96 Jobs für Clinical Trial Investigator
Stellenangebote Clinical Trial 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 [...]
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[...] 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 development of trial documents. ML drives execution for assigned projects in collaboration with Clinical Research teams and other cross-functional stakeholders. Key Responsibilities Provides medical input to Clinical Trial Protocol, Investigators Brochure, Informed Consent Form, Independent Data Monitoring Committee Charter, Statistical Analysis Plan, Medical Monitoring Plan, Clinical Trial Report, Clinical Trial Overview Statements [. .. ] 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 [...]
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[...] 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 responsibilities while [. .. ] 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 [...]
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[...] 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 reports, communication logs, and other required project documents as per SOPs and SMP, within required timelines. [. .. ]
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 [...]
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[...] 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 the following: Act as the main line of communication between the Sponsor or CRO and the site. Ensure response to feasibility [. .. ] 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 [...]
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[...] 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 of the following: Actas the main line of communication between the Sponsor or CRO and the site. Ensureresponse to feasibility questions [. .. ] 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 [...]
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[...] 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 above, with [. .. ]
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 [...]
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[...] 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 cooperation with Study Startup, Clinical Operations and Process Improvement. Project Responsibilities Conduct site identification activities, including discussion of clinical trial protocols and collection of site identification questionnaires during the startup phase of the clinical trials. Define the main study objectives and the optimal site profile. Create initial list of potential sites. Communicate with project teams on project/ regional level to fine-tune strategy and methodology of initial and follow-up [. .. ] 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 [...]
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[...] 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. [. .. ] to ensure IP is appropriately (re) labelled, imported and released/returned. 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, followup letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/ Site Management [. .. ]
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 [. .. ] 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 [. .. ] or clinical research organization clinical site contracting experience Good negotiating and communication skills with ability to challenge. Strong legal, financial and/or technical writing skills. Strong understanding of regulated clinical trial environment and knowledge of drug development process. Good understanding of clinical trial contract management. Fluent in English and German language IQVIA is a leading 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 [. .. ]
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 [...]
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[...] 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. [. .. ] to ensure IP is appropriately (re) labelled, imported and released/returned. 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, followup letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/ Site Management [. .. ]
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. [. .. ] to ensure IP is appropriately (re) labelled, imported and released/returned. 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, followup letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/ Site Management [. .. ]
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 [...]
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[...] 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 [. .. ] portfolio through scientific and clinical expertise. The Medical Strategy Lead will be charged with using his/ her clinical, scientific, and operational knowledge to harness the vast IQVIA data and clinical trial resources to develop innovative, data-driven, and patient-centered solutions for Dermatology trials. The Medical Strategy Lead will provide senior clinical and scientific expertise to all IQVIA divisions as requested and will collaborate closely with indication-specific teams to develop integrated strategies for Dermatology. The Medical Strategy Lead will also [. .. ] 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 [. .. ]
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 [...]
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[...] 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 [. .. ] portfolio through scientific and clinical expertise. The Medical Strategy Lead will be charged with using his/ her clinical, scientific, and operational knowledge to harness the vast IQVIA data and clinical trial resources to develop innovative, data-driven, and patient-centered solutions for Cardiovascular trials. The Medical Strategy Lead will provide senior clinical and scientific expertise to all IQVIA divisions as requested and will collaborate closely with indication-specific teams to develop integrated strategies for Cardiovascular clinical trials, mostly Phases 1-3. [. .. ] 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 [. .. ]
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 sites [...]
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[...] 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. Ensure response to feasibility questions are provided in due time. Assist in scheduling and preparation for all types [. .. ] 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
[. .. ] 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 [...]
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[...] 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 [. .. ] support to maintain focus on product performance and safety, ISS, grants, and scientific activities. In addition, Director will work cross functionally to support the review, implementation and publication of clinical trial results. This role provides input to establish the range plans and goals for clinical science, and is responsible for the implementation and maintenance of the clinical researchrelated policies, processes and procedures related to their respective functional areas. Director provides leadership and direction to product performance testing and evaluation, use clinical [. .. ] 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
[. .. ] 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 [. .. ] support to maintain focus on product performance and safety, ISS, grants, and scientific activities. In addition, Director will work cross functionally to support the review, implementation and publication of clinical trial results. This role provides input to establish the range plans and goals for clinical science, and is responsible for the implementation and maintenance of the clinical research-related policies, processes and procedures related to their respective functional areas. Director provides leadership and direction to product performance testing and evaluation, use [. .. ] 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 [. .. ] portfolio through scientific and clinical expertise. The Medical Strategy Lead will be charged with using his/ her clinical, scientific, and operational knowledge to harness the vast IQVIA data and clinical trial resources to develop innovative, data-driven, and patient-centered solutions for Cardiovascular trials. The Medical Strategy Lead will provide senior clinical and scientific expertise to all IQVIA divisions as requested and will collaborate closely with indication-specific teams to develop integrated strategies for Cardiovascular clinical trials, mostly Phases 1-3. [. .. ] 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 [. .. ]
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 [...]
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[...] 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 [. .. ] through scientific and clinical expertise. The CAGT Medical Strategy Lead will be charged with using his/ her clinical, scientific, and operational knowledge to harness the vast IQVIA data and clinical trial resources to develop innovative, data-driven, and patient-centered solutions for CAGT trials. The CAGT Medical Strategy Lead will provide clinical and scientific expertise to all IQVIA divisions as requested and will collaborate closely with indication-specific teams to develop integrated strategies for CAGT clinical trials and studies. 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 [. .. ]
Job am 21.02.2026 bei Jobleads gefunden
• 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 [...]
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[...] 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 [. .. ] through scientific and clinical expertise. The CAGT Medical Strategy Lead will be charged with using his/ her clinical, scientific, and operational knowledge to harness the vast IQVIA data and clinical trial resources to develop innovative, data-driven, and patient-centered solutions for CAGT trials. The CAGT Medical Strategy Lead will provide clinical and scientific expertise to all IQVIA divisions as requested and will collaborate closely with indication-specific teams to develop integrated strategies for CAGT clinical trials and studies. 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 [. .. ]
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 [. .. ] portfolio through scientific and clinical expertise. The Medical Strategy Lead will be charged with using his/ her clinical, scientific, and operational knowledge to harness the vast IQVIA data and clinical trial resources to develop innovative, data-driven, and patient-centered solutions for CNS trials. The Medical Strategy Lead will provide senior clinical and scientific expertise to all IQVIA divisions as requested and will collaborate closely with indication-specific teams to develop integrated strategies for CNS clinical trials, mostly Phases 1-3. [. .. ] 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 [. .. ]
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 [. .. ] portfolio through scientific and clinical expertise. The Medical Strategy Lead will be charged with using his/ her clinical, scientific, and operational knowledge to harness the vast IQVIA data and clinical trial resources to develop innovative, data-driven, and patient-centered solutions for Cardiovascular trials. The Medical Strategy Lead will provide senior clinical and scientific expertise to all IQVIA divisions as requested and will collaborate closely with indication-specific teams to develop integrated strategies for Cardiovascular clinical trials, mostly Phases 1-3. [. .. ] 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 [. .. ]
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 [...]
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[...] 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, [. .. ] on medical issuesproviding clear, informed guidance 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 [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Clinical Trial Physician, Oncology
• Baar, Zug
At Novocure, every role contributes to extending the lives of people living with cancer. As our new Senior Medical Director/ Medical Director,
Clinical Development, youll play a key part [...]
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[...] in this mission. As a key member of our multi-disciplinary oncology team, you will serve as a medical expert supporting Tumor Treating Fields (TT Fields) Therapy clinical programs. Depending on experience and level, you will either lead a clinical study (Medical Director) or [. .. ] the safety and efficacy of TT Fields delivered concomitantly with standard therapy in patients with cancer Drive clinical development strategy including protocol authoring, regulatory and ethics committee submissions, study initiation, investigator communication, safety and medical monitoring, data screening and analysis, and publication initiatives Author and oversee key clinical documents including study protocols and Clinical Study Reports (CSRs) , ensuring submission readiness and inspection/ audit preparedness Establish and lead physician teams and key opinion leader relationships to support study execution and overall [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Medical Science Liaison (MSL) Gastroenterology (with fluent written and spoken German)
• Zug
[. .. ] on their vantage point and perspective. Prioritize franchise customer-based initiatives and field responsibilities, while balancing administrative duties and project responsibilities. Leverages knowledge of standards of care and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Janssen company/ investigator sponsored clinical trials and competitor landscape to facilitate external-internal research communication. Engages with external investigators regarding unsolicited research inquiries and act as liaison to R D, Medical Affairs and operations teams. Provides clinical trial support to identify potential sites, resolve issues with enrolled sites, and participate in meetings as appropriate, including site initiation visits and investigator launch meetings. Qualifications Scientific degree in Medicine, Pharmacy, or Natural Sciences (MD or Ph D an asset) . Experience or strong interest in gastroenterology, immunology, and/or Medical Affairs. [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Site Director Clinical Research-Nuremberg (m/f/d)
• Nürnberg, Bayern
Führungs-/ Leitungspositionen
Future Meds was founded by a team with unparalleled SMO experience, united by a genuine passion for
clinical research, patients, and providing innovative pharma companies with best-in-class patient recruitment [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and retention. We believe that clinical research should be a treatment option for all patients. Future Meds is a growing network of modern, dedicated research sites providing both site management and patient recruitment services to pharma companies [. .. ] to the Managing Director Germany, with whom you will work very closely, and collaborate with our Berlin and Offenbach am Main sites, our sponsor and CRO partners, and the local investigator community. At the heart of this role is the partnership with your Principal Investigators. The Site Director PI relationship is fundamental to how a dedicated research site operates and succeeds. You will be the operational backbone that allows investigators to focus on the clinical and scientific aspects of each trial, and your ability to build that trust and working rhythm will be central to everything the site achieves. This is an ideal role for an ambitious clinical research professional who is ready to step into site leadership and make a real impact, combining operational, scientific, and people leadership in one [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical Trial Investigator pro Jahr?
Als Clinical Trial Investigator verdient man zwischen EUR 65.000,- bis EUR 95.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Trial Investigator Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 96 offene Stellenanzeigen für Clinical Trial Investigator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trial Investigator Jobs?
Aktuell suchen 25 Unternehmen nach Bewerbern für Clinical Trial Investigator Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Trial Investigator Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Trial Investigator Stellenangebote:
- IQVIA (10 Jobs)
- Dr. Falk Pharma GmbH (3 Jobs)
- PSI CRO (3 Jobs)
- Thermo Fisher Scientific (3 Jobs)
- Syneos Health (2 Jobs)
- Milestone One (2 Jobs)
In welchen Bundesländern werden die meisten Clinical Trial Investigator Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trial Investigator Jobs werden derzeit in Bayern (14 Jobs), Hessen (13 Jobs) und Berlin (12 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trial Investigator Jobs?
Clinical Trial Investigator Jobs gehören zum Berufsfeld Medizinisch-technische Assistenz / MTA.
