60 Jobs für Commercial Investigator
Stellenangebote Commercial Investigator Jobs
Neu Job vor 4 Std. bei Neuvoo.com gefunden
Jazz Pharmaceuticals
• Munich Muenchen
Führungs-/ Leitungspositionen
[. .. ] and career growth. Act as a role model for Jazzs cultural values, consistently demonstrating them in daily interactions and leadership. Serve as a strategic partner to cross-functional [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] teams, including Commercial, to drive alignment and collaboration. Execution of Medical Strategy and Scientific Excellence: Drive the effective execution of the medical strategy and associated plans. Maintain and continuously develop deep expertise in oncology-related clinical and scientific literature to position both yourself and the team as trusted subject matter experts. Strategically plan and engage with national Key External Experts (KEEs) to maximize scientific exchange and collaboration. Support data generation initiatives, including the reactive evaluation of Investigator Sponsored Trial (IST) proposals. Uphold the highest standards of pharmacovigilance, compliance, and adherence to SOPs. Ensure the delivery of accurate, high-quality medical information to both internal stakeholders and external customers. Strategic Cross-Functional Collaboration and Insight Integration: Ensure delivery of the German Oncology Medical Affairs field strategy and plan [. .. ]
Job vor 3 Tagen bei JobMESH gefunden
Jazz Pharmaceuticals
Associate Director, Head of MSL Oncology, Germany
• Bavorsko Mnichov
Führungs-/ Leitungspositionen
[. .. ] and career growth. Act as a role model for Jazzs cultural values, consistently demonstrating them in daily interactions and leadership. Serve as a strategic partner to cross-functional [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] teams, including Commercial, to drive alignment and collaboration. Execution of Medical Strategy and Scientific Excellence: Drive the effective execution of the medical strategy and associated plans. Maintain and continuously develop deep expertise in oncology-related clinical and scientific literature to position both yourself and the team as trusted subject matter experts. Strategically plan and engage with national Key External Experts (KEEs) to maximize scientific exchange and collaboration. Support data generation initiatives, including the reactive evaluation of Investigator Sponsored Trial (IST) proposals. Uphold the highest standards of pharmacovigilance, compliance, and adherence to SOPs. Ensure the delivery of accurate, high-quality medical information to both internal stakeholders and external customers. Strategic Cross-Functional Collaboration and Insight Integration: Ensure delivery of the German Oncology Medical Affairs field strategy and plan [. .. ]
Job vor 9 Tagen bei Mindmatch.ai gefunden
Gesellschaft für Virologie e. V.
• AT- 9 Wien
[. .. ] , demonstrated through national or international project cooperations with universities or research institutions) Outstanding, relevant publication track record Proof of successful acquisition of third-party funded research projects [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as Principal Investigator (PI) Demonstrable experience in the application, validation, and further development of state-of-the-art methods in the relevant subject area Didactic qualification or experience in teaching, supervision, and training of undergraduate and graduate students Good command of English (B2) Required general skills and abilities Excellent communication and presentation skills Strong leadership and social skills Gender and diversity management skills A commercial and strategic mindset Decision-making ability and assertiveness Strong commitment to the continuing success and development of Vetmeduni Additional desired qualifications and skills Experience in developing innovative teaching material Good command of German (non-German-speaking applicants are expected to reach at least level B1 within 2-3 years) What [. .. ]
Job vor 12 Tagen bei Mindmatch.ai gefunden
Blueprint Medicines, a Sanofi company
Field Medical Advisor, Alpine (Temporary)
• AT- 9 Wien
Homeoffice möglich
[. .. ] products. Works with colleagues of Blueprint Medicines International headquarter in Zug and other countries in the international region to ensure consistency of clinical programs from a medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] perspective. Ensures that Investigator Initiated Research studies are in line with the global strategy. Helps to detect need for and enables Real World Evidence generation when required for advancing therapeutic area a/ o for access needs. Collaborates closely with market access for HEOR access required information What minimum qualifications do we require Advanced Clinical/ [. .. ] of emotional intelligence displaying candor and integrity at all times combined with the ability to manage complexity ambiguity and paradoxes during the build out of the region. Understanding of pharmaceutical commercial access medical and scientific needs on a local basis. Experience with product launches. Solid knowledge of country level regulations guidelines codes of practices and Access requirements Operational excellence : management skills planning prioritization decision making objective setting and plan execution. Strong customer orientation; science-based but good understanding of marketing [. .. ]
Job vor 13 Tagen bei Mindmatch.ai gefunden
IQVIA Argentina
• AT- 9 Wien
[. .. ] completion of regulatory and contractual documents for individual sites. Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] (ICF) , and Investigator Pack (IP) release documents, in line with project timelines. Provide local expertise to SAMs and project team during initial and on-going project timeline planning. Perform quality control of documents provided by sites. May have direct contact with sponsors on specific initiatives. Qualifications B Sc Degree in Life Sciences or [. .. ] co-workers, managers and sponsors. Ability to work independently, to problem-solve collaboratively and to raise issues appropriately as needed. 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 J-18808-Ljbffr 70328842 [. .. ]
Job am 17.11.2025 bei Mindmatch.ai gefunden
IQVIA
Regulatory Start Up Specialist I, IQVIA Med Tech, Austria
• AT- 9 Wien
[. .. ] completion of regulatory and contractual documents for individual sites. Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] (ICF) , and Investigator Pack (IP) release documents, in line with project timelines. Provide local expertise to SAMs and project team during initial and on-going project timeline planning. Perform quality control of documents provided by sites. May have direct contact with sponsors on specific initiatives. Qualifications B Sc Degree in Life Sciences or [. .. ] co-workers, managers and sponsors. Ability to work independently, to problem-solve collaboratively and to raise issues appropriately as needed. 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 J-18808-Ljbffr 69813952 [. .. ]
Job am 17.11.2025 bei Mindmatch.ai gefunden
Syneos Health
• AT- 9 Wien
[. .. ] for Experienced Clinical Research Associate in Austria. Description Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model places the customer and the patient at the center of everything we do. We continuously look for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but easier to work [. .. ] provide recommendations, communicate/ escalate serious issues, and develop action plans. Verify informed consent procedures are performed and documented for each subject, protecting confidentiality and assessing safety and data integrity at investigator sites. Based on the Clinical Monitoring/ Site Management Plan, assess site processes, conduct source document review, verify CRF data accuracy, resolve queries remotely or onsite, support data capture and electronic data capture compliance. Perform IP inventory, reconciliation, storage and security review, and confirm correct dispensing and administration of study product. [. .. ]
Job am 14.10.2025 bei Mindmatch.ai gefunden
Syneos Health
CRA Austria
• AT- 9 Wien
[. .. ] among the first 25 applicants Description CRA Austria Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 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 vor 2 Tagen bei Jobleads gefunden
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] innovative professionals to ensure our customers achieve their goals. Key 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 : [. .. ] 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 [. .. ]
Job am 15.11.2025 bei Jobleads gefunden
Medical Director-Oncology, Home-Based (m/w/d)
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
[. .. ] as project team member: Provides medical and scientific input to clinical research programs including review of new business proposals, preclinical and/or clinical data, study protocols, training materials, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] informed consent, Investigator Drug Brochures, e CRFs, analysis plan designs, clinical study reports, regulatory approval submissions, serious and non-serious adverse event evaluation, and reporting. Ensures medical activities run according to GCP and operate with highest efficiency. Establishes and maintains a network of medical/ scientific consultants, etc. Supervises and manages Medical Director activities. Clinical [. .. ] Oncology/ Hematology Current or prior license to practice medicine; board certification/ eligibility ideal (Preference) Board Certified/Board Eligible: Oncology (Required) 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 IQVIA is a leading global provider of clinical research services, commercial insights and healthcare [. .. ]
Job am 05.11.2025 bei Jobleads gefunden
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
[. .. ] as project team member: Provides medical and scientific input to clinical research programs including review of new business proposals, preclinical and/or clinical data, study protocols, training materials, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] informed consent, Investigator Drug Brochures, e CRFs, analysis plan designs, clinical study reports, regulatory approval submissions, serious and non-serious adverse event evaluation, and reporting. Ensures medical activities run according to GCP and operate with highest efficiency. Establishes and maintains a network of medical/ scientific consultants, etc. Supervises and manages Medical Director activities. Clinical [. .. ] Oncology/ Hematology Current or prior license to practice medicine; board certification/ eligibility ideal (Preference) Board Certified/Board Eligible: Oncology (Required) 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 #J-18808-Ljbffr 68374450 [. .. ]
Job am 20.10.2025 bei Jobleads gefunden
Medical Director Oncology, Home-Based (mwd)
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
[. .. ] as project team member: Provides medical and scientific input to clinical research programs including review of new business proposals preclinical and/or clinical data study protocols training materials [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] informed consent Investigator Drug Brochures e CRFs analysis plan designs clinical study reports regulatory approval submissions serious and non-serious adverse event evaluation and reporting. Ensures medical activities run according to GCP and operate with highest efficiency. Establishes and maintains a network of medical/ scientific consultants etc. Supervises and manages Medical Director activities. Clinical [. .. ] prior license to practice medicine; board certification/ eligibility ideal (Preference) . Board Certified/Board Eligible : Oncology (Required) Additional Information 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 Required Experience : Director Key Skills EMR Systems Post Residency Experience Occupational Health [. .. ]
Job am 12.10.2025 bei Jobleads gefunden
Medical Director-Oncology, Home-Based (m/w/d)
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
[. .. ] as project team member: Provides medical and scientific input to clinical research programs including review of new business proposals, preclinical and/or clinical data, study protocols, training materials, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] informed consent, Investigator Drug Brochures, e CRFs, analysis plan designs, clinical study reports, regulatory approval submissions, serious and non-serious adverse event evaluation, and reporting. Ensures medical activities run according to GCP and operate with highest efficiency. Establishes and maintains a network of medical/ scientific consultants, etc. Supervises and manages Medical Director activities. Clinical [. .. ] Oncology/ Hematology Current or prior license to practice medicine; board certification/ eligibility ideal (Preference) Board Certified/Board Eligible: Oncology (Required) 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 #J-18808-Ljbffr 65746093 [. .. ]
Job am 16.09.2025 bei Jobleads gefunden
Associate Medical Director, Cardiology-Metabolic Diseases and Nephrology Experience (m/w/d)
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
[. .. ] review of the protocol, Investigative Drug Brochure (IDB) , and/or Case Report Forms (CRFs) . Provides therapeutic area/ indication training for the project clinical team. Attends and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] presents at Investigator Meetings. Performs review and clarification of trial-related Adverse Events (AEs) . May perform medical case review of Serious Adverse Events (SAEs) , including review of case documentation and patient narrative, in collaboration with the Pharmacovigilance department. May provide medical support for the Analysis of Similar Events (AOSE) , in [. .. ] in clinical medicine, in addition to 4 years clinical trials experience as an investigator or in the Pharma, CRO, or Biotech industry. Robust and current knowledge of scientific, clinical, regulatory, commercial and competitive landscape in applicable therapeutic area. Knowledge of applicable federal and local regulations and guidelines pertaining to clinical research. Business Acumen. A board-certification for the required therapeutic. Knowledge of cardiology, metabolic diseases and nephrology. Experience or knowledge in Phase I studies or early clinical development. Fluent English. Extensive [. .. ]
Job am 27.06.2025 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 gestern bei Jobleads gefunden
Medical Science Liaison-Switzerland
• Zug
[. .. ] and investigate new uses of Alnylams products in a fieldbased/virtual interactions focused role. Identify investigatorinitiated study (IIS) opportunities and act as the primary conduit and work directly [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with the investigator during the IIS. Report emerging clinical trends. In a projectbased set up assist in development of advisory boards, symposia and publication planning. Provide input to the Medical Affairs Manager and Medical Director to develop appropriate strategic and tactical plans (e. g. MAC) for the country. Be the team expert on all aspects of the MSL role including: process improvements and sharing of best practice. Foster a collaborative working relationship with Medical Representatives and Commercial colleagues to ensure strategies and business plans are both patient and business focused. Work with the Swiss team to bring the voice of the fieldbased MSL into strategy development and material creation. Provide accurate and fairbalanced medical and scientific education using literature, summaries of publications, education and presentation scientific materials [. .. ]
Job gestern bei Jobleads gefunden
• München, Bayern
Beratungs-/ Consultingtätigkeiten
[. .. ] field-based clinical/ medical insights in order to support the future strategy. This position will provide operational support for activities related to Medical Information and Communication, Medical Education [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and Training, Investigator Initiated Trials, Key Opinion Leader outreach bringing value via scientific exchange. The position will also provide Research Clinical Development support as needed. The RMA will support the Medical Director in all aspects, i. e. representation of company in scientific presentations, conferences, and support for the Commercial Organisation while ensuring compliance with all policies and procedures as well as local regulatory and legal requirements. Suitable applicants will have :-Advanced biomedical sciences degree (Dipl. , MD, Pharm D, Ph D) Experience of working in rare diseases advantageous but not essential Some experience of engaging with Key Opinion Leaders within [. .. ]
Job gestern bei Jobleads gefunden
Senior Regional Medical Advisor-Rare Disease (Central/ South)
• Düsseldorf, Nordrhein- Westfalen Duesseldorf
Beratungs-/ Consultingtätigkeiten
[. .. ] field-based clinical/ medical insights in order to support the future strategy. This position will provide operational support for activities related to Medical Information and Communication, Medical Education [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and Training, Investigator Initiated Trials, Key Opinion Leader outreach bringing value via scientific exchange. The position will also provide Research Clinical Development support as needed. The RMA will support the Medical Director in all aspects, i. e. representation of company in scientific presentations, conferences, and support for the Commercial Organisation while ensuring compliance with all policies and procedures as well as local regulatory and legal requirements. Suitable applicants will have :-Advanced biomedical sciences degree (Dipl. , MD, Pharm D, Ph D) Experience of working in rare diseases advantageous but not essential Some experience of engaging with Key Opinion Leaders within [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• Zürich Zuerich
[. .. ] regional Medical Affairs colleagues to support regional deliverables (e. g. , scientific support, internal/ external presentations) Monitor competitive activities and emerging trends within relevant therapeutic areas Provide [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] medical training for commercial Support clinical trial operations to ensure success with planned and ongoing clinical trials to include identifying, supporting, and regularly engaging clinical trial investigators, and sites External engagement insights (50 field based, covering all of Switzerland) Develop and maintain a KOL engagement plan that fosters collaborative relationships in Switzerland Provide medical/ [. .. ] medical congresses such as participation in clinical data presentations, scientific exchange at the medical affairs booth, and internal or external meetings Engage with external researchers as a primary contact for investigator-initiated trials (IITs) Ensure successful patient access initiatives by managing medical access programs and collaborating on regulatory and market access dossier Your profile Advanced degree (MD, Pharm D, Ph D) in a relevant scientific field Experience as Medical Science Liaison (MSL) and Medical Manager in a Swiss subsidiary of a smaller pharmaceutical [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Country Medical Lead, Switzerland Austria (remote)
• Burgenland
[. .. ] education, evidence generation and dissemination, HCP and KOL engagement, and internal knowledge and insights translation. The Medical Affairs Sr. Manager leads, aligns with and influences a number [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of crossfunctional partners (commercial, marketing, market access, regulatory, sales excellence) in Austria Switzerland to ensure proper execution of the medical plans. The Medical Affairs Sr. Manager is a key member of the DACH leadership team. They work closely with Insulets affiliate crossfunctional team to ensure the information, education, and research needs of HCPs are [. .. ] training with generation and delivery of medical content Inform strategize evidence generation plans, in answer to fulfil market access, regulatory and marketing needs Support the local execution of Insuletsponsored and Investigator Initiated trials Disseminate evidence within local markets Identify and engage with HCP to inform and seek advice on the companys solutions, through the execution of advisory boards, clinical activity, scientific Exchange and educational Events Establish and maintain credible peertopeer scientific relationships with national and regional KOLs Build confidence and advocacy [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Country Medical Lead, Switzerland Austria (remote)
• Schwyz
[. .. ] education, evidence generation and dissemination, HCP and KOL engagement, and internal knowledge and insights translation. The Medical Affairs Sr. Manager leads, aligns with and influences a number [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of crossfunctional partners (commercial, marketing, market access, regulatory, sales excellence) in Austria Switzerland to ensure proper execution of the medical plans. The Medical Affairs Sr. Manager is a key member of the DACH leadership team. They work closely with Insulets affiliate crossfunctional team to ensure the information, education, and research needs of HCPs are [. .. ] with generation and delivery of medical content Inform strategize evidence generation plans, in answer to fulfil market access, regulatory and marketing needs Support the local execution of Insulet-sponsored and Investigator-Initiated trials Disseminate evidence within local markets Identify and engage with HCP to inform and seek advice on the companys solutions, through the execution of advisory boards, clinical activity, scientific Exchange and educational Events Establish and maintain credible peertopeer scientific relationships with national and regional KOLs Build confidence and advocacy [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Sr Manager, Field Medical Affairs Hematology (West Germany)
[. .. ] 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 vor 11 Tagen bei Jobleads gefunden
Clinical Operations Specialist-Munich area
• München, Bayern
Clinical Operations Specialist-Munich area Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and
commercial insights into [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We continuously simplify and streamline our work to make Syneos Health easier to work with and easier to work for. Whether you join in [. .. ] Prepare and maintain site manuals, reference tools, and other documents. Maintain, update, and input clinical tracking information into databases. Track incoming and outgoing clinical and regulatory documents and updates for investigator sites, studies, project team, or client. Manage shared mailbox, process site requests, and route correspondence appropriately. Coordinate the ordering, packaging, shipping, and tracking of site supplies and materials. Assist with coordination of team meetings, attend meetings, and prepare accurate meeting minutes and action items. Handle receipt, tracking, and disposition of [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
Medical Affairs Diagnostic Solutions
• Berlin
Beratungs-/ Consultingtätigkeiten
[. .. ] (Country/ Hub) representative within the Medical Affairs team acting as a strategic liaison between the organization and external stakeholders. This role provides non-promotional product and scientific support [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to the commercial organization by leveraging clinical knowledge, academic credentials and scientific expertise in relevant therapeutic and diagnostic areas. Candidates must demonstrate a robust understanding of microbiology including disease states, diagnostic pathways, emerging clinical evidence and ongoing research. Experience in molecular diagnostics for infectious diseases is particularly valuable. The MAM also contributes to [. .. ] other healthcare partners. Serve as the primary source of clinical and scientific information for healthcare professionals (HCPs) within assigned scientific, clinical and diagnostic areas. Facilitate KOL participation in advisory boards, investigator meetings, educational symposia and sponsored promotional programs. Attend relevant scientific and medical congresses to gather insights and report key findings to internal partners. Act as Medical Reviewer/ Approver for promotional materials within the territory/ region as delegated by Business Unit Medical Affairs leadership. Serve as a liaison for Investigator Sponsored [. .. ]
Job am 18.11.2025 bei Jobleads gefunden
Sr Manager, Field Medical Affairs-Oncology (South-West Germany)
• Mannheim, Baden- Württemberg
[. .. ] 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 cancer care. A Typical Day Building and handling relationships with KOLs in Oncology. Acting as a primary clinical/ scientific contact for HCPs and investigators. Sharing [. .. ] 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 If You thrive on scientific exchange and are confident discussing complex data with KOLs. You have established connections in Oncology and understand the healthcare landscape. You enjoy balancing independent field work with cross-functional collaboration. You adapt easily to changing priorities [. .. ]
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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 60 offene Stellenanzeigen für Commercial Investigator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Commercial Investigator Jobs?
Aktuell suchen 11 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:
- wax. (11 Jobs)
- Jazz Pharmaceuticals (2 Jobs)
- Syneos Health (2 Jobs)
- Alimera (2 Jobs)
In welchen Bundesländern werden die meisten Commercial Investigator Jobs angeboten?
Die meisten Stellenanzeigen für Commercial Investigator Jobs werden derzeit in Bayern (11 Jobs), Nordrhein-Westfalen (7 Jobs) und Sachsen (4 Jobs) angeboten.
Zu welchem Berufsfeld gehören Commercial Investigator Jobs?
Commercial Investigator Jobs gehören zum Berufsfeld Revision.
