221 Jobs für Clinical Study Manager
Stellenangebote Clinical Study Manager Jobs
Job vor 9 Tagen bei Neuvoo gefunden
Bei Gene
[. .. ] When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer. General Description: [...]
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[...] Supports the Regional Clinical Study Manager in regional study delivery and ensures that delegated components of clinical studies are executed per expected and specified quality standards, within timelines and budget Builds solid knowledge of clinical trials operations in the region under guidance of the Regional Clinical Study Manager Supports the alignment of regional deliverables with overall [. .. ]
Job vor 12 Tagen bei Neuvoo gefunden
Bei Gene
Senior Clinical Research Associate
[. .. ] Act as the escalation point person for CRA (s) with site-related issues and concerns. May review visits reports, following-up on issue resolution and communicating with the Country/ [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Regional Clinical Study Manager on significant risk identified and action proposed. May serve as subject matter expert for clinical operations, country regulations and monitoring-related activities. Supervisory Responsibilities: Mentor/ Buddy for junior CRAs. Acts as the escalation point person for CRAs with site-related issues and concerns. May serve as subject matter expert for [. .. ]
Job am 24.01.2026 bei Neuvoo gefunden
Bei Gene
[. .. ] involved in study delivery on a regional level Collaborates with key stakeholders in the region and provides regular updates on study progress in the region to senior [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] management and Global Clinical Study Manager as required Represents the regional study team at internal meetings and at the cross-functional Clinical Study Team (CST) meetings Leads regional operations meetings with all regional study team members Timelines, Planning and Execution Leads planning and management of the assigned clinical study (ies) from feasibility through closeout activities for [. .. ]
Job vor 2 Tagen bei StepStone gefunden
Staburo GmbH
Sales Manager (f/m/d-part/ full-time)
• München Muenchen
Teilzeit
Staburo Gmb H is a data science company, specialized in statistical consulting, programming and bioinformatics for healthcare projects. Our core competencies include
Clinical Statistics, Translational Medicine Biomarkers, Phase I Pharmacokinetics/-Dynamics, [...]
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[...] Data Transparency Disclosure Services, Health Technology Assessment and Bioinformatics. Our customers are international pharmaceutical companies, CROs, biotech companies and medical device manufacturers. Our steadily growing team supports our clients efficiently from study design to data analysis and finally the disclosing and posting of trial results. Our new sales manager will collaborate directly with senior management across all business areas including the CEOs. The role is ideal for someone who is looking for a variety of tasks, from a basic technical understanding of our services to relationship building and communication as well as a certain level of travelling. Building relationships [. .. ]
Neu Job vor 6 Std. bei Jooble gefunden
Alimentiv
• Hamburg
Führungs-/ Leitungspositionen
Responsible for the
clinical operations of a project within a defined regional/ global level. Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and Investigator sites in accordance with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Monitoring Plan, Protocol, Good Clinical Practice (GCP) , ICH guidelines and local regulations. The COL acts as a primary liaison between the CRAs [. .. ] preparation of the monitoring plan and other structural documentation and the oversight of monitoring visit scheduling, site and monitoring performance metrics, issue escalation and corrective actions. The COL will develop study tools for site and CRA use, review visit reports, review and track protocol deviations, and support other objectives for clinical operations and the clinical project team. Project Oversight Overall oversight of (a group of) regional CRAs to ensure (site) compliance with study protocol, study plans, ICH-GCP, local regulations and [. .. ] for study-specific questions and issues. Escalates to PM and other functions as appropriate. Support line managers by providing status updates on utilization and performance of CRAs. Liaise with line manager for assigning sites to CRAs following line manager allocation of a CRA resource to the project. Conduct CRA Assessment visits per departmental requirements to assess the performance of the CRA against their monitoring responsibilities. Study Documents and Plans Develop training materials and study tools for sites and CRAs, including monitoring [. .. ]
Job gestern bei Jooble gefunden
Hello Better
Clinical Lead Ello (f/d/m)
• Berlin
Führungs-/ Leitungspositionen
[. .. ] combined our 10 years of digital therapeutics expertise with AI technology to make psychological support more accessible. For more information about Hello Better, see our Hello Better [...]
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[...] Handbook. As a Clinical Lead for Ello, your role is to bring clinical psychology expertise to AI. You ll be the clinical expert who ensures Ello provides safe, effective and evidence-based psychological support. This is a strategic clinical role that combines hands-on psychological work with cross-functional leadership-no coding or technical [. .. ] drive improvements whilst helping establish scientific standards for this emerging field. Own Psychological Safety: You ll support Ello s safety framework by working closely with our Senior Psychotherapist Medical Risk Manager responsible for established risk management principles, to ensure appropriate crisis detection and escalation protocols. You ll monitor for potential risks and ensure appropriate safety mechanisms whilst maintaining clear boundaries between wellness support and situations requiring clinical care. Communicate Clinical Value: You ll present Ello s approach and safety to potential [. .. ] identity, and people with disabilities to apply Privacy Policy for Applicants Interview Process Call with the People Team (30 mins) Technical Interview with Alena Elena (60 mins) Take-Home Case Study (2-3 hours) Team Interview with Tanja Vincent (30 mins) Founder Interview with C-Level (15-30 mins) About us Hello Better was founded under the name GET. ON Institut für Online Gesundheitstrainings Gmb H by internationally recognized researchers and psychologists in 2015. In more than 30 randomized-controlled studies, Hello [. .. ]
Job gestern bei Jooble gefunden
• München
Study Physician sponsor dedicated in 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] cardiology, pediatrics, emergency medicine are preferred) with following experience: Global Medical Monitor/ Study Physician/ Clinical Trial Physician managing phase I to IV clinical trials in CRO/ Pharma company. Global Project Manager/ Clinical Trial leader/ Project manager managing multiple countries in CRO/ Pharma company. Country Trial Manager/ Local Project Manager/ Project Manager USA in CRO/ Pharma company Global Safety Physician/ Risk Management Physician in Pharmacovigilance department in CRO/ Pharma company Additional Points: Clinical practice experience of minimum 4 yrs is mandatory. Normally [. .. ]
Job vor 4 Tagen bei Jooble gefunden
Sr CRA in oncology-Sponsor dedicated-Home Based Germany
• München
Sr CRA in oncology-Sponsor dedicated-Home Based Germany Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and commercial [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] site, and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelines Utilizes available hardware and software to support the effective conduct of the clinical study data review and capture. Verifies site compliance with electronic data capture requirements. May perform investigational product (IP) inventory, reconciliation and reviews storage and security. Verifies the IP has been dispensed and administered to subjects/ patients according to the protocol. Verifies issues or risks associated with blinded or randomized information related [. .. ] training and sign off visits for junior CRA staff, as assigned. May be mentored and assigned lead tasks under supervision of an experienced Clinical Operations Lead (COL) or operational line manager. This could include participation in business development proposals and/or defense meetings. Qualifications: Bachelors degree or RN in a related field or equivalent combination of education, training and experience Knowledge of Good Clinical Practice/ ICH Guidelines and other applicable regulatory requirements Preferably oncology experience Must demonstrate good computer skills and [. .. ]
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 activities as well as study conduct and site closure tasks. Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. Supports and/or conducts (accompanied) site qualification, initiation, [. .. ] experience. One year of clinically-related experience in a 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 [. .. ]
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 activities as well as study conduct and site closure tasks. Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. Supports and/or conducts (accompanied) site qualification, initiation, [. .. ] experience. One year of clinically-related experience in a 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 [. .. ]
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 activities as well as study conduct and site closure tasks. Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. Supports and/or conducts (accompanied) site qualification, initiation, [. .. ] experience. One year of clinically-related experience in a 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 [. .. ]
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 activities as well as study conduct and site closure tasks. Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. Supports and/or conducts (accompanied) site qualification, initiation, [. .. ] experience. One year of clinically-related experience in a 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 [. .. ]
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 activities as well as study conduct and site closure tasks. Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. Supports and/or conducts (accompanied) site qualification, initiation, [. .. ] experience. One year of clinically-related experience in a 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 [. .. ]
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 activities as well as study conduct and site closure tasks. Manages the activities of clinical investigative sites across multiple protocols and multiple therapeutic areas, with appropriate supervision. Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and [. .. ] and understanding of appropriate therapeutic indications as they relate 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 [. .. ]
Job vor 9 Tagen bei Jooble gefunden
• Berlin
Eb m/HEOR
Manager-all genders Arbeitsort: Berlin Office Unbefristete Festanstellung Attention: C2-level German proficiency is required for this position Attention: Home Office/ Remote contract cannot be offered About the job [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Our team The Eb m/HEOR vaccines team is an integral part of the Market Access team in Germany. We are responsible for [. .. ] studies, we address the evidence needs of key decision-makers such as the Standing Committee on Vaccination (STIKO) and other external stakeholders. Our focus lies on generating evidence regarding epidemiology, clinical and economic burden of vaccine-preventable diseases, public health impact, cost-effectiveness, and acceptance and uptake of our vaccines. Our methodological spectrum is broad and encompasses literature reviews, secondary data analyses (particularly health insurance claims data and EMR analyses) , economic evaluation, mathematical and decision-analytic modeling, as well as [. .. ] Conducting literature reviews and systematic reviews Performing secondary data analyses (statutory health insurance routine data, EMR data) Developing and applying mathematical and decision-analytic models Designing and implementing surveys Publishing study results in peer-reviewed journals Presenting findings to internal and external stakeholders, including at scientific conferences Supporting market access strategies with evidence-based insights Collaborating with cross-functional teams and external research partners Managing external service providers and research collaborations About you Education and Experience: Advanced degree (Master s or [. .. ]
Job vor 10 Tagen bei Jooble gefunden
Stryker
Associate Manager, Clinical Data Sciences
• Regierungsbezirk Freiburg
Grow Your Career at Stryker as an Associate
Manager,
Clinical Data Science As an Associate Manager for Clinical Data Sciences, you will lead a diverse team of experts [...]
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[...] and collaborate with internal and external stakeholders to implement and execute Clinical Data Sciences initiatives for the Instruments division. This role involves driving operational planning, building technical infrastructure to support excellence in [. .. ] ISO, FDA, and international standards. Strong quantitative analysis skills and project management expertise; ability to prioritize and manage multiple complex projects. Experience with healthcare real-world data sources and authoring study protocols, reports, abstracts, and publications. Knowledge of standard statistical software (e. g. , 78260167 [. .. ]
Job vor 10 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
[. .. ] information about Abb Vie, please visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Job Description The HTA Writer is [...]
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[...] responsible for providing clinical EUHTA document support to the JCA core team, ensuring successful preparation of high-quality submission-ready documents and effective implementation of the clinical writing process. Provides HTA writing expertise for multiple compounds and/or projects, expertise in HTA, oncology is a plus within a therapeutic area. Interfaces with JCA core [. .. ] per EU HTA regulations and guidance materials. Arranges and conducts review meetings with the team. Acts as interface to resolve issues and questions arising during the writing process. Works with manager throughout the document audit process and works with JCA Core team and manager to draft responses as necessary. Produces and maintains focusing on quality and compliance and ensures delivery within project timelines. Familiarity with HTA dossier regulations, requirements and guidance associated with EU HTA regulations. Qualifications A minimum of 3+ [. .. ] with a comprehensive knowledge of medical and scientific terminology across multiple therapeutic areas. Proficient in assimilating and analyzing complex data. Advanced understanding of HTA dossiers and HTA requirements, clinical research, study designs, biostatistics. Good understanding of regulatory requirements, and medical terminology cross functional teams and multiple contributors. Excellent English writing skills, effectively communicate and influence complex scientific and medical information to various stakeholders. Ability to collaborate with cross-functional teams. Strong organizational, time management, and problem-solving skills. Additional Information Abb [. .. ]
Job vor 12 Tagen bei Jooble gefunden
Alcedis GmbH
(Senior) Clinical Research Associate/ Klinischer Monitor/ Site Manager (m/w/d) - homebased (Region Berlin und Umgebung)
• Gießen
Homeoffice möglich Abgeschlossenes Studium
Flexible Arbeitszeiten 30+ Urlaubstage
(Senior)
Clinical Research Associate/ Klinischer Monitor/ Site
Manager (m/w/d) - homebased (Region Berlin und Umgebung) bei Alcedis Gmb H softgarden (Senior) Clinical Research Associate/ Klinischer Monitor/ Site Manager [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] (m/w/d) - homebased (Region Berlin und Umgebung) Vollzeit Remote Gießen, Deutschland Mit Berufserfahrung 23.01.26 Als (Senior) Clinical Research Associate/ Klinischer Monitor/ Site Manager (m/w/[. .. ] Kommunikation bzgl. Monitoring/ Site Management, Vertragsmanagement, Feasibility/ Site Selection, Erstellung Monitoringplan Wer du bist Du hast ein abgeschlossenes Studium aus dem Bereich der Naturwissenschaften oder Life Sciences, bzw. besitzt eine Study Nurse-oder vergleichbare Qualifikation Berufserfahrung (3 Jahre) in der Durchführung GCP-regulierter klinischer Studien innerhalb der Industrie (z. B. CRO, Pharma oder Biotech) ist als Lead-CRA verpflichtend Du arbeitest selbständig und vorausschauend bei Planung und Umsetzung Du besitzt eine hohe Sozialkompetenz und eine ausgeprägte Teamfähigkeit Du besitzt sehr gute [. .. ]
Job am 24.01.2026 bei Jooble gefunden
eppdata GmbH
• Hamburg
Work-Life-Balance
[. .. ] company bicycles, and more. Were committed to meeting individual needs and continuously expanding our benefits. About us Eppdata Gmb H is a growing service company offering information [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] technology services for supporting clinical studies in the field of Neuroradiology with more than twenty internal employees. We are simplifying imaging data collection and use advanced data analytics and AI, accelerating patient access to new therapies and supporting the clinical study lifecycle. We welcome individuals of all genders, nationalities, and backgrounds to join our team. Our goal is to bring together a group of talented individuals who can work collaboratively to make a positive impact on society through their work in the medical field. We are confident that you will find [. .. ]
Job am 24.01.2026 bei Jooble gefunden
Dr. Falk Pharma GmbH
Clinical Operations Manager Early Clinical Research (m/w/d)
• Regierungsbezirk Freiburg
Flexible Arbeitszeiten
[. .. ] und laufende Studien Hauptverantwortliches Führen des studienspezifischen elektronischen Trial Master Files (Veeva Vault) Übernahme IMP Management für Ph1 Studien und enge Zusammenarbeit mit dem pharmazeutischen Team Sponsor [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Oversight (u. a. Study Metrics, Review Monitoring Berichte) und Sicherstellung, dass Studien termingerecht, in hoher Qualität und compliant durchgeführt werden Organisation von und Teilnahme an Meetings Mitarbeit bei qualitätssichernden Maßnahmen (Überarbeitung von SOPs; Unterstützung bei der Vorbereitung von Audits) Ihre Qualifikation Abgeschlossene Berufsausbildung oder Studium mit Schwerpunkt im medizinischen, naturwissenschaftlichen oder pharmazeutischen Bereich Mehrjährige [. .. ]
Job am 24.01.2026 bei Jooble gefunden
TFS Health Science
Operational Strategy and Delivery Lead Internal Medicine and Neuroscience
• Mainz
Führungs-/ Leitungspositionen
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] service-capabilities, resourcing and Functional Service (FSP) solutions. Join Our Team as a Operational Strategy and Delivery Lead Internal Medicine and Neuroscience-home based in UK, Germany, Poland, Netherlands or Denmark. As part of our CDS Internal Medicine and Neuroscience team you will working alongside [. .. ] of client satisfaction for the assigned TFS CDS Business Unit. The Operational Strategy and Delivery Lead needs extensive knowledge and experience in how to design an operational solution to achieve study objectives and develop a level of credibility with clients to give them assurance that ideas and methodological approaches have a high chance of success as well as receive the required level of oversight to meet their objectives. The position works with service functions across the company to ensure that projects [. .. ] and competitive costing Studies Strategy and Delivery Participate in proposal and budget development for new opportunities Participate in and/or lead global process improvement initiatives Act as a key relationship manager for assigned customers Responsible for all the assigned BU projects across the portfolio and actively develop and be seen as the first point of escalation to resolve both project management and client issues Responsible to coordinate and lead creative project solutions, leveraging expertise, operational capabilities and technologies to ensure client [. .. ]
Job am 23.01.2026 bei Jooble gefunden
Clinical Trial Lead-single client-Austria, Germany or the UK
• München
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 outcomes to address modern [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] training; We are continuously building the company we all want to work for and our customers want to work with. Project Leadership and Delivery. Manages a project as a project manager overseeing interdisciplinary clinical research studies and ensures compliance with GCP, relevant SOPs, and regulatory requirements. Acts as a primary liaison between the Company and the Customer to ensure timely study launch, conduct, and closeout according to the Customers and the Companys contractual agreement. Lead project team to ensure quality, timelines and budget management. Accountable for the financial performance of each project. Coordinate activities and deliverables of all study conduct partners and proactively identify and manage issues. Ensure studies are conducted [. .. ]
Job am 17.01.2026 bei Jooble gefunden
Alira Health
Project Manager Senior
• München
[. .. ] roles by a connection in Alira Health? Join our global team dedicated to innovation and initiative, where physical walls and different time zones dont limit, but encourage, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] collaboration. The Project Manager (PM) is an important member of the Alira Health Clinical team. Manages clinical study functions, which may include investigational supply, IWRS/ IXRS, data management, biostatistics, pharmacovigilance, and central laboratory. Supervises and provides support to the Clinical team, including Clinical Assistants, In-house Clinical Research Associates, and Clinical Research Associates. Creates and reviews clinical study documents, including protocols, ICF templates, study budgets, site log/ form [. .. ]
Job am 17.01.2026 bei Jooble gefunden
Alira Health
Senior Manager, Project Management
• München
[. .. ] roles by a connection in Alira Health? Join our global team dedicated to innovation and initiative, where physical walls and different time zones dont limit, but encourage, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] collaboration. The Project Manager (PM) is an important member of the Alira Health Clinical team. Manages clinical study functions, which may include investigational supply, IWRS/ IXRS, data management, biostatistics, pharmacovigilance, and central laboratory. Supervises and provides support to the Clinical team, including Clinical Assistants, In-house Clinical Research Associates, and Clinical Research Associates. Creates and reviews clinical study documents, including protocols, ICF templates, study budgets, site log/ form [. .. ]
Job am 17.01.2026 bei Jooble gefunden
Alira Health
Senior Project Management Officer
• München
[. .. ] roles by a connection in Alira Health? Join our global team dedicated to innovation and initiative, where physical walls and different time zones dont limit, but encourage, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] collaboration. The Project Manager (PM) is an important member of the Alira Health Clinical team. Manages clinical study functions, which may include investigational supply, IWRS/ IXRS, data management, biostatistics, pharmacovigilance, and central laboratory. Supervises and provides support to the Clinical team, including Clinical Assistants, In-house Clinical Research Associates, and Clinical Research Associates. Creates and reviews clinical study documents, including protocols, ICF templates, study budgets, site log/ form [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical Study Manager pro Jahr?
Als Clinical Study Manager verdient man zwischen EUR 60.000,- bis EUR 90.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Study Manager Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 221 offene Stellenanzeigen für Clinical Study Manager Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Study Manager Jobs?
Aktuell suchen 41 Unternehmen nach Bewerbern für Clinical Study Manager Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Study Manager Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Study Manager Stellenangebote:
- Staburo GmbH (9 Jobs)
- TFS Health Science (9 Jobs)
- Alimentiv (8 Jobs)
- Abb Vie (7 Jobs)
- Herman Medical Staffing GmbH (7 Jobs)
- Alira Health (6 Jobs)
In welchen Bundesländern werden die meisten Clinical Study Manager Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Study Manager Jobs werden derzeit in Bayern (36 Jobs), Berlin (15 Jobs) und Baden-Württemberg (11 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Study Manager Jobs?
Clinical Study Manager Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
