157 Jobs für Clinical Study Manager
Stellenangebote Clinical Study Manager Jobs
Job vor 10 Tagen bei Neuvoo gefunden
Fraunhofer- Gesellschaft
• Lübeck, Schleswig- Holstein
Abgeschlossenes Studium
Flexible Arbeitszeiten Betriebliche Altersvorsorge Jobticket Tarifvertrag Vermögenswirksame Leistungen
[. .. ] klinischen Forschung (Studienkoordination, CRA, wissenschaftliche Mitarbeit) oder im Umfeld von Medizinprodukten/in-Vitro Diagnostika. Sie haben Kenntnisse der regulatorischen Anforderungen (z. B. MDR, IVDR, ISO 14155, ISO20916) und der [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Good Clinical Practice (GCP) . Ausgeprägte organisatorische Fähigkeiten und eine strukturierte Arbeitsweise. Sie sprechen fließend Deutsch und sehr gut Englisch in Wort und Schrift. Kommunikationsstärke und Freude an der Zusammenarbeit mit interdisziplinären Teams. Uns ist bewusst, dass jeder Lebenslauf einzigartig ist. Sollten Sie nicht alle Anforderungen erfüllen können, finden wir gemeinsam Lösungen, [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Manager Medical Science Liaison Oncology
• München, Bayern
[. .. ] as a field medical expert, delivering continuous medical education to HCPs in Germany and gathering actionable insights to inform strategy. Build and maintain scientific partnerships with key [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] opinion leaders, Cooperative Study Groups, medical associations, and research organizations in oncology. Develop and execute an Medical Science Liaison (MSL) Oncology strategy aligned with local and European medical affairs priorities. Build and expand relationships/ networks with key medical and scientific experts in the field of breast cancer and/or lung cancer. Support clinical trials by identifying study sites, participating in SIVs (Site Inviations Visits) , assisting with patient enrollment, and ensuring smooth information exchange. Identify research opportunities, including Investigator-Initiated Trials, Real-World Evidence, and other evidence-generation studies. Represent the organization at scientific conferences, advisory boards, and educational events, sharing insights and [. .. ]
Job am 07.12.2025 bei Jobleads gefunden
• Cham, Zug
[. .. ] Abb Vie Brand teams and external thought leaders using information that has been reviewed and approved by relevant local procedures, and under the direction, governance and oversight [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of the MSLs manager, therapeutic area Medical Manager, or Affiliate Medical Director as appropriate. This includes working with local Medical Information teams, as appropriate, to respond to unsolicited requests for off-label information on Abb Vie medicines. Develop and maintain collaborative relationships with thought leaders in Gastroenterology, to facilitate Abbvie research and educational priorities [. .. ] members of the Affiliate Brand Team to develop their scientific and technical expertise through the delivery of scientific update presentations. Assist in the initiation; oversight and follow up of assigned clinical studies and medical projects initiated within the therapeutic area for which the MSL carries responsibility (e. g. post marketing clinical activities such as registry/ database projects, epidemiological surveys, post-authorization studies (phase IV) . All such activities must comply with applicable local laws, guidelines, codes of practice, SOPs, and Abb Vie R D (GPRD) SOPs. Act as the point of contact with thought leaders to facilitate investigator initiated study (IIS) ideas and requests for support to the local and global medical teams as appropriate. Serve as a point of contact within the Medical Affairs team for thought leaders and external experts within western Switzerland in order to satisfy their needs for scientific knowledge in a therapeutic area and, when [. .. ]
Job am 23.11.2025 bei Jobleads gefunden
Medical Science Liaison Manager, Nephrology, North-West
• München, Bayern
[. .. ] within a geographic area. He/ she manages and maintains collegial and professional relationships with KOLs and identifies and facilitates collaboration opportunities with Alexion. He/ she combines strong [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] business acumen and clinical expertise and serves as a peer-to-peer liaison internally and externally. He/ she ensures a close working relationship with all functions in their region, including sales, and market access. You will be responsible for: Develop and maintain peer-to-peer collaborations with key medical experts in nephrology and adjacent [. .. ] in the region, manage questions, liaise with headquarters to ensure proper response has been provided and ensure that data is fair and balanced. In conjunction with clinical operations perform clinical study feasibility and support effective study implementation. Deliver quality medical education presentations in a variety of settings and obtain valuable feedback that can be disseminated throughout the organization e. g. Staff Meetings, Round Tables, Hospital Meeting activities. Serve as an Alexion-internal expert in therapeutic area demonstrating up-to-date and [. .. ]
Job am 23.11.2025 bei Jobleads gefunden
• München, Bayern
[. .. ] within a geographic area. He/ she manages and maintains collegial and professional relationships with KOLs and identifies and facilitates collaboration opportunities with Alexion. He/ she combines strong [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] business acumen and clinical expertise and serves as a peer-to-peer liaison internally and externally. He/ she ensures a close working relationship with all functions in their region, including sales, and market access. You will be responsible for: Develop and maintain peer-to-peer collaborations with key medical experts in nephrology and adjacent [. .. ] in the region, manage questions, liaise with headquarters to ensure proper response has been provided and ensure that data is fair and balanced. In conjunction with clinical operations perform clinical study feasibility and support effective study implementation. Deliver quality medical education presentations in a variety of settings and obtain valuable feedback that can be disseminated throughout the organization e. g. Staff Meetings, Round Tables, Hospital Meeting activities. Serve as an Alexion-internal expert in therapeutic area demonstrating up-to-date and [. .. ]
Job am 19.11.2025 bei Jobleads gefunden
Regional Market Access Manager Dermatology-West/ Mitte: Köln, Aachen, Darmstadt, Saarbrücken, Trier
• Neu- Isenburg, Hessen
Market Access
Manager, Germany LEO Pharma has embarked on an ambitious journey to become the preferred dermatology care partner improving peoples lives around the world and that is why we [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] need you. Responsibilities Definition and development of strategies to support medical personnel, especially regarding occupational dermatology and economic feasibility. Preparation of materials for [. .. ] the basis for targeted dialogue and credible relationships with relevant regional decision makers. Support of Market Access and HEOR Managers with national market access and reimbursement topics. Qualifications Completed university study in medicine, public health, natural sciences or comparable education. Industry experience in Market Access, health economics, marketing, sales, regulatory affairs or clinical research. Knowledge of the German healthcare system. Specific knowledge of the way of work in Market Access and reimbursement relevant stakeholders. Knowledge in target group appropriate communication. Sales experience. Relationship skills empathy. Stakeholder management network competence. Negotiation and closing security. Analytical competence data orientation. Argumentation and persuasion power. Project and [. .. ]
Job vor 11 Tagen bei Jobware gefunden
Fresenius Kabi Deutschland GmbH
• Bad Homburg
Werkstudenten
[. .. ] to effectively communicate our research findings. You will actively contribute to a variety of administrative tasks, ensuring smooth and efficient operations. Your profile You are currently enrolled [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in a full-time study program in Market Access, Health Economics, Nutrition Sciences, Pharmacy, Medicine, Biology, or a related field. Basic knowledge of End Note and MS Office (especially Power Point) is an advantage. You have an interest in reading and analyzing medical-scientific literature. In addition to your excellent communication skills, you work diligently [. .. ] Fresenius Kabi. Get involved and contribute your ideas to the development of groundbreaking products, services and therapies for the care of critically and chronically ill patients. Isabell Kuhn (Junior HR Manager) Fresenius Kabi is a global healthcare company that specializes in lifesaving medicines and technologies for infusion, transfusion and clinical nutrition. Our products and services are used to help care for critically and chronically ill patients. fresenius-kabi. com We seek talents and perspectives At Fresenius, we are convinced that combining different perspectives, opinions, experiences, cultures and values enables us to harness the potential that will make us even more successful. All [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
PhD-position at the University of Ulm, Germany (ENDOTRAIN) (DC9)
• Ulm, Baden- Württemberg
[. .. ] technologies. Global Collaboration: Extensive technical and physiological training, and the opportunity to build a professional network through world-leading international collaborations. Join us to translate complex biomedical data [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] into actionable clinical intelligence and shape the future of personalized medicine About the project/ work tasks: 19 Ph D Fellowships available in Digital Endocrinology in the Marie Skodowska-Curie Doctoral Network (ENDOTRAIN) . Join Europes first doctoral network in digital endocrinology integrating AI, sensor technology, omics, and clinical medicine to transform diagnosis and treatment [. .. ] of interdisciplinary experts who merge clinical endocrinology, AI, data science, engineering, ethics and law into an integrated field of digital endocrinology. The programme focuses on adrenal disorders as a case study for advancing digital health in Europe. This project is part of Work Package 2:Technologies for Multimodal Data of ENDOTRAIN, collaborating closely with an international network of clinical and technical experts across the ENDOTRAIN consortium. This includes mandatory secondments to maximize your practical exposure and network. Remote clinical trials, powered by [. .. ] host institutions for the position you are applying. General information Contact Informal enquiries should be addressed to Prof. Walter Karlen via. For questions about the ENDOTRAIN programme, please contact Programme Manager Elizabeth Farmer ( ) MSCA-Endotrain has a gender equality plan where gender balance among employees is therefore a goal. We encourage women to apply. If multiple applicants have approximately equivalent qualifications, the rules pertaining to moderate gender quotas shall apply. It is also a goal to recruit people with [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
• München, Bayern
[. .. ] moving forward the central monitoring function has become a top priority at PSI. We are looking for a person who would lead the risk-based monitoring approach implementation [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] on the clinical study and program level to ensure patient safety and data integrity. You will Lead and facilitate initial and ongoing study Risk Management Participate in selection and setup of the RBM platform Perform Centralized Monitoring for a study including review of Key Risk Indicators Statistical Analyses and Quality Tolerance Limits Present Centralized [. .. ] Communicate study challenges to Clinical Data Science group and work out data-driven solutions Qualifications College/ University degree or an equivalent combination of education training and experience Clinical Study Lead/Manager experience Strong communication presentation skills are essential Leadership and ability to work independently are essential Centralized Monitoring experience is a plus Critical thinking and analytical skills Ability to work with complex data and provide insight into risk reports and trends Ability to adapt to changing circumstances and learn quickly Knowledge [. .. ]
Job gestern bei Jobleads gefunden
Principal Lead Data Manager
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Job Description Acts as primary communication point for project teams and company [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] departments regarding clinical data management. Acts as primary communication point for clients/ vendors for all data management aspects of clinical projects and clinical data management reporting. Responsible for the supervision of all project data management activities of assigned studies. Coordinates data management activities within clinical projects including but not limited to EDC development, [. .. ] generation of final Data Management deliverables. Provides input into monitoring of project scope, budget, timelines, and deliverables. Responsible for clinical data management activities including, but not limited to: development of study documentation, User acceptance testing, User access management, Data review, e CRf/External data reconciliation, SAE reconciliation, Query management, Study Database Lock activities, Archival of CRFs QC coordination, Project status reporting, Data listings/ Patient profiles generation and delivery Maintains and QCs e TMF. Maintains and QCs Data Management working files. Participates in preparation [. .. ] or University degree or equivalent combination of training and experience that presents the required knowledge, skills, and abilities Minimum of five years of CRO industry experience as a Lead Data Manager or equivalent position At least 3years of experience using CDm/EDC systems (Medidata Rave or Oracle Inform preferable) Project data management experience is a plus Full working proficiency in English Organizational and managerialskills Additional Information Advance your career in clinical research and develop new skillsets whilst growing with the organization. [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Clinical Research Associate page is loaded # # Clinical Research Associatelocations: Germany Remotetime type: Full timeposted on: Posted 14 Days Agojob requisition id: R31245Be One continues to grow at [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who [. .. ] initiation, conduct (recruitment, quality data collection) and timely completion of oncology/ hematology clinical trials within the assigned region. The CRA is responsible for collaborating closely with the Regional Clinical Operations Manager to ensure study timelines are adhered to and required quality standards are maintained. Identify gaps and areas for improvement and propose CAPA. Supports start-up and provides local expertise. SSU experience is considered a plus CRA activities Perform feasibility, site identification, selection and evaluation, supporting initial list of sites and recruitment targets Provides protocol [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Medical Affairs Manager
• Essen, Nordrhein- Westfalen
Medical Affairs
Manager (m/f/D) Tasks Provide recommendation on Patient-Reported Outcomes (PRO) endpoints, instruments and assessment schedule based upon trial population, comparator and DS strategic objectives Contribute to Patient Experience [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Data (PED) / PRO-specific aspects of protocol profile, clinical trial protocol and informed consent form development Work with PRO implementation Lead to ensure PRO strategy is conducive to e PRO implementation capabilities Review trial statistical analysis plans for PROs to ensure that proposed analyses match with PRO endpoints as per protocol Review PRO-related TFL shells and actual results once finalized (PRO Team Lead to provide Senior Review) Review PRO outcomes in clinical study reports (PRO Team Lead to provide Senior Review) Respond to study team queries related to PED Respond to PRO-specific questions received in Requests for Information (RFIs) as part of EU CTR submissions Contribute to regulatory briefing documents as needed Contribute to HTA interactions as needed Consult the HEOR Asset [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• Leipzig, Sachsen
Medical Affairs
Manager (m/f/D) Tasks Provide recommendation on Patient-Reported Outcomes (PRO) endpoints, instruments and assessment schedule based upon trial population, comparator and DS strategic objectives Contribute to Patient Experience [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Data (PED) / PRO-specific aspects of protocol profile, clinical trial protocol and informed consent form development Work with PRO implementation Lead to ensure PRO strategy is conducive to e PRO implementation capabilities Review trial statistical analysis plans for PROs to ensure that proposed analyses match with PRO endpoints as per protocol Review PRO-related TFL shells and actual results once finalized (PRO Team Lead to provide Senior Review) Review PRO outcomes in clinical study reports (PRO Team Lead to provide Senior Review) Respond to study team queries related to PED Respond to PRO-specific questions received in Requests for Information (RFIs) as part of EU CTR submissions Contribute to regulatory briefing documents as needed Contribute to HTA interactions as needed Consult the HEOR Asset [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Future Opportunity: Clinical Research Start-up Project Manager
Future Opportunity: Start-up Project
Manager At Biomapas, we are continuously expanding our
Clinical Trial projects, and this means we are always on the lookout for talented Start-up Project [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Manager to join our team. While we may not have an immediate opening, we are proactively seeking experienced Start-up Project Manager who see themselves as part of our growing team. If you are [. .. ] Clinical Operations, Regulatory Affairs, Contracts Budgets, Vendor Management departments. Risk Time management: develop and maintain SSU strategy and timelines as per committed to Clients deliverables. Timely identify potential bottlenecks or study start up processes, suggest and implement mitigations strategies. Strong understanding oof EU CTR and CTIS submission process, proven experience of submissions done via CTIS (Part I and Part II) . Proven experience being a Start-up PM, Start-up lead within CRO, managing multicounty studies. Strong knowledge of ICH-GCP, [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Medical Affairs Manager
• Düsseldorf, Nordrhein- Westfalen Duesseldorf
Medical Affairs
Manager (m/f/D) Tasks Provide recommendation on Patient-Reported Outcomes (PRO) endpoints, instruments and assessment schedule based upon trial population, comparator and DS strategic objectives Contribute to Patient Experience [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Data (PED) / PRO-specific aspects of protocol profile, clinical trial protocol and informed consent form development Work with PRO implementation Lead to ensure PRO strategy is conducive to e PRO implementation capabilities Review trial statistical analysis plans for PROs to ensure that proposed analyses match with PRO endpoints as per protocol Review PRO-related TFL shells and actual results once finalized (PRO Team Lead to provide Senior Review) Review PRO outcomes in clinical study reports (PRO Team Lead to provide Senior Review) Respond to study team queries related to PED Respond to PRO-specific questions received in Requests for Information (RFIs) as part of EU CTR submissions Contribute to regulatory briefing documents as needed Contribute to HTA interactions as needed Consult the HEOR Asset [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Translational Executive
• München, Bayern
Translational Science Executive (Oncology) Overview I am working with a dynamic
clinical-stage biotechnology company that are looking urgently for a Translational Sciences Executive to provide scientific leadership across early [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] oncology programs. This is a senior, hands-on role for an experienced translational leader who has successfully taken oncology assets from preclinical development into first-in-human studies, and who thrives at [. .. ] my client is looking for the right fit for the business. Scope Own the translational strategy from late discovery through IND and early clinical development Bridge preclinical data with clinical study design and execution Provide scientific leadership across translational, biomarker and early development activities Act as a key cross-functional partner to research, clinical and regulatory teams Lead and develop a small, established translational science team (4 members) Experience Ph D or MD in Translational Medicine, Oncology, Pharmacology or related field 10+ [. .. ] oncology therapies Proven cross-functional leadership in early development settings Comfortable operating both strategically and hands on with scientific data Ideal Profile Senior scientific leader, not just a big company manager Able to guide teams while remaining close to the science Pragmatic, decisive, and data driven Clear communicator with strong stakeholder influence Whats Offered Senior leadership position with meaningful impact on early oncology programs Opportunity to shape translational strategy at a pivotal stage of development Competitive compensation including base salary, bonus [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• München, Bayern
[. .. ] into our product roadmap. What youll be doing Strategic Account Program Management Post Signature Leadership : Orchestrate the partner journey immediately following contract execution. You will act [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as the Project Manager for the deployment, ensuring seamless onboarding and integration of our foundational models. Scientific Advisory : Consult with client R D teams (ranging from bench scientists to Heads of R D) to diagnose their specific therapeutic challenges. Design and guide proofofconcept studies that demonstrate the clear utility of our models in [. .. ] Educational Background : Ph D in Computational Biology, Bioinformatics, Genomics, or a related field is required. Domain Expertise : Deep understanding of the biopharma R D value chain (target discovery to clinical trials) . You understand the specific pain points of drug developers. Technical Fluency : Extensive experience with multiomics datasets (singlecell, transcriptomics, proteomics) . You can comfortably discuss ML concepts (LLMs, benchmarking) with data scientists. Relationship Strategic Skills Stakeholder Management : Proven experience navigating complex, matrixed organizations (Big Pharma experience is [. .. ] the Hiring Manager to discuss your background, motivations, and the position in more detail. Interviews : Following a successful screening, you will be invited to a series of interviews: Case Study (60 min) : You will engage in a live, interactive case study focused on Business Development and Strategy. No prior preparation is required. We want to see how you think on your feet, how you structure complex problems in realtime, and how you approach strategic decisionmaking with our commercial team. [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Medical Affairs Manager
• Dortmund, Nordrhein- Westfalen
Medical Affairs
Manager (m/f/D) Tasks Provide recommendation on Patient-Reported Outcomes (PRO) endpoints, instruments and assessment schedule based upon trial population, comparator and DS strategic objectives Contribute to Patient Experience [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Data (PED) / PRO-specific aspects of protocol profile, clinical trial protocol and informed consent form development Work with PRO implementation Lead to ensure PRO strategy is conducive to e PRO implementation capabilities Review trial statistical analysis plans for PROs to ensure that proposed analyses match with PRO endpoints as per protocol Review PRO-related TFL shells and actual results once finalized (PRO Team Lead to provide Senior Review) Review PRO outcomes in clinical study reports (PRO Team Lead to provide Senior Review) Respond to study team queries related to PED Respond to PRO-specific questions received in Requests for Information (RFIs) as part of EU CTR submissions Contribute to regulatory briefing documents as needed Contribute to HTA interactions as needed Consult the HEOR Asset [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
[. .. ] deep therapeutic expertise, Amplity transforms how breakthrough treatments reach the people who need them. Regional Medical Science Liaison Oncology/ Breast Cancer Germany Client: Biotech, Oncology (Precision Medicine) [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Reports to: Field Manager at Amplity Health Primary Territory: Germany, Poland, Hungary, Check Republic, Switzerland and Austria Location: Germany RESPONSIBILITIES: Our client is a US based biopharmaceutical company fully dedicated to the research and development of medicines with the aim to improve the lives of patients. The company is looking for a driven and [. .. ] experience. The MSL is a member of a global field-based team of scientific experts who function as an extension of Medical Affairs. The MSL role focuses primarily on providing clinical, scientific, and educational support to healthcare professionals (HCPs) at clinical trial research sites (Principal Investigators PIs and their study teams) , and potential clinical trial sites, in addition to national and regional Key Opinion Leaders (KOLs) who have a key influence in the medical oncology communities. The MSL develops strong relationships within the respective oncology community and collects impactful insights to enhance the clients strategic objectives. This role will [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Medical Affairs Manager
• Hamburg
Medical Affairs
Manager (m/f/D) Tasks Provide recommendation on Patient-Reported Outcomes (PRO) endpoints, instruments and assessment schedule based upon trial population, comparator and DS strategic objectives Contribute to Patient Experience [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Data (PED) / PRO-specific aspects of protocol profile, clinical trial protocol and informed consent form development Work with PRO implementation Lead to ensure PRO strategy is conducive to e PRO implementation capabilities Review trial statistical analysis plans for PROs to ensure that proposed analyses match with PRO endpoints as per protocol Review PRO-related TFL shells and actual results once finalized (PRO Team Lead to provide Senior Review) Review PRO outcomes in clinical study reports (PRO Team Lead to provide Senior Review) Respond to study team queries related to PED Respond to PRO-specific questions received in Requests for Information (RFIs) as part of EU CTR submissions Contribute to regulatory briefing documents as needed Contribute to HTA interactions as needed Consult the HEOR Asset [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Clinical Operations Lead
• München, Bayern
Führungs-/ Leitungspositionen
This range is provided by Alimentiv. Your actual pay will be based on your skills and experience talk with your recruiter to learn more. Base pay range Responsible for the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 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, ICHGCP, local regulations and study [. .. ] 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 vor 4 Tagen bei Jobleads gefunden
Queensland State Manager
Work-Life-Balance
[. .. ] making visits to onsite clinics and working from home Remuneration : Competitive remuneration with up to 7, 500 PD budget + bonuses We are looking for a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategic engaging State Manager to lead, manage and grow our Early Intervention Onsite Physiotherapy services across Queensland-including Brisbane, Ipswich, Gold Coast, Townsville and Cairns You will be responsible formanaging key client relationships, developing coaching leads in your team and ensuring high quality service delivery from remote healthcare professionals across Queensland. You will be [. .. ] record in operational people leadership, including leading other leaders team members Proven account management business development skills A strategic mindset an active and agile driver of change Background in delivering clinical services across Medical, Allied Health or Occupational Health (e. g. Physiotherapy, Occupational Therapy) Current registration with Australian Health Practitioner Agency (AHPRA) Professional indemnity insurance Full Australian working rights Australian drivers license and access to your own private vehicle Why work for Axis? Axis is an industry-leading workplace health and [. .. ] pathways (APA titling, MBA etc) , weekly mentoring and support from the Axis Executive Leadership teams, bi-annual leadership days a promote from within culture Extra leave including 1 paid study day per year, option to purchaseadditional annual leave and proactive wellbeing pet leave Perks such as novated leasing options, free early intervention healthcare services and discounts for hundreds of retailers Even though its the festive season, rest assured our recruitment team is still here and actively reviewing applications throughout the [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Medical Affairs Manager
[. .. ] job poster from K-Recruiting Life Sciences We unite the people who make our world healthier by placing top experts with life sciences companies worldwide. Precise. Fast. Accurate. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Medical Affairs Manager (m/f/D) Tasks : Provide recommendation on Patient-Reported Outcomes (PRO) endpoints, instruments and assessment schedule based upon trial population, comparator and DS strategic objectives Contribute to Patient Experience Data (PED) / PRO-specific aspects of protocol profile, clinical trial protocol and informed consent form development Work with PRO implementation Lead to ensure PRO strategy is conducive to e PRO implementation capabilities Review trial statistical analysis plans for PROs to ensure that proposed analyses match with PRO endpoints as per protocol Review PRO-related TFL shells and actual results once finalized (PRO Team Lead to provide Senior Review) Review PRO outcomes in clinical study reports (PRO Team Lead to provide Senior Review) Respond to study team queries related to PED Respond to PRO-specific questions received in Requests for Information (RFIs) as part of EU CTR submissions Contribute to regulatory briefing documents as needed Contribute to HTA interactions as needed Consult the HEOR Asset [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Clinical Operations Lead
• Köln, Nordrhein- Westfalen Koeln
Führungs-/ Leitungspositionen
Alimentiv Cologne, North Rhine-Westphalia, Germany
Clinical Operations Lead Responsible for the clinical operations of a project within a defined regional/ global level. Provides oversight of project deliverables, assigned Clinical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Research Associate (CRAs) and Investigator sites in accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP) , ICH guidelines and local regulations. The COL acts as [. .. ] 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 [. .. ] CRAs for studyspecific 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 vor 4 Tagen bei Jobleads gefunden
Clinical Operations Lead
• Düsseldorf, Nordrhein- Westfalen Duesseldorf
Führungs-/ Leitungspositionen
Clinical Operations Lead 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] sites in accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP) , ICH guidelines and local regulations. The COL acts as [. .. ] 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. Base Pay Range This range is provided by Alimentiv. Your actual pay will be based on your skills and experience talk with your recruiter [. .. ] CRAs for studyspecific 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 [. .. ]
1 von 7Weiter » Weitere Suchergebnisse laden »
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 157 offene Stellenanzeigen für Clinical Study Manager Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Study Manager Jobs?
Aktuell suchen 18 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:
- Veeda Lifesciences (11 Jobs)
- Tubulis GmbH (11 Jobs)
- TFS Health Science (6 Jobs)
- Herman Medical Staffing GmbH (5 Jobs)
- Fresenius Kabi Deutschland GmbH (1 Job)
- Parexel (1 Job)
In welchen Bundesländern werden die meisten Clinical Study Manager Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Study Manager Jobs werden derzeit in Bayern (38 Jobs), Nordrhein-Westfalen (23 Jobs) und Berlin (10 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Study Manager Jobs?
Clinical Study Manager Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
