131 Jobs für Clinical Support Investigator
Stellenangebote Clinical Support Investigator Jobs
Job vor 2 Tagen bei StepStone gefunden
Dr. Falk Pharma GmbH
• Freiburg
Führungs-/ Leitungspositionen Homeoffice möglich
[. .. ] firmly believe that medical progress can only be achieved by working together. That is why we are looking for: Your tasks Serves as medical lead (ML) for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the company-sponsored clinical trials and development programs. Responsible for guiding the clinical development strategy and ensuring the scientific integrity of clinical trials. ML collaborates with Clinical Research teams and serves as a key liaison between Clinical Research and Global Safety teams. ML manages all medical aspects of clinical trials and contributes to the [. .. ] submitting necessary documentation to regulatory authorities, such as the FDA or EMA Supports Global Safety with medical expertise in the review of adverse events and safety issues, as requested Provides support in the review of scientific publications (abstracts, presentations, and manuscripts) Supports review of concepts for investigator-initiated studies Contributes to company-internal process improvement initiatives (e. g. SOP updates) Your qualification Physician/ medical license holder A minimum of 5 years of clinical development research, or related clinical research experience within the industry (pharmaceutical, biotech, CRO) at an international (Europe, USA, Australia) level is required Knowledge in [. .. ]
Neu Job vor 4 Std. 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 in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 and support to grow into full leadership [. .. ] 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 [. .. ]
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
Syneos Health
• AT- 9 Wien
Description On-site monitor open to diverse EMEA countries. Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to [. .. ] ability to perform activities for assigned sites working with study start-up and regulatory. Conduct of all remote and on-site monitoring activities through all study stages. Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness. Reconciles contents of the ISF with the Trial Master File (TMF) . Ensures the investigator/ physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations. Documents activities via confirmation letters, follow-up letters, trip [. .. ] (only as applicable) . Review data using data trend reports and knowledge of site practices. Ensure the resolution of data queries within agreed timelines. Utilize available hardware and software to support efficient study data collection and review. Maintain effective, accurate and timely communication with site staff and project team, and ensure appropriate issue escalation and resolution as per SOPs with a focus on issue prevention. Maintains clinical tracking and management systems. Ensure all assigned sites are trained and compliant with requirements [. .. ]
Job vor 7 Tagen bei Mindmatch.ai gefunden
Milestone One
Clinical Site Coordinator
• 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 in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 role may include, but not limited to, any/ all of [. .. ] 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 vor 12 Tagen bei Mindmatch.ai gefunden
PSI CRO
• AT- 9 Wien
Company Description 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 The Milestone One Site Coordinator role supports a Clinical Study Site in clinical trial related activities according to ICH-GCP, protocol requirements within Study specific defined timelines and enrollment goals. The function of the role may include, but not limited to, any/ all [. .. ] accountability and reconciliation of investigational products and clinical supplies. Collect, handleand maintainall site-specific regulatory documents as needed. Facilitateand support the contract and budget negotiations at the site level. Support Investigator and Site payments and processes as needed. Scheduleand/or performstudy procedures as per study requirements and delegation of responsibilities. Preparefor and participatein onsite study audits or regulatory agency inspections. Qualifications A university degree in Life Science, preferably in pharmacy, nursing or lab analytics. Minimum of 2 years of on-the-[. .. ]
Job am 06.03.2026 bei Mindmatch.ai gefunden
Alimentiv
Join our Talent Pool-Clinical Research Associates (Eastern Europe)
• 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 our side-note that this Talent Pool is not [. .. ] 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
• 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 [. .. ] any potential risks or issues to timelines or objectives. In cooperation with Legal, perform due diligence check of regulatory and legal limitations applicable to the 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
Syneos Health
CRA single sponsor-Germany
• AT- 9 Wien
Description CRA single sponsor-Germany Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and commercial insights into [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to [. .. ] each subject/ patient, as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/ patient. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol deviation/ violations and pharmacovigilance issues. For the Clinical Monitoring/ Site Management Plan (CMP/ SMP) : Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) is accurate and complete. Applies query resolution techniques remotely and on site, and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelines. Utilizes available hardware and software to support the effective conduct of the clinical project data review and capture. Verifies site compliance with electronic data capture requirements. May perform investigational product (IP) inventory, reconciliation and reviews storage and security. Verifies the IP has been dispensed and administered to subjects/ patients according to the protocol. Verifies issues or risks [. .. ]
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] budget 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 Scope of Work and Project Plan, within the agreed project [. .. ] 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 am 23.02.2026 bei Mindmatch.ai gefunden
Takko Mode Markt GmbH
• AT- 4 Linz
[. .. ] der CI/ CD-Methoden durch Einsatz von State-of-the-Art-Technologien wie Kubernetes, Docker/ Podman, Ansible, etc. Konzeption und Durchführung von Projekten im E-Learning Umfeld Inhaltliche Unterstützung des
Support-Teams Anfertigung [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] von technischer Dokumentation Administration klinischer, gesponserter und akademischer Studien an der Universitätsklinik für Kinder- und Jugendheilkunde Professionelle Betreuung von Patienten im Alter von 0-18 Jahren (Blutabnahmen, Kontrollen der Vitalfunktionen, Anamnesen etc. ) sowie Begleitung der Betreuungspersonen Organisatorische Unterstützung der klinisch und wissenschaftlich tätigen Prüfärzt innen bei der [. .. ] Studien: Koordination von : Patient innenflusssteuerung, Visitenvorbereitung, Dokumentation, Logistik, Datenmanagement, Monitoring Kooperation mit dem Kompetenzzentrum für Klinische Studien (KKS) an der Medizinischen Fakultät der JKU und dem Service Center for Clinical Research (SCCR) des Kepler Universitätsklinikums Organisation und Koordination von Diagnostik, Labor, Probenversand und gegebenenfalls Prüfmedikation Vorbereitung und Begleitung von Monitorbesuchen, Audits und Behördeninspektionen Kommunikation mit Sponsor innen, Studienzentralen, Principal Investigator innen, Behörden, Ethikkommission, etc Teilnahme an nationalen und internationalen Investigator innen Meetings Mitarbeit an sozial- und wirtschaftswissenschaftlichen Forschungsinfrastrukturen (u. a. AUSSDA The Austrian Social Science Data Archive, ISSP/ SSÖ Sozialer Survey Österreich, GGP. at Gender and Generations Programme Austria und Digital Skills Austria) Aufbereitung und Dokumentation von Forschungsdaten und Metadaten [. .. ]
Job am 22.02.2026 bei Mindmatch.ai gefunden
Syneos Health, Inc.
CRA Germany or Austria-single-client
• AT- 9 Wien
[. .. ] 9, 2025 Location: Vienna, 1, Austria Job ID: 25104265-OTHLOC-3538-2DR Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to [. .. ] each subject/ patient, as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/ patient. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol deviation/ violations and pharmacovigilance issues. Per the Clinical Monitoring/ Site Management Plan (CMP/ SMP) : Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) is accurate and complete. Applies query resolution techniques remotely and on site, and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelines. Utilizes available hardware and software to support the effective conduct of the clinical study data review and capture. Verifies site compliance with electronic data capture requirements. May perform investigational product (IP) inventory, reconciliation and reviews storage and security. Verifies the IP has been dispensed and administered to subjects/ patients according to the protocol. Verifies issues or risks [. .. ]
Job am 22.02.2026 bei Mindmatch.ai gefunden
Syneos Health, Inc.
• AT- 9 Wien
Updated: Yesterday Location: Vienna, 1, Austria Job ID: 25105750-OTHLOC-3538-2DR Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to [. .. ] each subject/ patient, as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/ patient. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol deviation/ violations and pharmacovigilance issues. Per the Clinical Monitoring/ Site Management Plan (CMP/ SMP) : Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) is accurate and complete. Applies query resolution techniques remotely and on site, and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelines. Utilizes available hardware and software to support the effective conduct of the clinical study data review and capture. Verifies site compliance with electronic data capture requirements. May perform investigational product (IP) inventory, reconciliation and reviews storage and security. Verifies the IP has been dispensed and administered to subjects/ patients according to the protocol. Verifies issues or risks [. .. ]
Job am 22.02.2026 bei Mindmatch.ai gefunden
IQVIA
Senior Director, Medical Strategy Lead-Dermatology
• AT- 9 Wien
Führungs-/ Leitungspositionen
The IQVIA Dermatology Center of Excellence, a hub of Dermatology
clinical innovation, is looking for exceptional Board-Certified physicians to join our team as a Medical Strategy Lead to help [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] us expand our Dermatology portfolio and advance this dynamic and rapidly expanding area of clinical development. The Dermatology Medical Strategy Lead is a subject matter expert with experience in clinical research [. .. ] design/ clinical development plan, mining data to address important clinical questions relevant to the study, reviewing the protocol for scientific/ regulatory soundness and feasibility, 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 strategy. Attends and presents at customer meeting, or bid defense or partnership meetings, as required. Participates in strategic business development activities including presentations [. .. ]
Job am 19.01.2026 bei Mindmatch.ai gefunden
IQVIA
• AT- 9 Wien
Führungs-/ Leitungspositionen
The IQVIA Cardiovascular Center of Excellence, a hub of Cardiovascular
clinical innovation, is looking for an exceptional Board-Certified cardiologist to join our team as a Medical Strategy Lead to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] help us expand our Cardiovascular portfolio and advance this dynamic and rapidly expanding area of clinical development. The Cardiovascular Medical Strategy Lead is a subject matter expert with experience in clinical [. .. ] design/ clinical development plan, mining data to address important clinical questions relevant to the study, reviewing the protocol for scientific/ regulatory soundness and feasibility, 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 Cardiovascular strategy. Attends and presents at customer meeting, or bid defense or partnership meetings, as required. Participates in strategic business development activities including [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Clinical Trials Site Coordinator
• Zug
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. Please submit CV in English. Job Description Milestone One Site Coordinator supports trial sites in all related activities according to ICHGCP, protocol requirements within studyspecific defined timelines and enrollment goals. Act as the main line of communication between the Sponsor or CRO and the site. [. .. ] 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. Build and sustain longlasting relationships with existing and potential clients (sponsors, CROs, medical institutions) . Qualifications College [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
• Eschborn, Hessen
Führungs-/ Leitungspositionen
[. .. ] Division Abbotts Heart Failure business is expanding its Global Medical Affairs organization, and we are seeking an experienced Director, Global Medical Affairs to help shape the future [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of mechanical circulatory support and hemodynamic management worldwide. This strategic leadership role reports directly to the Chief Medical Officer/ Divisional Vice President, Global Medical Affairs and will be based in Europe. Why This 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 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 vor 7 Tagen bei Jobleads gefunden
Director, Medical Affairs
• Eschborn, Hessen
Führungs-/ Leitungspositionen
[. .. ] Division Abbotts Heart Failure business is expanding its Global Medical Affairs organization, and we are seeking an experienced Director, Global Medical Affairs to help shape the future [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of mechanical circulatory support and hemodynamic management worldwide. This strategic leadership role reports directly to the Chief Medical Officer/ Divisional Vice President, Global Medical Affairs and will be based in Europe. Why This 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 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 10.03.2026 bei Jobleads gefunden
Senior Director, Medical Strategy Lead-Cardiologist
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
The IQVIA Cardiovascular Center of Excellence, a hub of Cardiovascular
clinical innovation, is looking for exceptional Board-Certified cardiologist to join our team as a Medical Strategy Lead to help [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] us expand our Cardiovascular portfolio and advance this dynamic and rapidly expanding area of clinical development. The Cardiovascular Medical Strategy Lead is a subject matter expert with experience in clinical research [. .. ] design/ clinical development plan, mining data to address important clinical questions relevant to the study, reviewing the protocol for scientific/ regulatory soundness and feasibility, 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 Cardiovascular strategy. Attends and presents at customer meeting, or bid defense or partnership meetings, as required. Participates in strategic business development activities including [. .. ]
Job am 24.02.2026 bei Jobleads gefunden
Senior Medical Director-Cell and Gene Therapy (m/w/d)
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Overview The IQVIA Cell and Gene Therapy Center of Excellence (CAGT COE) , a hub of CAGT
clinical innovation, is growing We are looking for an exceptional Board-Certified physician [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to join our team 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 [. .. ] 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 partnership meetings, as required. Participates in strategic business development activities including [. .. ]
Job am 21.02.2026 bei Jobleads gefunden
Senior Medical Director-Cell and Gene Therapy (m/w/d)
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
[. .. ] locations: Frankfurt, Hesse, Germanytime type: Full timeposted on: Posted Todayjob requisition id: R1529858Job Overview The IQVIA Cell and Gene Therapy Center of Excellence (CAGT COE) , a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] hub of CAGT clinical innovation, is growing We are looking for an exceptional Board-Certified physician to join our team 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 [. .. ] 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 partnership meetings, as required. Participates in strategic business development activities including [. .. ]
Job am 02.02.2026 bei Jobleads gefunden
Senior Director, Medical Strategic Lead-Psychiatrist
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Overview The IQVIA CNS Center of Excellence, a hub of CNS
clinical innovation, is looking for an exceptional Board-Certified psychiatrist to join our team as a Medical Strategy Lead [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to help us expand our CNS portfolio and advance this dynamic and rapidly expanding area of clinical development. The CNS Medical Strategy Lead is a subject matter expert with experience in clinical [. .. ] design/ clinical development plan, mining data to address important clinical questions relevant to the study, reviewing the protocol for scientific/ regulatory soundness and feasibility, 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 CNS strategy. Attends and presents at customer meeting, or bid defense or partnership meetings, as required. Participates in strategic business development activities including [. .. ]
Job am 02.02.2026 bei Jobleads gefunden
Country Medical Director (f/m/d) , Germany
• München, Bayern
Führungs-/ Leitungspositionen
A Typical Day Might Include The Following Serve as the key Regeneron medical representative in Germany for internal stakeholders (Medical Affairs,
Clinical Development, Operations, Regulatory, Commercial) and external stakeholders [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] (medical societies, academic institutions, key opinion leaders) . Represent Medical Affairs in crossfunctional internal meetings, partnering closely with global Therapeutic Area Medical Directors and Medical Affairs teams such as HEOR, Medical Education and Medical Information to optimize strategic and tactical planning. Provide medical leadership to clinical development in Germany, including identification of centers of excellence, key investigators, and relevant clinical sites; support investigator meetings and targeted recruitment efforts. Maintain deep scientific and clinical expertise in oncology/ hematology and a strong understanding of clinical decisionmaking and patient journeys. Lead scientific engagement with external experts to advance the understanding and appropriate use of Regeneron medicines. Bring the German patient and physician voice into crossfunctional strategy [. .. ]
Job am 19.01.2026 bei Jobleads gefunden
Senior Director, Medical Strategy Lead-Cardiologist
• Wien
Führungs-/ Leitungspositionen
The IQVIA Cardiovascular Center of Excellence, a hub of Cardiovascular
clinical innovation, is looking for an exceptional Board-Certified cardiologist to join our team as a Medical Strategy Lead to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] help us expand our Cardiovascular portfolio and advance this dynamic and rapidly expanding area of clinical development. The Cardiovascular Medical Strategy Lead is a subject matter expert with experience in clinical [. .. ] design/ clinical development plan, mining data to address important clinical questions relevant to the study, reviewing the protocol for scientific/ regulatory soundness and feasibility, 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 Cardiovascular strategy. Attends and presents at customer meeting, or bid defense or partnership meetings, as required. Participates in strategic business development activities including [. .. ]
Job am 15.01.2026 bei Jobleads gefunden
Senior/ Medical Director (Ophthalmology) 0.5 FTE
Führungs-/ Leitungspositionen
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] their clinical development journey. Join our team as a Senior/ Medical Director (Ophthalmology) . The Senior/ Medical Director is a key member of the Project Delivery team, working independently to manage safety and medical matters in line with company policies, standard operating procedures (SOPs) , and regulatory requirements. With deep medical expertise, [. .. ] 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 medical monitor in trials, perform literature reviews, and contribute to signal detection and interpretation. Regulatory Document Contributions: Offer expert medical insight into regulatory submissions and safety-[. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical Support Investigator pro Jahr?
Als Clinical Support Investigator verdient man zwischen EUR 45.000,- bis EUR 70.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Support Investigator Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 131 offene Stellenanzeigen für Clinical Support Investigator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Support Investigator Jobs?
Aktuell suchen 28 Unternehmen nach Bewerbern für Clinical Support Investigator Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Support Investigator Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Support Investigator Stellenangebote:
- IQVIA (11 Jobs)
- Dr. Falk Pharma GmbH (3 Jobs)
- PSI CRO (3 Jobs)
- GULP experts united (3 Jobs)
- Alexion Pharmaceuticals (3 Jobs)
- Syneos Health (2 Jobs)
In welchen Bundesländern werden die meisten Clinical Support Investigator Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Support Investigator Jobs werden derzeit in Bayern (22 Jobs), Hessen (15 Jobs) und Berlin (12 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Support Investigator Jobs?
Clinical Support Investigator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
