) Wohnort bundesweit
• Frankfurt, Hesse
Führungs-/ Leitungspositionen Homeoffice möglich
Medical Affairs Director Kardiologie (m/w/d) Wohnort bundesweit in Frankfurt am Main Sie arbeiten als Medical Affairs Director Kardiologie (m/w/d) für ein renommiertes, stark wachsendes Unternehmen aus der Medizintechnik mit [...]
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[...] internationalen Niederlassungen. Wohnort flexibel. Ihre Chancen: Abwechslungsreiche Tätigkeit mit professionellen und teamfähigen Kollegen Sehr gute Verdienstmöglichkeiten und flexible [. .. ] klinischen Studien und Daten sowie deren Auswirkung auf die medizinische Kommunikations- und Studienstrategie Erstellung, Prüfung und Freigabe medizinisch-wissenschaftlicher Inhalte (z. B. Broschüren, Präsentationen, Trainingsunterlagen) Planung, Vorbereitung und Koordination von Investigator-initiated Trials (IITs) und Sammlung klinischer Daten Beobachtung und Bewertung aktueller wissenschaftlicher Entwicklungen, Leitlinien und klinischer Trends im Bereich Kardiologie Ihr Profil: Abgeschlossenes naturwissenschaftliches oder medizinisches Studium (z. B. Medizin, Pharmazie, Biowissenschaften) Mehrjährige Berufserfahrung im Bereich Medical Affairs, idealerweise in der Medizintechnik bevorzugt in der Kardiologie (structural heart) Erfahrung in [. .. ]
Job am 04.04.2026 bei Jobleads gefunden
Medical Monitor (Gastroenterology)
• München, Bayern
[. .. ] a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Job [...]
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[...] Description PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients safety and well-being. Hybrid working based in Munich Responsibilities Serve as medical point of contact for internal project team, study sites and study sponsor for medical matters related to [. .. ] and per GCP guidelines Advise clients, project teams, sites, regulatory agencies and third-party vendors on medical matters Collaborate with internal departments in the preparation of clinical development plans, protocols, investigator brochures, annual reports, clinical study reports, patient narratives, and scientific presentations Review and analysis of clinical data to ensure the safety of study participants in clinical trials Ensure that the reported trial data is accurate, complete, and verifiable, and that the conduct of the trial is in compliance with the [. .. ]
Job am 24.02.2026 bei Jobleads gefunden
Senior Medical Director-Cell and Gene Therapy (m/w/d)
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
[. .. ] Therapy Center of Excellence (CAGT COE) , a hub of CAGT clinical innovation, is growing We are looking for an exceptional Board-Certified physician to join our team [...]
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[...] as a Medical Strategy Lead to help us expand our CAGT portfolio, with an emphasis on Gene Therapy/ Gene Editing platforms, and advance this dynamic and rapidly expanding area of clinical development. The CAGT Medical Strategy Lead is a subject matter expert with experience in clinical research and clinical trials in CAGT and [. .. ] development plan, mining data to address important clinical questions relevant to the study, reviewing the protocol for scientific/ regulatory soundness and feasibility, logistics challenges, identification of target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape. Support preparation of customer and bid defense meetings, e. g. training and preparation of the assigned project team; provide specific content; ensure presentation focus and content effectively conveys CAGT strategy. Attends and presents at customer meeting, or bid defense or [. .. ]
Job am 21.02.2026 bei Jobleads gefunden
Senior Medical Director-Cell and Gene Therapy (m/w/d)
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Senior
Medical Director-Cell and Gene Therapy (m/w/d) page is loaded # # Senior Medical Director-Cell and Gene Therapy (m/w/d) locations: Frankfurt, Hesse, Germanytime type: Full timeposted on: Posted Todayjob [...]
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[...] requisition id: R1529858Job Overview The IQVIA Cell and Gene Therapy Center of Excellence (CAGT COE) , a [. .. ] development plan, mining data to address important clinical questions relevant to the study, reviewing the protocol for scientific/ regulatory soundness and feasibility, logistics challenges, identification of target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape. Support preparation of customer and bid defense meetings, e. g. training and preparation of the assigned project team; provide specific content; ensure presentation focus and content effectively conveys CAGT strategy. Attends and presents at customer meeting, or bid defense or [. .. ]
Job am 15.01.2026 bei Jobleads gefunden
Senior/ Medical Director (Ophthalmology) 0.5 FTE
Führungs-/ Leitungspositionen
Overview Senior/
Medical Director (Ophthalmology) , 0.5 FTE. TFS Health Science is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical development journey. Join our team as a Senior/ Medical Director (Ophthalmology) . The Senior/ Medical Director is a key member of [. .. ] and answering complex questions related to medical, legal, and regulatory concerns. Responsibilities Expert Guidance: Provide advanced medical input on study design, measurement strategies, and trial protocols, including safety sections and investigator brochures. Comprehensive Safety Oversight: Review safety data such as adverse events, labs, vital signs, ECGs, and clinical trial reports from a medical perspective. Regulatory Risk Support: Conduct senior-level medical reviews of individual cases, cumulative listings, PSURs, PBRERs, DSURs, and Risk Management Plans. Medical Monitoring Signal Detection: Serve as a [. .. ]
Job am 11.12.2025 bei Jobleads gefunden
Medical Science Liaison Complement-Mediated Diseases
• München, Bayern
Medical Science Liaison Complement-Mediated Diseases Seniority level Associate Employment type Full-time Job function Other Pharmaceutical Manufacturing At Sobi, each person brings their unique talents to work as a team [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and make a difference. We are dedicated to developing and delivering innovative therapies to improve the lives of people who [. .. ] various activities locally and regionally. Provide local and regional feedback to HQ when performing Business Development Due Diligence. Deliver inputs to head office led medical programs ahead of launch. Coordinate Investigator Sponsored Studies (ISSs) as appropriate and support studies on the local level. Coordinate medical information enquiries in collaboration with MA/ SMA and HQ in Stockholm. Attend relevant local, regional and global congresses and symposia to represent Sobi and interact with appropriate stakeholders and customers. Represent the scientific interests in internal [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Medical Investigator pro Jahr?
Als Medical Investigator verdient man zwischen EUR 60.000,- bis EUR 90.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Medical Investigator Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 143 offene Stellenanzeigen für Medical Investigator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Medical Investigator Jobs?
Aktuell suchen 26 Unternehmen nach Bewerbern für Medical Investigator Jobs.
Welche Unternehmen suchen nach Bewerbern für Medical Investigator Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Medical Investigator Stellenangebote:
- Thermo Fisher Scientific (3 Jobs)
- TFS Health Science (2 Jobs)
- Helmholtz Association of German Research Centres (2 Jobs)
- Biontech (2 Jobs)
- ICON (2 Jobs)
- Incyte Corporation (2 Jobs)
In welchen Bundesländern werden die meisten Medical Investigator Jobs angeboten?
Die meisten Stellenanzeigen für Medical Investigator Jobs werden derzeit in Bayern (40 Jobs), Nordrhein-Westfalen (14 Jobs) und Niedersachsen (14 Jobs) angeboten.
Zu welchem Berufsfeld gehören Medical Investigator Jobs?
Medical Investigator Jobs gehören zum Berufsfeld Ärzte.
