172 Jobs für Clinical Investigator
Stellenangebote Clinical Investigator Jobs
Job vor 9 Tagen bei Jobleads gefunden
• Berlin
[. .. ] contract and budgets specialist to join our team in Germany. In this role you will be responsible for direct site facing contract and budget negotiations through contract [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] execution with assigned clinical investigator sites including initial agreements and amendments and oversight of other contracting professionals on assigned studies. This also includes managing the Per-Subject Cost (PSC) process for assigned studies, managing escalation and resolution for budget and non-legal term issues from other ICL or preferred Contract Research Organizations (p CRO) and collaborating [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
Medical Science Liaison Rare Disease (m/w/d) Region Nord
• Berlin
[. .. ] and 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] conferences, 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 vor 13 Tagen bei Jobleads gefunden
• Leipzig, Sachsen
[. .. ] and 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] conferences, 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 vor 14 Tagen bei Jobleads gefunden
Medical Science Liaison Rare Disease (m/w/d) Region Süd
• Heidelberg, Baden- Württemberg
[. .. ] aligned to strategy within the business Serve as an 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 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 11.03.2026 bei Jobleads gefunden
Medical Science Liaison Rare Disease (m/w/d) Region Nord
[. .. ] aligned to strategy within the business Serve as an 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 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 11.03.2026 bei Jobleads gefunden
Medical Science Liaison Rare Disease (m/w/d) Region Süd
• Frankfurt, Hesse
[. .. ] aligned to strategy within the business Serve as an 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 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 11.03.2026 bei Jobleads gefunden
• Nürnberg, Bayern
[. .. ] aligned to strategy within the business Serve as an 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 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 11.03.2026 bei Jobleads gefunden
Medical Science Liaison Rare Disease (m/w/d) Region Süd
• München, Bayern
[. .. ] aligned to strategy within the business Serve as an 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 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 07.03.2026 bei Jobleads gefunden
Medical Science Liaison Rare Disease (m/w/d) Region Süd
• Stuttgart, Baden- Württemberg
[. .. ] aligned to strategy within the business Serve as an 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 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 07.03.2026 bei Jobleads gefunden
Medical Science Liaison Rare Disease (m/w/d) Region Nord
• Bremen
[. .. ] aligned to strategy within the business Serve as an 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 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 05.03.2026 bei Jobleads gefunden
Medical Science Liaison Rare Disease (m/w/d) Region Nord
• Berlin
[. .. ] 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 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 Works to the highest ethical compliance, ethics and safety standards adhering to all local regulations and laws Maintains [. .. ]
Job am 05.03.2026 bei Jobleads gefunden
Medical Science Liaison Rare Disease (m/w/d) Region Nord
• Hannover, Niedersachsen
[. .. ] aligned to strategy within the business Serve as an 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 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 05.03.2026 bei Jobleads gefunden
Medical Science Liaison Rare Disease (m/w/d) Region Nord
• Kiel, Schleswig- Holstein
[. .. ] 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 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 Works to the highest ethical compliance, ethics and safety standards adhering to all local regulations and laws Maintains [. .. ]
Job am 12.02.2026 bei Neuvoo gefunden
Parexel
Site Contract and Budget Specialist-Remote-FSP
• Berlin
[. .. ] contract and budgets specialist to join our team in Germany. In this role you will be responsible for direct site facing contract and budget negotiations through contract [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] execution with assigned clinical investigator sites including initial agreements and amendments and oversight of other contracting professionals on assigned studies. This also includes managing the Per-Subject Cost (PSC) process for assigned studies, managing escalation and resolution for budget and non-legal term issues from other ICL or preferred Contract Research Organizations (p CRO) and collaborating [. .. ]
Job vor 2 Tagen bei StepStone gefunden
Dr. Falk Pharma GmbH
• Freiburg
Führungs-/ Leitungspositionen Homeoffice möglich
[. .. ] firmly believe that medical progress can only be achieved by working together. That is why we are looking for: Your tasks Serves as medical lead (ML) for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the company-sponsored clinical trials and development programs. Responsible for guiding the clinical development strategy and ensuring the scientific integrity of clinical trials. ML collaborates with Clinical Research teams and serves as a key liaison between Clinical Research and Global Safety teams. ML manages all medical aspects of clinical trials and contributes to the [. .. ] medical expertise in the review of adverse events and safety issues, as requested Provides support in the review of scientific publications (abstracts, presentations, and manuscripts) Supports review of concepts for investigator-initiated studies Contributes to company-internal process improvement initiatives (e. g. SOP updates) Your qualification Physician/ medical license holder A minimum of 5 years of clinical development research, or related clinical research experience within the industry (pharmaceutical, biotech, CRO) at an international (Europe, USA, Australia) level is required Knowledge in [. .. ]
Job vor 3 Tagen bei StepStone gefunden
Universität Bielefeld
Klinischer Studienkoordinatorin (m/w/d) / Study Nurse (m/w/d) für Investigator Initiated Trials-AG Translationale Pharmakologie
• Bielefeld
Homeoffice möglich Abgeschlossenes Studium
Flexible Arbeitszeiten
[. .. ] grundsätzlich auch eine Besetzung in Teilzeit erfolgen. In der Medizinischen Fakultät OWL ist die folgende Position zu besetzen: Klinischer Studienkoordinatorin (m/w/d) / Study Nurse (m/w/d) für
Investigator [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Initiated Trials-AG Translationale Pharmakologie Kennziffer: Tech26019 Start: nächstmöglich Vollzeit Vergütung je nach Qualifikation und Aufgabenübertragung bis zu E10 TV-L befristet Aufbau und regulatorische Leitung einer Studienambulanz (25 ) Mitarbeit bei der Anbahnung und Planung von Investigator Initiated Trials (wissenschaftsgetriebener klinischer Studien) in einem multidisziplinären Team organisatorische Leitung der [. .. ] Schrift) sichere Kenntnisse im Umgang mit MS Office Interesse an international vernetztem, wissenschaftlichem Arbeiten Das wünschen wir uns zertifizierte Qualifizierung zur Study Nurse/ Studienassistentin/ Studien Koordinatorin zertifizierte Weiterbildung in Good Clinical Practice Erfahrung in der Vorbereitung von Genehmigungsverfahren von klinischen Studien Qualifizierung zur venösen Blutentnahmen EDV-Kenntnisse (z. B. Klinische Studien Dokumentation) englische Sprachkenntnisse in Wort und Schrift weitere Sprachkenntnisse in Wort und Schrift Gefahrgutschulung (IATA) Vergütung je nach Qualifikation und Aufgabenübertragung bis zu E10 TV-L befristet auf 2 Jahre [. .. ]
Job vor 7 Tagen bei StepStone gefunden
Universitätsklinikum Ulm
• Ulm
Teilzeit
Betriebliche Altersvorsorge Tarifvertrag
[. .. ] (w/m/d) , Sponsoren (w/m/d) , Industriepartner (w/m/d) , CROs (w/m/d) und Patienten (w/m/d) Erhebung und Dokumentation studienrelevanter Daten Pflege des
Investigator Site Files (ISF) Vorbereitung und Teilnahme [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] an Studieninitiierungen, Monitorvisiten, Audits und Behördeninspektionen Medizinische Vorbildung in Form einer Ausbildung in einem Gesundheitsberuf (z. B. Gesundheits- und Krankenpflege, Medizinische Dokumentation) oder eine akademische Vorbildung im natur-oder gesundheitswissenschaftlichen Bereich (z. B. Informationsmanagement im Gesundheitswesen) Erfahrung im Bereich klinischer Studien/ Registerstudien wünschenswert Kenntnisse der gesetzlichen Anforderungen im Bereich klinischer Studien und Good Clinical Practice (GCP) wünschenswert Kenntnisse der medizinischen Terminologie Sehr gute Organisations-, Kommunikations- und Zeitmanagementfähigkeiten Gute Englischkenntnisse in Wort und Schrift Sicherer Umgang mit Standard-EDV (z. B. MS-Office) Verantwortungsbewusste Arbeitsweise und Freude am selbständigen Arbeiten Fundierte Einarbeitung unter fachlich kompetenter Anleitung in neue Themenbereiche Ein interessantes Aufgabengebiet mit vielfältigen [. .. ]
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
Fortrea
FSP Start Up Contract Finance Specialist based in Vienna
• AT- 9 Wien
We are looking for a
Clinical Start Up Contract Finance Specialist to support clinical trial startup activities across Austria. This role is an excellent opportunity for professionals with experience in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical startup operations, budget/ contract negotiations, and regulatory processes even if they have not previously worked in a Lead position. The successful candidate will receive development [. .. ] submissions and approvals for assigned protocols. Manage country-level deliverables, timelines, and outcomes to meet study commitments. Collaborate closely with sponsors, CROs, and site teams to streamline startup processes. Negotiate investigator budgets, manage financial forecasting, and track trialrelated expenses. Ensure timely delivery of clinical and financial contracts within fair market value through strong partnerships with local clinical teams. Oversee and track clinical researchrelated payments. Conduct payment reconciliation at study closeout. Qualifications University degree (life sciences preferred) or equivalent healthcarerelated certification. Fortrea [. .. ]
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
Syneos Health
• AT- 9 Wien
Description On-site monitor open to diverse EMEA countries. Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to [. .. ] ability to perform activities for assigned sites working with study start-up and regulatory. Conduct of all remote and on-site monitoring activities through all study stages. Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness. Reconciles contents of the ISF with the Trial Master File (TMF) . Ensures the investigator/ physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations. Documents activities via confirmation letters, follow-up letters, trip [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
MSD Österreich
Senior Director Medical Affairs (m/f/d)
• AT- 9 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 [. .. ] experience of the successful candidate. We are looking forward to receiving your application. 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 J-18808-Ljbffr 85459742 [. .. ]
Job vor 7 Tagen bei Mindmatch.ai gefunden
Milestone One
Clinical Site Coordinator
• AT- 9 Wien
Milestone One is a Site Enabling Services organization with global headquarters in Zug, Switzerland. We understand what
clinical study sites need and our overall mission is to support sites [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in stronger study delivery. Job Description The Milestone One Site Coordinator role supports a Clinical Study Site in clinical trial related activities according to ICHGCP, protocol requirements within Study specific defined timelines and enrollment goals. The function of the [. .. ] reconciliation of investigational products and clinical supplies. Collect, handle and maintain all sitespecific regulatory documents as needed. Facilitate and support the contract and budget negotiations at the site level. Support Investigator and Site payments and processes as needed. Schedule and/or perform study procedures as per study requirements and delegation of responsibilities. Prepare for and participate in onsite study audits or regulatory agency inspections. Qualifications A university degree in Life Science, preferably in pharmacy, nursing or lab analytics. Minimum of 2 [. .. ]
Job vor 12 Tagen bei Mindmatch.ai gefunden
PSI CRO
Clinical Site Coordinator
• AT- 9 Wien
Company Description Milestone One is a Site Enabling Services organization with global headquarters in Zug, Switzerland. We understand what
clinical study sites need and our overall mission is to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] support sites in stronger study delivery. Job Description The Milestone One Site Coordinator role supports a Clinical Study Site in clinical trial related activities according to ICH-GCP, protocol requirements within Study specific defined timelines and enrollment goals. The function of [. .. ] accountability and reconciliation of investigational products and clinical supplies. Collect, handleand maintainall site-specific regulatory documents as needed. Facilitateand support the contract and budget negotiations at the site level. Support Investigator and Site payments and processes as needed. Scheduleand/or performstudy procedures as per study requirements and delegation of responsibilities. Preparefor and participatein onsite study audits or regulatory agency inspections. Qualifications A university degree in Life Science, preferably in pharmacy, nursing or lab analytics. Minimum of 2 years of on-the-[. .. ]
Job am 06.03.2026 bei Mindmatch.ai gefunden
Alimentiv
Join our Talent Pool-Clinical Research Associates (Eastern Europe)
• AT- 9 Wien
[. .. ] quite matches what youre looking for, or not ready to make a move yet? Let us know We are proactively inviting qualified candidates to join our talent [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] pool for anticipated Clinical Research Associate needs (across multiple seniority levels) to support our Clinical Monitoring team. What the process looks like: A Talent Acquisition representative will contact selected candidates to schedule a qualifying call to learn more about your experience, and what your timeline looks like Well also share details about timelines on [. .. ] regulatory compliance. Assist/ lead (as appropriate) with query resolution, safety reviews, and adverse event follow-up throughout the study lifecycle. Support/ conduct (as appropriate) site startup and activation activities, including investigator coordination, trial material delivery, and recruitment support. Maintain accurate, timely, and complete TMF documentation, requesting updates as required. Provide day-to-day operational support to Senior CRA, and Lead CRAs. Participate in training, study meetings, and CRA development activities, building competencies required for role progression. Sr. Clinical Research Associate As [. .. ]
Job am 06.03.2026 bei Mindmatch.ai gefunden
PSI CRO
Site Identification Specialist
• AT- 9 Wien
[. .. ] committed to delivering high-quality, timely services across a wide range of therapeutic areas. Job Description We are in search of an experienced professional dedicated to developing strategic [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] relationships with clinical research sites, with the aim of optimizing and advancing the progress of clinical trials. Hybrid role in Vienna, Austria This is the main responsibility of a site ID specialist. Communicate and build relationship with clinical sites to identify potential centres for clinical trials. Maintain and refine internal site databases in [. .. ] recommended investigators or clinical sites. Support the project team throughout study startup and further on, whenever additional rounds of site identification are necessary, and/or additional information on the site/ investigator is needed. Qualifications University/ college degree (Md/Pharm D degree) , or an equivalent combination of education, training and experience. On-site monitoring experience is a plus. Understanding of Good Clinical Practice, local laws and applicable regulations in the region. Demonstrated ability to work in a dynamic environment, under compressed deadlines [. .. ]
Job am 02.03.2026 bei Mindmatch.ai gefunden
Syneos Health
CRA single sponsor-Germany
• AT- 9 Wien
Description CRA single sponsor-Germany Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and commercial insights into [...]
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 are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to [. .. ] each subject/ patient, as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/ patient. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol deviation/ violations and pharmacovigilance issues. For the Clinical Monitoring/ Site Management Plan (CMP/ SMP) : Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) is accurate and complete. [. .. ]
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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 172 offene Stellenanzeigen für Clinical Investigator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Investigator Jobs?
Aktuell suchen 39 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:
- IQVIA (11 Jobs)
- PSI CRO (4 Jobs)
- GULP experts united (4 Jobs)
- Dr. Falk Pharma GmbH (3 Jobs)
- Thermo Fisher Scientific (3 Jobs)
- Alexion Pharmaceuticals (3 Jobs)
In welchen Bundesländern werden die meisten Clinical Investigator Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Investigator Jobs werden derzeit in Bayern (29 Jobs), Hessen (19 Jobs) und Baden-Württemberg (18 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Investigator Jobs?
Clinical Investigator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
