54 Jobs für Clinical Trial Specialist
Stellenangebote Clinical Trial Specialist Jobs
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening [. .. ] Standard Operating Procedures (SOPs) and business processes, if applicable. Trains study site personnel on the protocol and applicable regulatory requirements in collaboration with pertinent project team members. Supports with Clinical Trial Application submissions, including relevant informed consent local changes and translations into local language as required. Supports remote monitoring, if and as applicable. Negotiates investigator/ hospital agreements with stakeholders. Supports new and innovative processes and technologies to increase the quality, productivity, and efficiency of Clinical Operations and conserve overall departmental operating [. .. ] medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive salary with an intensive onboarding process with a mentor at your [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
Senior Clinical Trial Assistant
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening [. .. ] Standard Operating Procedures (SOPs) and business processes, if applicable. Trains study site personnel on the protocol and applicable regulatory requirements in collaboration with pertinent project team members. Supports with Clinical Trial Application submissions, including relevant informed consent local changes and translations into local language as required. Supports remote monitoring, if and as applicable. Negotiates investigator/ hospital agreements with stakeholders. Supports new and innovative processes and technologies to increase the quality, productivity, and efficiency of Clinical Operations and conserve overall departmental operating [. .. ] medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive salary with an intensive onboarding process with a mentor at your [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening [. .. ] Standard Operating Procedures (SOPs) and business processes, if applicable. Trains study site personnel on the protocol and applicable regulatory requirements in collaboration with pertinent project team members. Supports with Clinical Trial Application submissions, including relevant informed consent local changes and translations into local language as required. Supports remote monitoring, if and as applicable. Negotiates investigator/ hospital agreements with stakeholders. Supports new and innovative processes and technologies to increase the quality, productivity, and efficiency of Clinical Operations and conserve overall departmental operating [. .. ] medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive salary with an intensive onboarding process with a mentor at your [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
Clinical Research Associate (CRA I) / Senior
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening [. .. ] Standard Operating Procedures (SOPs) and business processes, if applicable. Trains study site personnel on the protocol and applicable regulatory requirements in collaboration with pertinent project team members. Supports with Clinical Trial Application submissions, including relevant informed consent local changes and translations into local language as required. Supports remote monitoring, if and as applicable. Negotiates investigator/ hospital agreements with stakeholders. Supports new and innovative processes and technologies to increase the quality, productivity, and efficiency of Clinical Operations and conserve overall departmental operating [. .. ] medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive salary with an intensive onboarding process with a mentor at your [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening [. .. ] Standard Operating Procedures (SOPs) and business processes, if applicable. Trains study site personnel on the protocol and applicable regulatory requirements in collaboration with pertinent project team members. Supports with Clinical Trial Application submissions, including relevant informed consent local changes and translations into local language as required. Supports remote monitoring, if and as applicable. Negotiates investigator/ hospital agreements with stakeholders. Supports new and innovative processes and technologies to increase the quality, productivity, and efficiency of Clinical Operations and conserve overall departmental operating [. .. ] medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive salary with an intensive onboarding process with a mentor at your [. .. ]
Job vor 8 Tagen bei Jooble gefunden
Abb Vie
Clinical Research Associate I
• Wiesbaden
Work-Life-Balance
[. .. ] at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Job Description Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening [. .. ] study site conduct accurately and completely. Prepare and submit written reports, both monitoring and administrative, with appropriate supervision. Keep management informed of study progress through periodic updates. Supports with Clinical Trial Application submissions, including relevant informed consent local changes and translations into local language as required. Supports remote monitoring, if and as applicable. Assists in study budget preparation and clinical study agreement execution, including ensuring necessary payments are made according to executed agreements. Negotiates investigator/ hospital agreements with stakeholders. Maintains and [. .. ] to the conduct of clinical trials is preferred Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Knowledge related to ICH/ GCP Guidelines and applicable local regulations is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. Ability to work, understand and follow work processes within the assigned function. Strong analytical [. .. ]
Job am 24.01.2026 bei Jooble gefunden
Ciliatech
• Homeoffice
To support safe, consistent, high-quality adoption across
clinical and commercial environments, we are recruiting a Surgical Training Manager. You will be the go-to expert for surgical technique, responsible for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] training field teams, supporting surgeons during live cases, and ensuring that all clinical sites operate with the highest surgical and compliance standards. Location: United Kingdom or Germany (Remote) [. .. ] certification, and continuous training for internal field teams. Document all training and case support activities in internal systems. Surgical Case Support Provide live case support and coaching during surgeries (clinical trial and commercial) . Clinical Operations Support Support Site Initiation Visits (SIVs) and ensure consistent training across clinical sites. Ensure compliance with GCP, SOPs, regulatory requirements, and reporting obligations (AEs, complaints) . Support wet labs and represent Ciliatech at congresses. Clinical Application Specialist, surgical nurse, clinical support) . Fluent in written and spoken English. Full compliance mindset (GCP, SOPs, documentation) . Experience supporting clinical trials (training, monitoring, SIV support) . Experience in a medical device company. Ability to deliver training in another European language (Italian, Spanish, German, French) . 77787736 [. .. ]
Job am 24.01.2026 bei Jooble gefunden
Ciliatech
Facilitator (m/w/d)
• Homeoffice
To support safe, consistent, high-quality adoption across
clinical and commercial environments, we are recruiting a Surgical Training Manager. You will be the go-to expert for surgical technique, responsible for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] training field teams, supporting surgeons during live cases, and ensuring that all clinical sites operate with the highest surgical and compliance standards. Location: United Kingdom or Germany (Remote) [. .. ] certification, and continuous training for internal field teams. Document all training and case support activities in internal systems. Surgical Case Support Provide live case support and coaching during surgeries (clinical trial and commercial) . Clinical Operations Support Support Site Initiation Visits (SIVs) and ensure consistent training across clinical sites. Ensure compliance with GCP, SOPs, regulatory requirements, and reporting obligations (AEs, complaints) . Support wet labs and represent Ciliatech at congresses. Clinical Application Specialist, surgical nurse, clinical support) . Fluent in written and spoken English. Full compliance mindset (GCP, SOPs, documentation) . Experience supporting clinical trials (training, monitoring, SIV support) . Experience in a medical device company. Ability to deliver training in another European language (Italian, Spanish, German, French) . 77787735 [. .. ]
Job am 24.01.2026 bei Jooble gefunden
Ciliatech
• Homeoffice
To support safe, consistent, high-quality adoption across
clinical and commercial environments, we are recruiting a Surgical Training Manager. You will be the go-to expert for surgical technique, responsible for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] training field teams, supporting surgeons during live cases, and ensuring that all clinical sites operate with the highest surgical and compliance standards. Location: United Kingdom or Germany (Remote) [. .. ] certification, and continuous training for internal field teams. Document all training and case support activities in internal systems. Surgical Case Support Provide live case support and coaching during surgeries (clinical trial and commercial) . Clinical Operations Support Support Site Initiation Visits (SIVs) and ensure consistent training across clinical sites. Ensure compliance with GCP, SOPs, regulatory requirements, and reporting obligations (AEs, complaints) . Support wet labs and represent Ciliatech at congresses. Clinical Application Specialist, surgical nurse, clinical support) . Fluent in written and spoken English. Full compliance mindset (GCP, SOPs, documentation) . Experience supporting clinical trials (training, monitoring, SIV support) . Experience in a medical device company. Ability to deliver training in another European language (Italian, Spanish, German, French) . 77787737 [. .. ]
Job am 24.01.2026 bei Jooble gefunden
Ciliatech
Recruitment Training Manager:in
• Homeoffice
To support safe, consistent, high-quality adoption across
clinical and commercial environments, we are recruiting a Surgical Training Manager. You will be the go-to expert for surgical technique, responsible for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] training field teams, supporting surgeons during live cases, and ensuring that all clinical sites operate with the highest surgical and compliance standards. Location: United Kingdom or Germany (Remote) [. .. ] certification, and continuous training for internal field teams. Document all training and case support activities in internal systems. Surgical Case Support Provide live case support and coaching during surgeries (clinical trial and commercial) . Clinical Operations Support Support Site Initiation Visits (SIVs) and ensure consistent training across clinical sites. Ensure compliance with GCP, SOPs, regulatory requirements, and reporting obligations (AEs, complaints) . Support wet labs and represent Ciliatech at congresses. Clinical Application Specialist, surgical nurse, clinical support) . Fluent in written and spoken English. Full compliance mindset (GCP, SOPs, documentation) . Experience supporting clinical trials (training, monitoring, SIV support) . Experience in a medical device company. Ability to deliver training in another European language (Italian, Spanish, German, French) . 77787732 [. .. ]
Job am 24.01.2026 bei Jooble gefunden
Ciliatech
• Homeoffice
To support safe, consistent, high-quality adoption across
clinical and commercial environments, we are recruiting a Surgical Training Manager. You will be the go-to expert for surgical technique, responsible for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] training field teams, supporting surgeons during live cases, and ensuring that all clinical sites operate with the highest surgical and compliance standards. Location: United Kingdom or Germany (Remote) [. .. ] certification, and continuous training for internal field teams. Document all training and case support activities in internal systems. Surgical Case Support Provide live case support and coaching during surgeries (clinical trial and commercial) . Clinical Operations Support Support Site Initiation Visits (SIVs) and ensure consistent training across clinical sites. Ensure compliance with GCP, SOPs, regulatory requirements, and reporting obligations (AEs, complaints) . Support wet labs and represent Ciliatech at congresses. Clinical Application Specialist, surgical nurse, clinical support) . Fluent in written and spoken English. Full compliance mindset (GCP, SOPs, documentation) . Experience supporting clinical trials (training, monitoring, SIV support) . Experience in a medical device company. Ability to deliver training in another European language (Italian, Spanish, German, French) . 77787733 [. .. ]
Job am 24.01.2026 bei Jooble gefunden
Ciliatech
Surgical Training Manager-Europe
• Homeoffice
Ciliatech is expanding its European footprint with the launch of Intercil, a next-generation uveal spacer for glaucoma surgery. To support safe, consistent, high-quality adoption across
clinical and commercial environments, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] we are recruiting a Surgical Training Manager. This role is central to elevating surgical expertise internally and externally. You will be the go-to expert for surgical technique, responsible for training field teams, supporting surgeons during live cases, and ensuring that all clinical sites operate with the [. .. ] the OR, demonstrating best practices for Intercil implantation. Document all training and case support activities in internal systems. Surgical Case Support Provide live case support and coaching during surgeries (clinical trial and commercial) . Identify skill gaps and propose targeted training interventions. Clinical Operations Support Support Site Initiation Visits (SIVs) and ensure consistent training across clinical sites. Ensure compliance with GCP, SOPs, regulatory requirements, and reporting obligations (AEs, complaints) . Cross-Functional Collaboration Support wet labs and represent Ciliatech at congresses. Maintain awareness of industry developments and share insights with senior management PROFILE Required Skills Experience Minimum 5 years of experience in ophthalmic operating rooms (e. g. , Clinical Application Specialist, surgical nurse, clinical support) . Prior experience in a training, coaching, or educational function. Fluent in written and spoken English. Strong communication skills and high emotional intelligence. Ability to coach, influence, and lead without formal authority. Strong organization skills with high attention to detail. Full compliance mindset (GCP, SOPs, documentation) [. .. ]
Job am 16.01.2026 bei Jooble gefunden
Ascendis Pharma
• Heidelberg
Are you passionate aboutclinical disclosure and transparency? Do you have experiencewithinthe field? If so, now is your chance to join Ascendis Pharma as our new
Clinical Disclosure
Specialist. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Ascendis Pharmais a global biopharmaceutical company committed to making a meaningful difference in patients lives. Guided by our core values of Patients, Science, and Passion, we are applying our innovative Trans Con technology platform to fulfill our mission of developing new therapies thatdemonstratebest-in-class potential to address unmet medical [. .. ] working together to achieve extraordinary results. Youwill be joining the Global Regulatory Communicationsteamas the pioneer Clinical Disclosure Specialist in Ascendis, andbebasedin Copenhagen. Your key responsibilities willinclude: Overall responsibility for clinical trial disclosure activities Own CCI management processes Develop and implement relevant processes, including training of colleagues in requirements Monitor and interpret global and future CTD requirements Collaborate cross-functionally with clinical, regulatory, and other teams to meet disclosure requirements. Qualifications and Skills: You hold a relevant degreein a scientific discipline-preferably [. .. ]
Job am 14.01.2026 bei Jooble gefunden
FERCHAU GmbH
Clinical Study Specialist
• Biberach an der Riß
Mitarbeiterevents
Als
Clinical Trial Administrator:in unterstützt du spannende, internationale Studienprojekte. Bei uns hast du die Möglichkeit, aktiv an innovativen medizinischen Lösungen mitzuwirken und in einem Umfeld zu arbeiten, das deine Entwicklung [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] fördert. Unterstützung von Trial Managern für das eigenständige Management des CTSU-Studienteams innerhalb der Matrixstruktur Planung, Steuerung und Kontrolle von Zeitplänen, Kosten und [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Boston Scientific
• Düsseldorf
[. .. ] by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. Here, youll be supported in progressing whatever your ambitions. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] The Field Clinical Therapy Specialist will serve as the primary therapy expert for the Interventional Spine team across the EMEA region. This position is part of the Interventional Spine (IVS) team, supporting the Intracept procedure and will have responsibility for educating and training physicians and health care professional staff on Intracepts therapies to support clinical [. .. ] support the launch of new products and sales tools with comprehensive training materials. Assist the execution and delivery of procedural training to physicians and medical staff in support of clinical trial site initiation and qualification for ongoing and future clinical studies. Attend case coverage and technical support for clinical sites requiring supplemental training or education. Interact in the field and evaluate need for new learning programs, educational materials and hands-on equipment/ models to address unmet education needs for customers and [. .. ]
Job am 14.01.2026 bei Jooble gefunden
ICON
CRA II-Sponsor dedicated
• Frankfurt am Main
Work-Life-Balance
CRA II/ Senior CRA-sponsor dedicated ICON plc is a world-leading healthcare intelligence and
clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Clinical Research Associate II Specialist to join our diverse and dynamic team. As a Clinical Research Associate II Specialist at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of in Nvative treatments and therapies What you will be doing Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Collaborating with investigators and site staff to facilitate smooth study conduct. Performing data review and resolution of queries to maintain high-quality clinical data. Contributing to the preparation and review of study documentation, including protocols and clinical study reports Your profile Bachelors degree in a scientific or healthcare-related [. .. ]
Job am 14.01.2026 bei Jooble gefunden
ICON
• Frankfurt am Main
Work-Life-Balance
CRA II/ Senior CRA-Germany-office or remote ICON plc is a world-leading healthcare intelligence and
clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Clinical Research Associate II Specialist to join our diverse and dynamic team. As a Clinical Research Associate II Specialist at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies What You Will Be Doing: Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Collaborating with investigators and site staff to facilitate smooth study conduct. Performing data review and resolution of queries to maintain high-quality clinical data. Contributing to the preparation and review of study documentation, including protocols and clinical study reports Your Profile: Bachelors degree in a scientific or healthcare-related [. .. ]
Job am 15.01.2026 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, [. .. ] on medical issuesproviding clear, informed guidance 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 [. .. ] safety-related documentation. Team Client Engagement: Mentor junior medical staff, support SOP/ tool development, and join Commercial Operations in client meetings and presentations. Qualifications Medical Qualifications: Medical Doctor (MD) with specialist medical training in Ophthalmology and at least 5 years experience in clinical practice. Clinical Trial Expertise: Experience serving on safety data review boards or equivalent roles in clinical research. Regulatory Knowledge: Strong understanding of GCP, ICH guidelines, pharmacovigilance legislation, and internal SOPs. Adaptability: Comfortable working in fast-paced environments with [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
• München, Bayern
Sponsor Dedicated Study Start Up Lead with Finance expertise based in Munich We are looking for a sponsor-dedicated Country Start-Up Lead to oversee
clinical trial site activation, regulatory processes, and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] financial management. This is a well suited role for someone with experience in clinical start-up operations, budget negotiations, and regulatory compliance and who enjoys working collaboratively to drive progress. Key Responsibilities Responsible for execution and oversight of clinical trial country submissions and approvals for [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Principal Regulatory Affairs Specialist (m/f/d)
• München, Bayern
[. .. ] treat conditions we aspire to alter the course of lives. Responsibilities Participating on product development project teams to provide input to ensure that appropriate regulatory requirements for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] market clearance or clinical trials are built into project plans. Developing regulatory submission applications to introduce new or modified devices, new or expanded indications for use or changes to the manufacturing/ quality processes into the marketplace. Participating in meetings with regulatory officials for purposes related to market approval. Providing senior management practical operations-oriented [. .. ] procedures meet these requirements and, when necessary, identify compliant, effective and efficient approaches to fulfill such requirements. Understanding of basic clinical and regulatory principles including, but not limited to: clinical trial design and methodology and knowledgeable of world-wide clinical and regulatory environments we compete in. Pragmatic and result-oriented: capable to prioritize and plan activities with specific attention to understand expectations of internal personnel and external stakeholders. Time management: able to independently manage large technical writing projects to complete per [. .. ]
Job am 19.01.2026 bei Jobleads gefunden
Clinical Disclosure Specialist
• Heidelberg, Baden- Württemberg
Are you passionate aboutclinical disclosure and transparency? Do you have experiencewithinthe field? If so, now is your chance to join Ascendis Pharma as our new
Clinical Disclosure
Specialist. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Ascendis Pharmais a global biopharmaceutical company committed to making a meaningful difference in patients lives. Guided by our core values of Patients, Science, and Passion, we are applying our innovative Trans Con technology platform to fulfill our mission of developing new therapies thatdemonstratebest-in-class potential to address unmet medical [. .. ] cross-functional, global teams working together to achieve extraordinary results. Youwill be joining the Global Regulatory Communicationsteamas the pioneer Clinical Disclosure Specialist in Ascendis, andbebasedin Copenhagen. Responsibilities Overall responsibility forclinical trial disclosureactivities Own CC Imanagementprocesses Develop and implementrelevant processes, including training of colleaguesin requirements Monitorand interpret globalandfuture CT Drequirements Collaborate cross-functionallywith clinical, regulatory, and other teams to meet disclosure requirements. Qualifications and Skills You hold a relevant degreein a scientific discipline-preferably advance level-withminimum 5years of experience withinbiopharma and minimum [. .. ]
Job am 11.01.2026 bei Jobleads gefunden
Senior Medical Advisor
• München, Bayern
[. .. ] of MASH. It is the first and only medication approved by both the FDA and European Commission for the treatment of moderate to advanced fibrosis (F2F3) . [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] A Phase3 outcomes trial is evaluating Rezdiffra for compensated MASH cirrhosis (F4c) . Madrigal builds a dynamic, inclusive, and highperforming culture that values scientific excellence, operational rigor, and collaboration. We strengthen our workforce strategy to ensure the right talent at the right time in the right way. Position Summary The Medical Advisor will plan and lead prelaunch and launch activities in the therapeutic field of metabolic dysfunctionassociated steatohepatitis (MASLd/MASH) . The Advisor is the medical specialist in the field and an expert in the medical affairs landscape within the territory. A strong understanding of the healthcare system, diagnostic pathways, and stakeholder landscape is essential. The role represents Madrigal externally through scientific discussions with thought leaders, clinical trial investigators, and other healthcare professionals. Key Responsibilities Demonstrate support for clinical trials and engage with external experts on the generation of scientific data. Collaborate with clinical organizations to enhance patient enrollment in companysponsored clinical trials by identifying appropriate trial sites and interacting with investigators in ongoing trials. Deeply understand [. .. ]
Job am 02.01.2026 bei Jobleads gefunden
Senior Director Drug Discovery
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] is a handson leadership role. As the primary architect of our discovery engine, you will focus on the biological why and the technical how before a molecule [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ever reaches a clinical trial. Translate Research into Therapy: Leverage Deep Pictions understanding and knowhow of Long Covid disease mechanisms to pivot from highimpact research to a viable, differentiated, patentable therapeutic approach. Delivery Precision: Together with our experts, lead the integration of innovative delivery systems to ensure candidates reach the right targets, and build the [. .. ] hiding behind process. Experience with modern modalities, especially peptides, RNA (incl. m RNA) , targeted delivery, and AIenabled design, is a major plus. Nice to have: You are a Long Covid specialist with a proven track record of successful research and highimpact publications specifically on Long Covid. Your work has already contributed to a novel understanding of the disease. Why Join Us? You will work alongside a diverse, international team of toptier scientists and innovators who are as passionate about the science [. .. ]
Job am 23.12.2025 bei Jobleads gefunden
Clinical Operations Specialist Contracts (m/f/d)
• München, Bayern
Clinical Operations
Specialist Contracts (m/f/d) Site Name: Munich Prinzregentenplatz Posted Date: Dec 17 2025 Bei GSK haben wir ehrgeizige Ziele für Patienten und setzen uns dafür ein, die [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Gesundheit von 2, 5 Milliarden Menschen bis zum Ende des Jahrzehnts positiv zu beeinflussen. R D setzt sich dafür ein, innovative Impfstoffe und [. .. ] Konsistenz, Kostenoptimierung und Risikominimierung sicherzustellen. Budgetaktualisierungen in Verträgen aufgrund von Protokolländerungen und Beratung bei der Anpassung des Studienbudgets sowie Identifikation von Kostenabweichungen und Möglichkeiten zur Kostenvermeidung. Sicherstellung der Vollständigkeit der Trial Master File (TMF) für alle Budget- und Vertragsaktivitäten und Unterstützung bei weiteren Aufgaben im Studienverlauf gemäß absolviertem Training. Qualifikationen Fähigkeiten Bachelor-Abschluss oder gleichwertiger Abschluss in einem wissenschaftlichen Bereich wie Biowissenschaften, Medizin, klinische Forschung, Pharmazie oder einem verwandten Fachgebiet. Relevante Erfahrung in der klinischen Forschung Fundierte Kenntnisse im Erstellen und [. .. ]
Job am 21.12.2025 bei Jobleads gefunden
Clinical Specialist
Accompanying applications (
trial order of measurement parameters and products) in the field of non-invasive patient monitoring at the customers site Development and implementation of individual overall solutions for the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] customer together with the sales staff and subsequent continued support Training of clinical and nursing staff in the companys own training center or in hospitals Product presentation in workshops, at trade fairs and congresses Documentation and forwarding of customer feedback in the CRM system Collaboration with national and international teams such as Customer Service, Marketing and Technical Service Traveling in the assigned region [. .. ]
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Wieviel verdient man als Clinical Trial Specialist pro Jahr?
Als Clinical Trial Specialist verdient man zwischen EUR 50.000,- bis EUR 80.000,- im Jahr.
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Aktuell gibt es auf JobRobot 54 offene Stellenanzeigen für Clinical Trial Specialist Jobs.
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Aktuell suchen 20 Unternehmen nach Bewerbern für Clinical Trial Specialist Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Trial Specialist Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Trial Specialist Stellenangebote:
- Abb Vie (6 Jobs)
- Ciliatech (6 Jobs)
- Edwards Lifesciences (4 Jobs)
- ICON (3 Jobs)
- Thermo Fisher Scientific (2 Jobs)
- Siegfried (2 Jobs)
In welchen Bundesländern werden die meisten Clinical Trial Specialist Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trial Specialist Jobs werden derzeit in Bayern (11 Jobs), Niedersachsen (4 Jobs) und Nordrhein-Westfalen (3 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trial Specialist Jobs?
Clinical Trial Specialist Jobs gehören zum Berufsfeld Medizinisch-technische Assistenz / MTA.
