165 Jobs für Clinical Support Investigator
Stellenangebote Clinical Support Investigator Jobs
Neu Job vor 6 Std. bei Jooble gefunden
Alimentiv
• Hamburg
Führungs-/ Leitungspositionen
Responsible for the
clinical operations of a project within a defined regional/ global level. Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and
Investigator sites in accordance with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Monitoring Plan, Protocol, Good Clinical Practice (GCP) , ICH guidelines and local regulations. The COL acts as a primary liaison between the CRAs and the clinical project team. Additional responsibilities include project specific training of CRAs, conducting assessment visits with CRAs, implementation of enrollment and [. .. ] site and monitoring performance metrics, issue escalation and corrective actions. The COL will develop study tools for site and CRA use, review visit reports, review and track protocol deviations, and support other objectives for clinical operations and the clinical project team. Project Oversight Overall oversight of (a group of) regional CRAs to ensure (site) compliance with study protocol, study plans, ICH-GCP, local regulations and study timelines. Monitoring support visits (Co-monitoring) , per project requirements, to aid the site/ CRA [. .. ]
Job vor 3 Tagen bei Jooble gefunden
Medical Science Liaison Rare Disease-Ostdeutschland
• 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 local laws and regulations. The MSL will act as the medical representative across a large, complex environment with flexibility to support other countries as needed by the organisation. Responsibilities: Develop and maintain, in a self-driven manner, outstanding knowledge of cardiometabolic diseases and related areas, including specialised expertise in rare disease such as Familial Chylomicronemia Syndrome (FCS) and Severe Hypertriglyceridemia (SHTG) , along with comprehensive client and competitor product knowledge Understand [. .. ] 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 [. .. ]
Job vor 4 Tagen bei Jooble gefunden
• 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 [. .. ] Applies query resolution techniques remotely and on site, and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelines Utilizes available hardware and software to support the effective conduct of the clinical study data review and capture. Verifies site compliance with electronic data capture requirements. May perform investigational product (IP) inventory, reconciliation and reviews storage and security. Verifies the IP has been dispensed and administered to subjects/ patients according to the protocol. Verifies issues or risks [. .. ]
Job am 19.01.2026 bei Jooble gefunden
Helmholtz Association of German Research Centres
Scientist (f/m/x) in Adipocytes and Metabolism
• Deutschland
[. .. ] tissue dysfunction. In a modern laboratory environment equipped with state-of-the-art facilities and techniques, we aim to develop innovative strategies to decouple obesity from the metabolic syndrome. To [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] support our exciting and forward-looking research projects, we are seeking a highly motivated and dedicated individual to join our team. We look forward to your application. Your tasks Establishing nucleic acid-based tissue targeting vehicles Utilize in vivo and in vitro models to study restoration of adipocyte dysfunction through targeted delivery of small molecules or si RNAs Optimize nucleotide conjugation chemistry Biochemical analysis of human and murine cellular function in vivo and in vitro Develop concepts translating murine findings to clinical use Your profile Ph D in natural sciences Profound experience in molecular and cell biology, especially gene silencing methods and aptamer selection Knowledge of nucleic acid chemistry Experience or interest in metabolic phenotyping of mice High motivation, flexibility and topic specific publications If you fulfill all the requirements, you may be [. .. ] this reason, we established Career Development Centers for postdoctoral researchers in the Helmholtz Centers. This equips young researchers with the skills they need to go on to head a Helmholtz Investigator Group, for example. As an Investigator Group leader, junior scientists can independently set up their own group to conduct research in their specialist field and acquire management skills. Within its talent management strategy, the Helmholtz Association pays special attention to the increased recruitment of talented female scientists both from Germany [. .. ]
Job am 17.01.2026 bei Jooble gefunden
Alira Health
• München
[. .. ] team dedicated to innovation and initiative, where physical walls and different time zones dont limit, but encourage, collaboration. The Project Manager (PM) is an important member of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Alira Health Clinical team. Manages clinical study functions, which may include investigational supply, IWRS/ IXRS, data management, biostatistics, pharmacovigilance, and central laboratory. Supervises and provides support to the Clinical team, including Clinical Assistants, In-house Clinical Research Associates, and Clinical Research Associates. Creates and reviews clinical study documents, including protocols, ICF templates, study budgets, site log/ form templates, study manuals and plans, site binders, etc. Presents at project meetings such as investigator meetings and new client meetings. Updates management accurately and regularly through frequent communication. Manages subject accrual, retention, and compliance. Assists in TMF management and manages TMF reviews as needed. Complies with and ensures team compliance with ICH GCP guidelines, FDA regulations, and company SOPs. 3 years of experience in the [. .. ]
Job am 17.01.2026 bei Jooble gefunden
Alira Health
Senior Manager, Project Management
• München
[. .. ] team dedicated to innovation and initiative, where physical walls and different time zones dont limit, but encourage, collaboration. The Project Manager (PM) is an important member of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Alira Health Clinical team. Manages clinical study functions, which may include investigational supply, IWRS/ IXRS, data management, biostatistics, pharmacovigilance, and central laboratory. Supervises and provides support to the Clinical team, including Clinical Assistants, In-house Clinical Research Associates, and Clinical Research Associates. Creates and reviews clinical study documents, including protocols, ICF templates, study budgets, site log/ form templates, study manuals and plans, site binders, etc. Presents at project meetings such as investigator meetings and new client meetings. Updates management accurately and regularly through frequent communication. Manages subject accrual, retention, and compliance. Assists in TMF management and manages TMF reviews as needed. Complies with and ensures team compliance with ICH GCP guidelines, FDA regulations, and company SOPs. 3 years of experience in the [. .. ]
Job am 17.01.2026 bei Jooble gefunden
Alira Health
• München
[. .. ] team dedicated to innovation and initiative, where physical walls and different time zones dont limit, but encourage, collaboration. The Project Manager (PM) is an important member of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Alira Health Clinical team. Manages clinical study functions, which may include investigational supply, IWRS/ IXRS, data management, biostatistics, pharmacovigilance, and central laboratory. Supervises and provides support to the Clinical team, including Clinical Assistants, In-house Clinical Research Associates, and Clinical Research Associates. Creates and reviews clinical study documents, including protocols, ICF templates, study budgets, site log/ form templates, study manuals and plans, site binders, etc. Presents at project meetings such as investigator meetings and new client meetings. Updates management accurately and regularly through frequent communication. Manages subject accrual, retention, and compliance. Assists in TMF management and manages TMF reviews as needed. Complies with and ensures team compliance with ICH GCP guidelines, FDA regulations, and company SOPs. 3 years of experience in the [. .. ]
Job am 17.01.2026 bei Jooble gefunden
Alira Health
Project Manager
• 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, [. .. ] study functions, which may include investigational supply, IWRS/ IXRS, data management, biostatistics, pharmacovigilance, and central laboratory. Generates and presents frequent study status updates and reports to sponsor. Supervises and provides support to the Clinical team, including Clinical Assistants, In-house Clinical Research Associates, and Clinical Research Associates. Supervises and trains Associate PMs. Creates and reviews clinical study 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 17.01.2026 bei Jooble gefunden
Alira Health
• München
Führungs-/ Leitungspositionen
[. .. ] team dedicated to innovation and initiative, where physical walls and different time zones dont limit, but encourage, collaboration. The Project Manager (PM) is an important member of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Alira Health Clinical team. Manages clinical study functions, which may include investigational supply, IWRS/ IXRS, data management, biostatistics, pharmacovigilance, and central laboratory. Supervises and provides support to the Clinical team, including Clinical Assistants, In-house Clinical Research Associates, and Clinical Research Associates. Creates and reviews clinical study documents, including protocols, ICF templates, study budgets, site log/ form templates, study manuals and plans, site binders, etc. Presents at project meetings such as investigator meetings and new client meetings. Updates management accurately and regularly through frequent communication. Manages subject accrual, retention, and compliance. Assists in TMF management and manages TMF reviews as needed. Complies with and ensures team compliance with ICH GCP guidelines, FDA regulations, and company SOPs. 3 years of experience in the [. .. ]
Job am 17.01.2026 bei Jooble gefunden
Alira Health
Senior Project Management Coordinator
• München
[. .. ] team dedicated to innovation and initiative, where physical walls and different time zones dont limit, but encourage, collaboration. The Project Manager (PM) is an important member of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Alira Health Clinical team. Manages clinical study functions, which may include investigational supply, IWRS/ IXRS, data management, biostatistics, pharmacovigilance, and central laboratory. Supervises and provides support to the Clinical team, including Clinical Assistants, In-house Clinical Research Associates, and Clinical Research Associates. Creates and reviews clinical study documents, including protocols, ICF templates, study budgets, site log/ form templates, study manuals and plans, site binders, etc. Presents at project meetings such as investigator meetings and new client meetings. Updates management accurately and regularly through frequent communication. Manages subject accrual, retention, and compliance. Assists in TMF management and manages TMF reviews as needed. Complies with and ensures team compliance with ICH GCP guidelines, FDA regulations, and company SOPs. 3 years of experience in the [. .. ]
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 [. .. ] confidence for the years ahead Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80, 000 independent specialised professionals who are there to support you and your familys well-being Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others Visit our careers website to read more about the benefits of working at ICON: ICON, including subsidiaries, is an equal opportunity [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Freelance CRA Germany
• München
Freiberuflich
Freelance CRA Germany Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and commercial insights into outcomes [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to [. .. ] 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. Applies query resolution techniques remotely and on site, and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelines. Utilizes available hardware and software to support the effective conduct of the clinical study data review and capture. Verifies site compliance with electronic data capture requirements. May perform investigational product (IP) inventory, reconciliation and reviews storage and security. Verifies the IP has been dispensed and administered to subjects/ patients according to the protocol. Verifies issues or risks [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Incyte Corporation
• 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 [. .. ] processes and is part of respective brand teams Manages and lead the implementation of the medical/ non-promotional plans for respective products Reviews and critically appraise scientific literature and provide support and advice to medical and marketing groups in developing strategy and tactical implementation of planned activities Provides medical and scientific input to projects and manage related activities (e. g. educational programs, communication campaigns, scientific symposia etc. ) Ensures that Health Care Professionals (HCP) and educational activities are of high scientific [. .. ] 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
Incyte Corporation
Associate Director, Medical Affairs Dermatology (Atopic Dermatitis) (m/f/d)
• München
Führungs-/ Leitungspositionen
[. .. ] his/ her profound understanding of the respective treatment area and extensive network the Associate Director Medical Affairs Dermatology establishes and fosters collaborations with external partners and provides [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a bridge between clinical development, medical affairs and the commercial organization at a senior mastery level. He/ she provides critical insights into the countrys medical affairs plan for the respective disease areas, ensuring that it complements the companys development plan and adheres to the highest scientific standards. Constantly build and maintain expertise in the [. .. ] leadership and actively contributes to market access dossiers Oversee the agenda development, content creation, and execution for educational symposia, internal meetings/ summits and advisory boards Supports advisory board meetings and investigator meetings. Provides support for content development and delivering clinical presentations at medical meetings Develops and delivers presentations to colleagues and management as needed, provides strong input to briefing documents, written communications, Frequently Asked Questions documents, backgrounders, newsletters, slide decks, and medical information letters etc. MD, Pharm D or Ph D in life science Experience as [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Biontech
• Berlin
Jobticket
[. .. ] strategy 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] lung 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 [. .. ]
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 study close out, across commercial and government contracts. Together, we help clients define and develop clinical programs, minimize delays, and execute high-quality, cost-efficient clinical studies. The PPD FSP Solution: PPD s Functional Service Provider division partner with [. .. ] 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
• 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 [. .. ] 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 [. .. ]
Neu Job vor 6 Std. bei Jooble gefunden
Alimentiv
Operations Administrator-temp to perm
• Homeoffice
Responsible for the
clinical operations of a project within a defined regional/ global level. Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and
Investigator sites in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP) , ICH guidelines and local regulations. The COL acts as a primary liaison between the CRAs and the clinical project team. Additional responsibilities include project specific training of CRAs, conducting assessment visits with CRAs, implementation of enrollment and [. .. ] site and monitoring performance metrics, issue escalation and corrective actions. The COL will develop study tools for site and CRA use, review visit reports, review and track protocol deviations, and support other objectives for clinical operations and the clinical project team. Project Oversight Overall oversight of (a group of) regional CRAs to ensure (site) compliance with study protocol, study plans, ICH-GCP, local regulations and study timelines. Monitoring support visits (Co-monitoring) , per project requirements, to aid the site/ CRA [. .. ]
Neu Job vor 6 Std. bei Jooble gefunden
Alimentiv
• Homeoffice
Führungs-/ Leitungspositionen
Responsible for the
clinical operations of a project within a defined regional/ global level. Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and
Investigator sites in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP) , ICH guidelines and local regulations. The COL acts as a primary liaison between the CRAs and the clinical project team. Additional responsibilities include project specific training of CRAs, conducting assessment visits with CRAs, implementation of enrollment and [. .. ] site and monitoring performance metrics, issue escalation and corrective actions. The COL will develop study tools for site and CRA use, review visit reports, review and track protocol deviations, and support other objectives for clinical operations and the clinical project team. Project Oversight Overall oversight of (a group of) regional CRAs to ensure (site) compliance with study protocol, study plans, ICH-GCP, local regulations and study timelines. Monitoring support visits (Co-monitoring) , per project requirements, to aid the site/ CRA [. .. ]
Neu Job vor 6 Std. bei Jooble gefunden
Alimentiv
Operations Administrator (Permanent, Temporary)
• Homeoffice
Responsible for the
clinical operations of a project within a defined regional/ global level. Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and
Investigator sites in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP) , ICH guidelines and local regulations. The COL acts as a primary liaison between the CRAs and the clinical project team. Additional responsibilities include project specific training of CRAs, conducting assessment visits with CRAs, implementation of enrollment and [. .. ] site and monitoring performance metrics, issue escalation and corrective actions. The COL will develop study tools for site and CRA use, review visit reports, review and track protocol deviations, and support other objectives for clinical operations and the clinical project team. Project Oversight Overall oversight of (a group of) regional CRAs to ensure (site) compliance with study protocol, study plans, ICH-GCP, local regulations and study timelines. Monitoring support visits (Co-monitoring) , per project requirements, to aid the site/ CRA [. .. ]
Neu Job vor 6 Std. bei Jooble gefunden
Alimentiv
Clinical Operations Lead
• Frankfurt am Main
Führungs-/ Leitungspositionen
Responsible for the
clinical operations of a project within a defined regional/ global level. Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and
Investigator sites in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP) , ICH guidelines and local regulations. The COL acts as a primary liaison between the CRAs and the clinical project team. Additional responsibilities include project specific training of CRAs, conducting assessment visits with CRAs, implementation of enrollment and [. .. ] site and monitoring performance metrics, issue escalation and corrective actions. The COL will develop study tools for site and CRA use, review visit reports, review and track protocol deviations, and support other objectives for clinical operations and the clinical project team. Project Oversight Overall oversight of (a group of) regional CRAs to ensure (site) compliance with study protocol, study plans, ICH-GCP, local regulations and study timelines. Monitoring support visits (Co-monitoring) , per project requirements, to aid the site/ CRA [. .. ]
Neu Job vor 6 Std. bei Jooble gefunden
Alimentiv
Operations Administrator, Temp-Perm
• Homeoffice
Responsible for the
clinical operations of a project within a defined regional/ global level. Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and
Investigator sites in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP) , ICH guidelines and local regulations. The COL acts as a primary liaison between the CRAs and the clinical project team. Additional responsibilities include project specific training of CRAs, conducting assessment visits with CRAs, implementation of enrollment and [. .. ] site and monitoring performance metrics, issue escalation and corrective actions. The COL will develop study tools for site and CRA use, review visit reports, review and track protocol deviations, and support other objectives for clinical operations and the clinical project team. Project Oversight Overall oversight of (a group of) regional CRAs to ensure (site) compliance with study protocol, study plans, ICH-GCP, local regulations and study timelines. Monitoring support visits (Co-monitoring) , per project requirements, to aid the site/ CRA [. .. ]
Neu Job vor 6 Std. bei Jooble gefunden
Alimentiv
Operations Administrator-temp to perm (Permanent, Temporary)
• Homeoffice
Responsible for the
clinical operations of a project within a defined regional/ global level. Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and
Investigator sites in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP) , ICH guidelines and local regulations. The COL acts as a primary liaison between the CRAs and the clinical project team. Additional responsibilities include project specific training of CRAs, conducting assessment visits with CRAs, implementation of enrollment and [. .. ] site and monitoring performance metrics, issue escalation and corrective actions. The COL will develop study tools for site and CRA use, review visit reports, review and track protocol deviations, and support other objectives for clinical operations and the clinical project team. Project Oversight Overall oversight of (a group of) regional CRAs to ensure (site) compliance with study protocol, study plans, ICH-GCP, local regulations and study timelines. Monitoring support visits (Co-monitoring) , per project requirements, to aid the site/ CRA [. .. ]
Job vor 3 Tagen bei Jooble gefunden
Incyte Corporation
Medical Science Liaison Dermatology (m/f/d) - Frankfurt, Kassel, Saarbrücken
• Homeoffice
[. .. ] new chapter in Germany. With our expanding Inflammation Autoimmunity (IAI) portfolio, Germany stands as a top priority, and our Medical Affairs team is at the heart of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] this transformation. To support our ambition, we are looking for Medical Science Liaisons, who are eager to help shape this next phase scientifically and operationally. Job Summary Medical Science Liaisons (MSLs) are a team of field-based, highly trained professionals with strong clinical and/or scientific backgrounds and excellent communication skills. They represent the Medical Affairs organization to the broad scientific community. Essential Functions of The Job (Key Responsibilities) Represent the company and lead medical scientific exchanges within the respective community Develop and lead Key External Experts and investigators engagement plans identify, develop [. .. ] (i. e. dermatologists) . Systematically generate, prioritize and communicate medical insights to inform medical strategy and cross-functional decision-making Lead and support advisory board meetings, round table meetings and investigator meetings. Facilitate company sponsored and investigator sponsored trials (ISTs) Actively support real-world evidence generation activities, including non-interventional studies (NIS) , registries and collaborative research projects. Closely cooperate and align with KAM-team for all activities related to medical information for external groups. Act as point of contact for [. .. ]
Job vor 3 Tagen bei Jooble gefunden
Incyte Corporation
Medical Science Liaison Dermatology (m/f/d) - Münster, Dortmund, Bielefeld
• Homeoffice
[. .. ] new chapter in Germany. With our expanding Inflammation Autoimmunity (IAI) portfolio, Germany stands as a top priority, and our Medical Affairs team is at the heart of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] this transformation. To support our ambition, we are looking for Medical Science Liaisons, who are eager to help shape this next phase scientifically and operationally. Job Summary Medical Science Liaisons (MSLs) are a team of field-based, highly trained professionals with strong clinical and/or scientific backgrounds and excellent communication skills. They represent the Medical Affairs organization to the broad scientific community. Essential Functions of The Job (Key Responsibilities) Represent the company and lead medical scientific exchanges within the respective community Develop and lead Key External Experts and investigators engagement plans identify, develop [. .. ] (i. e. dermatologists) . Systematically generate, prioritize and communicate medical insights to inform medical strategy and cross-functional decision-making Lead and support advisory board meetings, round table meetings and investigator meetings. Facilitate company sponsored and investigator sponsored trials (ISTs) Actively support real-world evidence generation activities, including non-interventional studies (NIS) , registries and collaborative research projects. Closely cooperate and align with KAM-team for all activities related to medical information for external groups. Act as point of contact for [. .. ]
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Wieviel verdient man als Clinical Support Investigator pro Jahr?
Als Clinical Support Investigator verdient man zwischen EUR 45.000,- bis EUR 70.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Support Investigator Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 165 offene Stellenanzeigen für Clinical Support Investigator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Support Investigator Jobs?
Aktuell suchen 26 Unternehmen nach Bewerbern für Clinical Support Investigator Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Support Investigator Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Support Investigator Stellenangebote:
- Alimentiv (7 Jobs)
- Alira Health (6 Jobs)
- Regeneron (6 Jobs)
- IQVIA (6 Jobs)
- Incyte Corporation (4 Jobs)
- Thermo Fisher Scientific (4 Jobs)
In welchen Bundesländern werden die meisten Clinical Support Investigator Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Support Investigator Jobs werden derzeit in Bayern (29 Jobs), Nordrhein-Westfalen (10 Jobs) und Hessen (9 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Support Investigator Jobs?
Clinical Support Investigator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
