44 Jobs für Clinical Trial Monitor
Stellenangebote Clinical Trial Monitor Jobs
Job vor 13 Tagen bei Mindmatch.ai gefunden
ZOLL Medical Corporation
• AT- 5 Au
[. .. ] to introduce our advanced technologies, managing complex solutionbased sales cycles, and ensuring seamless support throughout the customer journeyfrom initial engagement to implementation and beyond. Your ability to [...]
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[...] deeply understand the clinical and operational needs of emergency care environments will be essential to your success. Working both autonomously and collaboratively with internal teams, you will be responsible for territory planning, sales execution, training and education, account development, and customer support. This role offers a unique opportunity to contribute to meaningful, lifesaving outcomes [. .. ] need to save lives. Key areas of accountability include Sales Performance Revenue Growth Achieve and exceed defined sales targets for capital equipment, consumables, and service offerings in the EMS sector. Monitor and manage sales performance through accurate forecasting, regular pipeline reviews, and proactive activity planning to maximise opportunities within the territory. Territory Management Planning Develop and execute a strategic territory business plan aligned with national and regional goals. This includes mapping out key customers and influencers, identifying new business opportunities, and [. .. ] accounts. Product Education Clinical Support Deliver comprehensive inservice training, product demonstrations, and education to ensure customer competency and confidence in using ZOLLs products. Act as the primary clinical resource during trial deployments and product evaluations. Support successful implementation and user adoption by collaborating closely with clinical educators, trainers, and product specialists. Market Development Opportunity Identification Identify emerging opportunities in the EMS market through continuous research, field engagement, and competitor analysis. Leverage market insights to expand ZOLLs footprint, introduce new solutions, and [. .. ]
Job am 17.11.2025 bei Mindmatch.ai gefunden
i- Pharm Consulting
Clinical Research Associate
• AT- 9 Wien
Work-Life-Balance
Job Title:
Clinical Research Associate (CRA) 0.8 FTE Location: Austria Duration: 12-Month Contract Travel: 6080 About the Company Join a leading global contract research organization (CRO) that partners with pharmaceutical, [...]
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[...] biotechnology, and medical device companies to advance innovative therapies. The organization is known for its commitment to high-quality clinical research [. .. ] supports employees in professional growth and development while contributing to meaningful medical advancements worldwide. Role Overview We are seeking an experienced Clinical Research Associate (CRA) to manage and coordinate clinical trial site activities in Austria on a 12-Month Contracted basis. In this role, you will ensure compliance with ICH GCP, FDA regulations, local laws, and company SOPs, while maintaining strong relationships with investigational sites and project teams. This is a 0.8 FTE position with significant travel (6080) . Key Responsibilities Conduct site visits to monitor clinical trial progress, protocol adherence, and regulatory compliance. Manage and maintain essential trial documentation to ensure data integrity and audit readiness. Represent the organization in the global clinical research community and maintain collaborative relationships with sites and client personnel. Assist project or clinical team managers on assigned projects and take [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
• Hamburg
Führungs-/ Leitungspositionen Freiberuflich
TFS Health Science is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire
clinical development journey. Our expertise includes full service-capabilities, [...]
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[...] resourcing and Functional Service (FSP) solutions. Join Our Team as a Freelance Senior/ Medical Director (Neurology-Bid Defense Support) . About this role TFS Health Science is seeking a highly flexible board-certified Neurology specialist to support upcoming Bid Defense Meetings. This [. .. ] a key scientific advisor in bid defense meetings (BDM) , RFP responses, and proposal development, ensuring compelling and medically sound strategies. Study Design Protocol Development : Provide expert input on trial design, patient recruitment, and regulatory strategy to optimize study success. Medical Oversight : Lead medical monitoring activities across assigned projects and step in as a handson medical monitor when needed. Scientific Advocacy : Represent TFS at client meetings, industry conferences, and scientific events, reinforcing our reputation as a trusted CRO partner. Team Leadership : Mentor crossfunctional teams, ensuring highquality execution of clinical programs. Qualifications Medical Degree. Boardcertified in Neurology. Deep knowledge of GCP, ICH guidelines, and regulatory requirements [. .. ]
Job gestern bei Jobleads gefunden
Senior/ Medical Director (Ophthalmology)
• München, Bayern
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 service-capabilities, [...]
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[...] resourcing and Functional Service (FSP) solutions. About this role As part of our Ophthalmology team you will working alongside passionate and innovative professionals to ensure our customers achieve their goals. Key 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 [. .. ]
Job am 27.09.2025 bei Jobleads gefunden
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] (IIR) programs, the management of the German Medical Science Liaisons (MSL) team and the medical review of Medical Affairs materials/ promotional materials. In addition, the role has [...]
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[...] oversight over the Clinical Operations team for Oncology/ Hematology and IAI/ Dermatology. Duties And Responsibilities Represent Germany in the Incyte International Medical Affairs Leadership Team, give appropriate feedback to global and regional initiatives Assure development of effective medical strategies and their local execution in accordance with local leadership team Develop, lead and manage German [. .. ] needed Serve as an expert on call to address call center questions from healthcare professionals Define and develop required team competencies (with HR) to recruit and retain local medical team Monitor team performance in terms of goals and delivery against medical plans; identify areas for development Allocate and oversee utilization of local medical budget Act as senior company representative both internally and externally Contribute positively to a strong culture in living the Incyte values and respecting business integrity and ethics Act [. .. ] in academic, clinical, or industry setting required Successful people management experience required with min 2+ years Hematology/ oncology experience required Familiarity with GCP/ ICH/ FDA requirements as well as clinical trial design, biostatistics, medical writing, product safety, and regulatory affairs Strong interpersonal, verbal and written communication skills. Strong public speaking skills Excellent leadership and management skills Ability to influence and work effectively across functions and operate in a matrix environment Ability to travel up to 30 of working time Disclaimer: The [. .. ]
Job am 27.06.2025 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 [...]
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[...] 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 [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
• Zug
Führungs-/ Leitungspositionen
[. .. ] profoundly impact health for humanity. Learn more at https:/ / Role Summary This outstanding data scientist will join the Neuroscience Data Science and Digital Health (DSDH) team [...]
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[...] to transform neurodegeneration clinical trials through cuttingedge AI, digital health technologies and advanced statistical methodologies. The role will work on the discovery, development and validation of novel digital endpoints and tools, enhancing patient screening, recruitment, monitoring, and engagement. By combining deep knowledge of neuroscience with expertise in data science and digital health, the role will ensure innovative, fitforpurpose solutions that enhance patientcentricity, streamline trial execution, and support regulatory and payer acceptance. Key Responsibilities Advancing our Digital Health Strategy Partner with crossfunctional teams to create strategic roadmaps that integrate digital health solutions throughout the patient journey ensuring clinical relevance and patientcentered outcomes. Monitor emerging technologies and trends to bring forward nextgeneration solutions for neurodegeneration research and development. Endpoint Digital Tool Development Contribute to evidence packages to support regulatory qualification of digital endpoints and tools. Partner with regulatory and medical affairs to engage health authorities and payers on the acceptance of digital health approaches. [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Associate Director, R D Neuroscience Data Science Digital Health Neurodegeneration
• Zug
Führungs-/ Leitungspositionen
[. .. ] candidate for consideration has been identified. However all applications will be considered. This outstanding data scientist will join the Neuroscience Data Science and Digital Health (DSDH) team [...]
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[...] to transform neurodegeneration clinical trials through cuttingedge AI digital health technologies and advanced statistical methodologies. This role will work on the discovery, development and validation of novel digital endpoints and tools enhancing patient screening, recruitment, monitoring and engagement. By combining deep knowledge of neuroscience with expertise in data science and digital health the role will ensure innovative fitforpurpose solutions that enhance patientcentricity, streamline trial execution and support regulatory and payer acceptance. This will be achieved by being an integral member of a matrixed team working closely with the Neuroscience Therapeutic Area Clinical Development, Quantitative Sciences, Regulatory and Patient Reported Outcomes and by establishing strategic external collaborations. Key Responsibilities Advancing our Digital Health Strategy Partner with crossfunctional teams to create strategic roadmaps that integrate digital health solutions throughout the patient journey ensuring clinical relevance and patientcentered outcomes. Monitor emerging technologies and trends to bring forward nextgeneration solutions for neurodegeneration research and development. Endpoint Digital Tool Development Monitor emerging technologies and trends to bring forward nextgeneration solutions for neurodegeneration research and development. Regulatory Evidence Generation Contribute to evidence packages to support regulatory qualification of digital endpoints and tools. Partner [. .. ]
Job gestern bei Jobleads gefunden
A leading
clinical research organization in Austria is looking for a Sponsor-Dedicated CRA to
monitor clinical
trial sites and ensure compliance with protocols and regulations. The ideal [...]
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[...] candidate will have solid monitoring experience and be fluent in both German and English. This role offers competitive salary, performance bonuses, and flexible work arrangements, contributing to a supportive work environment focused on career growth. #J-18808-Ljbffr 71596868 [. .. ]
Job gestern bei Jobleads gefunden
Clinical Research Associate Sponsor Dedicated in Austria
We are seeking a Sponsor-Dedicated CRA with solid monitoring experience. If you are eager to make an impact, this is your chance Key Responsibilities
Monitor clinical trial sites to ensure [...]
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[...] compliance with protocols, GCP, and regulatory requirements Build strong relationships with investigators and site staff Ensure high-quality data collection and patient safety Work closely with the sponsor, providing insights and updates on study progress Perform on-site monitoring visits Qualifications University or college degree, or certification [. .. ]
Job gestern bei Jobleads gefunden
• Zürich Zuerich
[. .. ] Regulatory) by providing medical expertise and to ensure alignment on strategic decision Collaborate with regional Medical Affairs colleagues to support regional deliverables (e. g. , scientific support, [...]
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[...] internal/ external presentations) Monitor competitive activities and emerging trends within relevant therapeutic areas Provide medical training for commercial Support clinical trial operations to ensure success with planned and ongoing clinical trials to include identifying, supporting, and regularly engaging clinical trial investigators, and sites External engagement insights (50 field based, covering all of Switzerland) Develop and maintain a KOL engagement plan that fosters collaborative relationships in Switzerland Provide medical/ scientific presentations to [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Senior Software Engineer, Medical Imaging
Were on a mission to change the future of
clinical research. At Perceptive, we help the biopharmaceutical industry bring medical treatments to the market, faster. Our mission is to [...]
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[...] change the world but to do this, we need people like you. As Senior Software Engineer, Medical Imaging you will contribute to the design and development of scalable, secure and compliant [. .. ] and develop microservices for medical imaging data processing and AI workloads. Implement auto-scaling and load balancing features for medical imaging datasets. Develop API endpoints and service integrations with clinical trial systems. Support platform scalability for concurrent clinical trials and imaging workflows. AI-Driven Medical Imaging Platform Development Implement AI/ ML model integrations for medical image analysis, including gen AI, computer vision and deep learning algorithms. Develop systems for real-time and batch processing of medical imaging data (DICOM, NIf TI, etc. ) [. .. ] development processes, and quality assurance. Collaborate in technical architecture reviews and system design decisions. Innovation Take an active interest in emerging technologies in medical imaging, AI/ ML, and cloud computing. Monitor the market to gather intelligence on emerging technologies. Share knowledge and insights with others. Functional Competencies (Technical knowledge/ Skills) : Knowledge of containerization and serverless architectures Knowledge of message queuing systems for high-throughput medical data processing Knowledge of DICOM networking protocols (DICOM C-STORE, C-FIND, C-MOVE) and [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• Zug
Führungs-/ Leitungspositionen
GSK Oncology Early
Clinical Development is seeking a highly skilled and motivated Early Clinical Development Medical Director-Oncology, to join our dynamic Oncology Research and Development team. In this role [...]
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[...] the successful candidate will create a strong link between Clinical Development and Pre-clinical/ Discovery teams to improve forward and reverse translation and, thereby, [. .. ] monitoring of studies, including patient eligibility assessment, study design questions, and addressing urgent safety questions (with inclusion of Safety/ PV as relevant) . Assume responsibility for medical review of clinical trial data, both directly as needed and/or via oversight of delegated medical review. Oversee review of data packages intended for internal and/or external IDMCs. Review/monitor safety data in collaboration with pharmacovigilance group for active clinical studies. Participate in the authoring of clinical study reports and regulatory documents and collaborate with colleagues in Regulatory Affairs, CMC, Toxicology, Research, Pharmacology to respond to health authority and ethics committee queries. Collaborate with Principal Investigators in the evaluation and [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
CTIS (Clinical Trial Information System) - Team Specialist-Fixed-term (1 year)
• Wien
Homeoffice möglich
[. .. ] we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. [...]
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[...] The Position The Clinical Trial Information System Team (part of Product Development Regulatory Operations) enables the development of organizational and people capabilities of the future, we support and optimize the delivery of projects and initiatives to the organization both on the molecule and molecule-enabling portfolio. We are responsible for enabling the future of clinical [. .. ] instructions from relevant functions for all CTA related submissions and manage execute submission of all CTAs related activities via CTIS and inform relevant functions of submissions and related review timelines Monitor CTIS for any incoming information from the HAs or ECs (e. g. questions) and interact with the different functions in order to address the information received. Update, track and archive relevant information in internal systems Drive overall process evolution: Assessment of automation opportunities for CTIS management and management of CTA [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
• Basel- Landschaft
Führungs-/ Leitungspositionen
Summary The
Clinical and Preclinical Quality Director (CQD) will lead the development, implementation, and communication of high-quality standards to ensure the delivery of global clinical studies. With a focus [...]
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[...] on proactive quality management, this role supports Clinical Development by driving quality excellence, safeguarding data integrity, and enabling R D objectives for the [. .. ] global clinical processes, procedural documents, and applicable Quality Compliance manual documents, in line with international guidelines, such as ICH-GCP, industry standards, and local regulations. Provide expert guidance on clinical trial regulations, monitor regulatory changes, and ensure local teams and processes remain current and compliant. Plan and conduct quality control activities in line with the annual quality plan, including performing accompanied site visits. Perform any required QC visits/ QC activities. Regularly reviews protocol deviations and ensures timely reporting of quality issues to local [. .. ]
Job vor 9 Tagen bei Jobleads gefunden
Director, Global Trial Lead
• Boudry, Neuenburg
Führungs-/ Leitungspositionen
[. .. ] our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers. bms. com/working-with-us Position Summary The Director, Global [...]
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[...] Trial Lead (GTL) is accountable for the strategic leadership and operational excellence of global clinical trials, driving delivery across all phases and therapeutic areas. This role sets the vision for successful trial execution, influences organizational strategy, and ensures alignment with business objectives, regulatory standards, and quality benchmarks. As a senior leader within Global Development Operations (GDO) , the Director GTL is responsible for critical decision [. .. ] and partner relationships at a strategic level, ensuring alignment with contractual terms and organizational standards. Sets and monitors performance metrics, proactively identifying and resolving operational challenges. Utilizes quality indicators to monitor and optimize trial execution. Maintains and ensures accurate data records in study management systems such as Veeva (i. e. CTMS, e TMF, etc. ) . Establishes and maintains studylevel project management tools, including action logs, decision trackers, issue registers, and risk mitigation plans. Develops and enforces trialspecific standards aligned with broader [. .. ]
Job am 20.11.2025 bei Jobleads gefunden
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] the batch was manufactured in accordance with approved manufacturing instructions Manufacture, import, test, and store medicinal products and investigational medicinal products in accordance with regulations and applicable [...]
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[...] marketing authorization or clinical trial authorization documents Check manufacturing records for accuracy and completeness and sign by suitable authorized persons before forwarding to the qualified person Make documents required for batch release (including import documentation for imported products) available to the qualified person in good time Maintain GMP-compliant qualification and requalification of all rooms, [. .. ] packaging in accordance with pharmaceutical law and provide valid package inserts or product information Validate manufacturing and packaging procedures and qualify relevant processes in accordance with valid SOPs Determine and monitor environmental conditions in all relevant areas (manufacturing, storage, packaging, shipping) and immediately address deviations Assist in selection, qualification, and monitoring of external manufacturers and import service providers (contract manufacturers, contract packagers, contract inspectors) Document, evaluate, and approve deviations in the area of responsibility in a timely manner and implement appropriate [. .. ]
Job am 16.11.2025 bei Jobleads gefunden
Medical Director Dermatology Clinical Development
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
[. .. ] we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. [...]
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[...] The Position Roches Clinical Development organization is structured by therapeutic area and is responsible for developing and executing the late development (Phase II III) clinical strategies and plans that deliver medically-differentiated therapies that provide meaningful improvement to patients. We have an opportunity for a Medical Director with a background in dermatology to join [. .. ] ; gathering and analyzing data and information necessary to create the CDP; you will participate in the design, development and execution of clinical studies. You will act as a medical monitor for assigned studies. You will collaborate with a variety of internal/ external partners stakeholders, as well as multidisciplinary internal groups, including business development, research, commercial, legal, etc. You may participate in meetings, reviews, discussions and other interactions regarding early development/ Phase I studies to provide clinical science input guidance; including [. .. ] have an MD, board-certified training in dermatology or substantial dermatology-specific research and clinical experience and have 2+ years of post-graduate relevant clinical/ scientific research and/or clinical trial experience You have knowledge of the pharma/ biotech industry, the multiple functions and roles involved in the drug development process. You have significant experience working with the principles and techniques of data analysis, interpretation and clinical relevance and demonstrated experience in scientific writing (e. g. manuscripts, grants, scientific protocols) You [. .. ]
Job am 11.11.2025 bei Jobleads gefunden
• Baden- Württemberg
[. .. ] stakeholders Build and maintain relationships with key regional stakeholders, providing local market intelligence to inform global strategic discussions Liaise with local affiliates to reflect local needs in [...]
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[...] Access strategy definition Monitor access landscape and pricing developments, sharing insights with the global team to identify opportunities and risks Contribute to the development of global health economic and value communication tools, ensuring local relevance Serve as a strategic partner to the global market access team and local (commercial) teams, supporting product launches and pricing activities Support global drug development efforts by providing regional insights relevant to clinical trial design, evidence generation, and reimbursement pathways University degree in Health Economics, Public Health, Life Sciences, Pharmacy, Economics, or a related field 5+ years of relevant experience in market access, pricing reimbursement, or health economics, ideally within an international context Market Access experience in the DACH and/or Benelux countries Knowledge [. .. ]
Job am 10.11.2025 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 [...]
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[...] and proactive Global Clinical Operations Lead (m/f/d) to manage and support clinical trials from initiation to closeout. This role will work closely with GC crossfunctional project teams, investigators, and Contract Research Organizations to ensure that studies are conducted in compliance with regulatory requirements, Good Clinical Practice (GCP) , and institutional policies. Reporting [. .. ] documents, IRB submissions, and study logs. Ensure compliance with GCP, ICH guidelines, and local regulatory requirements. Data Management Collect, enter, and manage clinical data in electronic data capture (EDC) systems. Monitor data quality and resolve discrepancies in collaboration with data management teams. Site Management Coordinate site visits, audits, and monitoring activities. Maintain study supplies, equipment, and documentation in auditready condition. Liaise with investigators, sponsors, CROs, and internal departments to ensure smooth study execution. Participate in study meetings, training sessions, and protocol [. .. ] clinical research or similar role and proven track record managing clinical trials in Europe and U. S. Mandatory experience in the medical device industry and standards. Strong knowledge of clinical trial processes, GCP, and global regulatory guidelines including ISO13485 and ISO14115. Excellent organizational and timemanagement skills. Strong interpersonal 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. [. .. ]
Job am 08.11.2025 bei Jobleads gefunden
Director, Clinical Study Management
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Responsible for providing leadership and oversight to support the global activities and timelines related to execution of full-service
clinical trials, including oversight of project management and project finance teams. [...]
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[...] As part of the senior leadership team, participate in the development and implementation of organizational strategies, technologies and best practices that ensure superior customer service, staff development, quality information management reporting and effective, efficient divisional short-and long-term goals [. .. ] participate in the project development process working with Sponsors and functional Directors to negotiate and deliver quality product (s) , assessing resource and financial and safety requirements, assigning resources, overseeing trial conduct, information, and data confidentiality, and supporting project teams by assisting the troubleshooting and resolution process while ensuring all align with corporate objectives. Responsible to ensure sufficient project level staffing and maintain utilization targets. Represent project operations on cross-department planning initiatives. Unit Leadership, Team Management and Engagement (30-40) [. .. ] during the budget and annual operational review processes. Maintain knowledge of financial and regulatory risks and requirements related to department service delivery and direct the development of methodologies to review, monitor, and manage risks and requirements. Work in conjunction with business development to prepare budgets and proposal text in response to requests for proposal, requests for information and statements of work. Oversee change order development for full-service projects ensuring realization of project costs are achieved in line with work performed. [. .. ]
Job am 26.10.2025 bei Jobleads gefunden
Sr/ Pr Biostatistician-Immunology Inflammation
• München, Bayern
[. .. ] Immunology Inflammation role at Syneos Health. Description Sr/ Pr Biostatistician-Immunology Inflammation Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We [...]
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[...] translate unique clinical, medical affairs and commercial 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 [. .. ] and datasets. Implement quality control to guarantee consistent, accurate deliverables. Represent biostatistics on project teams, interface with configuration and other departments. Manage scheduling, time constraints, and communicate progress to management. Monitor study activities against milestones; identify and address outofscope tasks. Support statistical programming as needed; participate in Data Safety Monitoring Board or Data Monitoring Committee activities. Lead integrated analyses, attend regulatory meetings, respond to queries. Follow SOPs, WIs, and regulatory guidelines (e. g. ICH) . Maintain organized, inspectionready documentation. Assist in [. .. ] past 5 years, we have worked with 94 of all Novel FDA Approved Drugs, 95 of EMA Authorized Products and over 200 studies across 73, 000 sites and 675, 000+ trial patients. No matter what your role is, youll take the initiative and challenge the status quo with us in a highly competitive and everchanging environment. Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive. Tasks may be reassigned at discretion. Equivalent experience and skills [. .. ]
Job am 24.10.2025 bei Jobleads gefunden
T2513-Clinical Development Quality Lead-Contractor 12 months
• Lausanne, Waadt
Clinical Development Quality Lead Contractor 12 months We are currently looking for a motivated and collaborative Clinical Development Quality professional to join our Quality Department based at our Headquarters [...]
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[...] in Lausanne, Switzerland as We are seeking an experienced and dedicated Clinical Development Quality Lead (CDQL) to provide expert quality oversight across [. .. ] contractor role is responsible for the proactive identification and mitigation of risks to maintain the highest standards of GCP compliance, protect patient safety, and ensure the integrity of our clinical trial data. If you thrive on providing strategic guidance, meticulous oversight, and driving continuous improvement, this is your opportunity. Your Mission 1. GCP Support and Continuous Oversight Provide expert GCP guidance and support to all clinical development stakeholders. Maintain and manage the GCP query log, ensuring timely logging, tracking, and resolution [. .. ] updates are current. 2. Quality Risk Management Trending Review and assess study risks in collaboration with stakeholders, facilitating the identification of study-specific critical data and processes. Develop, generate, and monitor Key Risk Indicators (KRIs) on a monthly/ quarterly basis through advanced analytics. Perform comprehensive trending analyses on KRIs, protocol deviations, and quality events to identify patterns and communicate potential quality issues, supporting mitigation planning. 3. Vendor Qualification and Quality Event Management Lead the qualification assessment of clinical vendors to ensure [. .. ]
Job am 24.10.2025 bei Jobleads gefunden
Medical Director-Dermatology Clinical Development
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
Medical Director-Dermatology
Clinical Development page is loaded # # Medical Director-Dermatology Clinical Developmentlocations: Baseltime type: Tempo integralposted on: Publicado hojejob requisition id: 202510-126736At Roche you can show up as [...]
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[...] yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, [. .. ] ; gathering and analyzing data and information necessary to create the CDP; you will participate in the design, development and execution of clinical studies. You will act as a medical monitor for assigned studies. You will collaborate with a variety of internal/ external partners stakeholders, as well as multidisciplinary internal groups, including business development, research, commercial, legal, etc. You may participate in meetings, reviews, discussions and other interactions regarding early development/ Phase I studies to provide clinical science input guidance; including [. .. ] have an MD, board-certified training in dermatology or substantial dermatology-specific research and clinical experience and have 2+ years of post-graduate relevant clinical/ scientific research and/or clinical trial experience You have knowledge of the pharma/ biotech industry, the multiple functions and roles involved in the drug development process. You have significant experience working with the principles and techniques of data analysis, interpretation and clinical relevance and demonstrated experience in scientific writing (e. g. manuscripts, grants, scientific protocols) You [. .. ]
Job am 21.10.2025 bei Jobleads gefunden
Regional Medical Science Liaison (MSL) - Breast Cancer/ Oncology-Germany
[. .. ] 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 [...]
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[...] 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 [. .. ] between client and CRO study project teams to ensure synergies occur between them and that all field-based clinical activities achieve global study team goals Liaise closely with client to monitor and measure study performance Support of ongoing and future company sponsored trials Liaison between corporate clinical operations and study sites e. g. , visit trial centers as required to provide updates on study, maintain client presence, enhance enrolment rates, patient retention, and assist in study closure Identify additional trial centers [. .. ]
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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 44 offene Stellenanzeigen für Clinical Trial Monitor Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trial Monitor Jobs?
Aktuell suchen 9 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:
- Sanofi (2 Jobs)
- PHOENIX Pharma SE (2 Jobs)
- OPTARES GmbH Co. KG (2 Jobs)
- ZOLL Medical Corporation (1 Job)
- i- Pharm Consulting (1 Job)
- Edwards Lifesciences (1 Job)
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), Baden-Württemberg (4 Jobs) und Berlin (4 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trial Monitor Jobs?
Clinical Trial Monitor Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
