105 Jobs für Clinical Safety Associate
Stellenangebote Clinical Safety Associate Jobs
Job vor 3 Tagen bei Jooble gefunden
Charles River Laboratories, Inc.
• Erkrath
[. .. ] another area, your skills will play an important role in the work we perform. Für die Abteilung Operations Support am Standort Erkrath suchen wir ab sofort unbefristet [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Shipping and Receiving Associate (m/w/d) der Unterstützung der operativen Einheiten als Zentrale Anlaufstelle für Versand Logistik der Beantwortung von Fragen zu Zollbestimmungen und Problemen bei der Ein-Ausfuhr der zu verschickenden Materialien, Prüfsubstanzen, Geräte, etc. (nach entsprechend erfolgten Schulungen) gute Kenntnisse von Microsoft Office (Word, Excel, Power Point) sowie gute deutsche und [. .. ] characterization, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products. Whether clients need stand-alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs. Each year more than 20, 000 biologic testing reports are sent each and over 200 licenses products are supported by our biologics testing solutions team. We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients clinical laboratory testing needs and manufacturing activities. Our client base includes global pharmaceutical companies, biotechnology companies, government [. .. ]
Job vor 4 Tagen bei Jooble gefunden
Sr CRA in oncology-Sponsor dedicated-Home Based Germany
• München
Sr CRA in oncology-Sponsor dedicated-Home Based Germany Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and commercial [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to [. .. ] has been adequately performed and documented for each subject/ patient as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/ patient. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol deviation/ violations and pharmacovigilance issues. Per the Clinical Monitoring/ Site Management Plan (CMP/ SMP) :Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report [. .. ] are met. Must be able to quickly adapt to changing priorities to achieve goals/ targets. May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and project-specific site team members are trained and compliant with applicable requirements. Prepares for and attends Investigator Meetings and/or sponsor face to face meetings. Participates in and may lead global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening [. .. ] well as study conduct and site closure tasks. Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. Supports and/or conducts (accompanied) site qualification, initiation, interim monitoring and study closeout visits for Phase 1-4 studies in accordance with local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, and Abb Vie Standard Operating Procedures (SOPs) and business processes, if applicable. Trains study site [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
Clinical Research Associate (CRA I) / Senior
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening [. .. ] well as study conduct and site closure tasks. Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. Supports and/or conducts (accompanied) site qualification, initiation, interim monitoring and study closeout visits for Phase 1-4 studies in accordance with local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, and Abb Vie Standard Operating Procedures (SOPs) and business processes, if applicable. Trains study site [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening [. .. ] well as study conduct and site closure tasks. Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. Supports and/or conducts (accompanied) site qualification, initiation, interim monitoring and study closeout visits for Phase 1-4 studies in accordance with local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, and Abb Vie Standard Operating Procedures (SOPs) and business processes, if applicable. Trains study site [. .. ]
Job vor 8 Tagen bei Jooble gefunden
Abb Vie
Clinical Research Associate I
• Wiesbaden
Work-Life-Balance
[. .. ] at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Job Description Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening [. .. ] protocols and multiple therapeutic areas, with appropriate supervision. Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. Ensures safety and protection of study subjects. Supports and/or conducts (accompanied) site qualification, initiation, interim monitoring and study closeout visits for Phase 1-4 studies in accordance with local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, and Abb Vie Standard Operating Procedures (SOPs) and [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Antal Sp. z o. o.
• Berlin
Clinical Research
Associate (CRA) Location: Germany (Remote ) Job Description: We are seeking a highly motivated Clinical Research Associate (CRA) to support multiple clinical studies. The Contractor will perform [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] monitoring and site management activities while ensuring patient safety, regulatory compliance, and high-quality data in accordance with applicable SOPs, study protocols, and ISO 14155:2020. Key Responsibilities: Conduct monitoring activities including visit preparation, on-site visits, follow-up, site contact, and report writing. Perform remote monitoring and interim site management as required. Support site start-up activities including EC/ [. .. ]
Job am 14.01.2026 bei Jooble gefunden
TFS Health Science
Clinical Research Associate
• Mainz
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 Clinical Research Associate. About this role As part of our FSP team you will working alongside passionate and innovative professionals to ensure our customers achieve their goals. This role is dedicated to one of our clients. This role is a full-time role based Germany. Key Responsibilities: Monitor clinical trial sites to ensure [. .. ] patients A Bit More About Us Our journey began 30 years ago in Sweden, in the city of Lund. As a global CRO with the ultimate goal of ensuring patients safety and well-being, we provide biotechnology and pharmaceutical companies with tailored clinical development solutions. We currently operate in 17 countries across Europe, North America, Asia Pacific and the Middle East. Our core values of Trust, Quality, Flexibility and Passion are what make TFS Healthscience the successful company it is today. [. .. ]
Job am 14.01.2026 bei Jooble gefunden
• München
Freiberuflich
Freelance CRA Germany Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and commercial insights into outcomes [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] has been adequately performed and documented for each subject/ patient, as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/ patient. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol deviation/ violations and pharmacovigilance issues. Per the Clinical Monitoring/ Site Management Plan (CMP/ SMP) : Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case [. .. ] are met. Must be able to quickly adapt to changing priorities to achieve goals/ targets. May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and project-specific site team members are trained and compliant with applicable requirements Prepares for and attends Investigator Meetings and/or sponsor face to face meetings. Participates in global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Antal Sp. z o. o.
Klinischer Monitor/ Clinical Research Associate
• Berlin
Clinical Research
Associate (CRA) Location: Germany (Remote ) We are seeking a highly motivated Clinical Research Associate (CRA) to support multiple clinical studies. The Contractor will perform monitoring [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and site management activities while ensuring patient safety, regulatory compliance, and high-quality data in accordance with applicable SOPs, study protocols, and ISO 14155:2020. Perform remote monitoring and interim site management as required. Support site start-up activities including EC/ CA submissions/ amendments, contract negotiation, and documentation preparation/ collection. Report non-compliance of investigators with their Clinical Study [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Antal Sp. z o. o.
• Berlin
Clinical Research
Associate (CRA) Location: Germany (Remote ) We are seeking a highly motivated Clinical Research Associate (CRA) to support multiple clinical studies. The Contractor will perform monitoring [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and site management activities while ensuring patient safety, regulatory compliance, and high-quality data in accordance with applicable SOPs, study protocols, and ISO 14155:2020. Perform remote monitoring and interim site management as required. Support site start-up activities including EC/ CA submissions/ amendments, contract negotiation, and documentation preparation/ collection. Report non-compliance of investigators with their Clinical Study [. .. ]
Job am 14.01.2026 bei Jooble gefunden
ICON
CRA II-Sponsor dedicated
• Frankfurt am Main
Work-Life-Balance
CRA II/ Senior CRA-sponsor dedicated ICON plc is a world-leading healthcare intelligence and
clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Clinical Research Associate II Specialist to join our diverse and dynamic team. As a Clinical Research Associate II Specialist at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of in Nvative treatments and therapies What you will be doing Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Collaborating with investigators and site staff to facilitate smooth study conduct. Performing data review and resolution of queries to maintain high-quality clinical data. Contributing to the preparation and review of study documentation, including protocols and clinical study reports Your profile Bachelors degree in a scientific [. .. ]
Job am 14.01.2026 bei Jooble gefunden
TFS Health Science
• Hamburg
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. We are currently looking for an experienced Clinical Research Associate (CRA) to support cell and gene therapy clinical trials at sites in Germany. Manage site start-up, initiation, monitoring (remote and onsite) , and close-out activities Ensure protocol, GCP, and regulatory compliance at site level Perform SDV/ SDR, CRF review, and data quality oversight according to the monitoring plan Support investigators and site staff through training and ongoing guidance Collaborate with data management, patient safety, and other stakeholders Support audits and regulatory inspections as required Bachelors degree in life sciences or a related field Proven CRA experience in Cell Gene Therapy (essential) Solid understanding of clinical trial processes, monitoring, and data management Experience with risk-based monitoring and remote monitoring approaches Fluency in English and [. .. ]
Job vor 4 Tagen bei Jooble gefunden
Sr CRA in oncology-Sponsor dedicated-Home Based Germany
• München
Sr CRA in oncology-Sponsor dedicated-Home Based Germany Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] has been adequately performed and documented for each subject/ patient as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/ patient. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol deviation/ violations and pharmacovigilance issues. Per the Clinical Monitoring/ Site Management Plan (CMP/ SMP) :Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report [. .. ] are met. Must be able to quickly adapt to changing priorities to achieve goals/ targets. May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and project-specific site team members are trained and compliant with applicable requirements. Prepares for and attends Investigator Meetings and/or sponsor face to face meetings. Participates in and may lead global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical [. .. ]
Job vor 10 Tagen bei Jooble gefunden
Abb Vie
• Ludwigshafen am Rhein
Führungs-/ Leitungspositionen
Work-Life-Balance
[. .. ] care into realities. Join a global powerhouse with over 50, 000 employees worldwide, including 3, 000 in Germany, where your expertise will address tomorrow s unmet medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] needs. As an Associate Director/ Director CMC Product Development you independently manage programs of various complexity utilizing a matrix approach. You lead Chemistry, Manufacturing and Controls (CMC) teams and Product Presentation and Device Strategy Teams (PPDST) of functional representatives from various departments and divisions for projects involving external collaboration partners per Pipeline Commercialization Model [. .. ] product. You serve as the spokesperson for all CMC functions and ensures information flow among AST and various line functions and stakeholders. You will also partner with key collaborators, incl. Clinical, Regulatory, Operations, Quality, Preclinical Safety, ADME and Commercial organizations. Apprises CMC and Stakeholder Management of strategies, plans and risks through regular communications and periodic reviews throughout development and in support of global filings and approvals. In addition you support and implement CMC functional initiatives and across-asset strategies. Make your mark by: Representing all CMC [. .. ]
Job vor 10 Tagen bei Jooble gefunden
Stryker
Clinical Specialist, Joint Replacement-Bangor, Maine Maine
• Augsburg
Clinical Specialist, Joint Replacement Insert Location Overview As a Clinical Specialist at Stryker, you will help improve orthopedic surgeries around the world and play a direct role in our [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] mission of making healthcare better. In this role, you will build deep clinical and technical expertise across both robotic (Mako Smart Robotics) [. .. ] seamless execution and a unified customer experience. Complete required trainings, competencies, and certifications. Provide on-call coverage during evenings, weekends, and holidays. What You Need Minimum Required: Bachelors degree OR Associate degree with 4 years of professional and/or related experience OR High school diploma with 6 years of professional and/or related experience Preferred: 1 year of relevant work experience. Previous clinical experience (nursing, physical therapy, surgical technology, athletic training, personal training, medical scribing, etc. ) . Extracurricular involvement such [. .. ] community service, leadership organizations, or athletic teams. Additional Information This position requires the handling of instruments that may have been contaminated by blood or bodily fluids. In compliance with Occupational Safety and Health Administration (OSHA) regulations, Stryker will provide a safe working environment for all employees. Ability to lift, push, pull, and carry up to 50 lbs. Ability to stand for extended periods. Ability to manage stressful OR situations with professionalism and focus Exerting up to 50 lbs of force occasionally [. .. ]
Job am 22.01.2026 bei Jooble gefunden
Charles River Laboratories, Inc.
• Frankfurt am Main
[. .. ] will play an important role in the work we perform. In return, well help you build a career that you can feel passionate about. Riepilogo del lavoro [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Reporting to the Associate Director Business Development Manager Europe, you will help in identifying new potential customers and/or unexplored markets in a focused portfolio set and lead operational activities including team management at client site. Working closely with Associate Director and client service team to create new pipeline to drive increases in business [. .. ] River is an early-stage contract research organization (CRO) . We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 20, 000 employees within 110 facilities in over 20 [. .. ]
Job am 14.01.2026 bei Jooble gefunden
ICON
CRA II/ Senior CRA
• Frankfurt am Main
Work-Life-Balance
CRA II/ Senior CRA-Germany-office or remote ICON plc is a world-leading healthcare intelligence and
clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Clinical Research Associate II Specialist to join our diverse and dynamic team. As a Clinical Research Associate II Specialist at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies What You Will Be Doing: Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Collaborating with investigators and site staff to facilitate smooth study conduct. Performing data review and resolution of queries to maintain high-quality clinical data. Contributing to the preparation and review of study documentation, including protocols and clinical study reports Your Profile: Bachelors degree in a scientific [. .. ]
Job am 14.01.2026 bei Jooble gefunden
• München
CRA-single sponsor-Germany Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and commercial insights into outcomes to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring [. .. ] GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance. immediately communicates/ escalates serious issues to the project team and develops action plans. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol deviation/ violations and pharmacovigilance issues. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) is accurate and complete. Utilizes available hardware and software to [. .. ] audit readiness standards and supports preparation for audit and required follow-up actions. For Real World Late Phase, the CRA II will use the business card title of Site Management Associate II. Site support throughout the study lifecycle from site identification through close-out. Chart abstraction activities and data collection Collaboration with Sponsor affiliates, medical science liaisons and local country staff. The SMA II may be requested to train junior staff. Identify and communicate out of scope activities to Lead CRA/ [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Freelance CRA Germany
• München
Freiberuflich
Freelance CRA Germany Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and commercial insights into outcomes [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] has been adequately performed and documented for each subject/ patient, as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/ patient. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol deviation/ violations and pharmacovigilance issues. Per the Clinical Monitoring/ Site Management Plan (CMP/ SMP) : Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case [. .. ] are met. Must be able to quickly adapt to changing priorities to achieve goals/ targets. May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and project-specific site team members are trained and compliant with applicable requirements Prepares for and attends Investigator Meetings and/or sponsor face to face meetings. Participates in global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Klinischer Monitor/ Clinical Research Associate (m/w/d)
• München
CRA-single sponsor-Germany Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and commercial insights into outcomes to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring [. .. ] GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance. immediately communicates/ escalates serious issues to the project team and develops action plans. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol deviation/ violations and pharmacovigilance issues. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) is accurate and complete. Utilizes available hardware and software to [. .. ] audit readiness standards and supports preparation for audit and required follow-up actions. For Real World Late Phase, the CRA II will use the business card title of Site Management Associate II. Site support throughout the study lifecycle from site identification through close-out. Chart abstraction activities and data collection Collaboration with Sponsor affiliates, medical science liaisons and local country staff. The SMA II may be requested to train junior staff. Identify and communicate out of scope activities to Lead CRA/ [. .. ]
Job am 14.01.2026 bei Jooble gefunden
CRA-single sponsor-Germany
• München
CRA-single sponsor-Germany Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and commercial insights into outcomes to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] has been adequately performed and documented for each subject/ patient, as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/ patient. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol deviation/ violations and pharmacovigilance issues. Per the Clinical Monitoring/ Site Management Plan (CMP/ SMP) : Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case [. .. ] are met. Must be able to quickly adapt to changing priorities to achieve goals/ targets. May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and project-specific site team members are trained and compliant with applicable requirements Prepares for and attends Investigator Meetings and/or sponsor face to face meetings. Participates in global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Clinical Research Associate/ Klinischer Monitor (m/w/d)
• München
CRA-single sponsor-Germany Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and commercial insights into outcomes to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring [. .. ] GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance. immediately communicates/ escalates serious issues to the project team and develops action plans. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol deviation/ violations and pharmacovigilance issues. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) is accurate and complete. Utilizes available hardware and software to [. .. ] audit readiness standards and supports preparation for audit and required follow-up actions. For Real World Late Phase, the CRA II will use the business card title of Site Management Associate II. Site support throughout the study lifecycle from site identification through close-out. Chart abstraction activities and data collection Collaboration with Sponsor affiliates, medical science liaisons and local country staff. The SMA II may be requested to train junior staff. Identify and communicate out of scope activities to Lead CRA/ [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Klinischer Monitor (m/w/d)
• München
CRA-single sponsor-Germany Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and commercial insights into outcomes to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring [. .. ] GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance. immediately communicates/ escalates serious issues to the project team and develops action plans. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol deviation/ violations and pharmacovigilance issues. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) is accurate and complete. Utilizes available hardware and software to [. .. ] audit readiness standards and supports preparation for audit and required follow-up actions. For Real World Late Phase, the CRA II will use the business card title of Site Management Associate II. Site support throughout the study lifecycle from site identification through close-out. Chart abstraction activities and data collection Collaboration with Sponsor affiliates, medical science liaisons and local country staff. The SMA II may be requested to train junior staff. Identify and communicate out of scope activities to Lead CRA/ [. .. ]
Job am 14.01.2026 bei Jooble gefunden
TFS Health Science
Research Associate
• Hamburg
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. We are currently looking for an experienced Clinical Research Associate (CRA) to support cell and gene therapy clinical trials at sites in Germany. Manage site start-up, initiation, monitoring (remote and onsite) , and close-out activities Ensure protocol, GCP, and regulatory compliance at site level Perform SDV/ SDR, CRF review, and data quality oversight according to the monitoring plan Support investigators and site staff through training and ongoing guidance Collaborate with data management, patient safety, and other stakeholders Support audits and regulatory inspections as required Bachelors degree in life sciences or a related field Proven CRA experience in Cell Gene Therapy (essential) Solid understanding of clinical trial processes, monitoring, and data management Experience with risk-based monitoring and remote monitoring approaches Fluency in English and [. .. ]
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Wieviel verdient man als Clinical safety associate pro Jahr?
Als Clinical safety associate verdient man zwischen EUR 40.000,- bis EUR 70.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Safety Associate Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 105 offene Stellenanzeigen für Clinical Safety Associate Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Safety Associate Jobs?
Aktuell suchen 12 Unternehmen nach Bewerbern für Clinical Safety Associate Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Safety Associate Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Safety Associate Stellenangebote:
- ICON (13 Jobs)
- TFS Health Science (7 Jobs)
- Abb Vie (5 Jobs)
- Antal Sp. z o. o. (3 Jobs)
- Fortrea (2 Jobs)
In welchen Bundesländern werden die meisten Clinical Safety Associate Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Safety Associate Jobs werden derzeit in Bayern (10 Jobs), Berlin (9 Jobs) und Hessen (8 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Safety Associate Jobs?
Clinical Safety Associate Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
