77 Jobs für Commercial Investigator
Stellenangebote Commercial Investigator Jobs
Job gestern bei Jooble gefunden
• München
Study Physician sponsor dedicated in 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] requirements too) Medical Monitoring experience preferred Pharma company experience preferred. However, CRO experience is fine. If no industry experience, the in addition to clinical practice they should have worked principal investigator/ sub investigator in clinical trials for a reasonable amount of time. Travel-15-20 depending on the study requirements. Key words to look for in potential CVs-Clinical Trial protocol-writing/ reviewing, Identify medically relevant critical data, Medical risks, risk mitigation/ monitoring plan, Medical quality review/clinical quality monitoring, Jreview, [. .. ]
Job vor 4 Tagen bei Jooble gefunden
Sr CRA in oncology-Sponsor dedicated-Home Based Germany
• München
[. .. ] CRA in oncology-Sponsor dedicated-Home Based Germany Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] 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 via [. .. ]
Job am 14.01.2026 bei Jooble gefunden
• München
Freiberuflich
Freelance CRA 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 to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 14.01.2026 bei Jooble gefunden
Incyte Corporation
(Senior) Medical Manager Dermatology (m/f/d)
• München
[. .. ] and supports the development of the local medical strategy and medical plans within the therapeutic area of dermatology. The role provides a bridge between Clinical Development, Medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Affairs and the commercial organization. The (Senior) Medical Manager Dermatology will play a key role in developing and executing the medical and scientific (non-promotional) strategy for the German Immunology portfolio/ therapeutic area and will be involved in a wide range of activities for Incyte IAI drugs both licensed as well as those in [. .. ] as registry/ database projects, epidemiological surveys, and PMOS studies) . Provide the required oversight to manage review, approval and conduct of IIR studies Collaborate with clinical trial teams and support investigator engagements (e. g. review new clinical study protocols, identifying potential investigators/ sites, conducting feasibility surveys) Supports adaptation of international/ local training and scientific material in collaboration with marketing and other internal stakeholders Supports development of publication plans and covers country data generation needs Provides scientific in-house training for MSLs, [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Incyte Corporation
• München
Führungs-/ Leitungspositionen
[. .. ] respective treatment area and extensive network the Associate Director Medical Affairs Dermatology establishes and fosters collaborations with external partners and provides a bridge between clinical development, medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] affairs and the commercial organization at a senior mastery level. He/ she provides critical insights into the countrys medical affairs plan for the respective disease areas, ensuring that it complements the companys development plan and adheres to the highest scientific standards. Constantly build and maintain expertise in the assigned areas IAI areas (dermatologic entities, [. .. ] leadership and actively contributes to market access dossiers Oversee the agenda development, content creation, and execution for educational symposia, internal meetings/ summits and advisory boards Supports advisory board meetings and investigator meetings. Provides support for content development and delivering clinical presentations at medical meetings Develops and delivers presentations to colleagues and management as needed, provides strong input to briefing documents, written communications, Frequently Asked Questions documents, backgrounders, newsletters, slide decks, and medical information letters etc. MD, Pharm D or Ph D in life [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Thermo Fisher Scientific
Local Clinical Trial Manager-FSP, Germany-6 month FTC (m/f/d)
• Homeoffice
[. .. ] global Clinical Operations colleagues within our PPD clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] across commercial and government contracts. Together, we help clients define and develop clinical programs, minimize delays, and execute high-quality, cost-efficient clinical studies. The PPD FSP Solution: PPD s Functional Service Provider division partner with and serve as an extension of our PPD team, supporting our customers key functions. We cover [. .. ] required, advises support/ develops and negotiates on contract development with Sites/ CRO/ Vendors ensuring legal input where required and may participate in budget/ contract negotiations with study vendors or clinical investigator sites. As required, selects manages local vendors in accordance with local practices in alignment with overall resourcing strategy for the study; accountable for local vendor management including oversight, agreements, payments, communications issue management. Manages the development of key study documents, plans manuals according to local requirements (monitoring plan, local informed [. .. ]
Job gestern bei Jooble gefunden
Study Physician sponsor dedicated in Germany
• München
Study Physician sponsor dedicated in Germany Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and
commercial [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] requirements too) Medical Monitoring experience preferred Pharma company experience preferred. However, CRO experience is fine. If no industry experience, the in addition to clinical practice they should have worked principal investigator/ sub investigator in clinical trials for a reasonable amount of time. Travel-15-20 depending on the study requirements. Key words to look for in potential CVs-Clinical Trial protocol-writing/ reviewing, Identify medically relevant critical data, Medical risks, risk mitigation/ monitoring plan, Medical quality review/clinical quality monitoring, Jreview, [. .. ]
Job vor 4 Tagen bei Jooble gefunden
Sr CRA in oncology-Sponsor dedicated-Home Based Germany
• München
[. .. ] CRA in oncology-Sponsor dedicated-Home Based Germany Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] 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 via [. .. ]
Job vor 8 Tagen bei Jooble gefunden
Regeneron
• München
Führungs-/ Leitungspositionen
[. .. ] Regenerons scientific presence in Germany. A Typical Day Might Include The Following: Serve as the key Regeneron medical representative in Germany for internal stakeholders (Medical Affairs, Clinical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Development, Operations, Regulatory, Commercial) and external stakeholders (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 vor 8 Tagen bei Jooble gefunden
Regeneron
Medical Manager/in (m/w/d)
• München
[. .. ] with global and international teams, and strengthen Regenerons scientific presence in Germany. Serve as the key Regeneron medical representative in Germany for internal stakeholders (Medical Affairs, Clinical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Development, Operations, Regulatory, Commercial) and external stakeholders (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. Bring the German patient and physician voice into crossfunctional strategy discussions, balancing scientific, clinical, and payer needs. Represent Regeneron at scientific congresses, symposia, and advisory boards, and support the development and localization of scientific content. Provide medical support to local clinical operations and ensure strong [. .. ]
Job vor 8 Tagen bei Jooble gefunden
Regeneron
• München
[. .. ] with global and international teams, and strengthen Regenerons scientific presence in Germany. Serve as the key Regeneron medical representative in Germany for internal stakeholders (Medical Affairs, Clinical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Development, Operations, Regulatory, Commercial) and external stakeholders (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. Bring the German patient and physician voice into crossfunctional strategy discussions, balancing scientific, clinical, and payer needs. Represent Regeneron at scientific congresses, symposia, and advisory boards, and support the development and localization of scientific content. Provide medical support to local clinical operations and ensure strong [. .. ]
Job vor 8 Tagen bei Jooble gefunden
Regeneron
Medical Affairs Director
• München
Führungs-/ Leitungspositionen
[. .. ] with global and international teams, and strengthen Regenerons scientific presence in Germany. Serve as the key Regeneron medical representative in Germany for internal stakeholders (Medical Affairs, Clinical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Development, Operations, Regulatory, Commercial) and external stakeholders (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. Bring the German patient and physician voice into crossfunctional strategy discussions, balancing scientific, clinical, and payer needs. Represent Regeneron at scientific congresses, symposia, and advisory boards, and support the development and localization of scientific content. Provide medical support to local clinical operations and ensure strong [. .. ]
Job vor 8 Tagen bei Jooble gefunden
Regeneron
• München
[. .. ] with global and international teams, and strengthen Regenerons scientific presence in Germany. Serve as the key Regeneron medical representative in Germany for internal stakeholders (Medical Affairs, Clinical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Development, Operations, Regulatory, Commercial) and external stakeholders (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. Bring the German patient and physician voice into crossfunctional strategy discussions, balancing scientific, clinical, and payer needs. Represent Regeneron at scientific congresses, symposia, and advisory boards, and support the development and localization of scientific content. Provide medical support to local clinical operations and ensure strong [. .. ]
Job vor 11 Tagen bei Jooble gefunden
Dr. Falk Pharma GmbH
Global Medical Science Manager-50 part-time (m/f/d)
• Regierungsbezirk Freiburg
[. .. ] We firmly believe that medical progress can only be achieved by working together. That is why we are looking for: Your tasks Falk Global Medical (GMED) bridges [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical development and commercial functions. We translate clinical science and communicate it externally and internally. GMED Science managers are working closely with their tandem GMED Affairs partners: GMED Science ensures a robust scientific foundation by providing medical-scientific and compliance expertise, while GMED Affairs focuses on market engagement, maintaining continuous interaction with healthcare professionals, [. .. ] and FDA) and clinical content and documentation, related to new drugs, clinical trials, as well as medical treatments (e. g. parts of clinical dossier module 2.5, scientific advice requests, investigator brochures clinical parts) - with focus on epidemiology, therapeutic area or indication background, national and international guidelines and patient journey/ medical need, based on study reports, medical-scientific publications and other literature and key external experts insights Answer and process internal and external medical inquiries from health care providers, patients, [. .. ]
Job am 15.01.2026 bei Jooble gefunden
• München
Führungs-/ Leitungspositionen
Senior Site Contracts Lead (Multiple location: Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and
commercial [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, youll collaborate with passionate problem solvers, innovating as a [. .. ] internal customers to seek assistance. Oversees negotiations of clinical study agreements (CTAs) on a study level and drives CTA document finalization and execution, including contractual language terms, financial attachments, and investigator grant budgets in collaboration with a global team of site contract budget negotiators. Advises study team and Sponsor stakeholders on industry trends, norms, and emergent developments surrounding site contract and budgetary negotiations. Provides consultation on potential risks and mitigation tactics for negotiation issues pertaining to overall study start-up needs. [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Klinischer Monitor/ Clinical Research Associate
• München
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 to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/[. .. ] and protocol compliance. immediately communicates/ escalates serious issues to the project team and develops action plans. 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. 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. Utilizes available hardware and software to support the effective conduct of the clinical [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Freelance CRA Germany
• München
Freiberuflich
Freelance CRA 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. 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 14.01.2026 bei Jooble gefunden
Klinischer Monitor/ Clinical Research Associate (m/w/d)
• München
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 to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/[. .. ] and protocol compliance. immediately communicates/ escalates serious issues to the project team and develops action plans. 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. 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. Utilizes available hardware and software to support the effective conduct of the clinical [. .. ]
Job am 14.01.2026 bei Jooble gefunden
• München
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 to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 14.01.2026 bei Jooble gefunden
Regeneron
Sr Manager, Field Medical Affairs Hematology (West Germany)
• Homeoffice
[. .. ] leaders, healthcare providers, and investigators, serving as a trusted scientific resource and strategic partner. Youll play a meaningful role in crafting the understanding of Regenerons therapies, supporting [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical development and investigator-initiated research, and contributing to impactful product launches. This is an exciting opportunity to work at the forefront of science while influencing the future of hematology care. A Typical Day: Building and handling relationships with KOLs in malignant hematology. Acting as a primary clinical/ scientific contact for HCPs and investigators. [. .. ] posters, and manuscripts to communicate data. Contributing to investigator-initiated study programs and research collaborations. Attending medical congresses to gather and report competitive intelligence. Partnering cross-functionally with Medical Affairs, Commercial, and Market Access. This Role May Be For You: You thrive on scientific exchange and are confident discussing complex data with KOLs. You have established connections in hematology and understand the oncology landscape. You enjoy balancing independent field work with cross-functional collaboration. You adapt easily to changing priorities and [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Clinical Research Associate/ Klinischer Monitor (m/w/d)
• München
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 to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/[. .. ] and protocol compliance. immediately communicates/ escalates serious issues to the project team and develops action plans. 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. 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. Utilizes available hardware and software to support the effective conduct of the clinical [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Klinischer Monitor (m/w/d)
• München
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 to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/[. .. ] and protocol compliance. immediately communicates/ escalates serious issues to the project team and develops action plans. 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. 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. Utilizes available hardware and software to support the effective conduct of the clinical [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Clinical Research Associate (Klinischer Monitor)
• München
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 to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/[. .. ] and protocol compliance. immediately communicates/ escalates serious issues to the project team and develops action plans. 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. 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. Utilizes available hardware and software to support the effective conduct of the clinical [. .. ]
Neu Job vor 6 Std. bei Mindmatch.ai gefunden
Syneos Health Commercial Solutions
Medical Science Liaison Rare Disease-Ostdeutschland
• AT- 2 Lavamünd
[. .. ] aligned to strategy within the business Serve as external, credible scientific expert on disease area and client products at HCP field meetings, key medical and scientific conferences, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] advisory boards, clinical investigator meetings and patient advocacy group meetings Facilitate clear communication between the client and investigators in investigator engagement for both client trials and investigator-sponsored studies and barriers to enrolment for pipeline assets Work to the highest ethical compliance, ethics and safety standards adhering to all local regulations and laws Maintain [. .. ]
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 [. .. ]
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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 77 offene Stellenanzeigen für Commercial Investigator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Commercial Investigator Jobs?
Aktuell suchen 13 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:
- Regeneron (6 Jobs)
- IQVIA (6 Jobs)
- Thermo Fisher Scientific (4 Jobs)
- Incyte Corporation (2 Jobs)
- Dr. Falk Pharma GmbH (2 Jobs)
- Syneos Health Commercial Solutions (1 Job)
In welchen Bundesländern werden die meisten Commercial Investigator Jobs angeboten?
Die meisten Stellenanzeigen für Commercial Investigator Jobs werden derzeit in Bayern (15 Jobs), Hessen (5 Jobs) und Sachsen-Anhalt (5 Jobs) angeboten.
Zu welchem Berufsfeld gehören Commercial Investigator Jobs?
Commercial Investigator Jobs gehören zum Berufsfeld Revision.
