74 Jobs für Commercial Investigator
Stellenangebote Commercial Investigator Jobs
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
Syneos Health
• AT- 9 Wien
[. .. ] 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 [...]
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 work with, but 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 [. .. ]
Job vor 3 Tagen bei Mindmatch.ai gefunden
Planet
Senior Software Engineer, Geometry
• AT- 3 St. Pölten
Homeoffice möglich
[. .. ] builds, and operates the largest constellation of imaging satellites in history. This constellation delivers an unprecedented dataset of empirical information via a revolutionary cloud-based platform to authoritative [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] figures in commercial, environmental, and humanitarian sectors. We are both a space company and data company all rolled into one. Customers and users across the globe use Planets data to develop new technologies, drive revenue, power research, and solve our worlds toughest obstacles. As we control every component of hardware design, manufacturing, data [. .. ] 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 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 [. .. ]
Job am 02.03.2026 bei Mindmatch.ai gefunden
Syneos Health
• 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 outcomes [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 work with, but 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. [. .. ]
Job am 25.02.2026 bei Mindmatch.ai gefunden
IQVIA
Contract Negotiator 2-FSP-German speaker
• AT- 9 Wien
Essential Functions Develop coordinate the development of
investigator grants and estimates, contracting strategies and proposal text to support the proposal development process. Develop contract language, payment language and budget templates [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] 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 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 [. .. ]
Job am 22.02.2026 bei Mindmatch.ai gefunden
Syneos Health, Inc.
• AT- 9 Wien
[. .. ] 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 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 work with, but 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. [. .. ]
Job am 22.02.2026 bei Mindmatch.ai gefunden
Syneos Health, Inc.
CRA single sponsor-Germany
• AT- 9 Wien
[. .. ] 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 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 work with, but 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. [. .. ]
Job am 22.02.2026 bei Mindmatch.ai gefunden
IQVIA
• AT- 9 Wien
Führungs-/ Leitungspositionen
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] an accredited and internationally recognized school is required 5 years and above of clinical research relevant experience in a CRO or pharma Robust and current knowledge of scientific, clinical, regulatory, commercial and competitive landscape in Dermatology Excellent skills in providing consultation and advice on multiple assignments are required, as well as initiative and flexibility. In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; e. g. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Demonstrated [. .. ]
Job am 19.01.2026 bei Mindmatch.ai gefunden
IQVIA
Senior Director, Medical Strategy Lead-Cardiologist
• AT- 9 Wien
Führungs-/ Leitungspositionen
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] and internationally recognized school is required. 2+ years clinical research relevant experience, including hands on operational delivery and/or drug development experience. Robust and current knowledge of scientific, clinical, regulatory, commercial and competitive landscape in Cardiovascular. Excellent skills in providing consultation and advice on multiple assignments are required, as well as initiative and flexibility. In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; e. g. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Demonstrated [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
• Eschborn, Hessen
Führungs-/ Leitungspositionen
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 guidance for the business group, including support to maintain focus on product performance and safety, ISS, grants, and scientific activities. [. .. ] 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
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 guidance for the business group, including support to maintain focus on product performance and safety, ISS, grants, and scientific activities. [. .. ] 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
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] and internationally recognized school is required 2+ years clinical research relevant experience, including hands on operational delivery and/or drug development experience Robust and current knowledge of scientific, clinical, regulatory, commercial and competitive landscape in Cardiovascular Excellent skills in providing consultation and advice on multiple assignments are required, as well as initiative and flexibility. In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; e. g. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Demonstrated [. .. ]
Job am 24.02.2026 bei Jobleads gefunden
Senior Medical Director-Cell and Gene Therapy (m/w/d)
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] least 5 years clinical research relevant experience, including hands on operational delivery and/or drug development experience in gene therapy/ gene editing. Robust and current knowledge of scientific, clinical, regulatory, commercial and competitive landscape in CAGT, especially in gene therapy/ gene editing. Excellent skills in providing consultation and advice on multiple assignments are required, as well as initiative and flexibility. In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; e. g. Good Clinical Practice (GCP) and International [. .. ]
Job am 21.02.2026 bei Jobleads gefunden
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] least 5 years clinical research relevant experience, including hands on operational delivery and/or drug development experience in gene therapy/ gene editing. Robust and current knowledge of scientific, clinical, regulatory, commercial and competitive landscape in CAGT, especially in gene therapy/ gene editing. Excellent skills in providing consultation and advice on multiple assignments are required, as well as initiative and flexibility. In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; e. g. Good Clinical Practice (GCP) and International [. .. ]
Job am 02.02.2026 bei Jobleads gefunden
Senior Director, Medical Strategic Lead-Psychiatrist
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] practice experience as a CNS physician. 5+ years clinical research relevant experience, including hands on operational delivery and/or drug development experience. Robust and current knowledge of scientific, clinical, regulatory, commercial and competitive landscape in psychiatry and other CNS indications. Excellent skills in providing consultation and advice on multiple assignments are required, as well as initiative and flexibility. In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; e. g. Good Clinical Practice (GCP) and International Conference on [. .. ]
Job am 02.02.2026 bei Jobleads gefunden
• 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
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] and internationally recognized school is required. 2+ years clinical research relevant experience, including hands on operational delivery and/or drug development experience. Robust and current knowledge of scientific, clinical, regulatory, commercial and competitive landscape in Cardiovascular. Excellent skills in providing consultation and advice on multiple assignments are required, as well as initiative and flexibility. In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; e. g. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Demonstrated [. .. ]
Job am 15.01.2026 bei Jobleads gefunden
Führungs-/ Leitungspositionen
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] detection and interpretation. Regulatory Document Contributions: Offer expert medical insight into regulatory submissions and safety-related documentation. Team Client Engagement: Mentor junior medical staff, support SOP/ tool development, and join Commercial Operations in client meetings and presentations. Qualifications Medical Qualifications: Medical Doctor (MD) with specialist medical training in Ophthalmology and at least 5 years experience in clinical practice. Clinical Trial Expertise: Experience serving on safety data review boards or equivalent roles in clinical research. Regulatory Knowledge: Strong understanding of GCP, ICH [. .. ]
Job am 13.01.2026 bei Jobleads gefunden
Senior Director, Medical Strategy Lead-Cardiologist
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
[. .. ] operational advice to internal stakeholders developing proposals: strategy to protocol design/ clinical development plan, mining data, reviewing protocol for scientific/ regulatory soundness and feasibility, identification of target [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape. Support preparation of customer and bid defense meetings, training and preparation of the assigned project team; provide specific content; ensure presentation focus and content effectively conveys cardiovascular strategy; attend and present at customer meetings, bid defense or partnership meetings. Participate [. .. ] accredited and internationally recognized school is required. 2+ years clinical research relevant experience, including handson operational delivery and/or drug development experience. Robust and current knowledge of scientific, clinical, regulatory, commercial and competitive landscape in cardiovascular. Excellent skills in providing consultation and advice on multiple assignments; initiative and flexibility. In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, e. g. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Demonstrated ability to understand customer needs; [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
• Baar, Zug
[. .. ] physicians (Senior Medical Director) , driving medical strategy, execution excellence, and cross-functional collaboration across our global organization. You will work closely with R D, global clinical operations, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] regulatory, and commercial partners to advance tumor-based programs from protocol development through submission readiness, ensuring scientific rigor, audit preparedness, and patient-focused impact. What Youll Do Serve as the medical expert and key technical contributor for a tumor-based clinical study or program evaluating 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 [. .. ]
Job gestern bei Jobleads gefunden
Director, MEG Lead Oncology, Medical Evidence Generation
• Boudry, Neuenburg
Führungs-/ Leitungspositionen
[. .. ] Evidence Generation (MEG) Lead in Oncology at Bristol Myers Squibb oversees evidence generation for the Oncology portfolio, including Clinical Research Collaborations (CRCs) , Medical Affairs Sponsored Studies [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] (MAST) , and Investigator-Sponsored Research Studies (ISRs) , ensuring alignment with internal strategies to accelerate pipeline development. Key responsibilities include fostering relationships with thought leaders, managing the lifecycle of CRCs and ISRs, and addressing evidence gaps by partnering with academic and professional networks. Responsibilities will include, but are not limited to, the following [. .. ] (MD, Ph D, or Pharm D or the equivalent) required with extensive, relevant scientific, and/or clinical experience. At least 7 years of experience in pharmaceutical clinical development, Medical Affairs or relevant Commercial experience; previous customer-facing role experience highly desirable. Demonstrated ability to strategically analyze data generation opportunities with minimal supervision Demonstrated ability to develop and sustain high-performing relationships with external thought leaders and internal matrix stakeholders Adeptness at building credibility with external investigators and collaborative partners competently balancing business and [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Senior Software Engineer, Geometry
• St. Pölten, Niederösterreich Niederoesterreich
Homeoffice möglich
[. .. ] builds, and operates the largest constellation of imaging satellites in history. This constellation delivers an unprecedented dataset of empirical information via a revolutionary cloud-based platform to authoritative [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] figures in commercial, environmental, and humanitarian sectors. We are both a space company and data company all rolled into one. Customers and users across the globe use Planets data to develop new technologies, drive revenue, power research, and solve our worlds toughest obstacles. As we control every component of hardware design, manufacturing, data [. .. ] 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 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 [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Senior Medical Science Liaison-South Central Region
• Darmstadt, Hessen
Spring Works Therapeutics, a healthcare company of Merck KGa A, Darmstadt, Germany, is a
commercial-stage biopharmaceutical company dedicated to improving the lives of patients with rare tumors. We developed [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and are commercializing the first and only FDA and EC approved medicine for adults with desmoid tumors and the first and only FDA and EC approved medicine for both adults and children with neurofibromatosis type [. .. ] data and clinical trendsto Medical Affairs andtranslate this information into strategic recommendations to enhance science and advance patient care Act as primary liaison to investigators interested in developing and performing investigator-initiated research Collaborate with the Clinical Operations organization to enhance patient enrollment in company-sponsored clinical trials by identifying appropriate clinical trial sites, supporting clinical trial awareness, and interacting with investigators in ongoing studies Serve as medical lead and provide scientific support at medical congresses, staff disease state booths, participate [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Senior Software Engineer, Geometry
• Berlin
Homeoffice möglich
[. .. ] builds, and operates the largest constellation of imaging satellites in history. This constellation delivers an unprecedented dataset of empirical information via a revolutionary cloud-based platform to authoritative [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] figures in commercial, environmental, and humanitarian sectors. We are both a space company and data company all rolled into one. Customers and users across the globe use Planets data to develop new technologies, drive revenue, power research, and solve our worlds toughest obstacles. As we control every component of hardware design, manufacturing, data [. .. ] 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 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, hybrid role which will require you to work from our Berlin office 3 days per week. Impact Youll Own Perform ongoing space imaging [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
Senior Software Engineer, Geometry
Homeoffice möglich
[. .. ] builds, and operates the largest constellation of imaging satellites in history. This constellation delivers an unprecedented dataset of empirical information via a revolutionary cloud-based platform to authoritative [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] figures in commercial, environmental, and humanitarian sectors. We are both a space company and data company all rolled into one. Customers and users across the globe use Planets data to develop new technologies, drive revenue, power research, and solve our worlds toughest obstacles. As we control every component of hardware design, manufacturing, data [. .. ] 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 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 [. .. ]
Job am 06.03.2026 bei Jobleads gefunden
Medical Science Liaison
• Lausanne, Waadt
[. .. ] dermatologists, and other relevant healthcare stakeholders Engage in high-level scientific exchange on products, clinical data, and therapeutic strategies in dermatology Present and discuss clinical trial data, including [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] support of Investigator-Initiated Studies (IIS) Support advisory boards, medical education events, and national/ international congresses Collaborate cross-functionally with Medical Affairs, Market Access, and Commercial teams in full compliance with regulatory requirements Gather and communicate medical insights from the field to inform strategic planning Your Profile Advanced scientific degree (e. g. , MD, Pharm D, Ph D, or equivalent in life sciences) Proven experience as an MSL or in a comparable medical affairs role within the pharmaceutical [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Commercial Investigator pro Jahr?
Als Commercial Investigator verdient man zwischen EUR 60.000,- bis EUR 90.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Commercial Investigator Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 74 offene Stellenanzeigen für Commercial Investigator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Commercial Investigator Jobs?
Aktuell suchen 15 Unternehmen nach Bewerbern für Commercial Investigator Jobs.
Welche Unternehmen suchen nach Bewerbern für Commercial Investigator Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Commercial Investigator Stellenangebote:
- IQVIA (10 Jobs)
- Abbott (7 Jobs)
- Syneos Health (2 Jobs)
- Planet (1 Job)
- Amplity Health (1 Job)
In welchen Bundesländern werden die meisten Commercial Investigator Jobs angeboten?
Die meisten Stellenanzeigen für Commercial Investigator Jobs werden derzeit in Hessen (16 Jobs), Sachsen-Anhalt (14 Jobs) und Bayern (11 Jobs) angeboten.
Zu welchem Berufsfeld gehören Commercial Investigator Jobs?
Commercial Investigator Jobs gehören zum Berufsfeld Revision.
