61 Jobs für Clinical Safety Associate
Stellenangebote Clinical Safety Associate Jobs
Job gestern bei Mindmatch.ai gefunden
Novamed
• AT- 6 Hengsberg
Teilzeit
[. .. ] is seeking an experienced Facilities Maintenance Manager to join our amazing team Job Title Facilities Maintenance Manager General Purpose of the Job Under the supervision of the [...]
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[...] Practice Administrator and Clinical Director the Facilities Maintenance Manager is responsible for the operation and maintenance of the Ambulatory Surgery Center (ASC) facilities, equipment and property. Oversees all buildingrelated activities. Performs overall housekeeping, building, grounds, safety, maintenance, custodial support, organization of events, ensuring that ASC operates efficiently by planning and directing building related services. Supervisory Responsibilities This position does not have any direct reports. Essential Job Duties And Responsibilities Monitors and maintains facility logbooks and all documentation in accordance with TX Department of Health/ CMS standards. [. .. ] meetings and educational trainings and activities as needed. Know, understand, and follow all HVSC policies and procedures. Performs any other duties as assigned. Qualifications High School Diploma or equivalent required. Associate degree (A. A. ) or equivalent from a twoyear college or technical school; or six months to one year related experience and/or training; or an equivalent combination of education and experience. Ability to perform duties under pressure and meet deadlines in a timely manner. Ability to effectively communicate with [. .. ]
Job vor 7 Tagen bei Mindmatch.ai gefunden
ICON
Clinical Research Associate
• AT- 9 Wien
Work-Life-Balance
Clinical Research
Associate-Remote-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 welcome you [...]
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[...] to join us on our mission to shape the future of clinical development. As a CRA I at ICON, you [. .. ] preparation and review of study documentation and feasibility studies for new proposals as required. Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff. Ensure patient safety by ensuring compliance with ICONs procedures, protocols, and regulatory requirements. Your Profile: University degree in medicine, science, or equivalent Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data Excellent written and verbal communication in English Good social skills enabling you to deal with queries in [. .. ]
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 activities, ensuring protocol adherence, data integrity, and subject safety. You will work closely with investigational sites and internal teams to oversee regulatory documentation, ethics committee and hospital submissions at site level, and trial conduct in accordance with SOPs, ICHGCP, and applicable regulatory requirements. All activities are performed with a strong focus on quality, inspection readiness, and timely delivery. If [. .. ]
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 [...]
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[...] 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 data accuracy and subject safety required by review of regulatory documents, medical records, reported data and device storage, if applicable. The CRA must be able to identify issues, present findings to the site staff, provide retraining if needed, provide problemsolving strategies and communicate findings to the study team and department management via escalation of issues [. .. ]
Job am 06.03.2026 bei Mindmatch.ai gefunden
Alimentiv
• AT- 9 Wien
[. .. ] quite matches what youre looking for, or not ready to make a move yet? Let us know We are proactively inviting qualified candidates to join our talent [...]
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[...] pool for anticipated Clinical Research Associate needs (across multiple seniority levels) to support our Clinical Monitoring team. What the process looks like: A Talent Acquisition representative will contact selected candidates to schedule a qualifying call to learn more about your experience, and what your timeline looks like Well also share details about timelines on our side-[. .. ] with SOPs, protocol, and GCP. Perform remote data and system reviews (EDC, CTMS, RBM, TMF) to ensure data quality, completeness, and regulatory compliance. Assist/ lead (as appropriate) with query resolution, safety reviews, and adverse event follow-up throughout the study lifecycle. Support/ conduct (as appropriate) site startup and activation activities, including investigator coordination, trial material delivery, and recruitment support. Maintain accurate, timely, and complete TMF documentation, requesting updates as required. Provide day-to-day operational support to Senior CRA, and Lead [. .. ]
Job am 02.03.2026 bei Mindmatch.ai gefunden
Octapharma Austria
Senior Scientist (m/w/d) - Scientific Operations Services-R D Plasma
• AT- 9 Wien
[. .. ] highquality scientific interpretations and conclusions Prepare, review and present reports, presentations, and scientific insights in accordance with internal standards to both internal and external stakeholders Coach, mentor, [...]
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[...] and supervise Scientists, Associate Scientists, and technical staff, supporting their growth and development Your expertise and ideal skill set University degree (MSc or Ph D) in biotechnology, biochemical engineering, biochemistry, biology, pharmaceutical sciences, or a related discipline Minimum 58 years of relevant experience in biopharmaceutical R D, including industrial exposure in Gx P regulated setting Expertise [. .. ] with a proactive, resultdriven and collaborative mindset Proficient in German and English (oral + written) Your department-where you make an impact We, the Research Development department, conduct preclinical and clinical research to develop new products and ensure their safe and effective use throughout their overall lifecycle. Our ultimate focus in our daily work is on increasing patient health and safety. Thrive with us Company restaurant meal subsidy Training further education Health promotion Parking spaces and good public transport connections Company and team events Enjoy these attractive benefits You can find all offers here: Benefits The minimum gross salary according to the collective agreement (chemical industry) is EUR 4, 270.14 [. .. ]
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 [...]
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[...] Science involvement 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 [. .. ] aspects of assigned projects. # # Provides medical support to investigative sites and project staff for protocol-related issues including protocol clarifications, inclusion/ exclusion determinations, and issues of patient safety and/or eligibility. # # Performs medical review of the protocol, Investigative Drug Brochure (IDB) , and/or Case Report Forms (CRFs) . # # Provides therapeutic area/ indication training for the project clinical team. # # Attends and presents at Investigator Meetings. # # Performs [. .. ]
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 [...]
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[...] of 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 [. .. ] medical and scientific aspects of assigned projects. Provides medical support to investigative sites and project staff for protocol-related issues including protocol clarifications, inclusion/ exclusion determinations, and issues of patient safety and/or eligibility. Performs medical review of the protocol, Investigative Drug Brochure (IDB) , and/or Case Report Forms (CRFs) . Provides therapeutic area/ indication training for the project clinical team. Attends and presents at Investigator Meetings. Performs review and clarification of trial-related Adverse Events (AEs) . May perform [. .. ]
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 [. .. ] 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 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 [. .. ]
Job vor 2 Tagen bei Jooble gefunden
Veeva Systems
Business Consultant-R D
• Berlin
Beratungs-/ Consultingtätigkeiten
[. .. ] measuring tangible business value. R D Business Consulting supports biopharma, medtech, animal and consumer health customers with solving business problems across the R D value chain but [...]
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[...] also specifically within Clinical, Pharmacovigilance and Regulatory domains. You will be part of a global team delivering meaningful and high-impact projects with a variety of organisations from Top 20 Pharma to small/ mid-sized organisations. What Youll Do Lead project workstreams from end-to-end, ensuring the high-quality design and delivery of customer solutions Solve complex problems for Life Sciences leaders, leveraging Veevas unique data and software insights Mentor and manage Associate Consultants, overseeing their work and professional development within your workstream Drive practice growth by contributing to business development and internal IP creation Requirements Experience: 3+ years in Life Sciences Consulting (Business or Management Consulting preferred) Domain Knowledge: Proven expertise in Clinical Data/ Operations, Regulatory or Pharmacovigilance/ Drug Safety Analytical Rigor: A strong mindset for both quantitative and qualitative reasoning Communication: Ability to articulate complex ideas clearly to senior stakeholders Education: Bachelors degree or higher Not a perfect match yet? If you have 35 years of life sciences experience, a recent advanced degree, or a military background, Master Class [. .. ]
Job vor 3 Tagen bei Jooble gefunden
Charles River Laboratories, Inc.
• Kreis Mettmann; Regierungsbezirk Düsseldorf; Westfalen Duesseldorf
Work-Life-Balance
[. .. ] 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 [...]
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[...] 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 [. .. ] 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 [. .. ]
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 [...]
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[...] coordinates 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 [. .. ] planning and conduct of the Investigator s Meeting. Ensure that each site has the necessary material to adequately perform the study (e. g. , investigational product, study supplies, special equipment, safety lab kits, etc. ) . Lead study start-up activities including trial kick-off, TMF setup, site selection and activation, vendor set-up timelines, and site contracting and budgeting. Collaborate with Regulatory Affairs to ensure timely submissions and completeness of essential documents prior to site initiation and throughout the study. [. .. ] 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. [. .. ] 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 trial integrity and patient safety. Activities around regulatory affairs, site activation and study-startup. Requirements To be successful you will possess: Youre an experienced CRA ready to take the next step with a company that truly values your expertise and independence. You thrive in an agile, collaborative environment and want to be part of a [. .. ]
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 [...]
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[...] 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 [. .. ] 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 vor 9 Tagen bei Jooble gefunden
Linical
• Deutschland Deutschland, DE
The
Clinical Research
Associate is responsible for the feasibility, initiation, monitoring, and close-out of investigative sites. Major responsibilities include ensuring the
safety and well-being of study participants [...]
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[...] at assigned sites, ensuring site compliance with Good Clinical Practice (GCPs) , applicable regulations, the protocol and study plans; ensuring data integrity through source data verification and monitoring process, and ensuring site compliance with all Investigational Product (IP) storage, inventory, dispensing, dosing, and disposition [. .. ]
Job am 16.04.2026 bei Jooble gefunden
TFS Health Science
Clinical Research Associate (CRA)
• Regierungsbezirk Darmstadt; Hessen Frankfurt am Main, DE
TFS Health Science is a global, mid-sized contract research organization (CRO) partnering with biotechnology and pharmaceutical companies across the full
clinical development lifecycle. Our expertise spans full-service clinical development, [...]
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[...] project-based support, strategic resourcing, and Functional Service Provider (FSP) solutions, matching experienced professionals to roles where they deliver the greatest impact. 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 expertise includes full service capabilities, resourcing and Functional Service (FSP) solutions. The Clinical Research Associate (CRA) plays a key role in ensuring highquality clinical trial execution across all study phases. You will work directly with investigative sites to support patient safety, data integrity, and protocol compliance. This position is wellsuited for someone who enjoys site collaboration, problemsolving, and maintaining strong operational oversight throughout the study lifecycle. Key Responsibilities Manage site start-up, initiation, monitoring (remote and onsite) , and close-out activities Ensure protocol, GCP, and regulatory compliance at site level [. .. ]
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 [. .. ] 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 15.04.2026 bei Jooble gefunden
Sr CRA Oncology Germany
• 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 [. .. ] 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 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 [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Biontech
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern München, DE
Führungs-/ Leitungspositionen
Your main responsibilities are: Design, build, maintain, and optimize scalable, secure, and resilient data pipelines using Spark, Databricks, Delta Lake, and AWS Support data flow across
clinical systems (EDC, [...]
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[...] CTMS, IRT, Rave, biosample systems, BRIMS, PV, MDM) and build transformations aligned with CDISC standards (CDASH, ODM, SDTM, ADa M) Implement frameworks for data quality, testing, monitoring, and performance optimization; perform clinical data cleaning, reconciliation, validation, and QC Partner with Platform, Cloud, and Dev Ops teams to evolve the [. .. ] engineering initiatives, serving as a senior engineering leader and mentoring engineers on best practices, coding standards, automation, and reproducibility Integrate data across R D lifecycle domains (translational science, clinical development, safety, regulatory, realworld evidence) , including AP Ibased ingestion (REST, Graph QL) and metadata management Collaborate with crossfunctional teams (QA, Data Analysts, Data Scientists, Cloud Ops, Biostats, Clinical Ops) , CROs, and external vendors, fostering an open, respectful, and inclusive team culture Engage with governance, compliance, and security to ensure Gx P, CSV, [. .. ] you have to offer: Bachelors or masters degree in computer science, engineering, a related field, or equivalent practical experience 6 to 10+ years of data engineering experience (Senior Data Engineer/ Associate Director) with productiongrade data pipelines and largescale distributed systems 2 to 6+ years of experience with Databricks and AWS, plus ETL/ ELT tools and cloud data lake/ warehouse solutions Experience in biotech/ pharma regulated or complex scientific environments, including Gx P/ CSV and data governance (privacy, data ethics) Strong SQL, Py [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Veeva Systems
Business Consultant-R D (Remote)
• Berlin Berlin, DE
Beratungs-/ Consultingtätigkeiten
[. .. ] Veeva. We work with senior customer stakeholders, as the partner of choice for 85 of the top 20 Pharmaceutical companies, to define and realize the strategic value [...]
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[...] of Regulatory Affairs, Clinical Strategy Operations as well as Quality and Safety (eg. Pharmacovigilance) . As a Consultant, you will manage workstreams on consulting projects for Veeva customers in R D planning, organizing, and tracking all aspects of delivery. You will analyze problems, build insightful solutions, and develop close working relationships with customer stakeholders (through face-to-face discussions, workshops, email, etc. [. .. ] the customer Be a primary client contact for operational project questions, developing the relationship through face-to-face discussions, workshops, phone, and email contact Manage the work and priorities of Associate Consultants in your workstream Support and mentor Associates in developing skills and professional capabilities Build trusted relationships with customer stakeholders Bring to your customers a good level of industry/ market/ functional insights Input into business development opportunities and proposals Help develop and disseminate thought leadership Requirements Bachelor s or Masters [. .. ]
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 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 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 [. .. ] 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 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 [...]
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[...] oversight of the safety surveillance activities for the assigned program (s) . The Safety Scientist ensures that all processes are conducted according to Bio NTech s written [. .. ] 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, [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Jobgether
Associate Director, PKPD Programmer
• Deutschland Deutschland, DE
Führungs-/ Leitungspositionen
Work-Life-Balance
This position is posted by Jobgether on behalf of a partner company. We are currently looking for an
Associate Director, PKPD Programmer in Germany. The Associate Director, PKPD Programmer [...]
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[...] will lead a team of programming specialists to deliver high-quality pharmacokinetic and pharmacodynamic analyses that support drug development and regulatory submissions. This role combines technical expertise with leadership responsibilities, overseeing dataset construction, analysis programs, and quality assurance for PPK, [. .. ] a team of PKPD programmers, providing guidance, training, and mentorship to enhance technical skills and efficiency. Oversee the preparation and management of datasets for PPK, PKPD, exposure-response (efficacy and safety) , C-QTc, and NCA analyses, ensuring compliance with CDISC ADa m/SDTM standards. Develop, maintain, and optimize high-quality R and SAS programs to facilitate dataset construction and analyses. Conduct exploratory analyses to support modeling and reporting, ensuring accuracy and scientific rigor. Interface directly with clients on dataset specifications, data [. .. ] Ph D, Pharm D, or equivalent in Pharmaceutical Sciences, Pharmacology, Toxicology, Statistics, Mathematics, or related fields. Minimum 10 years of experience in PKPD programming, analysis, reporting, and regulatory submissions. Strong knowledge of clinical drug development, pharmacokinetics, pharmacology, and PKPD methodologies. Expertise in R and SAS for dataset construction and analysis, with familiarity in CDISC ADa m/SDTM standards. Proven experience in multiple therapeutic areas and global regulatory contexts. Excellent verbal and written communication skills in English, with experience presenting technical findings to cross-functional [. .. ]
Job am 08.04.2026 bei Jooble gefunden
CRA-Future Roles (Germany)
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern München, DE
CRA Future Roles (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 [...]
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[...] outcomes to address modern market realities. Every day we perform better because of how we work together, as one team, each the best at what we do. We bring a wide range of talented experts together across a wide range of business-critical services [. .. ] 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. For 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 [. .. ] oversight of the Lead CRA, to changing priorities to achieve goals/ targets. May act as primary liaison with project site personnel, or in collaboration with another CRA or Central Monitoring Associate (CMA) . 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 [. .. ]
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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.
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Aktuell gibt es auf JobRobot 61 offene Stellenanzeigen für Clinical Safety Associate Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Safety Associate Jobs?
Aktuell suchen 17 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 (2 Jobs)
- Veeva Systems (2 Jobs)
- Indero (2 Jobs)
- Biontech (2 Jobs)
- Novamed (1 Job)
- Gouya Insights (1 Job)
In welchen Bundesländern werden die meisten Clinical Safety Associate Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Safety Associate Jobs werden derzeit in Bayern (14 Jobs), Niedersachsen (9 Jobs) und Berlin (7 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Safety Associate Jobs?
Clinical Safety Associate Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
