127 Jobs für Clinical Trial Investigator
Stellenangebote Clinical Trial Investigator Jobs
Job vor 2 Tagen bei StepStone gefunden
Universitätsklinikum Tübingen
• Tübingen Tuebingen
Führungs-/ Leitungspositionen Teilzeit Homeoffice möglich
Flexible Arbeitszeiten Work-Life-Balance
[. .. ] der KTQ zertifiziert. Über die Abteilung Das Nationale Centrum für Tumorerkrankungen (NCT Südwest, Standort Tübingen) in Verbindung mit der Abteilung Innere Medizin VIII, Medizinische Onkologie und Pneumologie, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] sucht Prüfärzte/ Principal Investigator/ Sub-Investigator zur Betreuung von frühen Onkologischen Studien. In unserem NCT Clinical Trial Center (CTC) und in unserer Early Clinical Trial Unit (ECTU) werden vielfältige klinische Studien mit Schwerpunkten in den Bereichen Molekulare Tumortherapien und Immuntherapien durchgeführt. Oberärztin/ Oberarzt oder Fachärztin/ Facharzt onkologische Studien (w/m/d) Medizinische Universitätsklinik, Nationales Centrum für Tumorerkrankungen und Medizinische Onkologie und Pneumologie, Kennz. 7231 Voll-/ Teilzeit: 50-[. .. ]
Job gestern bei Jooble gefunden
Study Physician sponsor dedicated in Germany
• München
Study Physician sponsor dedicated in 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] Doctors (Candidates who completed fellowship, residency, specialization e. g. Internal medicine, oncology, neurology, immune-oncology, cardiology, pediatrics, emergency medicine are preferred) with following experience: Global Medical Monitor/ Study Physician/ Clinical Trial Physician managing phase I to IV clinical trials in CRO/ Pharma company. Global Project Manager/ Clinical Trial leader/ Project manager managing multiple countries in CRO/ Pharma company. Country Trial Manager/ Local Project Manager/ Project Manager USA in CRO/ Pharma company Global Safety Physician/ Risk Management Physician in Pharmacovigilance department in [. .. ] requirements too) Medical Monitoring experience preferred Pharma company experience preferred. However, CRO experience is fine. If no industry experience, the in addition to clinical practice they should have worked principal investigator/ sub investigator in clinical trials for a reasonable amount of time. Travel-15-20 depending on the study requirements. Key words to look for in potential CVs-Clinical Trial protocol-writing/ reviewing, Identify medically relevant critical data, Medical risks, risk mitigation/ monitoring plan, Medical quality review/clinical quality monitoring, Jreview, [. .. ]
Job vor 3 Tagen bei Jooble gefunden
• Berlin
The Regional Medical Science Liaison (MSL) serves as the primary field-based point of contact with healthcare providers (HCPs) including
clinical investigators on a range of clinical and scientific issues. The [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] primary role is to deliver and facilitate medical education and communications, research, and scientific insight gathering activities of the client. This includes the provision of scientific and medical data on both licensed and unlicensed products and indications as permissible by [. .. ] aligned to strategy within the business Serves as external, credible scientific expert on disease area and client products at HCP field meetings, key medical and scientific conferences, advisory boards, clinical investigator meetings and patient advocacy group meetings Facilitate clear communication between the client and investigators in investigator engagement for both client trials and investigator-sponsored studies and barriers to enrolment for pipeline assets Works to the highest ethical compliance, ethics and safety standards adhering to all local regulations and laws Maintains [. .. ] or rare disease experience preferred or experience in endocrinology or lipidology experience Knowledge of clinical research design and GCP in the cardiology area Demonstrate a strong understanding of clinical research trial design and study analysis including cost effectiveness and other high-level HEOR evidence approaches Demonstrate ability to develop trust and maintain integrity with KOLs/ External Clinical and Scientific Experts, investigators, HCPs, and institutions, as well as with peers, and others Ability to convey complex scientific concepts and information appropriately tailored [. .. ]
Job vor 4 Tagen bei Jooble gefunden
Sr CRA in oncology-Sponsor dedicated-Home Based Germany
• München
Sr CRA in oncology-Sponsor dedicated-Home Based Germany Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and commercial [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to [. .. ] 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 via [. .. ] 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 vor 4 Tagen bei Jooble gefunden
Universitätsklinikum Tübingen
• Tübingen
Flexible Arbeitszeiten Tarifvertrag Work-Life-Balance
[. .. ] der KTQ zertifiziert. Über die Abteilung Das Nationale Centrum für Tumorerkrankungen (NCT Südwest, Standort Tübingen) in Verbindung mit der Abteilung Innere Medizin VIII, Medizinische Onkologie und Pneumologie, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] sucht Prüfärzte/ Principal Investigator/ Sub-Investigator zur Betreuung von frühen Onkologischen Studien. In unserem NCT Clinical Trial Center (CTC) und in unserer Early Clinical Trial Unit (ECTU) werden vielfältige klinische Studien mit Schwerpunkten in den Bereichen Molekulare Tumortherapien und Immuntherapien durchgeführt. Kontakt bei Fragen Prof. Ulrich Lauer 0172 7491027 Bewerbungsadresse Herrn Prof. Ulrich Lauer Kennziffer: 7231 Gewünschte Bewerbungsunterlagen: Lebenslauf, Motivationsschreiben Bewerbungsfrist: 28.02.2026 Wir wenden den [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
Contract Clinical Research Associate
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening [. .. ] Standard Operating Procedures (SOPs) and business processes, if applicable. Trains study site personnel on the protocol and applicable regulatory requirements in collaboration with pertinent project team members. Supports with Clinical Trial Application submissions, including relevant informed consent local changes and translations into local language as required. Supports remote monitoring, if and as applicable. Negotiates investigator/ hospital agreements with stakeholders. Supports new and innovative processes and technologies to increase the quality, productivity, and efficiency of Clinical Operations and conserve overall departmental operating costs. Appropriate life-science or healthcare-related qualification or experience or equivalent work experience. One year of clinically-related experience in a medical profession, [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening [. .. ] Standard Operating Procedures (SOPs) and business processes, if applicable. Trains study site personnel on the protocol and applicable regulatory requirements in collaboration with pertinent project team members. Supports with Clinical Trial Application submissions, including relevant informed consent local changes and translations into local language as required. Supports remote monitoring, if and as applicable. Negotiates investigator/ hospital agreements with stakeholders. Supports new and innovative processes and technologies to increase the quality, productivity, and efficiency of Clinical Operations and conserve overall departmental operating costs. Appropriate life-science or healthcare-related qualification or experience or equivalent work experience. One year of clinically-related experience in a medical profession, [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
Clinical Study Specialist (Contract)
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening [. .. ] Standard Operating Procedures (SOPs) and business processes, if applicable. Trains study site personnel on the protocol and applicable regulatory requirements in collaboration with pertinent project team members. Supports with Clinical Trial Application submissions, including relevant informed consent local changes and translations into local language as required. Supports remote monitoring, if and as applicable. Negotiates investigator/ hospital agreements with stakeholders. Supports new and innovative processes and technologies to increase the quality, productivity, and efficiency of Clinical Operations and conserve overall departmental operating costs. Appropriate life-science or healthcare-related qualification or experience or equivalent work experience. One year of clinically-related experience in a medical profession, [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening [. .. ] Standard Operating Procedures (SOPs) and business processes, if applicable. Trains study site personnel on the protocol and applicable regulatory requirements in collaboration with pertinent project team members. Supports with Clinical Trial Application submissions, including relevant informed consent local changes and translations into local language as required. Supports remote monitoring, if and as applicable. Negotiates investigator/ hospital agreements with stakeholders. Supports new and innovative processes and technologies to increase the quality, productivity, and efficiency of Clinical Operations and conserve overall departmental operating costs. Appropriate life-science or healthcare-related qualification or experience or equivalent work experience. One year of clinically-related experience in a medical profession, [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
Clinical Senior Research Associate
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening [. .. ] Standard Operating Procedures (SOPs) and business processes, if applicable. Trains study site personnel on the protocol and applicable regulatory requirements in collaboration with pertinent project team members. Supports with Clinical Trial Application submissions, including relevant informed consent local changes and translations into local language as required. Supports remote monitoring, if and as applicable. Negotiates investigator/ hospital agreements with stakeholders. Supports new and innovative processes and technologies to increase the quality, productivity, and efficiency of Clinical Operations and conserve overall departmental operating costs. Appropriate life-science or healthcare-related qualification or experience or equivalent work experience. One year of clinically-related experience in a medical profession, [. .. ]
Job vor 8 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Job Description Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening [. .. ] study site conduct accurately and completely. Prepare and submit written reports, both monitoring and administrative, with appropriate supervision. Keep management informed of study progress through periodic updates. Supports with Clinical Trial Application submissions, including relevant informed consent local changes and translations into local language as required. Supports remote monitoring, if and as applicable. Assists in study budget preparation and clinical study agreement execution, including ensuring necessary payments are made according to executed agreements. Negotiates investigator/ hospital agreements with stakeholders. Maintains and completes own expense reports as per local and applicable guidelines. Supports new and innovative processes and technologies to increase the quality, productivity, and efficiency of Clinical Operations and conserve overall departmental operating costs. Qualifications Appropriate life-science or healthcare-related qualification or experience or [. .. ]
Job vor 14 Tagen bei Jooble gefunden
Thermo Fisher Scientific
Clinical Trial Coordinator II (m/f/d) - Germany
• Karlsruhe
[. .. ] safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on now and in the future. Location/ Division Specific Information Our clinical department defines, develops and delivers clinical programmes. We ensure the highest-quality review of data and effective interaction with study sites, [. .. ] We invite you to re-imagine health promoting protocols with us, working alongside our dedicated, forward-thinking and upbeat teams. A day in the Life: Performs PPD clinical research services investigator file reviews and logging of outstanding issues in project related tracking tools Reviews regulatory documents for proper content Liaises with monitor and investigative sites to resolve outstanding regulatory issues identified Disseminates study related information, including project tracking updates to Clients, clinical study teams and other PPD clinical research services departments [. .. ]
Job am 17.01.2026 bei Jooble gefunden
Alira Health
• München
[. .. ] values: be courageous, be accountable, be honest, be inclusive and elevate others. Job Description Summary Job Description ROLE The Project Manager (PM) is an important member of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Alira Health Clinical team. The PM ensures the efficient implementation of one or more study protocols, works closely with all Clinical team members, and communicates directly with study sponsors and vendors. KEY RESPONSABILITIES Manages clinical research studies to ensure studies are conducted in accordance with approved scope of work/ budget, ICH GCP guidelines, [. .. ] documents, including protocols, ICF templates, study budgets, site log/ form templates, study manuals and plans, site binders, etc. Drives and facilitates clinical teamwork and communications to ensure timely attainment of trial milestones. Ensures accuracy of reports and material work product. Provides monthly billing information to finance team. Presents at project meetings such as investigator meetings and new client meetings. Updates management accurately and regularly through frequent communication. Identifies issues and develops problem-solving strategies to ensure study timelines are met. Manages subject accrual, retention, and compliance. Assists in TMF management and manages TMF reviews as needed. Prepares for and participates in third-party audits [. .. ]
Job am 15.01.2026 bei Jooble gefunden
IGES GmbH
Wissenschaftliche Projektassistenz (m/w/d)
• Berlin
30+ Urlaubstage
[. .. ] CRO der IGES Gruppe erschließen wir ein breites Spektrum von Real World Daten. Wir forschen im Auftrag unserer Kunden darüber hinaus auch zu den Themen Inanspruchnahme, Medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Need, Patientenpräferenzen und Clinical Pathways. Zur Verstärkung und Unterstützung unseres Teams im Bereich der klinischen Forschung suchen wir zum nächstmöglichen Zeitpunkt eine Wissenschaftliche Projektassistenz (m/w/d) in Berlin. Ihre Aufgaben Mitarbeit bei der Erstellung von Kalkulationen und Angeboten Korrespondenz mit Behörden, Studienzentren und Auftraggebern Erstellung und Pflege des Trial Master Files (TMF) und Investigator Site Files (ISF) Mitwirkung an der Erstellung und Überprüfung von Studiendokumenten Mitarbeit bei Projekten im Qualitätsmanagement Einreichungen der klinischen Studien bei Ethik Kommissionen Pflege von Studiendaten in Datenbanken, Erstellung und Versand von Statusberichten Bestellung von Studienmaterial sowie Versand von Studiendokumenten Vor- und Nachbereitung von Meetings (inkl. Protokollführung) Ihre Qualifikation Hochschulabschluss [. .. ]
Job am 14.01.2026 bei Jooble gefunden
ICON
• Homeoffice
Work-Life-Balance
ICON plc is a world-leading healthcare intelligence and
clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve [. .. ] activities to meet the business objectives Maintain active/ frequent communication with internal/ external partners and/or investigators and internal departments regarding research contracts throughout the contract lifecycle Assist in developing investigator baseline budgets Review and negotiate the terms and conditions for various types of incoming and outgoing contracts and budgets in accordance with internal policy and ICH-GCP regulations Prepare subsequent contract amendments, note to files and other contract activities, as needed Develop and maintain status trackers, prepare start-up and [. .. ] all electronic records are kept up to date with the most current documentation and information You are: Previous experience working within a CRO/ Pharmaceutical organisation with specific experience negotiating clinical trial agreements with sites Exemplary communication skills including a fluency in English and German Excellent planning, prioritization and organization skills Ability to work as a team and develop relationships with others internally and externally Proactive attitude, perseverance and commitment to continuous development Law degree or training is nice to have What [. .. ]
Job am 14.01.2026 bei Jooble gefunden
(Junior-) Field Medical Advisor-Rare Oncology North
• Berlin
Absolventen, Einsteiger, Trainees
[. .. ] gifted cultivator of new and exciting opportunities grounded in science? The (Junior-) Field Medical Advisor serves as the primary field-based point of contact with healthcare providers (HCPs) [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] including clinical investigators on a range of clinical and scientific issues. The primary role is to deliver and facilitate medical education and communications, research, and scientific insight gathering activities of the client. This includes the provision of scientific and medical data on both licensed and unlicensed products and indications as permissible by [. .. ] aligned to strategy within the business Serves as external, credible scientific expert on disease area and client products at HCP field meetings, key medical and scientific conferences, advisory boards, clinical investigator meetings and patient advocacy group meetings Identify key field insights related to client products, activities and the disease area and effectively disseminate and collaborate with cross-functional partners Facilitate clear communication between the business and investigators in investigator engagement for both client trials and investigator-sponsored studies and barriers to [. .. ] Pharm D Demonstrable experience in an MSL function with oncology desired) Knowledge of clinical research design and GCP in the oncology/ immune oncology area Demonstrate a strong understanding of clinical research trial design and study analysis including cost effectiveness and other high-level HEOR evidence approaches Demonstrate ability to develop trust and maintain integrity with KOLs/ External Clinical and Scientific Experts, investigators, HCPs, and institutions; as well as with peers, and others Ability to convey complex scientific concepts and information appropriately tailored [. .. ]
Job am 14.01.2026 bei Jooble gefunden
• München
Freiberuflich
Freelance CRA Germany Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and commercial insights into outcomes [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to [. .. ] 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 am 14.01.2026 bei Jooble gefunden
Incyte Corporation
(Senior) Medical Manager Dermatology (m/f/d)
• München
[. .. ] Medical Affairs Inflammation Autoimmunity (IAI) Team and supports the development of the local medical strategy and medical plans within the therapeutic area of dermatology. The role provides [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a bridge between Clinical Development, Medical Affairs and the commercial organization. The (Senior) Medical Manager Dermatology will play a key role in developing and executing the medical and scientific (non-promotional) strategy for the German Immunology portfolio/ therapeutic area and will be involved in a wide range of activities for Incyte IAI drugs both [. .. ] marketing clinical activities such as registry/ database projects, epidemiological surveys, and PMOS studies) . Provide the required oversight to manage review, approval and conduct of IIR studies Collaborate with clinical trial teams and support investigator engagements (e. g. review new clinical study protocols, identifying potential investigators/ sites, conducting feasibility surveys) Supports adaptation of international/ local training and scientific material in collaboration with marketing and other internal stakeholders Supports development of publication plans and covers country data generation needs Provides scientific in-house training for MSLs, [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Biontech
• Berlin
Jobticket
[. .. ] aligned with local and European medical affairs priorities. Build and expand relationships/ networks with key medical and scientific experts in the field of breast cancer and/or lung [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] cancer. Support clinical trials by identifying study sites, participating in SIVs (Site Inviations Visits) , assisting with patient enrollment, and ensuring smooth information exchange. Identify research opportunities, including Investigator-Initiated Trials, Real-World Evidence, and other evidence-generation studies. Represent the organization at scientific conferences, advisory boards, and educational events, sharing insights and preparing reports for internal stakeholders. Ensure timely documentation of HCP interactions, compliance with local policies, and accurate reporting of insights and safety information. What you have [. .. ] Germany. Minimum 3 years of experience and an established network in Breast Cancer and/or Lung Cancer therapeutic areas, ideally within a pharmaceutical company. Strong expertise in GCP-compliant clinical trial support, with a solid understanding of trial design and execution. Exceptional ability to process, communicate, and present complex medical and scientific information effectively. Proven self-management and project management skills to independently plan and execute stakeholder engagement. Highest ethical standards with knowledge of clinical regulations, industry standards, and German codes [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Thermo Fisher Scientific
Local Clinical Trial Manager-FSP, Germany-6 month FTC (m/f/d)
• Homeoffice
[. .. ] safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on now and in the future. Our global Clinical Operations colleagues within our PPD clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to [. .. ] required, advises support/ develops and negotiates on contract development with Sites/ CRO/ Vendors ensuring legal input where required and may participate in budget/ contract negotiations with study vendors or clinical investigator sites. As required, selects manages local vendors in accordance with local practices in alignment with overall resourcing strategy for the study; accountable for local vendor management including oversight, agreements, payments, communications issue management. Manages the development of key study documents, plans manuals according to local requirements (monitoring plan, local informed [. .. ]
Job am 14.01.2026 bei Jooble gefunden
ICON
Manager, Site Engagement Liaison
• Homeoffice
Work-Life-Balance
As a Manager, Site Engagement Liaison, you will be joining the worlds largest most comprehensive
clinical research organisation, powered by healthcare intelligence. The Site Engagement Liaison Manager is a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] field based expert who supports the conduct and the patient recruitment of the client global clinical trials at investigative sites, through local and relational support. What you will be doing: Participate in study-level feasibility activities through providing key country/ regional and site specific knowledge including patient pathways and operational execution. Interface and act as a local client Trial Ops representative, an expert on the clinical trial protocol (s) and SME providing the sites with knowledge and awareness about the current and upcoming clinical trials. Lead and engage in local site, KOL and network engagement initiatives in view of the clinical trials. Contribute to the trial specific site feasibility/ [. .. ] signature as needed. Proactively work to fully understand all matters that impact the successful patient recruitment and high quality conduct of the clinical trial at each site, eg the Principle Investigator (PI) and site preferences and best practices on clinical trials, standard of care treatments, competing studies etc. Ensure a supportive relationship with clinical sites and trial personnel. Proactively work to fully understand the patient voice, preferences and pathway (s) . Closely work with the client GPA team. Speak to patient [. .. ]
Job gestern bei Jooble gefunden
Study Physician sponsor dedicated in Germany
• München
Study Physician sponsor dedicated in Germany Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and commercial [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to [. .. ] Doctors (Candidates who completed fellowship, residency, specialization e. g. Internal medicine, oncology, neurology, immune-oncology, cardiology, pediatrics, emergency medicine are preferred) with following experience: Global Medical Monitor/ Study Physician/ Clinical Trial Physician managing phase I to IV clinical trials in CRO/ Pharma company. Global Project Manager/ Clinical Trial leader/ Project manager managing multiple countries in CRO/ Pharma company. Country Trial Manager/ Local Project Manager/ Project Manager USA in CRO/ Pharma company Global Safety Physician/ Risk Management Physician in Pharmacovigilance department in [. .. ] requirements too) Medical Monitoring experience preferred Pharma company experience preferred. However, CRO experience is fine. If no industry experience, the in addition to clinical practice they should have worked principal investigator/ sub investigator in clinical trials for a reasonable amount of time. Travel-15-20 depending on the study requirements. Key words to look for in potential CVs-Clinical Trial protocol-writing/ reviewing, Identify medically relevant critical data, Medical risks, risk mitigation/ monitoring plan, Medical quality review/clinical quality monitoring, Jreview, [. .. ]
Job vor 3 Tagen bei Jooble gefunden
Medical Science Liaison Rare Disease-Ostdeutschland
• Schwerin
The Regional Medical Science Liaison (MSL) serves as the primary field-based point of contact with healthcare providers (HCPs) including
clinical investigators on a range of clinical and scientific issues. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] The primary role is to deliver and facilitate medical education and communications, research, and scientific insight gathering activities of the client. This includes the provision of scientific and medical data on both licensed and unlicensed products and indications as permissible by [. .. ] aligned to strategy within the business Serves as external, credible scientific expert on disease area and client products at HCP field meetings, key medical and scientific conferences, advisory boards, clinical investigator meetings and patient advocacy group meetings Facilitate clear communication between the client and investigators in investigator engagement for both client trials and investigator-sponsored studies and barriers to enrolment for pipeline assets Works to the highest ethical compliance, ethics and safety standards adhering to all local regulations and laws Maintains [. .. ] or rare disease experience preferred or experience in endocrinology or lipidology experience Knowledge of clinical research design and GCP in the cardiology area Demonstrate a strong understanding of clinical research trial design and study analysis including cost effectiveness and other high-level HEOR evidence approaches Demonstrate ability to develop trust and maintain integrity with KOLs/ External Clinical and Scientific Experts, investigators, HCPs, and institutions, as well as with peers, and others Ability to convey complex scientific concepts and information appropriately tailored [. .. ]
Job vor 4 Tagen bei Jooble gefunden
Sr CRA in oncology-Sponsor dedicated-Home Based Germany
• München
Sr CRA in oncology-Sponsor dedicated-Home Based Germany Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to [. .. ] 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 via [. .. ] 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 vor 7 Tagen bei JobMESH gefunden
Thermo Fisher Scientific
Assistant CRA (m/f/d)
• Baden- Wurttemberg
[. .. ] safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] therapies. With clinical trials conducted in 100 countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on now and in the future. Location/ Division Specific Information We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD, [. .. ] specific guidelines. Raises manual queries in EDC when applicable. Remotely reviews study logs as deemed necessary. Conducts and documents site management calls/ contacts according to the monitoring plan. Participates in investigator meetings. Investigates and follows-up on centralized monitoring findings. Evaluates PI oversight (e. g. , protocol adherence) , subject safety and study processes to assess sites ability to conduct study on a regular basis. Conducts remote investigations into site performance using a risk based monitoring approach: applying root cause analysis [. .. ]
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Häufig gestellte Fragen
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.
Wieviele offene Stellenangebote gibt es für Clinical Trial Investigator Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 127 offene Stellenanzeigen für Clinical Trial Investigator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trial Investigator Jobs?
Aktuell suchen 20 Unternehmen nach Bewerbern für Clinical Trial Investigator Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Trial Investigator Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Trial Investigator Stellenangebote:
- Thermo Fisher Scientific (8 Jobs)
- Abb Vie (6 Jobs)
- IQVIA (6 Jobs)
- Bei Gene (3 Jobs)
- ICON (2 Jobs)
In welchen Bundesländern werden die meisten Clinical Trial Investigator Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trial Investigator Jobs werden derzeit in Bayern (22 Jobs), Hessen (6 Jobs) und Sachsen-Anhalt (6 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trial Investigator Jobs?
Clinical Trial Investigator Jobs gehören zum Berufsfeld Medizinisch-technische Assistenz / MTA.
