Medical Trials Stellenangebote in Essen


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11 Jobs für Medical Trials in Essen


Stellenangebote Medical Trials in Essen Jobs


Job am 17.10.2025 bei Jobleads gefunden

Associate Medical Director/ Medical Director

• Essen, 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 [. .. ]

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Job am 05.10.2025 bei Jobleads gefunden

Clinical Scientist-Manager/ Senior Manager (m/f/d)

• Essen, Nordrhein- Westfalen [. .. ] (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 trials. [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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, [. .. ] study 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. Responsibilities 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. [. .. ]

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Job am 27.09.2025 bei Jobleads gefunden

Global Head of Pharmacovigilance

• Essen, Nordrhein- Westfalen Führungs-/ Leitungspositionen [. .. ] compliance for oncology drug products across clinical development and commercialization phases, and is central to ensuring safe, compliant, and successful oncology drug development and to maximizing 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 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 [. .. ]

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Job vor 8 Tagen bei Neuvoo gefunden TFS Health Science

Senior Clinical Research Associate

• Essen, North Rhine- Westphalia [. .. ] dedicated to one sponsor. Please, keep in mind that this is a Freelance opportunity for approximately 0.7 FTE with sites in both Germany and Switzerland. Key Responsibilities [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Monitor clinical trials on-site and remotely in accordance with TFS/ client SOPs, FDA regulations, and GCP/ ICH guidelines Review CRFs (paper or electronic) and subject source documentation for validity and accuracy; generate queries to resolve data issues Identify site problems or deficiencies and report them to management through trip reports, memos, and [. .. ] CTMS with site and study information Audit data in tables and text of clinical summaries (as applicable) Qualifications: Bachelors degree, preferably in life sciences or nursing, or equivalent Experience in Medical Devices Solid understanding of Good Clinical Practice (GCP) regulations and ICH guidelines Ability to work independently and within a team/matrix organization Excellent written and verbal communication skills Strong organizational skills Ability and willingness to travel Experience with Medical Device submissions in both Germany and Switzerland is mandatory. What We [. .. ]

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Job am 27.11.2025 bei Neuvoo.com gefunden wax.

Senior Regional Medical Advisor-Rare Disease (Central/ South)

• Essen 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 [. .. ]

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Job am 20.11.2025 bei Neuvoo.com gefunden Tigermed

Contractor PM-Tigermed Jyton-Germany (MJ000034)

• Essen 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) [. .. ]

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Job am 20.11.2025 bei Neuvoo.com gefunden Tigermed

Contractor CRA-Tigermed Jyton-Germany (MJ000035)

• Essen [. .. ] 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. 70064962 [. .. ]

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Job am 11.11.2025 bei Neuvoo.com gefunden Tubulis GmbH Clinical Scientist-Manager/ Senior Manager (m/f/d) • Essen [. .. ] (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. [. .. ]

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Job am 11.11.2025 bei Neuvoo.com gefunden Tubulis GmbH Associate Medical Director/ Medical Director • Essen 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 [. .. ]

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Job am 14.10.2025 bei Neuvoo.com gefunden Bio Talent Global Head of Pharmacovigilance • Essen 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, [. .. ]

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Job am 14.10.2025 bei Neuvoo.com gefunden Tigermed Contractor CRA-Tigermed Jyton-Germany • Essen [. .. ] 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. 65912943 [. .. ]

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Jobs



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 Essen bei unserer Jobsuche?

Aktuell gibt es auf JobRobot 11 offene Stellenanzeigen für Medical Trials Jobs in Essen.


Wieviele Unternehmen suchen nach Bewerbern für Medical Trials Jobs in Essen?

Aktuell suchen 6 Unternehmen nach Bewerbern für Medical Trials Jobs in Essen.


Welche Unternehmen suchen nach Bewerbern für Medical Trials Stellenangebote in Essen?

Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Medical Trials Stellenangebote in Essen:


  • Tigermed (3 Jobs)
  • Tubulis GmbH (2 Jobs)
  • TFS Health Science (1 Job)
  • wax. (1 Job)
  • Bio Talent (1 Job)


Zu welchem Berufsfeld gehören Medical Trials Jobs in Essen?

Medical Trials Jobs in Essen gehören zum Berufsfeld Forschung, Lehre, Wissenschaft.


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Forschung, Lehre, Wissenschaft

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