55 Jobs für Clinical Trial Monitor
Stellenangebote Clinical Trial Monitor Jobs
Job vor 8 Tagen bei Jobleads gefunden
[. .. ] degree RN, certified medical technologist) . Minimum of 8+ years relevant clinical research (or related) experience. 6+ years experience in monitoring and site management of industry sponsored [...]
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[...] clinical research (CRA, Clinical Trial Monitor, or equivalent) . Thorough understanding of the drug development and clinical trial process. Ability to assess selected CROs monitoring performance and provide constructive feedback and remediation as necessary. Ability to participate in preparation, conduct and follow up of audits and site inspections. Active management experience of countries and sites in [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
Senior/ Medical Director (Ophthalmology)
• Hamburg
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 vor 13 Tagen bei Jobleads gefunden
• München, Bayern
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 am 06.12.2025 bei Jobleads gefunden
Medical Director
Führungs-/ Leitungspositionen
[. .. ] development, with multiple programs advancing across solid tumours, AML and lung cancer. This role is ideal for a Medical Director who wants to combine scientific depth, strategic [...]
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[...] influence and handson clinical impact. Why This Role Matters The Medical Director will play a central role in clinical strategy and trial execution. Youll lead protocol development, engage investigators globally and help guide oncology programs through key stages of development. This is a position where your expertise directly shapes patient outcomes. What You Will Be Doing Acting as Medical Monitor and Safety Physician across cuttingedge oncology studies Leading protocol development for pivotal and earlyphase programs Building strong partnerships with global investigators and KOLs Collaborating closely with Clinical Operations, Regulatory and R D Providing scientific and strategic insight to optimise study design and execution Who Were Looking For Medical Doctor (preferred) [. .. ]
Job am 06.12.2025 bei Jobleads gefunden
Führungs-/ Leitungspositionen
A leading biotech company in Austria is seeking a Medical Director to drive
clinical strategy in oncology drug development. This role combines scientific expertise and hands-on impact to shape patient [...]
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[...] outcomes. You will act as Medical Monitor, lead protocol development, and build strong global partnerships. The ideal candidate is a Medical Doctor with oncology experience and a strong background in clinical trial design and strategic thinking. Join us in making a difference in oncology. #J-18808-Ljbffr 71757232 [. .. ]
Job am 04.12.2025 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, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 27.06.2025 bei Jobleads gefunden
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
GCP QA Consultant
• Berlin
Beratungs-/ Consultingtätigkeiten
Champion compliance and precision-help deliver life-changing therapies. Proclinical is seeking a GCP QA Consultant to support quality assurance activities for oncology-focused
clinical trials. This role involves overseeing quality processes [...]
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[...] for phase 2-3 studies, ensuring compliance with ICH-GCP and regulatory requirements, and managing risk-based quality plans. You will collaborate with internal teams and external partners to maintain high standards of clinical trial execution and inspection readiness. This is a fully remote position, open to candidates located anywhere within Europe. Responsibilities Develop and oversee study quality-related plans, including Oversight Quality and Audit Plans. Collaborate with third parties to formalize Investigator Site Audits (ISA) and agendas. Oversee quality activities for phase 2-3 [. .. ] and endpoint de-risking. Conduct risk-based reviews of study documents to ensure compliance with protocols, ICH-GCP, and regulatory requirements. Act as the Clinical Quality Assurance Representative in weekly monitor-site meetings. Monitor site performance, ensuring adherence to monitoring plans, tracking deviations, and recommending improvements. Ensure internal operations align with study plans, SOPs, and maintain transparent communication regarding quality events. Maintain and update Clinical Trial Oversight Plans and Clinical Quality Plans. Ensure proper documentation and adherence to Clinical Trial Agreements, [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Beratungs-/ Consultingtätigkeiten
[. .. ] top-tier QA talent with groundbreaking life sciences opportunities Champion compliance and precisionhelp deliver lifechanging therapies. Proclinical is seeking a GCP QA Consultant to support quality assurance activities [...]
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[...] for oncologyfocused clinical trials. This role involves overseeing quality processes for phase 23 studies, ensuring compliance with ICHGCP and regulatory requirements, and managing riskbased quality plans. You will collaborate with internal teams and external partners to maintain high standards of clinical trial execution and inspection readiness. This is a fully remote position, open to candidates located anywhere within Europe. Responsibilities Develop and oversee study qualityrelated plans, including Oversight Quality and Audit Plans. Collaborate with third parties to formalize Investigator Site Audits (ISA) and agendas. Oversee quality activities for phase 23 trials, focusing [. .. ] management and endpoint derisking. Conduct riskbased reviews of study documents to ensure compliance with protocols, ICHGCP, and regulatory requirements. Act as the Clinical Quality Assurance Representative in weekly monitorsite meetings. Monitor site performance, ensuring adherence to monitoring plans, tracking deviations, and recommending improvements. Ensure internal operations align with study plans, SOPs, and maintain transparent communication regarding quality events. Maintain and update Clinical Trial Oversight Plans and Clinical Quality Plans. Ensure proper documentation and adherence to Clinical Trial Agreements, site feasibility, qualification, [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Clinical Operations Area Head, Canada EMEA region
• Basel, Basel- Stadt
The Position At Roche/ Genentech Pharma Product Development Global
Clinical Operations (PDG) we are determined to transform drug development and realize our Pharma Ambition to deliver 20 transformative medicines [...]
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[...] addressing diseases with the highest societal burden by 2029. Location: Canada, Russia, South Africa, Switzerland, Turkey, Ukraine, United Kingdom. The Opportunity Are you a strategic leader with a passion for clinical operations? We are looking for a Clinical Operations Area Head to lead and oversee clinical trial execution across multiple countries in Canada EMEA. In this senior leadership role you will act as the bridge between country clinical operations teams and global study leadership, ensuring our studies are delivered with excellence in performance, quality, and speed. Youll drive operational excellence and compliance while fostering a culture of [. .. ] that enable faster, smoother study delivery. Advocate for countries: Represent the needs and perspectives of country teams in global forums, making sure their voices are heard. Drive performance through data: Monitor and analyze key performance metrics to identify trends and opportunities using datadriven insights to optimize trial execution. Forge strong partnerships: Collaborate with other functional heads, senior leaders, and external stakeholders to achieve business objectives and ensure clinical trial success. Who You Are You are a proven leader with a strong [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• Wien
Führungs-/ Leitungspositionen
[. .. ] Business Leadership Communications team, and respective Oncology and Precision Medicine leaders. Oversee relevant strategic internal communications activities in support of critical business priorities, including major product regulatory [...]
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[...] milestones, HTA and clinical trial developments. Colead EMEA execution of joint flagship campaigns in Oncology Haematology Partner with the Haematology CPA Lead to develop and execute comprehensive Oncologywide communication strategies (e. g. , In Front of Cancer campaign) that resonate with the EMEA region while aligning with global campaign objectives. Identify and leverage opportunities for [. .. ] for local Operating Companies needs. Lead Research and Insights Generate and leverage key insights from audience research to continuously refine and improve impact of PCPA and PEA strategies in Oncology. Monitor and analyze industry and reputational trends and competitive benchmarks to drive competitiveness. Implement and track standardized metrics (KPIs) aligned with global CPA and EMEA CPA Measurement Framework to monitor performance and refine strategies. Lead Issues Communications and Crisis Management Provide strategic counsel and lead coordination of local or regional Oncology [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Senior Data Scientist II-Therapeutic Modality Insights Competitor Intelligence (all genders)
• Ludwigshafen am Rhein, Rheinland- Pfalz
[. .. ] knowledge and insights mining and analysis, as well as designing and building innovative selfservice solutions for insights generation from published resources and internal knowledge. This includes literature, [...]
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[...] patent, conference, news, clinical trial, and competitive intelligence data such as competitor pipelines. As a Senior Data Scientist on the Solutions for Published Insights Client Enablement (SPICE) team, you will serve as the lead data scientist focused on advancing Abb Vies competitiveness by driving Therapeutic Modality Knowledge Intelligence Solutions. You will lead the creation of [. .. ] agentic workflows) that address significant scientific and strategic trends and knowledge gaps in therapeutic modalities. Develop and deliver innovative, highquality intelligence solutions that systematically extract, analyze, summarize, integrate and proactively monitor key knowledge about novel therapeutic modalities (such as gene/ cell therapies and innovative RNA or antibodybased drugs) to address urgent scientific and business needs. Apply broad expertise in knowledge information science, Generative AI/ NLP, data warehousing, and software development to build robust data pipelines and analytical workflows for large and [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
[. .. ] 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 [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Sponsor-Focused Clinical Research Associate-Remote/ Hybrid
• Wien
A
clinical research organization in Austria is seeking a Clinical Research Associate to
monitor clinical
trial sites and ensure compliance with protocols and safety regulations. The ideal [...]
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[...] candidate will possess a university degree in a related field and be fluent in both German and English. This role offers a competitive salary, performance bonuses, and flexible work arrangements. If youre ready to advance your CRA career, apply [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
Executive Director,
Clinical Operations, Europe Join to apply for the Executive Director, Clinical Operations, Europe role at Revolution Medicines Revolution Medicines is a clinical-stage precision oncology company focused on [...]
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[...] developing novel targeted therapies to inhibit frontier targets in RA Saddicted cancers. The companys R D pipeline comprises RAS (ON) Inhibitors designed to [. .. ] who will play a critical role in driving the implementation and execution of the R D strategic vision in the Europe region. The incumbent will be responsible for implementing clinical trial strategy and management of all clinical studies in close collaboration with the Clinical Development Sciences functions and crossfunctional partners. Expected to support clinical growth, the individual will also be responsible for overseeing the operating activities in drug development spanning across all human trial activities from Phase1 trials through Phase3 and [. .. ] reports to senior management on a regular basis. Implement process improvements, in conjunction with trial teams in response to trial or project needs, client and team feedback and quality audits. Monitor and provide oversight on CRO performance according to functional metrics and protocol amendments. Maintain a positive, resultsoriented work environment by building partnerships, modelling teamwork, motivating team members, and communicating to the study team in an open, balanced, and objective manner. Ensure compliance with all applicable regulations. Ability to travel domestically [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Site Relationship Manager
• Essen, Nordrhein- Westfalen
About this role 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 [...]
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[...] expertise includes full service capabilities, resourcing and Functional Service (FSP) solutions. The Site Relationship Manager (SRM) covers multiple indications within the assigned country throughout the full life cycle of the trial. The key focus areas are to facilitate optimal clinical trial setup, execution, and quality by understanding the local environment, creating and maintaining strong, longterm relationships with sites, and supporting applicable Sponsor Teams in CRO and Sponsor site oversight activities. As part of our SRS/ FSP team, you will be dedicated [. .. ] Bachelors or Masters degree in Life Sciences. Minimum 7 years of experience in the pharmaceutical or clinical research industry. At least 5 years of experience as a Clinical Research Associate, Monitor, or similar role. Proven clinical research and site management experience within Pharma, Biotech, or CRO settings. Direct experience collaborating with investigator sites and investigators. Strong knowledge of ICH GCP guidelines. Demonstrated ability to build and maintain site relationships both inperson and remotely. Excellent networking, communication, and problemsolving skills. Experience in [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
• Hamburg
[. .. ] Relationship Manager role at TFS Health Science. 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 entire clinical development journey. Our expertise includes full service capabilities, resourcing and Functional Service (FSP) solutions. About This Role The Site Relationship Manager (SRM) covers multiple indications within the assigned country throughout the full life cycle of the trial. The key focus areas are to facilitate optimal clinical trial setup, execution, and quality by: understanding the local environment, creating and maintaining strong, longterm relationships with sites, supporting applicable Sponsor Teams in CRO and Sponsor site oversight activities. As part of our SRS/ FSP team, you will be dedicated to [. .. ] Bachelors or Masters degree in Life Sciences. Minimum 7 years of experience in the pharmaceutical or clinical research industry. At least 5 years of experience as a Clinical Research Associate, Monitor, or similar role. Proven clinical research and site management experience within Pharma, Biotech, or CRO settings. Direct experience collaborating with investigator sites and investigators. Strong knowledge of ICH GCP guidelines. Demonstrated ability to build and maintain site relationships both inperson and remotely. Excellent networking, communication, and problemsolving skills. Experience in [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Senior Data Scientist II Therapeutic Modality Insights Competitor Intelligence (all genders)
• Ludwigshafen am Rhein, Rheinland- Pfalz
Work-Life-Balance
[. .. ] knowledge and insights mining and analysis, as well as designing and building innovative selfservice solutions for insights generation from published resources and internal knowledge. This includes literature, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] patent, conference, news, clinical trial, and competitive intelligence data such as competitor pipelines. As a Senior Data Scientist on the Solutions for Published Insights Client Enablement (SPICE) team, you will serve as the lead data scientist focused on advancing Abb Vies competitiveness by driving Therapeutic Modality Knowledge Intelligence Solutions. You will lead the creation of [. .. ] workflows) that address significant scientific and strategic trends and knowledge gaps in therapeutic modalities. Develop and deliver innovative, high-quality intelligence solutions that systematically extract, analyze, summarize, integrate and proactively monitor key knowledge about novel therapeutic modalities (such as gene/ cell therapies and innovative RNA or antibody-based drugs) to address urgent scientific and business needs. Apply broad expertise in knowledge information science, Generative AI/ NLP, data warehousing, and software development to build robust data pipelines and analytical workflows for large [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Site Relationship Manager
• Kassel, Hessen
About this role 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 [...]
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[...] expertise includes full service capabilities, resourcing and Functional Service (FSP) solutions. The Site Relationship Manager (SRM) covers multiple indications within the assigned country throughout the full life cycle of the trial. The key focus areas are to facilitate optimal clinical trial setup, execution, and quality by understanding the local environment, creating and maintaining strong, longterm relationships with sites, and supporting applicable Sponsor Teams in CRO and Sponsor site oversight activities. As part of our SRS/ FSP team, you will be dedicated [. .. ] Bachelors or Masters degree in Life Sciences. Minimum 7 years of experience in the pharmaceutical or clinical research industry. At least 5 years of experience as a Clinical Research Associate, Monitor, or similar role. Proven clinical research and site management experience within Pharma, Biotech, or CRO settings. Direct experience collaborating with investigator sites and investigators. Strong knowledge of ICH GCP guidelines. Demonstrated ability to build and maintain site relationships both inperson and remotely. Excellent networking, communication, and problemsolving skills. Experience in [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
Director Project Delivery
Führungs-/ Leitungspositionen
TFS Health Science is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire
clinical development journey. Our expertise includes full [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] service-capabilities, resourcing and Functional Service (FSP) solutions. Join Our Team as a Director Project Delivery-home based in Poland, Portugal, Italy, Sweden or UK. About this role We are seeking an experienced and dedicated Line Manager to lead our Trial Master File (TMF) and Clinical Research Associate (CRA) functional teams within the dynamic Ophthalmology Business Unit. This critical role involves strategic oversight, team leadership and operational management to ensure the efficient execution of clinical trials and the maintenance of regulatory compliance. Key Responsibilities Team Leadership Line Management Provide strong leadership, [. .. ] clinical studies to ensure project milestones are met efficiently. Oversee performance management processes, including goal setting, regular feedback, career development planning, and conducting annual performance reviews. Oversight of KPIs Establish, monitor, and report on corporate and role-based Key Performance Indicators (KPIs) for both the TMF and CRA teams. Utilize KPI data to identify trends, drive process improvements, and ensure functional teams are meeting performance targets and quality standards. TMF Strategy Budgeting Hold responsibility for supporting TMF-related activities during the [. .. ]
Job vor 8 Tagen bei Jobleads gefunden
Manager 1, Projects Clinical Operations
• Allschwil, Basel- Landschaft
[. .. ] America, Titusville, New Jersey, United States of America Job Description: The Innovative Health (IH) Organization has been created to drive meaningful impact to participant health and wellbeing [...]
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[...] by reinventing the clinical trial experience. The Innovative Health organization connects teams across development to novel capabilities and solutions, unleashing the potential of innovation to drive broader access to innovative medicines, and enriching the healthcare experience for all. The IH team is seeking an innovation leader who will be a forward-thinker, able to imagine [. .. ] and/or reduce cost. Collaborate with internal and external cross-functional teams to validate hypotheses. Collaborate with cross-functional teams to execute the projects, develop project plans, set milestones, and monitor progress to ensure timely evaluation and decision making for launch. Generate conclusive results to support the business case for launch or adoption of these new methods. Proactively identifying potential roadblocks and taking a solutions-driven approach for complex and undefined projects that may not be addressed by existing policies, procedures, [. .. ]
Job vor 8 Tagen bei Jobleads gefunden
Manager 1, Projects Clinical Operations
• Allschwil, Basel- Landschaft
Manager 1, Projects
Clinical Operations Johnson Johnson Innovative Medicine At Johnson Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where [...]
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[...] complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and [. .. ] Titusville, New Jersey, United States of America Job Description The Innovative Health (IH) Organization has been created to drive meaningful impact to participant health and wellbeing by reinventing the clinical trial experience. The Innovative Health organization connects teams across development to novel capabilities and solutions, unleashing the potential of innovation to drive broader access to innovative medicines, and enriching the healthcare experience for all. The IH team is seeking an innovation leader who will be a forwardthinker, able to imagine and [. .. ] cycle times, and/or reduce cost. Collaborate with internal and external crossfunctional teams to validate hypotheses. Collaborate with crossfunctional teams to execute the projects, develop project plans, set milestones, and monitor progress to ensure timely evaluation and decision making for launch. Generate conclusive results to support the business case for launch or adoption of these new methods. Proactively identify potential roadblocks and take a solutionsdriven approach for complex and undefined projects that may not be addressed by existing policies, procedures, or [. .. ]
Job vor 8 Tagen bei Jobleads gefunden
Site Relationship Manager
• Mainz, Rheinland- Pfalz
About this role 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] expertise includes full service capabilities, resourcing and Functional Service (FSP) solutions. The Site Relationship Manager (SRM) covers multiple indications within the assigned country throughout the full life cycle of the trial. The key focus areas are to facilitate optimal clinical trial setup, execution, and quality by understanding the local environment, creating and maintaining strong, longterm relationships with sites, and supporting applicable Sponsor Teams in CRO and Sponsor site oversight activities. As part of our SRS/ FSP team, you will be dedicated [. .. ] Bachelors or Masters degree in Life Sciences. Minimum 7 years of experience in the pharmaceutical or clinical research industry. At least 5 years of experience as a Clinical Research Associate, Monitor, or similar role. Proven clinical research and site management experience within Pharma, Biotech, or CRO settings. Direct experience collaborating with investigator sites and investigators. Strong knowledge of ICH GCP guidelines. Demonstrated ability to build and maintain site relationships both inperson and remotely. Excellent networking, communication, and problemsolving skills. Experience in [. .. ]
Job vor 8 Tagen bei Jobleads gefunden
Senior Clinical Data Team Lead (Senior DTL) - FSP
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Senior
Clinical Data Team Lead (Senior DTL) - FSP Be among the first 25 applicants. The Sr. CDM will lead and contribute to data management activities in support of [...]
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[...] Clients studies across all stages of clinical drug development. Summary of Key Responsibilities Contribute to data management activities as a lead study data manager in support of Clients clinical studies. Lead database build activities including leading crossfunctional review of e CRF content, review of edit check specifications, and perform user acceptance testing. Monitor data collection, coding, and cleaning by vendors through tracking of study metrics and targeted data reviews. Oversight of database lock activities and ultimate archiving of study data. Collaborate with internal and external partners, including Biostatistics, Statistical Programming, Clinical Operations, Medical, Quality Assurance, Global Patient Safety and Risk Management, Regulatory Affairs, [. .. ] an outsourced CRO model; experience with drug development in rare genetic diseases preferred. Expert knowledge of e Clinical processes, efficient design/ build of an EDC data management system and other Clinical Trial/ Data Management Systems. Knowledge and understanding of regulations and industry/ adopted data standards such as CDISC, SDTM, and CDASH. Experience working with Medidata Rave. Experience using standardized medical terminology, including Med DRA and WHO Drug. Experience working with MS Office Suite (Excel, Word, Power Point) and familiarity with MS Project. Excellent [. .. ]
Job vor 9 Tagen bei Jobleads gefunden
Site Relationship Manager
• München, Bayern
About this role 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] expertise includes full service capabilities, resourcing and Functional Service (FSP) solutions. The Site Relationship Manager (SRM) covers multiple indications within the assigned country throughout the full life cycle of the trial. The key focus areas are to facilitate optimal clinical trial setup, execution, and quality by: understanding the local environment, creating and maintaining strong, longterm relationships with sites, supporting applicable Sponsor Teams in CRO and Sponsor site oversight activities. As part of our SRS/ FSP team, you will be dedicated to [. .. ] Bachelors or Masters degree in Life Sciences. Minimum 7 years of experience in the pharmaceutical or clinical research industry. At least 5 years of experience as a Clinical Research Associate, Monitor, or similar role. Proven clinical research and site management experience within Pharma, Biotech, or CRO settings. Direct experience collaborating with investigator sites and investigators. Strong knowledge of ICH GCP guidelines. Demonstrated ability to build and maintain site relationships both in person and remotely. Excellent networking, communication, and problemsolving skills. Experience [. .. ]
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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 55 offene Stellenanzeigen für Clinical Trial Monitor Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trial Monitor Jobs?
Aktuell suchen 7 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:
- TFS Health Science (5 Jobs)
- Abb Vie (2 Jobs)
- PHOENIX Pharma SE (2 Jobs)
- Proclinical (1 Job)
- SCIRENT Clinical Research and Science (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), Hamburg (4 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.
