117 Jobs für Clinical Trial Investigator
Stellenangebote Clinical Trial Investigator Jobs
Job vor 2 Tagen bei Stellenanzeigen.de gefunden
Fraunhofer- Institut für Translationale Medizin und Pharmakologie ITMP
• Niedersachsen 37075
Teilzeit Homeoffice möglich
Jobticket 30+ Urlaubstage Tarifvertrag Vermögenswirksame Leistungen
[. .. ] Nervensystems in Folge gestörter Funktionen des Immunsystems. Die von uns gewonnenen Erkenntnisse sollen möglichst bald den Weg in die klinische Anwendung finden. Ergebnisse der Grundlagenforschung können durch [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] unsere Fraunhofer Early Clinical Trial Unit (ECTU) am Universitätsklinikum Göttingen zügig Bench to Bedside in neue Therapieansätze überführt werden. Hier sorgen Sie für Veränderung Für unsere Abteilung ECTU suchen wir Sie als Studienassistenz/ Study Nurse. Hier arbeiten Sie aktiv bei der Umsetzung der Projekte und in der Organisation des Stationsbereichs mit. Ihre Mitarbeit umfasst die [. .. ] etc. ) , Entnahme, Aufbereitung und Versand von Blutproben sowie Meldung unerwünschter Ereignisse an die Studienleitung Organisation und Koordination von klinischen Prüfungen in der Neurologie Qualitätssicherung, Datenbankpflege und Pflege des Investigator Site Files sowie Verwaltung und Archivierung der Prüfarztordner und CRFs Vor- und Nachbereitung sowie Begleitung von Schulungen, Initiierungen, Monitorbesuchen und Behördeninspektionen Korrespondenz und Terminkoordination mit Studienpatientinnen und Ärztinnen Hiermit bringen Sie sich ein Abgeschlossene medizinische Berufsausbildung zum/zur Gesundheits- und Krankenpflegerin, Arzthelferin oder Medizinisch-technischen Assistentin (MTA) Praxis im klinischen [. .. ]
Job vor 2 Tagen bei Neuvoo.com gefunden
Jazz Pharmaceuticals
Associate Director, Head of MSL Oncology, Germany
• Munich Muenchen
Führungs-/ Leitungspositionen
[. .. ] alignment and collaboration. Execution of Medical Strategy and Scientific Excellence: Drive the effective execution of the medical strategy and associated plans. Maintain and continuously develop deep expertise [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in oncology-related clinical and scientific literature to position both yourself and the team as trusted subject matter experts. Strategically plan and engage with national Key External Experts (KEEs) to maximize scientific exchange and collaboration. Support data generation initiatives, including the reactive evaluation of Investigator Sponsored Trial (IST) proposals. Uphold the highest standards of pharmacovigilance, compliance, and adherence to SOPs. Ensure the delivery of accurate, high-quality medical information to both internal stakeholders and external customers. Strategic Cross-Functional Collaboration and Insight Integration: Ensure delivery of the German Oncology Medical Affairs field strategy and plan in close [. .. ]
Job vor 2 Tagen bei JobMESH gefunden
Jazz Pharmaceuticals
• Bavorsko Mnichov
Führungs-/ Leitungspositionen
[. .. ] alignment and collaboration. Execution of Medical Strategy and Scientific Excellence: Drive the effective execution of the medical strategy and associated plans. Maintain and continuously develop deep expertise [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in oncology-related clinical and scientific literature to position both yourself and the team as trusted subject matter experts. Strategically plan and engage with national Key External Experts (KEEs) to maximize scientific exchange and collaboration. Support data generation initiatives, including the reactive evaluation of Investigator Sponsored Trial (IST) proposals. Uphold the highest standards of pharmacovigilance, compliance, and adherence to SOPs. Ensure the delivery of accurate, high-quality medical information to both internal stakeholders and external customers. Strategic Cross-Functional Collaboration and Insight Integration: Ensure delivery of the German Oncology Medical Affairs field strategy and plan in close [. .. ]
Job vor 2 Tagen bei Stellen-Online.de gefunden
Fraunhofer- Institut für Translationale Medizin und Pharmakologie ITMP
Studienassistenz/ Study Nurse (all genders) - Teilzeit
• Göttingen, 37081 Goettingen
Teilzeit
Jobticket 30+ Urlaubstage Tarifvertrag Vermögenswirksame Leistungen
[. .. ] Nervensystems in Folge gestörter Funktionen des Immunsystems. Die von uns gewonnenen Erkenntnisse sollen möglichst bald den Weg in die klinische Anwendung finden. Ergebnisse der Grundlagenforschung können durch [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] unsere Fraunhofer Early Clinical Trial Unit (ECTU) am Universitätsklinikum Göttingen zügig Bench to Bedside in neue Therapieansätze überführt werden. Hier sorgen Sie für Veränderung Für unsere Abteilung ECTU suchen wir Sie als Studienassistenz/ Study Nurse. Hier arbeiten Sie aktiv bei der Umsetzung der Projekte und in der Organisation des Stationsbereichs mit. Ihre Mitarbeit umfasst die [. .. ] etc. ) , Entnahme, Aufbereitung und Versand von Blutproben sowie Meldung unerwünschter Ereignisse an die Studienleitung Organisation und Koordination von klinischen Prüfungen in der Neurologie Qualitätssicherung, Datenbankpflege und Pflege des Investigator Site Files sowie Verwaltung und Archivierung der Prüfarztordner und CRFs Vor- und Nachbereitung sowie Begleitung von Schulungen, Initiierungen, Monitorbesuchen und Behördeninspektionen Korrespondenz und Terminkoordination mit Studienpatientinnen und Ärztinnen Hiermit bringen Sie sich ein Abgeschlossene medizinische Berufsausbildung zum/zur Gesundheits- und Krankenpflegerin, Arzthelferin oder Medizinisch-technischen Assistentin (MTA) Praxis im klinischen [. .. ]
Job vor 11 Tagen bei Mindmatch.ai gefunden
Blueprint Medicines, a Sanofi company
• AT- 9 Wien
Homeoffice möglich
[. .. ] role in driving the success of Blueprints mission to improve and extend the lives of as many patients as possible through precision therapy. You will be a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] reliable bridge between clinical research market access and commercialization and within the overall organization building strong relationships and collaboration with external and internal stakeholders. As a Field Medical Advisor you will be living and sharing our core values and will be driven by the pursuit of new ideas new innovations and new ways of [. .. ] of Blueprint Medicines company sponsored symposia and other activities. Reviews and signs off local educational and promotional material as the responsible information officer for the corresponding indication and of clinical trial treatment plans and protocols of Phase IV projects in line with local compliance regulations. Supports interventional and non-Interventional clinical trials in close collaboration with with Clinical development Clinical Operations and Global Medical Affairs teams. Ensures a strategic approach to such programs and the development of clinical data to support [. .. ] products. Works with colleagues of Blueprint Medicines International headquarter in Zug and other countries in the international region to ensure consistency of clinical programs from a medical perspective. Ensures that Investigator Initiated Research studies are in line with the global strategy. Helps to detect need for and enables Real World Evidence generation when required for advancing therapeutic area a/ o for access needs. Collaborates closely with market access for HEOR access required information What minimum qualifications do we require Advanced Clinical/ [. .. ]
Job vor 11 Tagen bei Mindmatch.ai gefunden
bio Mrieux
Medical Scientific Liaison (MSL) for Austria and Switzerland (m/f/d)
• AT- 9 Wien
[. .. ] understand patient care pathways and their needs in terms of unmet medical needs, medical information and medical education. Contribute to evidence generation by participating in company-sponsored postmarket [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] studies, supporting Investigator Initiated Trials (IITs) in line with global strategy and according to Medtech requirements and bio Mrieux SOPs, and supporting clinical development initiatives including site identification, trial recruitment, registry and presentation of final approved data. Provide operational and medical support to marketing and sales teams (Account Managers, Clinical Education Managers, Business Developers) . Qualifications Academic degree in Medicine or Pharmacology. Advanced scientific degree (MD, Ph D, Pharm D) with relevant industry experience is desirable. Experience in the therapy area [. .. ]
Job vor 12 Tagen bei Mindmatch.ai gefunden
IQVIA Argentina
• AT- 9 Wien
[. .. ] completion of regulatory and contractual documents for individual sites. Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] (ICF) , and Investigator Pack (IP) release documents, in line with project timelines. Provide local expertise to SAMs and project team during initial and on-going project timeline planning. Perform quality control of documents provided by sites. May have direct contact with sponsors on specific initiatives. Qualifications B Sc Degree in Life Sciences or related field 1-3 years clinical research experience German language proficiency is essential for direct communication with the Competent Authority and Ethics Committees. Good interpersonal communication and organizational skills. Good technology skills and knowledge of MS Office applications. Good attention to detail. General awareness clinical trial environment and drug development process. Ability to work on multiple projects. Ability to establish and maintain effective working relationships with co-workers, managers and sponsors. Ability to work independently, to problem-solve collaboratively and to raise issues appropriately as needed. IQVIA is a leading global provider of clinical research services, [. .. ]
Job am 17.11.2025 bei Mindmatch.ai gefunden
Syneos Health
Experienced CRA Austria
• AT- 9 Wien
Experienced CRA Austria Syneos Health Application open. Position sought for Experienced
Clinical Research Associate in Austria. Description Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model places the customer and the patient at the center of [. .. ] provide recommendations, communicate/ escalate serious issues, and develop action plans. Verify informed consent procedures are performed and documented for each subject, protecting confidentiality and assessing safety and data integrity at investigator sites. Based on the Clinical Monitoring/ Site Management Plan, assess site processes, conduct source document review, verify CRF data accuracy, resolve queries remotely or onsite, support data capture and electronic data capture compliance. Perform IP inventory, reconciliation, storage and security review, and confirm correct dispensing and administration of study product. Review Investigator Site File accuracy and completeness, reconcile with the Trial Master File, and ensure compliance with archiving regulations. Document activities via letters, reports, logs per SOPs, support subject recruitment and retention, enter data into tracking systems with ongoing status and action items. Understand project scope, budgets, and timelines; manage sitelevel activities to meet objectives and adapt to changing priorities. Act [. .. ]
Job am 17.11.2025 bei Mindmatch.ai gefunden
IQVIA
Regulatory Start Up Specialist I, IQVIA Med Tech, Austria
• AT- 9 Wien
[. .. ] completion of regulatory and contractual documents for individual sites. Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] (ICF) , and Investigator Pack (IP) release documents, in line with project timelines. Provide local expertise to SAMs and project team during initial and on-going project timeline planning. Perform quality control of documents provided by sites. May have direct contact with sponsors on specific initiatives. Qualifications B Sc Degree in Life Sciences or related field 1-3 years clinical research experience German language proficiency is essential for direct communication with the Competent Authority and Ethics Committees. Good interpersonal communication and organizational skills. Good technology skills and knowledge of MS Office applications. Good attention to detail. General awareness clinical trial environment and drug development process. Ability to work on multiple projects. Ability to establish and maintain effective working relationships with co-workers, managers and sponsors. Ability to work independently, to problem-solve collaboratively and to raise issues appropriately as needed. IQVIA is a leading global provider of clinical research services, [. .. ]
Job am 14.10.2025 bei Mindmatch.ai gefunden
Syneos Health
CRA Austria
• AT- 9 Wien
2 days ago Be among the first 25 applicants Description CRA Austria Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to [. .. ] 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 form (CRF) is accurate and complete. [. .. ] to ensure IP is appropriately (re) labelled, imported and released/returned. Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness. Reconciles contents of the ISF with the Trial Master File (TMF) . Ensures the investigator/ physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations. Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/ Site [. .. ]
Job gestern bei Jobleads gefunden
• München, Bayern
Führungs-/ Leitungspositionen
TFS Health Science is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire
clinical development journey. Our expertise includes full [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] service-capabilities, resourcing and Functional Service (FSP) solutions. About this role As part of our Ophthalmology team you will working alongside passionate and innovative professionals to ensure our customers achieve their goals. Key Responsibilities Expert Guidance : Provide advanced medical input on study design, measurement strategies, and trial protocols, including safety sections and investigator brochures. Comprehensive Safety Oversight : Review safety data such as adverse events, labs, vital signs, ECGs, and clinical trial reports from a medical perspective. Regulatory Risk Support : Conduct senior-level medical reviews of individual cases, cumulative listings, PSURs, PBRERs, DSURs, and Risk Management Plans. Medical Monitoring Signal Detection : [. .. ]
Job am 20.10.2025 bei Jobleads gefunden
Clinical Site Contracts Lead client-based in Munich
• München, Bayern
Führungs-/ Leitungspositionen
Clinical Site Contracts Lead clientbased in Munich Are you ready to take your expertise in clinical contracts and budgeting to the next level? At Fortrea, we are looking for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a detailoriented and strategic professional to join our FSP team as a Site Contract Lead. In this role, you will be at the forefront of clinical trial execution, ensuring that contracts and budgets are aligned with operational goals and regulatory standards. This role offers a hybrid model (50 at clients office in Munich) . Key Responsibilities Serve as the primary point of contact for study teams on all matters related to clinical trial budgets and contracts. Prepare [. .. ] Clinical Trial Management Systems and contract management platforms. Identify and elevate business risks appropriately while supporting internal teams with contractrelated guidance. Support payment tracking, invoice preparation, and financial reconciliation for investigator sites as needed. Required Qualifications Bachelors degree in life sciences, business, or a related field; equivalent experience may be considered. Minimum of 2 years experience negotiating legal and/or financial agreements, preferably in clinical research or the pharmaceutical industry. Strong understanding of ICHGCP guidelines, clinical trial startup processes, and site [. .. ]
Job am 10.10.2025 bei Jobleads gefunden
• München, Bayern
Firmenwagen 30+ Urlaubstage
[. .. ] global specialty pharma business and a preferred partner for innovator pharma companies, instigating a paradigm shift in the life cycle management of iconic medicines. We seek to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] extensively engage with clinical communities to communicate product improvements and prioritise environmental, social, and governance considerations across the business and workforce. Pharmanovias therapeutic areas include Cardiovascular, Oncology, Endocrinology and Neurology. About the role: Reporting to the Medical Department, you will be a member of MSL team, whose primary responsibility is to interact with influential stakeholders and healthcare providers. You will collaborate with physicians and other medical experts to support trial management, RWE initiatives, interact with patient organisations, and ensure that healthcare professionals have the most up-to-date information about medical and clinical benefits of Pharmanovias products. Setting up strategies to target the most relevant HCPs for Pharmanovias therapeutic efforts and coordinate and align key messages to position Pharmanovia as [. .. ] and maintaining professional relationships with national/ regional KOLs, establishing peer-to-peer collaborations with key medical experts in the therapeutic areas covered by Pharmanovia Supporting evidence generation initiatives including potential investigator site identification, trial recruitment, registries, and presentation of final approved data, involving experts to generate scientific data including investigator-initiated trials Collaborating with physicians on medical affairs initiatives including publication and communication plans, advisory boards, medical education opportunities, webinars, training, and speaker development Serving as a scientific peer-to-peer [. .. ]
Job am 27.09.2025 bei Jobleads gefunden
Medical Director Hematology Oncology, Country Medical Director Germany (m/f/d)
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] Overview This person will actively participate/ lead a broad range of medical affairs activities in Oncology/ Hematology such as the development of medical strategies for Germany, the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] preparation support of investigator initiated research (IIR) programs, the management of the German Medical Science Liaisons (MSL) team and the medical review of Medical Affairs materials/ promotional materials. In addition, the role has oversight over the Clinical Operations team for Oncology/ Hematology and IAI/ Dermatology. Duties And Responsibilities Represent Germany in the Incyte International Medical Affairs Leadership Team, give appropriate feedback to global and regional initiatives Assure development of effective medical strategies and their local execution in accordance with local leadership team Develop, lead and manage German [. .. ] in academic, clinical, or industry setting required Successful people management experience required with min 2+ years Hematology/ oncology experience required Familiarity with GCP/ ICH/ FDA requirements as well as clinical trial design, biostatistics, medical writing, product safety, and regulatory affairs Strong interpersonal, verbal and written communication skills. Strong public speaking skills Excellent leadership and management skills Ability to influence and work effectively across functions and operate in a matrix environment Ability to travel up to 30 of working time Disclaimer: The [. .. ]
Job am 16.09.2025 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] involvement on assigned trials. Serve as a medical expert during project delivery lifecycle. Provide therapeutic and medical expertise to business development activities. Essential Functions Medical Monitoring: Primarily serves as Global Medical Advisor on [. .. ] 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 medical case review of Serious Adverse Events (SAEs) , including review of case documentation and patient narrative, in collaboration with the Pharmacovigilance department. May provide medical support for the Analysis of Similar Events (AOSE) , in collaboration with or on behalf of Pharmacovigilance [. .. ]
Job am 27.06.2025 bei Jobleads gefunden
Senior/ Medical Director (Ophthalmology) 0.5 FTE
Führungs-/ Leitungspositionen
[. .. ] Senior/ Medical Director (Ophthalmology) , 0.5 FTE. TFS Health Science is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] their clinical development journey. Join our team as a Senior/ Medical Director (Ophthalmology) . The Senior/ Medical Director is a key member of the Project Delivery team, working independently to manage safety and medical matters in line with company policies, standard operating procedures (SOPs) , and regulatory requirements. With deep medical expertise, [. .. ] on medical issuesproviding clear, informed guidance and answering complex questions related to medical, legal, and regulatory concerns. Responsibilities Expert Guidance: Provide advanced medical input on study design, measurement strategies, and trial protocols, including safety sections and investigator brochures. Comprehensive Safety Oversight: Review safety data such as adverse events, labs, vital signs, ECGs, and clinical trial reports from a medical perspective. Regulatory Risk Support: Conduct senior-level medical reviews of individual cases, cumulative listings, PSURs, PBRERs, DSURs, and Risk Management Plans. Medical Monitoring Signal Detection: Serve as a [. .. ]
Job gestern bei Jobleads gefunden
• Zürich Zuerich
[. .. ] Affairs colleagues to support regional deliverables (e. g. , scientific support, internal/ external presentations) Monitor competitive activities and emerging trends within relevant therapeutic areas Provide medical training [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] for commercial Support clinical trial operations to ensure success with planned and ongoing clinical trials to include identifying, supporting, and regularly engaging clinical trial investigators, and sites External engagement insights (50 field based, covering all of Switzerland) Develop and maintain a KOL engagement plan that fosters collaborative relationships in Switzerland Provide medical/ scientific presentations to [. .. ] medical congresses such as participation in clinical data presentations, scientific exchange at the medical affairs booth, and internal or external meetings Engage with external researchers as a primary contact for investigator-initiated trials (IITs) Ensure successful patient access initiatives by managing medical access programs and collaborating on regulatory and market access dossier Your profile Advanced degree (MD, Pharm D, Ph D) in a relevant scientific field Experience as Medical Science Liaison (MSL) and Medical Manager in a Swiss subsidiary of a smaller pharmaceutical [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Sr Manager, Field Medical Affairs Hematology (West Germany)
[. .. ] with key opinion leaders, healthcare providers, and investigators, serving as a trusted scientific resource and strategic partner. Youll play a meaningful role in crafting the understanding of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Regenerons therapies, supporting clinical development and investigator-initiated research, and contributing to impactful product launches. This is an exciting opportunity to work at the forefront of science while influencing the future of hematology care. A Typical Day: Building and handling relationships with KOLs in malignant hematology. Acting as a primary clinical/ scientific contact for HCPs and investigators. Sharing medical insights to advise strategy and development plans. Supporting clinical trial execution by identifying investigators and trial sites. Collaborating on abstracts, posters, and manuscripts to communicate data. Contributing to investigator-initiated study programs and research collaborations. Attending medical congresses to gather and report competitive intelligence. Partnering cross-functionally with Medical Affairs, Commercial, and Market Access. This Role May Be For You: [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Clinical Scientist-Manager/ Senior Manager (m/f/d) Direct message the job poster from Tubulis Gmb H Be part of our team As a Clinical Scientist (m/f/d) and member of our Clinical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Development team, you will support the planning and execution of full life-cycle development of our antibody-drug conjugates (ADCs) global clinical trials. You will support the review, analysis, and interpretation of clinical trial data, contribute to the development of critical clinical trial documents, and take an active role in risk monitoring and mitigation. You will be part of a highly collaborative and crossfunctional team involved with site evaluation, study startup, study execution and management, and study closeout of our trials. This position will [. .. ] of study data to ensure timely and highquality data entry, including review of case report forms, assist in coding, analysis, and proper and complete documentation of clinical data. Participate in investigator meetings, investigator engagement, including assisting in the preparation of Advisory Board meetings. Support the Medical Director in managing sites to ensure study treatment discontinuation or other safety decisions are made per protocol and align with stakeholders within the study team. Support the Medical Director to coordinate relevant and timely data [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Associate Director-Early Development Lead
Führungs-/ Leitungspositionen
[. .. ] are looking for an Associate Director, Early Development Lead who is a strategic safety leader responsible for designing and implementing safety surveillance and risk management strategies for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] preclinical and early clinical assets. Apply scientific and medical judgement to analyse safety data, develop risk mitigation plans, and contribute to regulatory submissions. Be the safety representative on research and early development teams, ensuring understanding of regulatory, company, and stakeholder safety expectations. Your Role: Develop and implement risk mitigation strategies for early development assets [. .. ] setup and evaluation of preclinical data packages, identify new risks, and determine needs for supplementary data. Respond promptly to regulatory agency safety requests. Ensure risk mitigations are reflected in clinical trial documents (protocols, investigator brochures, informed consent forms) . Provide guidance on safety issues and facilitate internal/ external safety reviews (e. g. , DMCs) . Represent GSPV in crossfunctional teams and chair safety management teams. Your Experience: PHD degree or medical degree (Doctors) with exposure to basic research work Minimum 5 years in pharmaceutical/ [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
Clinical and Preclinical Quality Director
• Basel- Landschaft
Führungs-/ Leitungspositionen
Summary The
Clinical and Preclinical Quality Director (CQD) will lead the development, implementation, and communication of high-quality standards to ensure the delivery of global clinical studies. With a focus [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] on proactive quality management, this role supports Clinical Development by driving quality excellence, safeguarding data integrity, and enabling R D objectives for the [. .. ] global clinical processes, procedural documents, and applicable Quality Compliance manual documents, in line with international guidelines, such as ICH-GCP, industry standards, and local regulations. Provide expert guidance on clinical trial regulations, monitor regulatory changes, and ensure local teams and processes remain current and compliant. Plan and conduct quality control activities in line with the annual quality plan, including performing accompanied site visits. Perform any required QC visits/ QC activities. Regularly reviews protocol deviations and ensures timely reporting of quality issues [. .. ] preferably in a life science discipline. Minimum 10 years of relevant experience in clinical and preclinical Quality, including significant experience in a GCP-regulated environment with clinical trial management and investigator site compliance ICH-GCP, ISO 9001, or CCRP certifications preferred. GMP knowledge preferred. Excellent working knowledge of international ICH-GCP guidelines and relevant local regulations, GLP regulations, and preclinical expectations. Strong understanding of the drug development process and related GXP activities. Solid understanding of the skills and knowledge required for [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
Clinical Operations Specialist-Munich area
• München, Bayern
Clinical Operations Specialist-Munich area 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything [. .. ] and Work Instructions. Assist Clinical Monitoring staff with site management activities, acting as a Sponsor representative for assigned studies and communicating with sites to ensure protocol compliance. Create and maintain Trial Master Files (TMF) and project files, including participation in file audits. Prepare and maintain site manuals, reference tools, and other documents. Maintain, update, and input clinical tracking information into databases. Track incoming and outgoing clinical and regulatory documents and updates for investigator sites, studies, project team, or client. Manage shared mailbox, process site requests, and route correspondence appropriately. Coordinate the ordering, packaging, shipping, and tracking of site supplies and materials. Assist with coordination of team meetings, attend meetings, and prepare accurate meeting minutes and action items. Handle receipt, tracking, and disposition of [. .. ]
Job vor 14 Tagen bei Jobleads gefunden
Clinical Research Associate
• Darmstadt, Hessen
Homeoffice möglich
Clinical Research Associate # Clinical Research Associate Darmstadt Vollzeit Kein Home Office möglich Clinical Research Associate Veeda Lifesciences is seeking a Clinical Research Associate (CRA) based in Germany for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] its growing international hematology/ oncology Clinical Trials program. This is a full-time job. Job overview: The CRA is responsible for ensuring that the conduct of a clinical trial at selected Investigational Sites is according to the currently approved protocol/ amendments, ICH GCP guidelines, the applicable Standard Operating Procedures (SOPs) and the applicable laws and regulations. He/ she is the primary responsible person for communication on operational study related activities between the Sponsor, the Investigator and other study personnel to build and maintain successful working relationships. The most important responsibility is to ensure that the subjects rights are respected and that all collected clinical trial data are accurate, complete, and verifiable from source documents. Main responsibilities:-Acknowledges, follows ensures compliance with the Companys Quality and [. .. ]
Job vor 14 Tagen bei Jobleads gefunden
Clinical Scientist-Manager/ Senior Manager (m/f/d)
• Köln, Nordrhein- Westfalen
Be part of our team As a
Clinical Scientist (m/f/d) and member of our Clinical Development team, you will support the planning and execution of full life-cycle development of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] our antibodydrug conjugates (ADCs) global clinical trials. You will support the review, analysis, and interpretation of clinical trial data, contribute to the development of critical clinical trial documents, and take an active role in risk monitoring and mitigation. You will be part of a highly collaborative and crossfunctional team involved with site evaluation, study startup, study execution and management, and study closeout of our trials. This position will [. .. ] of study data to ensure timely and highquality data entry, including review of case report forms, assists in coding, analysis, and proper and complete documentation of clinical data. Participate in investigator meetings, investigator engagement, including assisting in the preparation of Advisory Board meetings. Support the Medical Director in managing sites to ensure study treatment discontinuation or other safety decisions are made per protocol and align with stakeholders within the study team. Support the Medical Director to coordinate relevant and timely data [. .. ]
Job vor 14 Tagen bei Jobleads gefunden
Clinical Scientist-Manager/ Senior Manager (m/f/d)
• Düsseldorf, Nordrhein- Westfalen
Be part of our team As a
Clinical Scientist (m/f/d) and member of our Clinical Development team, you will support the planning and execution of full life-cycle development of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] our antibodydrug conjugates (ADCs) global clinical trials. You will support the review, analysis, and interpretation of clinical trial data, contribute to the development of critical clinical trial documents, and take an active role in risk monitoring and mitigation. You will be part of a highly collaborative and crossfunctional team involved with site evaluation, study startup, study execution and management, and study closeout of our trials. This position will [. .. ] of study data to ensure timely and highquality data entry, including review of case report forms, assists in coding, analysis, and proper and complete documentation of clinical data. Participate in investigator meetings, investigator engagement, including assisting in the preparation of Advisory Board meetings. Support the Medical Director in managing sites to ensure study treatment discontinuation or other safety decisions are made per protocol and align with stakeholders within the study team. Support the Medical Director to coordinate relevant and timely data [. .. ]
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Wieviel verdient man als Clinical Trial Investigator pro Jahr?
Als Clinical Trial Investigator verdient man zwischen EUR 65.000,- bis EUR 95.000,- im Jahr.
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Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Trial Investigator Stellenangebote:
- Tigermed (32 Jobs)
- Tubulis GmbH (11 Jobs)
- Medpace (8 Jobs)
- Jazz Pharmaceuticals (2 Jobs)
- Syneos Health (2 Jobs)
In welchen Bundesländern werden die meisten Clinical Trial Investigator Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trial Investigator Jobs werden derzeit in Nordrhein-Westfalen (23 Jobs), Bayern (18 Jobs) und Niedersachsen (10 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trial Investigator Jobs?
Clinical Trial Investigator Jobs gehören zum Berufsfeld Medizinisch-technische Assistenz / MTA.
