61 Jobs für Clinical Trial Monitor
Stellenangebote Clinical Trial Monitor Jobs
Job vor 7 Tagen bei Mindmatch.ai gefunden
Teleflex
• AT- 9 Wien
Homeoffice möglich
[. .. ] the study team and department management via escalation of issues and/or within the monitoring visit report. The CRA has a minimum of two years of work experience [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as a clinical trial monitor and assists the Management Team with training needs. Principal Responsibilities Conducts monitoring within timelines and according to the monitoring plan and Teleflex procedures. Works cooperatively with Research Coordinators and Investigators to schedule and conduct monitoring visits including site qualification, site initiation, routine monitoring and site closure visits. Evaluates quality and [. .. ]
Job am 11.03.2026 bei Jobleads gefunden
Clinical Research Associate
• Wien
[. .. ] the study team and department management via escalation of issues and/or within the monitoring visit report. The CRA has a minimum of two years of work experience [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as a clinical trial monitor and assists the Management Team with training needs. Principal Responsibilities Conducts monitoring within timelines and according to the monitoring plan and Teleflex procedures. Works cooperatively with Research Coordinators and Investigators to schedule and conduct monitoring visits including site qualification, site initiation, routine monitoring and site closure visits. Evaluates quality and [. .. ]
Job gestern bei Jooble gefunden
Verbatim Pharma
• Deutschland
Comparator Strategic Sourcing Manager
Clinical Trial Supplies/ Comparator Sourcing Remote (Europe) An established and growing pharmaceutical sourcing organization is seeking an experienced Strategic Comparator Sourcing Manager to strengthen and expand [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] its European supplier network within the clinical trial supplies sector. This is a highly visible role for someone with strong industry relationships who enjoys building partnerships, [. .. ] Negotiate commercial agreements and secure competitive supply solutions. Support sourcing strategies for clinical trial comparator and reference products. Work closely with commercial and operational teams to deliver successful client outcomes. Monitor market dynamics, supplier capabilities, and sourcing opportunities. Represent the business at industry conferences and networking events. Ideal Background Experience within comparator sourcing, clinical trial supplies, clinical supply chain, pharmaceutical procurement, or strategic sourcing. Existing network of pharmaceutical manufacturers, wholesalers, distributors, and sourcing partners across Europe. Strong commercial negotiation and relationship [. .. ]
Job gestern bei Jooble gefunden
Tigermed
CRA/ Klinischer Monitor (m/w/d)
• Deutschland
[. .. ] Qualifications 1. Bachelor degree in biomedical/ medical science or equivalent (e. g. medical, Nurse, Pharmacology) 2. At least 1 year of CRA experiences. 3. Good understanding and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] knowledge of Good Clinical Practice and clinical trial operation processes/ procedures. 4. Language: Fluent in English and German 5. Experience in medical practice is a plus. 96372634 [. .. ]
Job gestern bei Jooble gefunden
Tigermed
• Deutschland
[. .. ] Qualifications 1. Bachelor degree in biomedical/ medical science or equivalent (e. g. medical, Nurse, Pharmacology) 2. At least 1 year of CRA experiences. 3. Good understanding and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] knowledge of Good Clinical Practice and clinical trial operation processes/ procedures. 4. Language: Fluent in English and German 5. Experience in medical practice is a plus. 96372636 [. .. ]
Job gestern bei Jooble gefunden
Tigermed
Klinischer Monitor-CRA (m/w/d)
• Deutschland
[. .. ] Qualifications 1. Bachelor degree in biomedical/ medical science or equivalent (e. g. medical, Nurse, Pharmacology) 2. At least 1 year of CRA experiences. 3. Good understanding and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] knowledge of Good Clinical Practice and clinical trial operation processes/ procedures. 4. Language: Fluent in English and German 5. Experience in medical practice is a plus. 96372635 [. .. ]
Job gestern bei Jooble gefunden
Verbatim Pharma
• Deutschland
Führungs-/ Leitungspositionen
Comparator Strategic Sourcing Manager
Clinical Trial Supplies/ Comparator Sourcing Remote (Europe) An established and growing pharmaceutical sourcing organization is seeking an experienced Strategic Comparator Sourcing Manager to strengthen and expand [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] its European supplier network within the clinical trial supplies sector. This is a highly visible role for someone with strong industry relationships who enjoys building partnerships, [. .. ] Negotiate commercial agreements and secure competitive supply solutions. Support sourcing strategies for clinical trial comparator and reference products. Work closely with commercial and operational teams to deliver successful client outcomes. Monitor market dynamics, supplier capabilities, and sourcing opportunities. Represent the business at industry conferences and networking events. Ideal Background Experience within comparator sourcing, clinical trial supplies, clinical supply chain, pharmaceutical procurement, or strategic sourcing. Existing network of pharmaceutical manufacturers, wholesalers, distributors, and sourcing partners across Europe. Strong commercial negotiation and relationship [. .. ]
Job gestern bei Jooble gefunden
Verbatim Pharma
Global Strategic Sourcing Manager
• Deutschland
Comparator Strategic Sourcing Manager
Clinical Trial Supplies/ Comparator Sourcing Remote (Europe) An established and growing pharmaceutical sourcing organization is seeking an experienced Strategic Comparator Sourcing Manager to strengthen and expand [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] its European supplier network within the clinical trial supplies sector. This is a highly visible role for someone with strong industry relationships who enjoys building partnerships, [. .. ] Negotiate commercial agreements and secure competitive supply solutions. Support sourcing strategies for clinical trial comparator and reference products. Work closely with commercial and operational teams to deliver successful client outcomes. Monitor market dynamics, supplier capabilities, and sourcing opportunities. Represent the business at industry conferences and networking events. Ideal Background Experience within comparator sourcing, clinical trial supplies, clinical supply chain, pharmaceutical procurement, or strategic sourcing. Existing network of pharmaceutical manufacturers, wholesalers, distributors, and sourcing partners across Europe. Strong commercial negotiation and relationship [. .. ]
Job vor 5 Tagen bei Mindmatch.ai gefunden
IQVIA
• AT- 9 Wien
Führungs-/ Leitungspositionen
The IQVIA
Clinical Functional Service Partnerships (Clinical FSP) department is providing highly skilled professionals to our clients project team to set-up and execute clinical trials. As Clinical
Trial Leader (m/w/d) [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] you will be accountable for the operational performance of the trial (preparation, initiation, conduct, closeout and reporting) . As such you will manage crossfunctional trial teams at the customer, acting as that accountable point for delivery and quality whilst maintaining financial control. You will be supported [. .. ] problemsolving to ensure global alignment and adoption of process and technology tools. Support staff in achieving project deliverables on time and within budget, ensuring quality and compliance with contractual obligations. Monitor and guide financial aspects of trials including scope, budget, schedule, and change control. Plan trial quality and risk monitoring/ mitigation. Identify and address quality issues within studies, implementing corrective and preventive actions as needed. Perform continuous review, risk identification, evaluation/ analysis and communication on a trial level as applicable. Train [. .. ]
Job vor 7 Tagen bei Mindmatch.ai gefunden
Roche
Clinical Site Manager (Study Start Up/in Vitro Diagnostic Regulation)
• AT- 9 Wien
[. .. ] where every voice matters. The Position At Roche Diagnostics Solutions (RDS) , our mission is clear: to diagnose earlier, develop faster, and personalise treatment because every patient [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] is unique. Our Clinical Development Medical Affairs (CDMA) team drives innovation to improve healthcare outcomes globally. We see ourselves and our customers as a team that can only reach its full potential together. By listening closely to patients and physicians, and leveraging digitalisation and new technologies, we get closer to their realworld needs. This [. .. ] study startup activities, driving site selection, activation, and qualification assessments to ensure clinical trials launch efficiently and are complianceready Manage Ethics Committee (EC) and Competent Authority (CA) submissions, ensuring all trial documentation is available, local contracts, Ethics Committee and Competent Authority approvals meet stringent regulatory requirements Provide robust CRO oversight, monitoring external partner deliverables, tracking milestones, and escalating any issues Act as the primary contact and clinical trial expert for assigned study site personnel, for execution of the study including training [. .. ] navigating the early phases of clinical trials, specifically managing Ethics Committee (EC) and Competent Authority (CA) regulatory submissions Vendor Management: Demonstrated experience in CRO oversight, with the ability to effectively monitor external partner deliverables and keep study timelines on track IVDR Regulatory Knowledge: Understanding of In Vitro Diagnostic Regulation (IVDR) frameworks alongside global standards such as ICHGCP guidelines Stakeholder Engagement: Exceptional verbal and written communication skills (English) with a proven ability to build trusted relationships and influence crossfunctional partners Nice to [. .. ]
Job am 29.05.2026 bei Mindmatch.ai gefunden
IQVIA Argentina
• AT- 9 Wien
Führungs-/ Leitungspositionen
Vienna, Austria Full time Home-based R1546726 To lead Local Study Teams (LSTs) at country level to deliver committed components of
clinical studies according to agreed resources, budget and timelines [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] complying with Sponsor Procedural Documents, international guidelines such as ICHGCP as well as relevant local regulations. In addition to leading LST (s) , the Local Study Associate Director may perform site monitoring as needed to support the flexible capacity model. The Local [. .. ] Consent Form (MICF) and subsequent site level ICFs, as required, including any relevant translations, and in line with relevant Sponsor SOPs and local regulations. Ensures all country and site level trial essential documents required by ICHGCP prior to study start have been collected and verified for correctness, prior to setting sites ready to enrol, and in line with Sponsor SOPs. Plans and coordinates applicable local drug activities (from local purchase or reimbursement to drug destruction) . Sets up and maintains the [. .. ] activation through to study closure at country and site level in accordance with the Monitoring Plans. Reviews monitoring visit reports (as required and following Sponsor SOPs) and proactively advises the monitor (s) on study related matters. Performs any required comonitoring, Accompanied Site Visits/ training visits with study CRAs. Proactively identifies risks and facilitates resolution of complex study problems and issues. Organises regular Local Study Team meetings on an agenda driven basis. Actively works towards achieving good personal relationships with all Local [. .. ]
Job am 29.05.2026 bei Mindmatch.ai gefunden
IQVIA Argentina
Local Study Associate Director
• AT- 9 Wien
Führungs-/ Leitungspositionen
Vienna, Austria Full time Home-based R1546726 To lead Local Study Teams (LSTs) at country level to deliver committed components of
clinical studies according to agreed resources, budget and timelines [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] complying with Sponsor Procedural Documents, international guidelines such as ICHGCP as well as relevant local regulations. In addition to leading LST (s) , the Local Study Associate Director may perform site monitoring as needed to support the flexible capacity model. The Local [. .. ] Consent Form (MICF) and subsequent site level ICFs, as required, including any relevant translations, and in line with relevant Sponsor SOPs and local regulations. Ensures all country and site level trial essential documents required by ICHGCP prior to study start have been collected and verified for correctness, prior to setting sites ready to enrol, and in line with Sponsor SOPs. Plans and coordinates applicable local drug activities (from local purchase or reimbursement to drug destruction) . Sets up and maintains the [. .. ] activation through to study closure at country and site level in accordance with the Monitoring Plans. Reviews monitoring visit reports (as required and following Sponsor SOPs) and proactively advises the monitor (s) on study related matters. Performs any required comonitoring, Accompanied Site Visits/ training visits with study CRAs. Proactively identifies risks and facilitates resolution of complex study problems and issues. Organises regular Local Study Team meetings on an agenda driven basis. Actively works towards achieving good personal relationships with all Local [. .. ]
Job am 25.05.2026 bei Mindmatch.ai gefunden
Syneos Health, Inc.
• AT- 9 Wien
[. .. ] (SOPs) and Work Instructions (WIs) . Assure compliance with local regulations and appropriate guidance for assigned study design/ classification, including Good Pharmacoepidemiology Practices (GPP) and International Conference [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] on Harmonisation Good Clinical Practice (ICHGCP) . Conduct site management activities as per agreed Scope of Work (So W) , Site Management Plan (SMP) and relevant guidelines. Site identification contact sites to gauge interest, confirm contact details, and obtain relevant documents. Site qualification. Ensure selection of appropriate sites for assigned studies. Site startup with minimal [. .. ] regulatory teams. Conduct all remote and onsite monitoring activities through all study stages. Routinely review the Investigator Site File (ISF) for accuracy, timeliness and completeness; reconcile its contents with the Trial Master File (TMF) ; and ensure sites archive essential documents per local guidelines. Document activities via confirmation letters, followup letters, trip reports, communication logs, and other required project documents per SOPs and SMP; support subject recruitment, retention, and awareness strategies; and enter data into tracking systems to monitor observations, status, and action items. Demonstrate diligence in protecting the confidentiality of each subject or patient. Review assigned site data, assist with data query resolution and missing data followup; analyze data using trend reports and site practices; ensure timely resolution of data queries; and use available hardware and software to [. .. ]
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 Monitoring Signal Detection: Serve as a medical monitor in trials, perform literature reviews, and contribute to signal detection and interpretation. Regulatory Document Contributions: Offer expert medical insight into regulatory submissions and 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 [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
[. .. ] upon request of Healthcare Professionals. Facilitate responses to unsolicited requests for medical information, often in collaboration with Be One Medical Information Services personnel. Present data on Be [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] One products, including clinical, development, and publication data, and data outside the scope of marketing authorization during adhoc field engagements or scientific meetings. Support, attend, and follow up on local, national, regional, and international scientific congresses and events. Support enterprise activities such as booth duty, session coverage, and insight gathering and participate in the [. .. ] institutional networks in the assigned therapeutic area and location. Establish, develop, and maintain longterm professional relationships with HCPs and cooperative groups in Be Ones therapeutic areas. Propose, initiate, implement, and monitor scientific partnerships in line with the crossfunctional strategy for key clinical sites and hospitals in the assigned region. Participate in the planning, organization, and execution of medical events (e. g. , congresses and advisory boards) according to needs. Evidence Generation Clinical Support Identify and support the identification and verification of [. .. ] to or conduct monitoring on developments in the therapeutic area landscape and standards of care. In collaboration with clinical operations, participate in site feasibility assessments, planning and onboarding of clinical trial sites, and continuous followup of sites and ongoing trials in the assigned region. Serve as the primary territory liaison for the receipt, preliminary review, and submission of Investigator Sponsored Research proposals, facilitating the process from concept submission through publication. Medical Insights Strategic Input Collect, analyze, and communicate fieldbased medical insights [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Clinical Research Associate
Job Title: Field
Clinical Research Associate This role supports the Clinical Operations team by overseeing clinical studies, ensuring high-quality human study data collection, and facilitating collaboration between internal study [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] teams, contract research organizations, and clinical sites. You will take ownership of site monitoring and study oversight for multiple clinical studies, with a focus [. .. ] and contribute to impactful research that supports cuttingedge technology development. Responsibilities Assist with clinical study closure activities, including preparing and collecting closeout documentation and organizing study files for longterm storage. Monitor clinical sites for multiple clinical studies, ensuring compliance with study protocols, Good Clinical Practice (GCP) , and ICH guidelines. Collaborate closely with contract research organizations and university sites to facilitate training of site and vendor personnel and support clinical trial execution. Track and maintain regulatory documentation and ensure that all required records are complete, accurate, and up to date. Work with incoming study data to reconcile data reports, identify discrepancies, and generate reports for invoicing and other operational needs. Resolve data queries and delinquencies in a timely manner, coordinating with [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
• Wien
We are looking for a Manager, Clin Ops at Orpha Care to drive the successful planning, execution, and oversight of
clinical investigations for innovative Class III medical devices. In [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] this role, you will act as the operational lead across all clinical trial activitiesfrom study startup to closeoutensuring highquality, compliant, and timely delivery in line with regulatory requirements and company standards. You will work crossfunctionally and with external partners to translate clinical strategy into operational excellence. What Your Day To Day Will Look Like Lead end-to-end operational planning, execution, and oversight [. .. ] ensure effective communication and training Ensure studies are conducted in accordance with ISO 14155, EU MDR, ICHGCP, and internal SOPs Drive vendor and CRO selection, contracting, onboarding, and performance management Monitor vendor deliverables, KPIs, budgets, and timelines in collaboration with internal stakeholders Coordinate crossfunctional teams (e. g. , Clinical, RA, QA, Data, Statistics, Safety, R D) Ensure inspection readiness and support audits and regulatory inspections Identify and elevate risks related to quality, timelines, or compliance Maintain study trackers, documentation, and operational [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
Site Management Lead m/w/d
• München, Bayern
Führungs-/ Leitungspositionen
The Site Management Lead (SML) is a key member of the
Clinical Study Team (CST) , responsible for overseeing all site management and monitoring activities conducted by the Contract [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Research Organization (CRO) in a clinical study. SML ensures high-quality execution of site-related processes from site selection through to site closure, while maintaining compliance with regulatory standards and study protocols. SML collaborates closely with Clinical Trial Lead (CTL) , CST and the CRO to develop study-specific operational plans, including the Clinical Monitoring Plan, and plays a critical role in identifying and mitigating study-level risks. Responsibilities Serve as the primary liaison between the CST and the CRO for all site management activities. Oversee CRO performance [. .. ] and other study-specific operational plans in collaboration with the CST. Identify study-level risks and contribute to the development and implementation of risk management and mitigation strategies. Manage and monitor site identification, feasibility assessments, and site selection processes. Ensure timely and complete submissions to Ethics Committees (ECs) and Institutional Review Boards (IRBs) by the CRO. Support and review site budget negotiations and contract finalizations. Ensure site readiness for initiation, including training, documentation, and logistical preparedness. Oversee and support site initiation [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
• Ingelheim am Rhein, Rheinland- Pfalz
[. .. ] dedicated Patient Safety teams are seeking experienced (Senior) Patient Safety Physicians to join us on our journey. Youll have the chance to work on a variety of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] products, either in clinical development or post-marketing drug safety. Were particularly interested in physicians with expertise in Inflammatory Diseases, Dermatology, Gastroenterology, Rheumatology or Pulmonology. If youre ready to take on this challenge and make a real difference in patient safety, we look forward to receiving your application Tasks Responsibilities In this role as [. .. ] contributing to proactive patient-centric RM strategies for assigned compounds; Planning, managing/ performing and monitoring all PV activities for assigned drugs, including: Set-up of safety analyses in the clinical trial and safety databases for monitoring In this role, you will continuously monitor and further develop the product safety and benefit/ risk profile Managing safety issues will be one of your key responsibilities Collaborating with various departments, including Clinical Development and Global Patient Engagement, you will develop patient-centric benefit-risk profile assessment strategies for developmental compounds Together with Global Epidemiology and Medical [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
Clinical Site Manager (Study Start Up/in Vitro Diagnostic Regulation)
• Wien
[. .. ] where every voice matters. The Position At Roche Diagnostics Solutions (RDS) , our mission is clear: to diagnose earlier, develop faster, and personalise treatment because every patient [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] is unique. Our Clinical Development Medical Affairs (CDMA) team drives innovation to improve healthcare outcomes globally. We see ourselves and our customers as a team that can only reach its full potential together. By listening closely to patients and physicians, and leveraging digitalisation and new technologies, we get closer to their realworld needs. This [. .. ] study startup activities, driving site selection, activation, and qualification assessments to ensure clinical trials launch efficiently and are complianceready Manage Ethics Committee (EC) and Competent Authority (CA) submissions, ensuring all trial documentation is available, local contracts, Ethics Committee and Competent Authority approvals meet stringent regulatory requirements Provide robust CRO oversight, monitoring external partner deliverables, tracking milestones, and escalating any issues Act as the primary contact and clinical trial expert for assigned study site personnel, for execution of the study including training [. .. ] navigating the early phases of clinical trials, specifically managing Ethics Committee (EC) and Competent Authority (CA) regulatory submissions Vendor Management: Demonstrated experience in CRO oversight, with the ability to effectively monitor external partner deliverables and keep study timelines on track IVDR Regulatory Knowledge: Understanding of In Vitro Diagnostic Regulation (IVDR) frameworks alongside global standards such as ICHGCP guidelines Stakeholder Engagement: Exceptional verbal and written communication skills (English) with a proven ability to build trusted relationships and influence crossfunctional partners Nice to [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
Global Clinical Operations Lead (m/f/d)
• Luzern
Führungs-/ Leitungspositionen
[. .. ] health. If youre looking to join a successful, global company with real career opportunities, wed love to meet you. About the Role We are seeking an experienced [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and proactive Global Clinical Operations Lead (f/m/d) to manage and oversee clinical trials/ clinical studies/ clinical investigations from initiation to close-out. This role will work closely with GC crossfunctional project teams, investigators, and Contract Research Organizations (CRO) to ensure that studies are conducted in compliance with applicable regulatory requirements, Good Clinical [. .. ] 14155:2026, EU MDR 2017/ 745, and applicable local regulatory requirements. Data Management Able to collect, enter, and manage clinical data in electronic data capture (EDC) systems provided by the CRO. Monitor data quality and resolve discrepancies in collaboration with data management teams. Site Management Coordinate site visits, audits, and monitoring activities with CRO. Maintain study supplies, equipment, and documentation in audit-ready condition. Liaise with investigators, sponsors, CROs, and internal departments to ensure compliant study execution. Participate in study meetings, training [. .. ] Strong knowledge of clinical investigation processes, GCP, and global regulatory guidelines including ISO14155. Excellent organizational and time management skills. Strong diplomatic and communication skills. Proficiency in Microsoft Office and clinical trial management systems. Excellent command of English is required; knowledge of additional languages will be considered an asset. Willingness to travel internationally as required. Preferred Qualifications Certification as a Clinical Research Coordinator recognized in the US or Europe. Proficiency in class III dental medical devices. Experience with clinical trials preparation, monitoring, [. .. ]
Job am 07.06.2026 bei Jobleads gefunden
Professorship in Clinical Computational Cancer Biology (W3) (f/m/d)
University of Cologne Faculty of Medicine Professorship in
Clinical Computational Cancer Biology (W3) (f/m/d) The University of Cologne and the German Cancer Research Center (DKFZ) are jointly appointing a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] University Professor for Clinical Computational Cancer Biology. The chair will be established at the NCT West, Campus Cologne. The primary mission is the design, preparation, and conduct of [. .. ] developed to better understand tumor heterogeneity, evolution, chromosomal instability, risk stratification and early detection. You will play a leading role in establishing suitable datasets in the NCT/ SUDO databases to monitor trial parameters, and provide key elements for big and deepdata analyses from clinical trials and tumor tissue sample databases. The program will be integrated into the DKFZ Data Science Faculty to enable complex genomic analyses in primary tumors and metastases and address challenges through adaptive study design. At the Cologne campus, [. .. ]
Job am 03.06.2026 bei Jobleads gefunden
Associate Director EU CTR Strategy Operations Excellence Lead
• Baar, Rheinland- Pfalz
Führungs-/ Leitungspositionen
[. .. ] The Associate Director, EU CTR Strategy Operations Excellence supports the Head of EU CTR in providing leadership and strategic oversight for the implementation, optimization, and continuous improvement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of all EU Clinical Trials Regulation (EU CTR) processes within the organization. This role ensures consistent process execution, compliance, and operational excellence across CTIS (Clinical Trials Information System) submissions and lifecycle management activities. Acting as the process owner and operations excellence lead, the role focuses on developing and maintaining frameworks, training programs, and controls [. .. ] member states. Strategic Process Governance and Oversight Define and maintain the EU CTR operating model, standard procedures, RACI frameworks, and control mechanisms. Establish oversight routines, KPIs, and performance dashboards to monitor compliance and operational effectiveness. Align EU CTR operational processes with corporate regulatory strategies and global process standards. Coordinate process control reviews and readiness assessments to drive continuous improvement and ensure adherence to EU CTR requirements. Operational Process Control Maintain end-to-end EU CTR process maps, workflows, and control points for submissions and trial maintenance activities. Monitor process execution through quality reviews, deviation tracking, and performance metrics to identify risks and improvement areas. Support audit readiness and act as a subject matter expert (SME) during inspections, internal audits, and CAPA development. Learning and Capability Building Develop and oversee EU CTR learning and competency programs [. .. ]
Job am 03.06.2026 bei Jobleads gefunden
Associate Director EU CTR Strategy Operations Excellence Lead
• Baar, Zug
Führungs-/ Leitungspositionen
[. .. ] The Associate Director, EU CTR Strategy Operations Excellence supports the Head of EU CTR in providing leadership and strategic oversight for the implementation, optimization, and continuous improvement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of all EU Clinical Trials Regulation (EU CTR) processes within the organization. This role ensures consistent process execution, compliance, and operational excellence across CTIS (Clinical Trials Information System) submissions and lifecycle management activities. Acting as the process owner and operations excellence lead, the role focuses on developing and maintaining frameworks, training programs, and controls [. .. ] EU CTR in defining and maintaining the EU CTR operating model, including standard procedures, RACI frameworks, and control mechanisms. Lead the establishment of oversight routines, KPIs, and performance dashboards to monitor compliance and operational effectiveness. Ensure alignment of EU CTR operational processes with corporate regulatory strategies and global process standards. Coordinate process control reviews and readiness assessments to drive continuous improvement and ensure adherence to EU CTR requirements. Operational Process Control: Maintain end-to-end EU CTR process maps, workflows, and control points for submissions and trial maintenance activities. Monitor process execution through quality reviews, deviation tracking, and performance metrics to identify risks and improvement areas. Support audit readiness and act as a subject matter expert (SME) during inspections, internal audits, and CAPA development. Learning and Capability Building: Develop and oversee EU CTR learning and competency programs [. .. ]
Job am 02.06.2026 bei Jobleads gefunden
Manager Theranostics Strategy Portfolio Business Development (f/m/d)
• Erlangen, Bayern
[. .. ] with the Radiopharma business objectives. Identify, prioritize, and manage theranostics opportunities, including diagnostic and therapeutic radiopharmaceuticals, new isotopes, and emerging technologies. Develop longterm portfolio roadmaps and corresponding [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] investment strategies. Continuously monitor market trends, the competitive landscape, and regulatory developments. Manufacturing Network Development Define requirements and specific considerations to develop a global manufacturing and supply network that supports theranostics programs. Define the site strategy, capacity planning, and investment roadmap for theranostic products, ensuring close alignment and collaboration with technical operations, quality, and capital programmes. Ensure that manufacturing capabilities effectively support both clinical trial and commercial supply requirements. Align the network design with regulatory, quality, and logistical constraints. Business Development Partnerships Lead business development activities with pharmaceutical, biotech, and academic partners. Position Siemens Healthineers Radiopharma as a CDMO and strategic partner for theranostics development and manufacturing. Structure and negotiate agreements for clinical trials and [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical trial monitor pro Jahr?
Als Clinical trial monitor verdient man zwischen EUR 45.000,- bis EUR 70.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Trial Monitor Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 61 offene Stellenanzeigen für Clinical Trial Monitor Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trial Monitor Jobs?
Aktuell suchen 18 Unternehmen nach Bewerbern für Clinical Trial Monitor Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Trial Monitor Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Trial Monitor Stellenangebote:
- IQVIA (6 Jobs)
- Verbatim Pharma (4 Jobs)
- Tigermed (3 Jobs)
- Parexel (3 Jobs)
- IQVIA Argentina (2 Jobs)
- Thermo Fisher Scientific (2 Jobs)
In welchen Bundesländern werden die meisten Clinical Trial Monitor Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trial Monitor Jobs werden derzeit in Bayern (8 Jobs), Berlin (7 Jobs) und Rheinland-Pfalz (4 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trial Monitor Jobs?
Clinical Trial Monitor Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
