Clinical Investigator Stellenangebote


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228 Jobs für Clinical Investigator


Stellenangebote Clinical Investigator Jobs


Job vor 3 Tagen bei Jobleads gefunden

(Junior-) Field Medical Advisor-Rare Oncology South

• München, Bayern Absolventen, Einsteiger, Trainees [. .. ] and aligned to strategy within the business Serves as external, credible scientific expert on disease area and client products at HCP field meetings, key medical and scientific [...]
MEHR INFOS ZUM STELLENANGEBOT[...] conferences, advisory boards, clinical investigator meetings and patient advocacy group meetings Identify key field insights related to client products, activities and the disease area and effectively disseminate and collaborate with cross-functional partners Facilitate clear communication between the business and investigators in investigator engagement for both client trials and investigator-sponsored studies and barriers to [. .. ]

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Job am 30.10.2025 bei Jobleads gefunden Medical Science Liaison, North Germany • Köln, Nordrhein- Westfalen [. .. ] permissible by local laws and regulations. Serves as external, credible scientific expert on disease area and Exact Sciences products at HCP field meetings, key medical and scientific [...]
MEHR INFOS ZUM STELLENANGEBOT[...] conferences, advisory boards, clinical investigator meetings and patient advocacy group meetings. Responds to unsolicited requests for medical information on Exact Sciences products in a credible, balanced/objective manner. Participate in the development and execution of a KOL outreach plans. Identify and map KOL, other stakeholder, key accounts as well as patient referral patterns and pathways. [. .. ]

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Job vor 3 Tagen bei StepStone gefunden Sigmund Freud Privatuniversität Wien

Professor of Molecular Medicine (m/f/x)

• Wien [. .. ] researchers and medical specialists. The mission of medical research at SFU is to foster innovation in healthy aging and preventive medicine across all fields of human medicine. [...]
MEHR INFOS ZUM STELLENANGEBOT[...] We actively support investigator-initiated clinical studies and translational research within SFU and its partner hospitals, as well as collaborative projects with external senior scientists, always with the goal of translating research outcomes directly into patient care. Our laboratories are equipped with a broad range of state-of-the-art instruments supporting molecular and cellular biology [. .. ]

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Job vor 4 Tagen bei StepStone gefunden Miltenyi Biotec B. V. Co. KG Lead Medical Writer (m f d) • Bergisch Gladbach Führungs-/ Leitungspositionen Homeoffice möglich Miltenyi Biomedicine is a biopharmaceutical company committed to advancing personalized cell and gene therapies. We are pioneering groundbreaking therapies for serious life-threatening diseases, and reshaping their accessibility for clinical professionals [...]
MEHR INFOS ZUM STELLENANGEBOT[...] and patients worldwide with the aim to improve and extend patients lives. We are currently focusing on difficult-to-treat hematological cancers using CAR-T and other technologies, while also exploring treatments for other diseases. Our lead candidate, a tandem CAR-T cell product, is currently undergoing pivotal clinical [. .. ] review, revision and finalization of clinical documents for submission to regulatory authorities. You lead the development, authoring, and submission of regulatory documents (e. g. , CTD modules, clinical study reports, investigator brochures, INDs/ IMPDs, NDAs/ MAAs, and briefing documents) . Your responsibility includes ensuring that all documents are scientifically sound, strategically aligned, and compliant with global regulatory standards. In addition, you manage document timelines, coordinate internal reviews, and ensure on-time delivery. Collaborating closely within cross-functional teams (clinical, regulatory, biostatistics, [. .. ]

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Neu Job vor 3 Std. bei JobMESH gefunden Fraunhofer- Institut für Translationale Medizin und Pharmakologie ITMP

Studienassistenz/ Study Nurse (all genders)

• Niedersachsen Jobticket 30+ Urlaubstage Tarifvertrag Vermögenswirksame Leistungen [. .. ] Nervensystems in Folge gestörter Funktionen des Immunsystems. Die von uns gewonnenen Erkenntnisse sollen möglichst bald den Weg in die klinische Anwendung finden. Ergebnisse der Grundlagenforschung können durch [...]
MEHR INFOS ZUM STELLENANGEBOT[...] unsere Fraunhofer Early Clinical Trial Unit (ECTU) am Universitätsklinikum Göttingen zügig Bench to Bedside in neue Therapieansätze überführt werden. Hier sorgen Sie für Veränderung Für unsere Abteilung ECTU suchen wir Sie als Studienassistenz/ Study Nurse. Hier arbeiten Sie aktiv bei der Umsetzung der Projekte und in der Organisation des Stationsbereichs mit. Ihre Mitarbeit umfasst [. .. ] etc. ) , Entnahme, Aufbereitung und Versand von Blutproben sowie Meldung unerwünschter Ereignisse an die Studienleitung Organisation und Koordination von klinischen Prüfungen in der Neurologie Qualitätssicherung, Datenbankpflege und Pflege des Investigator Site Files sowie Verwaltung und Archivierung der Prüfarztordner und CRFs Vor- und Nachbereitung sowie Begleitung von Schulungen, Initiierungen, Monitorbesuchen und Behördeninspektionen Korrespondenz und Terminkoordination mit Studienpatientinnen und Ärztinnen Hiermit bringen Sie sich ein Abgeschlossene medizinische Berufsausbildung zum/zur Gesundheits- und Krankenpflegerin, Arzthelferin oder Medizinisch-technischen Assistentin (MTA) Praxis im klinischen [. .. ]

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Job vor 3 Tagen bei Jobleads gefunden Manager Medical Science Liaison Oncology • München, Bayern [. .. ] aligned with local and European medical affairs priorities. Build and expand relationships/ networks with key medical and scientific experts in the field of breast cancer and/or lung [...]
MEHR INFOS ZUM STELLENANGEBOT[...] cancer. Support clinical trials by identifying study sites, participating in SIVs (Site Inviations Visits) , assisting with patient enrollment, and ensuring smooth information exchange. Identify research opportunities, including Investigator-Initiated Trials, Real-World Evidence, and other evidence-generation studies. Represent the organization at scientific conferences, advisory boards, and educational events, sharing insights and preparing reports for internal stakeholders. Ensure timely documentation of HCP interactions, compliance with local policies, and accurate reporting of insights and safety information. Qualifications Advanced degree [. .. ]

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Job vor 12 Tagen bei Jobleads gefunden

Medical Science Liaison Complement-Mediated Diseases

• München, Bayern [. .. ] various activities locally and regionally. Provide local and regional feedback to HQ when performing Business Development Due Diligence. Deliver inputs to head office led medical programs ahead [...]
MEHR INFOS ZUM STELLENANGEBOT[...] of launch. Coordinate Investigator Sponsored Studies (ISSs) as appropriate and support studies on the local level Coordinate medical information enquiries in collaboration with MA/ SMA and HQ in Stockholm. Attend relevant local, regional and global congresses and symposia to represent Sobi and interact with appropriate stakeholders and customers. Represent the scientific interests in internal [. .. ] Sc. , D. N. P. , Ph. D. , or M. D. / D. O. ) Consideration will be given to candidates with an advanced health degree and extensive industry or clinical experience. Ability to understand and effectively communicate scientific information; respond to inquiries and address needs of key stakeholders A minimum of 1 year of MSL experience Demonstrated success managing internal/ external stakeholders and leading or influencing cross-functional teams in a matrixed environment including strong teamwork and collaboration Proven track [. .. ]

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Job vor 12 Tagen bei Jobleads gefunden Senior/ Medical Director (Ophthalmology) • Hamburg Führungs-/ Leitungspositionen TFS Health Science is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full [...]
MEHR INFOS ZUM STELLENANGEBOT[...] service-capabilities, resourcing and Functional Service (FSP) solutions. About this role As part of our Ophthalmology team you will working alongside passionate and 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 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 : [. .. ]

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Job am 07.12.2025 bei Jobleads gefunden

MSL Gastroenterology Region West

• Cham, Zug [. .. ] members of the Affiliate Brand Team to develop their scientific and technical expertise through the delivery of scientific update presentations. Assist in the initiation; oversight and follow [...]
MEHR INFOS ZUM STELLENANGEBOT[...] up of assigned clinical studies and medical projects initiated within the therapeutic area for which the MSL carries responsibility (e. g. post marketing clinical activities such as registry/ database projects, epidemiological surveys, post-authorization studies (phase IV) . All such activities must comply with applicable local laws, guidelines, codes of practice, SOPs, and Abb Vie R D (GPRD) SOPs. Act as the point of contact with thought leaders to facilitate investigator initiated study (IIS) ideas and requests for support to the local and global medical teams as appropriate. Serve as a point of contact within the Medical Affairs team for thought leaders and external experts within western Switzerland in order to satisfy their needs for scientific knowledge in a therapeutic area [. .. ]

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Job am 06.12.2025 bei Jobleads gefunden Chief Scientific Officer (CSO) Switzerland, 80 100 (Ref. 2605) - Member of the executive Board • Bern Führungs-/ Leitungspositionen [. .. ] of the Executive Board role at Auriga Vision AG. Our client is the Swiss Cancer Institute (former SAKK) , a non-profit organization focused on the development and [...]
MEHR INFOS ZUM STELLENANGEBOT[...] implementation of clinical trials in oncology based in Berne, Switzerland. As part of the teams expansion, we are looking for a Member of the executive Board. Responsibilities Leadership : Leading the Clinical Science team (Senior Scientific Director, Head of Clinical Development, Medical Science Liaison) , approximately 10 Clinical Scientists and Medical Advisors; active [. .. ] Proven leadership experience (with direct reports) . Knowing how to collaborate in the field of public health, industry and development/ research. Proven track record in oncology/ hematology, with experience in Investigator Initiated Trials (academic record in leading clinical research is a strong plus) . Experience in setting up and handling clinical trials in Switzerland. Fluent in English plus German and/or French. Susanne Rietiker is looking forward to receiving your application documents via our job portal (CV, diploma, reference letters; no [. .. ]

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Job am 04.12.2025 bei Jobleads gefunden

Senior/ Medical Director (Ophthalmology)

• München, Bayern Führungs-/ Leitungspositionen TFS Health Science is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full [...]
MEHR INFOS ZUM STELLENANGEBOT[...] service-capabilities, resourcing and Functional Service (FSP) solutions. About this role As part of our Ophthalmology team you will working alongside passionate and 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 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 : [. .. ]

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Job am 24.11.2025 bei Jobleads gefunden Senior Director Medical Affairs (mfd) • Wien Führungs-/ Leitungspositionen Homeoffice möglich [. .. ] D. degree required MPH, Ph. D. , MBA degree in Health Administration or Economics is seen as a plus Proven experience in global biopharmaceutical industry in Medical [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Affairs and/or Clinical Development Solid people management experience running a large matrix organization of healthcare professionals Experience in one of the following fields : Oncology (strong plus) Infectious Diseases Treatment Vaccines or Specialty care Strong leadership skills demonstrated effective organizational skills including ability to set goals and align priorities Business acumen ethics and [. .. ] recognition bonuses during the year Discounted fitness offer Pharmacy discounts wholesale discounts etc. Required Skills Advisory Board Development Clinical Development Clinical Medicine Decision Making Healthcare Education Healthcare Marketing Infectious Disease Investigator-Initiated Studies (IIS) Job Placement Leadership Management Process Medical Affairs Medical Care Medical Marketing Strategy People Leadership Results Oriented Scientific Communications Specialty Care Stakeholder Engagement Strategic Planning Strategic Thinking Writing Job Descriptions Preferred Skills Current Employees apply HERE Current Contingent Workers apply HERE Job Details Employee Status : Regular Relocation [. .. ]

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Job am 23.11.2025 bei Jobleads gefunden

Medical Science Liaison Manager, Nephrology, North-West

• München, Bayern [. .. ] within a geographic area. He/ she manages and maintains collegial and professional relationships with KOLs and identifies and facilitates collaboration opportunities with Alexion. He/ she combines strong [...]
MEHR INFOS ZUM STELLENANGEBOT[...] business acumen and clinical expertise and serves as a peer-to-peer liaison internally and externally. He/ she ensures a close working relationship with all functions in their region, including sales, and market access. You will be responsible for: Develop and maintain peer-to-peer collaborations with key medical experts in nephrology and adjacent [. .. ] medical community with up-to-date medical and scientific information Identify and execute collaboration opportunities between expert KOLs in nephrology and Alexion medical affairs and clinical development such as publications, investigator-initiated trials, regional advisory boards, training and speaker development programs. Communicate experts opinion, feedback on new data and clinical trends to Alexion Medical Affairs, therapeutic area (TA) franchises and translate this information into strategic recommendations to enhance science and advance patient care. Respond to unsolicited medical information requests in the [. .. ]

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Job am 23.11.2025 bei Jobleads gefunden Medical Science Liaison Manager, Nephrology, South • München, Bayern [. .. ] within a geographic area. He/ she manages and maintains collegial and professional relationships with KOLs and identifies and facilitates collaboration opportunities with Alexion. He/ she combines strong [...]
MEHR INFOS ZUM STELLENANGEBOT[...] business acumen and clinical expertise and serves as a peer-to-peer liaison internally and externally. He/ she ensures a close working relationship with all functions in their region, including sales, and market access. You will be responsible for: Develop and maintain peer-to-peer collaborations with key medical experts in nephrology and adjacent [. .. ] medical community with up-to-date medical and scientific information Identify and execute collaboration opportunities between expert KOLs in nephrology and Alexion medical affairs and clinical development such as publications, investigator-initiated trials, regional advisory boards, training and speaker development programs. Communicate experts opinion, feedback on new data and clinical trends to Alexion Medical Affairs, therapeutic area (TA) franchises and translate this information into strategic recommendations to enhance science and advance patient care. Respond to unsolicited medical information requests in the [. .. ]

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Job am 18.11.2025 bei Jobleads gefunden

Medical Science Liaison Oncology

• Stuttgart, Baden- Württemberg [. .. ] the primary field contact for the companys Medical Affairs. Engage thought leaders in a compliant manner developing strategic engagement plans. Disseminate scientific information accurately and fairly addressing [...]
MEHR INFOS ZUM STELLENANGEBOT[...] medical inquiries. Manage investigator-initiated research interests and support clinical development activities. Lead advisory board meetings and provide internal/ external training. Represent the company at medical conferences contributing to scientific discussions in Oncology. About you: Degree in life sciences discipline 3 years of medical affairs experience preferably in Oncology/ Hematology. Fluent German good professional English Car driving licence Key Skills [. .. ]

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Job am 17.11.2025 bei Jobleads gefunden Medical Science Liaison (m/w/d) Dermatology-Süd • Stuttgart, Baden- Württemberg [. .. ] Moderation indikationsbezogener Vorträge, wissenschaftlicher Fortbildungen sowie Unterstützung ärztlicher Referenten bei Präsentationen Organisation und Umsetzung regionaler Fortbildungen und Experten-Meetings inklusive Budgetverantwortung Mitarbeit bei klinischen Studienprojekten: Studienunterstützung in Zusammenarbeit [...]
MEHR INFOS ZUM STELLENANGEBOT[...] mit Global Clinical Operations, Betreuung nicht-interventioneller Studien (NIS) sowie Begleitung von Investigator Initiated Studies (IIS) Teilnahme an Kongressen und Symposien, Erstellung von Kongressberichten und wissenschaftlicher Support vor Ort Bewertung und Diskussion präklinischer und klinischer Projektanträge sowie aktive Mitwirkung an laufenden medizinischen Projekten Identifikation regionaler Versorgungslücken und Ableitung von Maßnahmen zur Verbesserung der Versorgungssituation gemeinsam mit Experten, Fachgesellschaften und Verbänden Planung und Durchführung [. .. ]

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Job am 14.11.2025 bei Jobleads gefunden

Medical Science Liaison (mwd) Immunologie

• Düsseldorf, Nordrhein- Westfalen Abgeschlossenes Studium Firmenwagen Flexible Arbeitszeiten 30+ Urlaubstage [. .. ] Markterfolg innovativer Therapien bei. Deine Aufgaben Aufbau und Pflege von Beziehungen zu Key Opinion Leaders (KOLs) Studienzentren und medizinischen Fachgesellschaften Präsentation wissenschaftlicher Daten und Studienergebnisse zu immunologischen [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Therapien Unterstützung von Investigator Initiated Trials (IITs) und klinischen Studienprogrammen Durchführung wissenschaftlicher Schulungen für interne Teams (z. B. Vertrieb Marketing Medical Affairs) Beobachtung und Bewertung aktueller Forschungsergebnisse Trends und Publikationen im Bereich Immunologie Teilnahme an medizinischen Kongressen Symposien und Advisory Boards Unterstützung der medizinisch-wissenschaftlichen Kommunikation im Rahmen von Markteinführungen Das bringst du mit [. .. ] einem dynamischen forschungsnahen Umfeld Interesse Dann sende uns deinen CV an Oder melde dich direkt über Linked In wir freuen uns auf den Austausch Key Skills Presentation Skills, Time Management, Clinical Research, Communication skills, GCP, Infusion Experience, Managed Care, Hospice Care, Conflict Management, Clinical Trials, Research Experience, Home Care Employment Type: Full Time Experience: years Vacancy: 1 #J-18808-Ljbffr 69377191 [. .. ]

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Job am 10.10.2025 bei Jobleads gefunden Medical Science Liaison • München, Bayern Firmenwagen 30+ Urlaubstage [. .. ] innovative global specialty pharma business and a preferred partner for innovator pharma companies, instigating a paradigm shift in the lifecycle management of iconic medicines. We seek to [...]
MEHR INFOS ZUM STELLENANGEBOT[...] extensively engage with clinical communities to communicate product improvements and prioritise environmental, social, and governance considerations across the business and workforce. Pharmanovias therapeutic areas include Cardiovascular, Oncology, Endocrinology and Neurology. About The Role Reporting to the Medical Department, you will be a member of the MSL team, whose primary responsibility is to interact with [. .. ] Identifying, developing, and maintaining professional relationships with national/ regional KOLs, establishing peertopeer collaborations with key medical experts in the therapeutic areas covered by Pharmanovia. Supporting evidence generation initiatives including potential investigator site identification, trial recruitment, registries, and presentation of final approved data, involving experts to generate scientific data including investigatorinitiated trials. Collaborating with physicians on medical affairs initiatives including publication and communication plans, advisory boards, medical education opportunities, webinars, training, and speaker development. Serving as a scientific peertopeer resource to external [. .. ]

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Job am 27.06.2025 bei Jobleads gefunden

Senior/ Medical Director (Ophthalmology) 0.5 FTE

Führungs-/ Leitungspositionen [. .. ] Senior/ Medical Director (Ophthalmology) , 0.5 FTE. TFS Health Science is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout [...]
MEHR INFOS ZUM STELLENANGEBOT[...] their clinical development journey. Join our team as a Senior/ Medical Director (Ophthalmology) . The Senior/ Medical Director is a key member of the Project Delivery team, working independently to manage safety and medical matters in line with company policies, standard operating procedures (SOPs) , and regulatory requirements. With deep medical expertise, [. .. ] and answering complex questions related to medical, legal, and regulatory concerns. Responsibilities Expert Guidance: Provide advanced medical input on study design, measurement strategies, and trial protocols, including safety sections and investigator brochures. Comprehensive Safety Oversight: Review safety data such as adverse events, labs, vital signs, ECGs, and clinical trial reports from a medical perspective. Regulatory Risk Support: Conduct senior-level medical reviews of individual cases, cumulative listings, PSURs, PBRERs, DSURs, and Risk Management Plans. Medical Monitoring Signal Detection: Serve as a [. .. ]

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Neu Job vor 3 Std. bei Jobleads gefunden Clinical Research Associate-12 months monitoring experience required • Frankfurt (Oder) , Brandenburg Senior CRA ICON plc is a worldleading healthcare intelligence and clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to [...]
MEHR INFOS ZUM STELLENANGEBOT[...] join us on our mission to shape the future of clinical development. Role: Clinical Research Associate (12+ months monitoring experience required) Location: Must be based in the UK, ideally in the Midlands [. .. ] corrective actions are implemented within specified timelines. Identify issues at sites, resolve and escalate as appropriate; collaborate with stakeholders to manage data query resolution for accurate data entry. Ensure the Investigator Folder is up to date and maintain TMFs. Negotiate investigator remuneration, prepare financial contracts, and trigger payments to investigational sites. You will need the following: Right to work in the UK. Up to 2years of pharmaceutical industry experience or other relevant experience (NHS or Academic) . Good knowledge of the [. .. ]

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Job gestern bei Jobleads gefunden Junior Clinical Research Associate Absolventen, Einsteiger, Trainees The Clinical Research Associate at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development. For those with medical [...]
MEHR INFOS ZUM STELLENANGEBOT[...] and/or health/ life science interest and background who want to explore the research field, travel throughout Germany, Austria, Switzerland, and be part [. .. ] monitoring, and closeout visits for research sites in compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians and their site staff; Verifying adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP and applicable regulatory [. .. ]

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Job gestern bei Jobleads gefunden GCP QA Consultant • Berlin Beratungs-/ Consultingtätigkeiten Champion compliance and precision-help deliver life-changing therapies. Proclinical is seeking a GCP QA Consultant to support quality assurance activities for oncology-focused clinical trials. This role involves overseeing quality processes [...]
MEHR INFOS ZUM STELLENANGEBOT[...] for phase 2-3 studies, ensuring compliance with ICH-GCP and regulatory requirements, and managing risk-based quality plans. You will collaborate with internal teams and external partners to maintain high standards of clinical trial execution and inspection readiness. This is a fully remote position, open to candidates located anywhere within Europe. Responsibilities Develop and oversee study quality-related plans, including Oversight Quality and Audit Plans. Collaborate with third parties to formalize Investigator Site Audits (ISA) and agendas. Oversee quality activities for phase 2-3 trials, focusing on risk management and endpoint de-risking. Conduct risk-based reviews of study documents to ensure compliance with protocols, ICH-GCP, and regulatory requirements. Act as the Clinical Quality Assurance Representative in weekly monitor-site meetings. [. .. ]

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Job gestern bei Jobleads gefunden Principal Lead Data Manager • München, Bayern Führungs-/ Leitungspositionen [. .. ] employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Job Description Acts as primary communication point for project teams and company [...]
MEHR INFOS ZUM STELLENANGEBOT[...] departments regarding clinical data management. Acts as primary communication point for clients/ vendors for all data management aspects of clinical projects and clinical data management reporting. Responsible for the supervision of all project data management activities of assigned studies. Coordinates data management activities within clinical projects including but not limited to EDC development, [. .. ] findings pertaining to Data Management. Trains Lead Data Managers, Data Managers and Assistant Data Managers. Conducts project-specific training of the clinical team in CRF completion and presents at the Investigator Meetings. Provides input into proposals and assists with Business Development activities. Participates in process improvement activities at corporate/ departmental level. Qualifications College or University degree or equivalent combination of training and experience that presents the required knowledge, skills, and abilities Minimum of five years of CRO industry experience as a [. .. ]

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Job gestern bei Jobleads gefunden GCP QA Consultant Beratungs-/ Consultingtätigkeiten [. .. ] top-tier QA talent with groundbreaking life sciences opportunities Champion compliance and precisionhelp deliver lifechanging therapies. Proclinical is seeking a GCP QA Consultant to support quality assurance activities [...]
MEHR INFOS ZUM STELLENANGEBOT[...] for oncologyfocused clinical trials. This role involves overseeing quality processes for phase 23 studies, ensuring compliance with ICHGCP and regulatory requirements, and managing riskbased quality plans. You will collaborate with internal teams and external partners to maintain high standards of clinical trial execution and inspection readiness. This is a fully remote position, open to candidates located anywhere within Europe. Responsibilities Develop and oversee study qualityrelated plans, including Oversight Quality and Audit Plans. Collaborate with third parties to formalize Investigator Site Audits (ISA) and agendas. Oversee quality activities for phase 23 trials, focusing on risk management and endpoint derisking. Conduct riskbased reviews of study documents to ensure compliance with protocols, ICHGCP, and regulatory requirements. Act as the Clinical Quality Assurance Representative in weekly monitorsite meetings. Monitor site performance, ensuring adherence [. .. ]

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Job gestern bei Jobleads gefunden Medical Science Liaison, Immunology (IBD) , Germany • Berlin Work-Life-Balance [. .. ] supports colleagues to manage all aspects of their wellbeing by focusing on a holistic approach What Youll Be Doing In this role you will support activities across [...]
MEHR INFOS ZUM STELLENANGEBOT[...] both Medical Affairs Clinical Development objectives for the portfolio of pipeline products in inflammatory bowel disease. You will serve as a key interface with clinical trial sites across all development programs, working closely with Clinical Development and Clinical Operations. Additionally, you will collaborate with Medical Affairs to identify and engage key opinion leaders within [. .. ] meetings Sharing important clinical and scientific insights that you have gathered from fieldwork to cross-functional teams Acting as an internal and external scientific expert Adhering to compliance requirements Supporting investigator-initiated studies What Youll Need To Be Successful An advanced doctoral degree (MD, Ph D, Pharm D) is preferred Relevant therapeutic area knowledge in the field of immunology or immuno-oncology, experience in gastroenterology is a plus. Post graduate therapeutic area experience is preferred Fluency in English and local language 3+ [. .. ]

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Häufig gestellte Fragen

Wieviel verdient man als Clinical Investigator pro Jahr?

Als Clinical Investigator verdient man zwischen EUR 60.000,- bis EUR 90.000,- im Jahr.


Wieviele offene Stellenangebote gibt es für Clinical Investigator Jobs bei unserer Jobsuche?

Aktuell gibt es auf JobRobot 228 offene Stellenanzeigen für Clinical Investigator Jobs.


Wieviele Unternehmen suchen nach Bewerbern für Clinical Investigator Jobs?

Aktuell suchen 18 Unternehmen nach Bewerbern für Clinical Investigator Jobs.


Welche Unternehmen suchen nach Bewerbern für Clinical Investigator Stellenangebote?

Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Investigator Stellenangebote:


  • Tigermed (32 Jobs)
  • Veeda Lifesciences (11 Jobs)
  • wax. (11 Jobs)
  • Tubulis GmbH (11 Jobs)
  • TFS Health Science (10 Jobs)
  • LEO Pharma (3 Jobs)


In welchen Bundesländern werden die meisten Clinical Investigator Jobs angeboten?

Die meisten Stellenanzeigen für Clinical Investigator Jobs werden derzeit in Bayern (38 Jobs), Nordrhein-Westfalen (36 Jobs) und Niedersachsen (17 Jobs) angeboten.


Zu welchem Berufsfeld gehören Clinical Investigator Jobs?

Clinical Investigator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.


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Dauer: 0.0626 s., Vers. V.2025-d-2009-Ind-141