14 Jobs für Medical Trials in Düsseldorf
Stellenangebote Medical Trials in Düsseldorf Jobs
Job am 14.11.2025 bei Jobleads gefunden
• Düsseldorf, Nordrhein- Westfalen
Abgeschlossenes Studium
Firmenwagen Flexible Arbeitszeiten 30+ Urlaubstage
Medical Science Liaison (m/w/d) Immunologie Düsseldorf Vollzeit Ab sofort Über uns Cube4 Consulting ist spezialisiert auf Recruitment Prozessberatung in regulierten Branchen wie Pharma Biotechnologie und Medizintechnik. Wir unterstützen Unternehmen bei [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] der Besetzung von Schlüsselpositionen mit qualifizierten Fach- und Führungskräften und begleiten unsere Kandidaten auf ihrem nächsten Karriereschritt. Deine Mission [. .. ] 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 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 Abgeschlossenes Studium [. .. ]
Job am 17.10.2025 bei Jobleads gefunden
• Düsseldorf, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] Be part of a multidisciplinary and focused team, that works towards getting novel promising ADCs to patients with solid and hematological cancers. Be Part of Our Team [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] As an Associate Medical Director/ Medical Director and member of our Clinical Development team, you will support the planning and execution of full life-cycle development of our antibody-drug conjugates (ADCs) global clinical trials. You will lead all clinical aspects of clinical trials, provide support to the Clinical Trial Team (CTT) , ensure patient safety, and support the company in clinical development and in medical aspects of early development. You will be responsible for clinical trial execution and analysis and serve as a key [. .. ]
Job am 28.09.2025 bei Jobleads gefunden
• Düsseldorf, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] oncology drug products across clinical development and commercialisation Phases. This leadership role is central to ensuring safe, compliant, and successful oncology drug development and to maximising patient [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] safety from clinical trials to post-marketing surveillance. This position will report to the Chief Medical Officer and can be based on a hybrid basis from the company office in Germany or remotely. Your mission Develop and execute the overall drug safety and pharmacovigilance (PV) strategy aligned with company and global regulatory requirements, especially for oncology assets. Oversee safety surveillance, signal detection, risk assessment, and risk [. .. ]
Job am 05.12.2025 bei Jobleads gefunden
• Düsseldorf, Nordrhein- Westfalen
Beratungs-/ Consultingtätigkeiten
Our client has a fantastic opportunity for a Senior
Medical Science Liaison (MSL) / Regional Medical Advisor to join the Medical team. This role will focus on the Central/ Southern [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] part of Germany. This role will support their portfolio of products and relay 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 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 [. .. ]
Job am 21.11.2025 bei Jobleads gefunden
• Düsseldorf, Nordrhein- Westfalen
[. .. ] Scientist (m/f/d) and member of our Clinical Development team, you will support the planning and execution of full life-cycle development of our antibodydrug conjugates (ADCs) global clinical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] trials. You will support the review, analysis, and interpretation of clinical trial data, contribute to the development of critical clinical trial documents, and take an active role in risk monitoring and mitigation. You will be part of a highly collaborative and crossfunctional team involved with site evaluation, study startup, study execution [. .. ] study closeout of our trials. This position will report to the VP, Clinical and Translational Development and will be based in Munich or remotely in Germany. Your mission Support the Medical Director in the oversight of clinical studies including review and interpretation of clinical trial data and timely execution of deliverables in collaboration with relevant internal and external partners. Take a lead role in writing protocol amendments, informed consents, and other protocolrelated documents for the operational execution of clinical studies. Participate [. .. ]
Job am 13.11.2025 bei Jobleads gefunden
Overview Join to apply for the Senior
Medical Affairs Specialist-Region West-Mainz, Köln, Düsseldorf (m/w/d) role at Dexcom. Dexcom Corporation (NASDAQ: DXCM) is a pioneer and a global leader in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] continuous glucose monitoring (CGM) . We aim to improve human health by providing accessible information and insights that lead to better health outcomes. Our future [. .. ] updates on current research and clinical practices during product launches, customer meetings and training sessions. Clinical Research Support Support the clinical research teams to identify sites and investigators for clinical trials. Data Dissemination and Insights Gather information from KOLs on how they are using our products. Provide feedback to marketing and sales to help develop marketing materials and commercial strategy. Represent the company at scientific conferences, meetings, and advisory boards, communicating data and engaging in scientific discussions. Compliance and Reporting Ensure [. .. ]
Job am 07.09.2025 bei Jobleads gefunden
• Düsseldorf, Nordrhein- Westfalen
[. .. ] an experienced Senior Clinical Research Associate to join an innovative, fast-growing biopharmaceutical organisation advancing nextgeneration cell and gene therapies. You will play a key role in overseeing [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] complex clinical trials, ensuring highquality monitoring, and driving operational excellence across German study sites. This is an opportunity to work at the cutting edge of science, supporting transformative therapies that have the potential to redefine treatment outcomes for patients with severe and rare diseases. Key Responsibilities Perform independent onsite and remote monitoring activities [. .. ] industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including : Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/ Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/ belief, sexual orientation or age. #J-18808-Ljbffr 61332110 [. .. ]
Job am 27.11.2025 bei Neuvoo.com gefunden
wax.
Senior Regional Medical Advisor-Rare Disease (Central/ South)
• Düsseldorf
Our client has a fantastic opportunity for a Senior
Medical Science Liaison (MSL) / Regional Medical Advisor to join the Medical team. This role will focus on the Central/ [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Southern part of Germany. This role will support their portfolio of products and relay 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 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 [. .. ]
Job am 20.11.2025 bei Neuvoo.com gefunden
Tigermed
• Düsseldorf
[. .. ] all studies. Conduct monitoring visit according to monitoring plan and SOP; address issues with sites and complete monitoring visit report in a timely manner. Ensure timely coordination [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of study materials (medical device, IVD, drug, non-drug, equipment) to the site for start-up and throughout the study. 2. Training Provide ongoing training to site staff with regards to GCP, study protocol and requirements. Conduct site initiation to ensure that the site has a thorough understanding of the study protocol and requirements. [. .. ] processes/ procedures. Good working and proactive attitude. Ability to work in team. 3. Working Experience: At least 2 years of CRA experiences. Experience in at least 3 medical device clinical trials. 4. Language ability: Good written and oral English. 5. Computer: Proficient Microsoft Word, Excel, PPT and Outlook, etc 6. Other abilities such as Communication skills Information-gathering skills Knowledge and/or experience in medical practice is a plus. 70058366 [. .. ]
Job am 20.11.2025 bei Neuvoo.com gefunden
Tigermed
• Düsseldorf
1. Job Purpose To implement project management of clinical
trials effectively, and to ensure success of clinical trials. 2. Responsibilities Make the project management plan: To draft and implement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] feasible project management plan according to SOPs, ICH GCP Guidelines, ISO14155 and other applicable regulations. Ensure the trial in managed under the project management plan. Make monitoring plan: To draft and [. .. ] Manage site feasibility, site selection, initiation, monitoring, and close-out activities. Client Maintenance: Keep positive relationship with sponsor and investigator. 3. Minimum Qualifications a Academic/ Major: Bachelor degree or above in Medical, Pharmacology or Biology related majors. b) Professional Skills Adequate knowledge of medical device development, including local regulation, GCP. GCP certificate required. (c) Working Experience At least 5 years clinical trial experience, at least 3 years of independent project management experience. Experience of at least 3 medical device clinical trials. (d) [. .. ]
Job am 09.11.2025 bei Neuvoo.com gefunden
Tubulis GmbH
Associate Medical Director/ Medical Director
• Düsseldorf
Führungs-/ Leitungspositionen
[. .. ] Be part of a multidisciplinary and focused team, that works towards getting novel promising ADCs to patients with solid and hematological cancers. Be Part of Our Team [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] As an Associate Medical Director/ Medical Director and member of our Clinical Development team, you will support the planning and execution of full life-cycle development of our antibody-drug conjugates (ADCs) global clinical trials. You will lead all clinical aspects of clinical trials, provide support to the Clinical Trial Team (CTT) , ensure patient safety, and support the company in clinical development and in medical aspects of early development. You will be responsible for clinical trial execution and analysis and serve as a key [. .. ]
Job am 14.10.2025 bei Neuvoo.com gefunden
Tubulis GmbH
Clinical Scientist-Manager/ Senior Manager (m/f/d)
• Düsseldorf
[. .. ] (m/f/d) and member of our Clinical Development team, you will support the planning and execution of full life-cycle development of our antibody-drug conjugates (ADCs) global clinical
MEHR INFOS ZUM STELLENANGEBOT
[...] class=highlight_text>trials. You will support the review, analysis, and interpretation of clinical trial data, contribute to the development of critical clinical trial documents, and take an active role in risk monitoring and mitigation. You will be part of a highly collaborative and cross-functional team involved with site evaluation, study start-up, [. .. ] close-out of our trials. This position will report to the VP, Clinical and Translational Development and will be based in Munich or remotely in Germany. Your mission Support the
Medical Director in the oversight of clinical studies including review and interpretation of clinical trial data and timely execution of deliverables in collaboration with relevant internal and external partners. Take a lead role in writing protocol amendments, informed consents, and other protocol-related documents for the operational execution of clinical studies. [. .. ]
▶ Zur Stellenanzeige
Job am 14.10.2025 bei Neuvoo.com gefunden
Tigermed
Contractor CRA-Tigermed Jyton-Germany
• Düsseldorf
[. .. ] all studies. Conduct monitoring visit according to monitoring plan and SOP; address issues with sites and complete monitoring visit report in a timely manner. Ensure timely coordination [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of study materials (medical device, IVD, drug, non-drug, equipment) to the site for start-up and throughout the study. 2. Training Provide ongoing training to site staff with regards to GCP, study protocol and requirements. Conduct site initiation to ensure that the site has a thorough understanding of the study protocol and requirements. [. .. ] processes/ procedures. Good working and proactive attitude. Ability to work in team. 3. Working Experience: At least 2 years of CRA experiences. Experience in at least 3 medical device clinical trials. 4. Language ability: Good written and oral English. 5. Computer: Proficient Microsoft Word, Excel, PPT and Outlook, etc 6. Other abilities such as Communication skills Information-gathering skills Knowledge and/or experience in medical practice is a plus. 65906870 [. .. ]
Job am 14.10.2025 bei Neuvoo.com gefunden
Bio Talent
Global Head of Pharmacovigilance
• Düsseldorf
Führungs-/ Leitungspositionen
[. .. ] oncology drug products across clinical development and commercialisation phases. This leadership role is central to ensuring safe, compliant, and successful oncology drug development and to maximising patient [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] safety from clinical trials to post-marketing surveillance. This position will report to the Chief Medical Officer and either work on a hybrid basis from the company office in Germany or on a remote basis. Your mission Develop and execute the overall drug safety and pharmacovigilance (PV) strategy aligned with company and global regulatory requirements, especially for oncology assets. Oversee safety surveillance, signal detection, risk assessment, [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Medical Trials pro Jahr?
Als Medical Trials verdient man zwischen EUR 40.000,- bis EUR 70.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Medical Trials Jobs in Düsseldorf bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 14 offene Stellenanzeigen für Medical Trials Jobs in Düsseldorf.
Wieviele Unternehmen suchen nach Bewerbern für Medical Trials Jobs in Düsseldorf?
Aktuell suchen 5 Unternehmen nach Bewerbern für Medical Trials Jobs in Düsseldorf.
Welche Unternehmen suchen nach Bewerbern für Medical Trials Stellenangebote in Düsseldorf?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Medical Trials Stellenangebote in Düsseldorf:
- Tigermed (3 Jobs)
- Tubulis GmbH (2 Jobs)
- wax. (1 Job)
- Bio Talent (1 Job)
Zu welchem Berufsfeld gehören Medical Trials Jobs in Düsseldorf?
Medical Trials Jobs in Düsseldorf gehören zum Berufsfeld Forschung, Lehre, Wissenschaft.
