Clinical Trials Management Stellenangebote in Hamburg

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Stellenangebote Clinical Trials Management Hamburg Jobs bei Mindmatch.ai

Neu Job heute gefunden Pharmiweb

Director Clinical Affairs

• Hamburg, HH Führungs-/ Leitungspositionen

MEHR

Job Description Position : Director of Clinical Affairs Role Overview : The Director of Clinical Affairs is responsible for driving the strategic direction and execution of the organizations clinical research initiatives, ensuring adherence to international standards and regulatory guidelines. This role involves global leadership across clinical operations, partnering with data management, regulatory teams, clinical research professionals, and other stakeholders. Key responsibilities include designing and overseeing clinical studies, managing clinical documentation, engaging with opinion leaders and site staff, and contributing to scientific publications to advance the organizations clinical objectives. Required Qualifications : Advanced degree in a relevant clinical, medical, or biomedical discipline. 5- 10 years of experience managing clinical trials, preferably in the medical device sector with an emphasis on cardiovascular studies. A minimum of 5 years leading cross- functional [...]

Neu Job heute gefunden Pharmiweb

Clinical Trial Site Relationship Coordinator

• Hamburg, HH

MEHR

Our clinical activities are growing rapidly, and we are currently seeking a full- time Clinical Trial Site Relationship Coordinator to join our [...] where you can grow your potential, then this is the opportunity for you. Responsibilities Provide ongoing support of sites, including identifying and discussing future new business opportunities and feasibility assessments; Develop effective plans for site contact and follow- up; Support management in expediting feasibility, site selection and study start- up; and May be responsible for other projects and responsibilities as assigned. [...] site information; and May be responsible for other projects and responsibilities as assigned, including site Qualification Visits, prepping/ consultation support for site audits, etc. Qualifications Minimum a Bachelor of Science in health- related field; Minimum 1 years site and clinical trials experience (more experience for the more senior positions required) ; CRA experience is an asset; Knowledge of drug development, clinical [...]

Stellenangebote Clinical Trials Management Hamburg Jobs bei Jobleads

Job vor 2 Tagen gefunden

Prüfärztin/ Prüfarzt (all genders)

• Hamburg, Berlin Jobticket Krisensicher

MEHR

[...] erfolgreiches und erfüllendes Arbeiten im Einklang mit den persönlichen Bedürfnissen und individuellen Lebensentwürfen der Mitarbeitenden stehen sollte. Und so unterschiedlich diese sind, so vielfältig ist unser Angebot an individuellen Lösungen. Ärztin/ Arzt als Prüfärztin/ Prüfarzt (all genders) für klinische Studien/ Clinical Trials In der Kinderneurologie des Kinder- UKE werden mehrere Phase- I- IV- Studien bei Kindern und Jugendlichen aller Altersklassen mit seltenen [...] Tätigkeiten als Prüfärzt:in (gemäß AMG) in Phase I- IV Studien, Härtefallprogrammen und klinischen Forschungsprojekten medizinische Betreuung der Studienteilnehmenden unter Supervision Erhebung und Dokumentation studienbezogener Daten: Anamneseerhebung, Untersuchung, Aufklärung, Einholen der Einwilligungserklärungen etc. Verarbeitung und Versand von Laborproben Blutentnahmen, Lumbalpunktionen Query- Management Pflege regulatorischer Dokumente Mitarbeit an der kontinuierlichen Qualitäts- und Prozessverbesserung Die Position ist zum nächstmöglichen Zeitpunkt mit ca. 20- 30 [...]
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Job vom 16.12.2024

Clinical Research Associate

• Hamburg, Berlin

MEHR

TFS Health Science is a leading global mid- size Contract Research Organization (CRO) dedicated to partnering with biotechnology and pharmaceutical companies throughout their entire clinical development journey. With expertise in full- service capabilities, resourcing, and Functional Service (FSP) solutions, we re looking for a talented [...] Associate with TFS Health Science, you will be a vital part of our SRS/ FSP team, working exclusively with a world- renowned global pharmaceutical/ biotech sponsor. You will play a crucial role in ensuring the quality and integrity of clinical trials, driving them forward from start to finish. Key Responsibilities Submission Amendment Support: Assist with initial and ongoing submissions, including amendments to ethics committees. Regulatory Reporting: Manage periodic reporting to ethics committees, including the reporting of safety events. Pre- activation SIV Support: Contribute to site pre- activation activities and support Site Initiation Visits (SIVs) . Monitoring Site Management: Conduct both onsite monitoring and periodic central monitoring to ensure trial integrity; manage site relationships and processes. Documentation Closeout: Maintain [...]
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Job vom 10.12.2024

Team Lead Copywriting (f/m/d)

• Hamburg, Berlin Führungs-/ Leitungspositionen

MEHR

[...] creation projects from concept to delivery, working closely with project stakeholders to ensure high- quality, on- time deliverables. Being responsible for error- free quality control of all medical copy deliverables. Overseeing development of medical copy concepts for marketing materials promoting clinical trials, such as patient brochures, leaflets, websites, banner ads etc. Serving as the primary point of contact for clients regarding all copy matters, managing expectations through effective communication. Continuously improving the management of medical copy concepts and deliverables, ensuring effective prioritization, planning and forecasting the team s capacity, along with timely delivery. [...]

Job vom 23.11.2024

Medical Science Liaison

• Hamburg, Niedersachsen, Berlin

MEHR

Updated: November 20, 2024 Location: Hamburg, Lower Saxony, Germany Job ID: 6719- OTHLOC- CVJw YfwS The Regional Medical Science Liaison (MSL) serves as the primary field- based point of contact with healthcare providers (HCPs) including clinical investigators on a range of clinical and scientific issues. The primary role is to deliver and facilitate medical education and [...] products, activities, and the disease area, and ensure these insights are effectively brought back to internal teams, disseminated, and leveraged through collaboration 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 enrolment for pipeline assets. REQUIREMENTS Advanced Degree MD, PhD, PharmD. Demonstrable experience in [...]
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Job vom 07.11.2024

Senior Proposal Specialist

• Berlin, Hamburg, Köln, Düsseldorf, Frankfurt, Nordrhein- Westfalen, Hesse

MEHR

The Senior Proposal Specialist will assist the BD team on the preparation of proposal responses associated with high priority, high complexity business development opportunities and will work closely and often independently with the clinical subject matter experts to create customized, comprehensive responses and budgets for Sponsors. This person will support the BD team in [...] 6 years of related experience preferred) Minimum Post- secondary certificate/ diploma (College, Training Institute, etc. ) (Bachelors degree preferred) Fluent in English (Verbal and Written) Additional knowledge/ skills Science degree/ diploma preferred Previous budget building experience in CRO and clinical trials mandatory Advanced user ability with Excel and proficient with other MS Office tools High degree of detail orientation Logical and process thinking mindset Good written and verbal communication skills and project management skills. 50, 500- 84, 500 a year + Bonus Accommodations for persons with disabilities are available on request in respect [...]

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Stellenangebote Clinical Trials Management Hamburg Jobs bei Neuvoo

Job vom 10.12.2024 TFS Health Science

Senior Clinical Research Associate (m/f/d)

• Hamburg

MEHR

Scientific . 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 service- capabilities, resourcing and Functional Service (FSP) solutions. Join Our Team as a Senior [...] a Project Team and is responsible for the initiation, on- site and/ or remote monitoring and close out of study sites during study conduct, according to company policies, SOPs and regulatory requirements. Key Responsibilities: Monitor on- site and remotely clinical trials in accordance with TFS and/ or sponsor Standard Operating Procedures GCP and ICH guidelines and applicable regulatory regulations. Perform all [...] and ensure subjects safety, data integrity and quality. Verify the protection of study participants by informed consent procedures and protocol requirements that follow appropriate regulations. Review CRFs (electronic or paper) and subject source documentation for validity and accuracy Verify proper management and accountability of Investigational Product Timely reporting of actions taken during monitoring visits in Monitoring Visit Report including findings, corrective [...]

Stellenangebot Clinical Trials Management Hamburg Job bei Clariness GmbH

Job vom 05.12.2024 Clariness GmbH Team Lead Copywriting (f/m/d) • Hamburg Führungs-/ Leitungspositionen

MEHR

[...] creation projects from concept to delivery, working closely with project stakeholders to ensure high- quality, on- time deliverables. Being responsible for error- free quality control of all medical copy deliverables. Overseeing development of medical copy concepts for marketing materials promoting clinical trials, such as patient brochures, leaflets, websites, banner ads etc. . Serving as the primary point of contact for clients, regarding all copy matters, managing expectations through effective communication. Continuously improving the management of medical copy concepts and deliverables, ensuring effective prioritization, planning and forecasting the team s capacity, along with timely delivery. [...]

Job vom 20.11.2024 Edwards Lifesciences

(Senior) Manager, Medical Science Liaison, Therapy Development, Transcatheter Mitral and Tricuspid Therapies (Germany)

• Hamburg

MEHR

[...] care. Patients with mitral and tricuspid heart valve disease often have complex conditions with limited treatment options. Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address a patient s unmet clinical needs. It s our driving force to help patients live longer and healthier lives. Join us and be part of [...] and on- site support for patient selection, screening, imaging, Heart Team concept and clinical data across BU (TMTT mitral and tricuspid therapies) Define areas of opportunity along the Heart Team referral pathway to maximize their patient access to key clinical trials Identify, influence and meet with existing HCPs to identify clinical needs and constraints related to BU clinical trial protocol adoption [...] timelines and key deliverables to align with overall business objective. Provide technical guidance on a variety of projects including identifying trial site specific bottlenecks and work with clinical affairs to refer to cross- functional partners (e. g. , training, trial management, screening etc. ) Identify and differentiate root cause of patient access restrictions between outreach and patient pathway; Accurate tracking and [...]
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Job vom 25.10.2024 Edwards Lifesciences (Sr. ) CRA Germany • Hamburg

MEHR

[...] SIVs, IMVs and COVs independently. Has a solid working knowledge of the regulatory environment : ISO, MDR and GCP. Is familiar with maintaining ISFs and the study e TMF. Background in pharma or medical devices. Experience in cardiology/ cardiac therapy clinical trials. Ideal locations : North or Central Germany Responsible for remotely supporting field clinical research associate/ site activities to ensure the [...] handlingo Identifying and reporting adverse events and device- related complications in accordance with regulatory and internal requirements Identifies and supports process improvement opportunities and implementation Ensures Audit readiness for internal, external and site Audits Other incidental duties as assigned by management Education and Experience:Bachelors Degree in in related field, 3 years experience of previous related medical device and/ or clinical experience [...]

Job vom 10.10.2024 TFS Health Science Clinical Research Associate • Hamburg

MEHR

Scientific . TFS Health Science is a leading global mid- size Contract Research Organization (CRO) dedicated to partnering with biotechnology and pharmaceutical companies throughout their entire clinical development journey. With expertise in full- service capabilities, resourcing, and Functional Service (FSP) solutions, we re looking for a talented [...] Associate with TFS Health Science, you will be a vital part of our SRS/ FSP team, working exclusively with a world- renowned global pharmaceutical/ biotech sponsor. You will play a crucial role in ensuring the quality and integrity of clinical trials, driving them forward from start to finish. Key Responsibilities Submission Amendment Support: Assist with initial and ongoing submissions, including amendments to ethics committees. Regulatory Reporting: Manage periodic reporting to ethics committees, including the reporting of safety events. Pre- activation SIV Support: Contribute to site pre- activation activities and support Site Initiation Visits (SIVs) . Monitoring Site Management: Conduct both onsite monitoring and periodic central monitoring to ensure trial integrity; manage site relationships and processes. Documentation Closeout: Maintain [...]

Job vom 07.08.2024 Marken Project Manager, Kit Operations • Hamburg

MEHR

Description Title:Project Manager, Kit Operations (all genders) Job Purpose:The main purpose of the Project Manager s role is the overall responsibility for the successful planning, execution, monitoring, control and closure of kit operation activities for clinical supply projects. Main Duties and Responsibilities:The role is highly people oriented and entails dealing directly with clients and internal operational [...] identification and escalation of any risks to meet performance of quality control activities per the appropriate process/ requirementsThe assisting in client audits Outside of client project support, the Project Manager is expected to be an engaged member of the Project Management team, contributing to training, business process documentation, departmental activities, budget and project forecasting, SOP development and the similar which will [...] to manage multiple projects proactively across a multi- disciplinary team. Understanding of a clinical trial protocol Strong work ethics Team- oriented way of working Ability to adapt to changes Minimum of 2 years project management experience, ideally in a clinical trials environment Graduation e. g. in Life Sciences or Logistics or other supply chain related industry or 2 years professional experience [...]
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Jobs aus dasauge.de

Stellenangebote Clinical Trials Management Hamburg Jobs bei dasauge.de

Job vom 17.12.2024 Clariness GmbH Team Lead Copywriting (f/m/d) • D- 22767 Hamburg Führungs-/ Leitungspositionen

MEHR

[...] creation projects from concept to delivery, working closely with project stakeholders to ensure high- quality, on- time deliverables. Being responsible for error- free quality control of all medical copy deliverables. Overseeing development of medical copy concepts for marketing materials promoting clinical trials, such as patient brochures, leaflets, websites, banner ads etc. . Serving as the primary point of contact for clients, regarding all copy matters, managing expectations through effective communication. Continuously improving the management of medical copy concepts and deliverables, ensuring effective prioritization, planning and forecasting the team s capacity, along with timely delivery. [...]

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