67 Jobs für Clinical Trials Associate
Stellenangebote Clinical Trials Associate Jobs
Job vor 8 Tagen bei jobanzeigen.de gefunden
Universität Wien
• 1010, Wien, Österreich
[. .. ] processes and policy design. The Theory Testing Lab at the University of Vienna focuses on empirical analyses of pharmaceutical innovation, developing and leveraging large-scale datasets (e. g. [...]
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[...] , patents, clinical trials, molecular data) to study how innovation trajectories emerge and are shaped. The position offers the opportunity to contribute to internationally visible, frontier research. You will have the chance to help build and shape a high-impact interdisciplinary research group while working on your own research. The group is led by Prof. Stefan Wagner, who publishes in leading international journals and serves as Associate Editor at Management Science. Your responsibilities:As a Postdoctoral Research you will:Conduct independent and collaborative empirical research on pharmaceutical innovation and technological trajectories Build, manage, and analyse large-scale datasets (e. g. , patent data, clinical trials, molecular and firm-level data) Apply advanced econometric methods to study innovation processes and [. .. ]
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
Universität Wien
Scientific project assistant postdoc
• AT- 9 Innere Stadt
[. .. ] processes and policy design. The Theory Testing Lab at the University of Vienna focuses on empirical analyses of pharmaceutical innovation, developing and leveraging large-scale datasets (e. g. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] , patents, clinical trials, molecular data) to study how innovation trajectories emerge and are shaped. The position offers the opportunity to contribute to internationally visible, frontier research. You will have the chance to help build and shape a high-impact interdisciplinary research group while working on your own research. The group is led by Prof. Stefan Wagner, who publishes in leading international journals and serves as Associate Editor at Management Science. Your responsibilities:As a Postdoctoral Research you will:Conduct independent and collaborative empirical research on pharmaceutical innovation and technological trajectories Build, manage, and analyse large-scale datasets (e. g. , patent data, clinical trials, molecular and firm-level data) Apply advanced econometric methods to study innovation processes and [. .. ]
Job vor 8 Tagen bei Mindmatch.ai gefunden
Gouya Insights
• AT- 9 Wien
Job Description
Clinical Research
Associate (CRA) at GOUYA INSIGHTS Are you an experienced Clinical Research Associate (CRA) looking to further strengthen your expertise in clinical trial execution? Gouya Insights is [...]
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[...] seeking a motivated and handson CRA to join our growing clinical operations team. In this role, you will be responsible for onsite and remote monitoring [. .. ] medical device sponsors worldwide. We provide endtoend support across the clinical development lifecycle, acting as an interface between sponsors, clinical operations, and regulatory stakeholders to ensure highquality and inspectionready clinical trials. J-18808-Ljbffr 90248584 [. .. ]
Job am 11.03.2026 bei Mindmatch.ai gefunden
Teleflex
Clinical Research Associate
• AT- 9 Wien
Expected Travel: More than 50 Requisition ID: 13617 Position Summary The
Clinical Research
Associate (CRA) is responsible for scheduling and conducting on-site and remote monitoring visits in compliance with applicable [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] regulatory standards (MDR, ISO 14155, ICH/ GCP guidelines, Teleflex procedures and IRB/ EC policies) . The CRA conducts monitoring visits as identified by the monitoring plan, study team or department needs to evaluate [. .. ] Cardiology and/or Peripheral Vascular Intervention is an advantage. Specialized Skills/ Other Requirements Strong working knowledge, understanding and ability to apply MDR, ISO 14155 and ICH/ GCP guidelines governing clinical trials. Strong compliance focus. Demonstrated aptitude and knowledge in relevant therapeutic areas and ability to learn and integrate new therapeutic areas knowledge. Ability to train and mentor Clinical Studies personnel for remote and onsite monitoring visits. Ability to train onsite staff on the protocol, GCPs, data entry and other pertinent regulations. [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Job Overview The
Associate Medical Director/ Medical Director will provide medical,
clinical and scientific advisory expertise to all IQVIA divisions as requested. Participate in all aspects of Medical Science involvement [...]
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[...] on assigned trials. Serve as a medical expert during project delivery lifecycle. Provide therapeutic and medical expertise to business development activities. Essential Functions The role includes predominantly Medical Monitoring responsibilities with Medical Strategic input involvement as requested. Medical Monitoring: # # Primarily serves as Global and/or Regional Medical Advisor on assigned [. .. ]
Job vor 9 Tagen bei Jobleads gefunden
Medical Director-Psychiatry (m/w/d)
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Job Overview The
Associate Medical Director/ Medical Director will provide medical,
clinical and scientific advisory expertise to all IQVIA divisions as requested. They will participate in all aspects of [...]
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[...] medical science involvement on assigned trials, serve as a medical expert during the project delivery lifecycle, and provide therapeutic and medical expertise to business development activities. Essential Functions Primarily responsible for medical monitoring with input into medical strategy as requested. Medical Monitoring Primarily serves as Global and/or Regional Medical Advisor on assigned projects. Serves as [. .. ]
Job vor 2 Tagen bei Jooble gefunden
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern
[. .. ] organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, youll collaborate with passionate problem [. .. ] are met. Must be able to quickly adapt to changing priorities to achieve goals/ targets. May act as primary liaison with project 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, and may, with supervision, lead, global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends [. .. ] Lead (COL) , or operational line manager. Qualifications: Bachelors degree or RN in a related field or equivalent combination of education, training and experience Experience as a CRA in oncology trials. Knowledge of Good Clinical Practice/ ICH Guidelines and other applicable regulatory requirements Must demonstrate good computer skills and be able to embrace new technologies Excellent communication, presentation and interpersonal skills. Basic level of critical thinking skills expected. Fluency in German and English Ability to manage required travel of up to [. .. ]
Job vor 2 Tagen bei Jooble gefunden
Abb Vie
Project Data Manager/ Associate Scientist II (all genders) (full-or parttime, temporary for 18 months)
• Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz Ludwigshafen am Rhein, DE
Teilzeit
Work-Life-Balance
[. .. ] your expertise? In a challenging work environment that offers opportunities of developing and increasing your own skills? Youve come to the right place Moving mountains together as [...]
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[...] Project Data Manager/ Associate Scientist II (all genders) Your tasks and responsibilities: Support cross-functional laboratory sample and data operations in all stages of Abb Vie clinical trials and in compliance with GCP/ GLP requirements Initiate, coordinate and revise documents for setting up projects/ services with vendors, for example on the external storage of clinical trial samples Support sample data curation, intake, reconciliation and transfer using bioanalytical LIMS and ELN software Support internal and external sample storage management [. .. ]
Job vor 3 Tagen bei Jooble gefunden
Biontech
• Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz Mainz, DE
Führungs-/ Leitungspositionen
As
Associate Director Audit Management, you will play a pivotal role in ensuring the quality and compliance of Bio NTechs
clinical trials and processes. As part of the Global [...]
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[...] Development Quality Assurance team, you will lead audits across Good Clinical Practice (GCP) , Good Laboratory Practices (GLP) , Good Pharmacovigilance Practice (GVP) , and Information Technology (IT) domains. Your work will directly contribute to advancing Bio NTechs mission by ensuring adherence to regulatory [. .. ]
Job vor 4 Tagen bei Jooble gefunden
Indero
Project Manager II (Germany)
• Unstrut- Hainich- Kreis; Thüringen Thueringen
Description The project manager II has the overall responsibility for the successful initiation, planning, execution, monitoring, controlling and closure of assigned
clinical trials. The project manager II oversees and coordinates [...]
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[...] study resources to ensure compliance with the study budget, project scope and timelines and in accordance with applicable standard operating procedures (SOPs) , good clinical practices, regulatory and study-specific requirements. Project Manager II acts as the main line of communication to relevant [. .. ] functional departments, and senior management. Manage and report on recruitment status and highlight initiatives needed to meet recruitment timelines. Project team leadership Lead the core project team which may include: Associate Project Managers, Project Coordinators, Project Assistants. Ensure all team members have adequate training on the project. Work closely with vendors and the following internal teams to ensure all tasks and deliverables are completed on time, according to plans and according to applicable standards: Site Selection, Regulatory Affairs, Data Management, Clinical [. .. ]
Job vor 5 Tagen bei Jooble gefunden
Allucent
• Regierungsbezirk Köln; Westfalen Koeln
[. .. ] a last impact on patients worldwide. Together we. Find more information about our values. The role Bring your monitoring expertise to the forefront of innovation. We are [...]
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[...] looking for a Clinical Research Associate (CRA) to join our A-team. As a CRA at Allucent, you will independently control and monitor investigational sites, pro-actively detect issues, provide solutions to ensure clinical studies are performed according to the trial protocol and in compliance with SOPs, applicable regulations, and the principles of Good Clinical Practice. [. .. ] site activation processesincluding contracting and start-up activitiesto ensure smooth and compliant study execution. You will travel throughout Germany. Main responsibilities: Independently manage all aspects of monitoring for assigned clinical trials across study phases, including site initiation, routine monitoring, and close-out visits. Ensure compliance with protocols, GCP, ICH, SOPs, and applicable regulatory requirements. Build strong site relationships, acting as a primary point of contact and ensuring high-quality data collection. Identify and resolve site issues, escalating as needed to maintain [. .. ]
Job vor 5 Tagen bei Jooble gefunden
CRA II Germany-eastern Germany (Leipzig, Halle, Berlin)
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern
[. .. ] organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, youll collaborate with passionate problem [. .. ] 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 [. .. ] remote monitoring of trial sites to verify compliance with regulatory requirements and clinical protocols. Utilizes data analytics and risk-based monitoring techniques to identify potential issues and trends, ensuring that trials are conducted in accordance with established clinical practices. Collaborates with site teams to develop and implement tools, procedures, and processes that enhance quality monitoring and support the overall success of clinical trials. Impact and Contribution Individual contributors with responsibility in a professional or technical discipline or specialty, but may manage [. .. ]
Job am 25.04.2026 bei Jooble gefunden
Biontech
• Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz Mainz, DE
Führungs-/ Leitungspositionen
As
Associate Director Statistical Programming you will be responsible for representing Statistics in all assigned cross-functional
clinical study teams and other projects and holding accountability for all statistical [...]
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[...] aspects, as well as for providing statistical input into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate deliverables. Your main responsibilities are: Work as part of a collaborative, cross-functional team [. .. ] staff (internal as well as outsourced) and in representing Biostatistics in a matrix organization and in a multidisciplinary team Experiences in planning, conducting and analyses of oncology or infectious diseases trials from phase I-IV, including scientific publications Experience in answering health authority questions (FDA, EMA) and in leadings statistics on regulatory submissions, including developing ISE/ ISS packages Good knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian is a Plus) , regulatory guidelines [. .. ]
Job am 15.04.2026 bei Jooble gefunden
CRA II Germany-eastern Germany (Leipzig, Halle, Dresden)
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern München, DE
[. .. ] organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, youll collaborate with passionate problem [. .. ] 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 [. .. ] remote monitoring of trial sites to verify compliance with regulatory requirements and clinical protocols. Utilizes data analytics and risk-based monitoring techniques to identify potential issues and trends, ensuring that trials are conducted in accordance with established clinical practices. Collaborates with site teams to develop and implement tools, procedures, and processes that enhance quality monitoring and support the overall success of clinical trials. Impact and Contribution Individual contributors with responsibility in a professional or technical discipline or specialty, but may manage [. .. ]
Job am 15.04.2026 bei Jooble gefunden
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern München, DE
[. .. ] organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, youll collaborate with passionate problem [. .. ] are met. Must be able to quickly adapt to changing priorities to achieve goals/ targets. May act as primary liaison with project 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, and may, with supervision, lead, global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends [. .. ] related field or equivalent combination of education, training and experience Knowledge of Good Clinical Practice/ ICH Guidelines and other applicable regulatory requirements Three years monitoring experience Experience in monitoring oncology trials Must demonstrate good computer skills and be able to embrace new technologies Excellent communication, presentation and interpersonal skills. Basic level of critical thinking skills expected. Fluency in German and proficient in English Ability to manage required travel of up to 75 on a regular basis throughout Germany. Occasional visits to [. .. ]
Job am 08.04.2026 bei Jooble gefunden
ICON
CRA II
• Homeoffice Homeoffice, DE
Homeoffice möglich
Work-Life-Balance
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 welcome you to join us [...]
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[...] on our mission to shape the future of clinical development. As a Clinical Research Associate II at ICON, youll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II IV, ensuring adherence to applicable regulations and principles of ICH-GCP. You will be [. .. ] efficiency Preparation and review of study documentation and feasibility studies for new proposals Potential to assist in training and mentoring fellow CRAs You are: 18 months of experience in clinical trials Degree in medicine, science, or equivalent Previous monitoring experience in medium-sized studies, including study start-up and close-out Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data Excellent written and verbal communication in both English and German Ability to work to tight deadlines Availability [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Clin Choice
• Deutschland Deutschland, DE
[. .. ] of both worlds and we think youll agree. Clin Choice is a rapidly growing global contract research organization. Were currently expanding our CRA network in Germany and [...]
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[...] are seeking skilled Clinical Research Associates (CRA II and Senior CRA) interested in partnering with some of the worlds leading pharmaceutical companies in the field of biomedicine. If that sounds like you, we encourage you to submit your resume via our website wed love to hear from you Position Overview Clinical Research Associate As a CRA, youll manage clinical study activities across multiple sites within one or more projects, with a focus on medical devices. You will oversee site performance, conduct company-initiated clinical studies, and ensure high-quality deliverables through site visits, monitoring, and effective communication. Key Requirements: Willingness to travel to sites and surrounding countries (50-80 travel) . Fluent in German is required. Prior experience in monitoring clinical trials and site management. Join a dynamic, global team that values growth, collaboration, and making a difference in clinical research. Skills and Qualifications: Bachelor s Degree or equivalent University Degree in scientific and/or medical or paramedical disciplines; Nursing degree or relevant degree or background preferred. In some cases, an equivalency, [. .. ]
Job am 08.04.2026 bei Jooble gefunden
IQVIA
Experienced Clinical Research Associate (m/w/d) , Multi-Sponsor, Germany
• Regierungsbezirk Darmstadt; Hessen Frankfurt am Main, DE
Homeoffice möglich
Join IQVIA as a CRA II/ Sr CRA (m/w/d) in our
Clinical Site Management department home-based throughout Germany. You will focus on a comprehensive clinical trial management in a [...]
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[...] variety of indications and learn about the diverse scientific approach of the sponsors. Beside establishing strong relationships with the global study team and the involved investigators, you will conduct monitoring on complex clinical trials for different pharma companies and assure their adherence to good clinical practices and study protocols. With strategic site relationship managers supporting you throughout your role, this is a fantastic opportunity for you to embed yourself in the wider clinical operations team and work on ground-breaking new medicine development. Your [. .. ]
Job am 08.04.2026 bei Jooble gefunden
ICON
• Homeoffice Homeoffice, DE
Homeoffice möglich
Work-Life-Balance
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 welcome you to join us [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] on our mission to shape the future of clinical development. As a Clinical Research Associate I at ICON, youll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II IV, ensuring adherence to applicable regulations and principles of ICH-GCP. You will be [. .. ] efficiency Preparation and review of study documentation and feasibility studies for new proposals Potential to assist in training and mentoring fellow CRAs You are: 12 months of experience in clinical trials Degree in medicine, science, or equivalent Previous monitoring experience in medium-sized studies, including study start-up and close-out Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data Excellent written and verbal communication in both English and German Ability to work to tight deadlines Availability [. .. ]
Job am 08.04.2026 bei Jooble gefunden
ICON
CRA II-Sponsor dedicated
• Regierungsbezirk Darmstadt; Hessen Frankfurt am Main, DE
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 [...]
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[...] 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 [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Position CRA-single sponsor-Western Germany (Düsseldorf, Köln, Essen)
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern München, DE
[. .. ] organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, youll collaborate with passionate problem [. .. ] 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 [. .. ] remote monitoring of trial sites to verify compliance with regulatory requirements and clinical protocols. Utilizes data analytics and risk-based monitoring techniques to identify potential issues and trends, ensuring that trials are conducted in accordance with established clinical practices. Collaborates with site teams to develop and implement tools, procedures, and processes that enhance quality monitoring and support the overall success of clinical trials. Impact and Contribution Individual contributors with responsibility in a professional or technical discipline or specialty, but may manage [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Thermo Fisher Scientific
CRA II/ Sr CRA-FSP-Germany (m/f/d)
• Homeoffice Homeoffice, DE
Homeoffice möglich
Work-Life-Balance
[. .. ] discover meaningful work that makes a positive impact on a global scale. Our Mission is to enable our customers to make the world healthier, cleaner and safer. [...]
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[...] Through our PPD clinical research services, we support clinical trials in more than 100 countries, delivering laboratory, digital and decentralized solutions that help bring life-changing therapies to patients faster. Our goal-driven teams combine and deliver startup activities for the clinical trials, collaborating to improve processes, cycle and flexibility. We partner with our sites, businesses and colleagues around the [. .. ] Complete documentation, system updates, and administrative tasks Education Experience Bachelors degree in a life sciences related field or equivalent qualification Minimum 2 + years of experience as a Clinical Research Associate/ Monitor Valid drivers license Full right to work in Germany Fluency in German and English (C1 level) interviews will be conducted in German Knowledge, Skills Abilities Strong clinical monitoring skills with hands-on RBM experience Excellent understanding and application of ICH-GCP and applicable regulations Solid therapeutic area knowledge and [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Hays Professional Solutions GmbH
Clinical Trial Associate für den Bereich Quality Assurance (m/f/d)
• Regierungsbezirk Darmstadt; Hessen Frankfurt am Main, DE
Angebote von Zeitarbeitsunternehmen
Ihre Aufgaben: Quality Oversight Systems Management: Monitor compliance with quality guidelines in
clinical business areas and implement regional quality plans Identify potential gaps, recommend solutions, and escalate relevant issues [...]
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[...] Assist in maintaining and improving quality documents and processes Audit Inspection: Lead and support audit and inspection preparations, including document management and response coordination Ensure trial sites and teams are inspection-ready Consultation Collaboration:Serve [. .. ] to identify gaps and recommend corrective actions to enhance compliance and efficiency Ihre Qualifikationen: Education Experience: Bachelor s degree in science, technology, or healthcare; experience in quality systems within clinical trials is required Project Management: Strong ability to prioritize and effectively manage multiple tasks Communication: Excellent communication skills and ability to influence various stakeholders Analytical Skills: Problem-solving abilities and attention to detail for risk assessment and process optimization Teamwork Flexibility: Independent yet collaborative work style within global teams Preferred: Experience [. .. ]
Job am 08.04.2026 bei Jooble gefunden
TFS Health Science
Senior Clinical Research Associate
• Regierungsbezirk Darmstadt; Hessen Frankfurt am Main, DE
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. In this position, you will play a key role in the operational execution of clinical studies, contributing to the safe, effective, and responsible development of new therapies. You may also take on Study Lead responsibilities for national and international trials, depending on project needs. Key Responsibilities Independently plan, conduct, and follow up on pre-study, site initiation, routine monitoring, and close-out visits, both on-site and remotely, in line with the applicable monitoring plan Oversee study site performance, including recruitment progress, and provide ongoing support to sites on study-[. .. ] discipline, or completed vocational training in a relevant healthcare or medical field Additional training in clinical research or CRA certification, combined with several years of experience as a Clinical Research Associate Strong knowledge of GCP, ICH guidelines, and clinical research processes, with a high level of accuracy in handling study data and regulatory requirements Fluent German and English language skills, both written and spoken, with willingness to travel nationally and internationally as required What We Offer We provide opportunities for personal [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Biontech
Associate Director, Safety Scientist
• Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz Mainz, DE
Führungs-/ Leitungspositionen
The
Associate Director, Safety Sciences provides scientific expertise for medical safety tasks. Core responsibilities include safety data review and analysis from different sources, periodic report authoring and the oversight [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of the safety surveillance activities for the assigned program (s) . The Safety Scientist ensures that all processes are conducted according to Bio NTech [. .. ] regulations. The Associate Director Safety Sciences participates in audits and inspections as Subject Matter Expert and works in close collaboration with the Safety Physician to author relevant safety sections of clinical trial documents for the assigned program (s) . Your Contribution: Perform cumulative safety data reviews across trials or programs to assess safety profiles and identify emerging risks or trends Oversee the Safety Surveillance activities, including signal detection, literature reviews, and aggregate safety data analysis using tools like Safety Dashboards, Spotfire, and Elluminate Collaborate with Safety Physicians to review and align on safety data conclusions for informed decision-[. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical Trials Associate pro Jahr?
Als Clinical Trials Associate verdient man zwischen EUR 40.000,- bis EUR 60.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Trials Associate Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 67 offene Stellenanzeigen für Clinical Trials Associate Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trials Associate Jobs?
Aktuell suchen 14 Unternehmen nach Bewerbern für Clinical Trials Associate Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Trials Associate Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Trials Associate Stellenangebote:
- Biontech (4 Jobs)
- ICON (3 Jobs)
- Thermo Fisher Scientific (2 Jobs)
- Gouya Insights (1 Job)
- Teleflex (1 Job)
In welchen Bundesländern werden die meisten Clinical Trials Associate Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trials Associate Jobs werden derzeit in Bayern (14 Jobs), Sachsen-Anhalt (9 Jobs) und Niedersachsen (7 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trials Associate Jobs?
Clinical Trials Associate Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
