88 Jobs für Clinical Trial Investigator
Stellenangebote Clinical Trial Investigator Jobs
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
Syneos Health, Inc.
• AT- 9 Wien
[. .. ] (SOPs) and Work Instructions (WIs) . Assure compliance with local regulations and appropriate guidance for assigned study design/ classification, including Good Pharmacoepidemiology Practices (GPP) and International Conference [...]
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[...] on Harmonisation Good Clinical Practice (ICHGCP) . Conduct site management activities as per agreed Scope of Work (So W) , Site Management Plan (SMP) and relevant guidelines. Site identification contact sites to gauge interest, confirm contact details, and obtain relevant documents. Site qualification. Ensure selection of appropriate sites for assigned studies. Site startup with minimal supervision, working with study startup and regulatory teams. Conduct all remote and onsite monitoring activities through all study stages. Routinely review the Investigator Site File (ISF) for accuracy, timeliness and completeness; reconcile its contents with the Trial Master File (TMF) ; and ensure sites archive essential documents per local guidelines. Document activities via confirmation letters, followup letters, trip reports, communication logs, and other required project documents per SOPs and SMP; support subject recruitment, retention, and awareness strategies; and enter data into tracking systems to monitor observations, status, [. .. ]
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
IQVIA LLC
Clinical Associate Regulatory Submissions, Austria, IQVIA Biotech
• AT- 9 Wien
Clinical Associate Regulatory Submissions, Austria, IQVIA Biotech page is loaded # # Clinical Associate Regulatory Submissions, Austria, IQVIA Biotechlocations: Vienna, Austriatime type: Full timeposted on: Posted Todayjob requisition id: R1522611 [...]
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[...] Clinical Associate Submissions Regulatory Homebased Austria IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across [. .. ] and review for completeness and accuracy, along with reviewing, tracking, and following up the progress, the approval and execution of documents, questionnaires, CDA/ SIF, regulatory, ethics, Informed Consent Form, and Investigator Pack release documents, in line with project timelines. Coupled with informing team members of completion of feasibility, site ID, regulatory and contractual documents for individual sites, and providing local expertise to SAMs and project team during initial and on-going project timeline planning. Along with performing quality control of documents [. .. ] skills. Ability to work independently and to effectively prioritize tasks. Ability to manage multiple projects. Knowledge and ability to apply GCP/ ICH and applicable regulatory guidelines. Understanding of regulated clinical trial environment and knowledge of drug development process. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population [. .. ]
Job am 26.03.2026 bei Mindmatch.ai gefunden
Fortrea
• AT- 9 Wien
We are looking for a
Clinical Start Up Contract Finance Specialist to support clinical
trial startup activities across Austria. This role is an excellent opportunity for professionals with experience in [...]
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[...] clinical startup operations, budget/ contract negotiations, and regulatory processes even if they have not previously worked in a Lead position. The successful candidate will receive development and support to grow into full leadership responsibilities while [. .. ] submissions and approvals for assigned protocols. Manage country-level deliverables, timelines, and outcomes to meet study commitments. Collaborate closely with sponsors, CROs, and site teams to streamline startup processes. Negotiate investigator budgets, manage financial forecasting, and track trialrelated expenses. Ensure timely delivery of clinical and financial contracts within fair market value through strong partnerships with local clinical teams. Oversee and track clinical researchrelated payments. Conduct payment reconciliation at study closeout. Qualifications University degree (life sciences preferred) or equivalent healthcarerelated certification. Fortrea [. .. ]
Job am 19.03.2026 bei Mindmatch.ai gefunden
Milestone One
Clinical Site Coordinator
• AT- 9 Wien
Milestone One is a Site Enabling Services organization with global headquarters in Zug, Switzerland. We understand what
clinical study sites need and our overall mission is to support sites in [...]
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[...] stronger study delivery. Job Description The Milestone One Site Coordinator role supports a Clinical Study Site in clinical trial related activities according to ICHGCP, protocol requirements within Study specific defined timelines and enrollment goals. The function of the role may include, but not limited to, any/ all of the following: Act as the main line of communication between the Sponsor or CRO and the site. Ensure response to feasibility [. .. ] reconciliation of investigational products and clinical supplies. Collect, handle and maintain all sitespecific regulatory documents as needed. Facilitate and support the contract and budget negotiations at the site level. Support Investigator and Site payments and processes as needed. Schedule and/or perform study procedures as per study requirements and delegation of responsibilities. Prepare for and participate in onsite study audits or regulatory agency inspections. Qualifications A university degree in Life Science, preferably in pharmacy, nursing or lab analytics. Minimum of 2 [. .. ]
Job am 11.03.2026 bei Mindmatch.ai gefunden
Teleflex
• AT- 9 Wien
Expected Travel: More than 50 Requisition ID: 13617 Position Summary The
Clinical Research Associate (CRA) is responsible for scheduling and conducting on-site and remote monitoring visits in compliance with applicable [...]
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[...] regulatory standards (MDR, ISO 14155, ICH/ GCP guidelines, Teleflex procedures and IRB/ EC policies) . The CRA conducts monitoring visits as identified by the monitoring plan, study team or department needs [. .. ] study team and department management via escalation of issues and/or within the monitoring visit report. The CRA has a minimum of two years of work experience as a clinical trial monitor and assists the Management Team with training needs. Principal Responsibilities Conducts monitoring within timelines and according to the monitoring plan and Teleflex procedures. Works cooperatively with Research Coordinators and Investigators to schedule and conduct monitoring visits including site qualification, site initiation, routine monitoring and site closure visits. Evaluates quality [. .. ] visit preparation. Conducts monitoring visits per the department SOP, WIs and monitoring plans. Applies MDR, ISO 14155, ICH/ GCP guidelines and Teleflex SOP and WIs to monitoring activities. Completes the Investigator Files with all appropriate documentation. Ensures all required documentation is completed prior to site initiation, during enrollment and followup, and at site close out. Provides findings to site staff, clear directions for resolution, appropriate retraining, and reviews data queries with site staff to ensure they are understood and can be [. .. ]
Job am 06.03.2026 bei Mindmatch.ai gefunden
Alimentiv
Join our Talent Pool-Clinical Research Associates (Eastern Europe)
• AT- 9 Wien
[. .. ] quite matches what youre looking for, or not ready to make a move yet? Let us know We are proactively inviting qualified candidates to join our talent [...]
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[...] pool for anticipated Clinical Research Associate needs (across multiple seniority levels) to support our Clinical Monitoring team. What the process looks like: A Talent Acquisition representative will contact selected candidates to schedule a qualifying call to learn more about your experience, and what your timeline looks like Well also share details about timelines on [. .. ] regulatory compliance. Assist/ lead (as appropriate) with query resolution, safety reviews, and adverse event follow-up throughout the study lifecycle. Support/ conduct (as appropriate) site startup and activation activities, including investigator coordination, trial material delivery, and recruitment support. Maintain accurate, timely, and complete TMF documentation, requesting updates as required. Provide day-to-day operational support to Senior CRA, and Lead CRAs. Participate in training, study meetings, and CRA development activities, building competencies required for role progression. Sr. Clinical Research Associate As above, with [. .. ]
Job am 06.03.2026 bei Mindmatch.ai gefunden
PSI CRO
• AT- 9 Wien
[. .. ] committed to delivering high-quality, timely services across a wide range of therapeutic areas. Job Description We are in search of an experienced professional dedicated to developing strategic [...]
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[...] relationships with clinical research sites, with the aim of optimizing and advancing the progress of clinical trials. Hybrid role in Vienna, Austria This is the main responsibility of a site ID specialist. Communicate and build relationship with clinical sites to identify potential centres for clinical trials. Maintain and refine internal site databases in cooperation with Study Startup, Clinical Operations and Process Improvement. Project Responsibilities Conduct site identification activities, including discussion of clinical trial protocols and collection of site identification questionnaires during the startup phase of the clinical trials. Define the main study objectives and the optimal site profile. Create initial list of potential sites. Communicate with project teams on project/ regional level to fine-tune strategy and methodology of initial and follow-up [. .. ] recommended investigators or clinical sites. Support the project team throughout study startup and further on, whenever additional rounds of site identification are necessary, and/or additional information on the site/ investigator is needed. Qualifications University/ college degree (Md/Pharm D degree) , or an equivalent combination of education, training and experience. On-site monitoring experience is a plus. Understanding of Good Clinical Practice, local laws and applicable regulations in the region. Demonstrated ability to work in a dynamic environment, under compressed deadlines [. .. ]
Job am 25.02.2026 bei Mindmatch.ai gefunden
IQVIA
Contract Negotiator 2-FSP-German speaker
• AT- 9 Wien
Essential Functions Develop coordinate the development of
investigator grants and estimates, contracting strategies and proposal text to support the proposal development process. Develop contract language, payment language and budget [...]
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[...] templates as required as applicable to the position. Utilize and maintain contracting systems, tools, processes, and training materials for selected sponsors, studies or multi-protocol programs according to the [. .. ] RSU Management Plan. Provide specialist legal, operational and financial contracting support to the Study Teams, as applicable to site agreements to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements. Ensure overall contracting efficiency and adherence to project timelines and financial goals as applicable to site agreements. Report contracting performance metrics and out of scope contracting activities as required. Work with Quality Management to ensure appropriate contract management and quality standards. Mentor and [. .. ] or clinical research organization clinical site contracting experience Good negotiating and communication skills with ability to challenge. Strong legal, financial and/or technical writing skills. Strong understanding of regulated clinical trial environment and knowledge of drug development process. Good understanding of clinical trial contract management. Fluent in English and German language IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Job Overview The Associate Medical Director/ Medical Director will provide medical,
clinical and scientific advisory expertise to all IQVIA divisions as requested. Participate in all aspects of Medical Science [...]
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 The role includes predominantly Medical Monitoring responsibilities with Medical [. .. ] 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 [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Clinical Trials Lead Site Coordinator
• Zug
Führungs-/ Leitungspositionen
Overview Milestone One is a Site Enabling Services organization with global headquarters in Zug, Switzerland. We understand what
clinical study sites need and our overall mission is to support [...]
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[...] sites in stronger study delivery. Job Description Milestone One Site Coordinator supports trial sites in all related activities according to ICH-GCP, protocol requirements within study-specific defined timelines and enrollment goals. Responsibilities Act as the main line of communication between the Sponsor or CRO and the site. Ensure response to feasibility questions are provided in due time. Assist in scheduling and preparation [. .. ] of investigational products and clinical supplies. Collect, handle and maintain all site-specific regulatory documents as needed. Facilitate and support the contract and budget negotiations at the site level. Support Investigator and Site payments and processes as needed. Schedule and/or perform study procedures as per study requirements and delegation of responsibilities. Prepare for and participate in onsite study audits or regulatory agency inspections. Build and sustain long-lasting relationships with existing and potential clients (sponsors, CROs, medical institutions) . Qualifications [. .. ]
Job vor 9 Tagen bei Jobleads gefunden
Medical Director-Psychiatry (m/w/d)
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Job Overview The Associate Medical Director/ Medical Director will provide medical,
clinical and scientific advisory expertise to all IQVIA divisions as requested. They will participate in all aspects of [...]
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[...] medical science involvement on assigned trials, serve as a medical expert during the project delivery lifecycle, and provide therapeutic and medical expertise to business development activities. Essential Functions Primarily responsible for medical monitoring [. .. ] 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 17.04.2026 bei Jobleads gefunden
Director, Medical Affairs (m/f/d)
• Eschborn, Hessen
Führungs-/ Leitungspositionen
[. .. ] Role Matters This is a highimpact position at the forefront of advancing innovative therapies for patients living with heart failure. The Director will play a key role [...]
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[...] in guiding the clinical and scientific strategy across a rapidly evolving portfolio, partnering closely with Clinical Affairs, R D, Market Access, Marketing, and Commercial teams. The role requires a significant global presence (approx. 60 travel) to engage with investigators, clinical sites, and internal stakeholders. This position will manage Clinical Research professionals to provide medical [. .. ] support to maintain focus on product performance and safety, ISS, grants, and scientific activities. In addition, Director will work cross functionally to support the review, implementation and publication of clinical trial results. This role provides input to establish the range plans and goals for clinical science, and is responsible for the implementation and maintenance of the clinical research-related policies, processes and procedures related to their respective functional areas. Director provides leadership and direction to product performance testing and evaluation, use [. .. ] product safety processes and procedures for new products and technologies as clinical studies are implemented, worldwide regulatory approvals are obtained and new products are commercialized. Key responsibilities Regionally responsible for Investigator Initiated Study and Research Grant programs Develop the priorities for the Global Abbott HF ISS strategy Responsible for medical affairs contributions to physician level professional education on advanced HF, MCS and hemodynamic management Work with professional societies on increasing awareness and knowledge about advanced HF and hemodynamic management Assists the [. .. ]
Job am 17.04.2026 bei Jobleads gefunden
• Zürich
Führungs-/ Leitungspositionen
Discover Intenarnational is partnered with a Swiss Biotech in their search for an experienced Medical Director Oncology to provide medical and
clinical leadership across a portfolio of innovative oncology [...]
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[...] assets within a fast-growing biotech group. This role will lead oncology clinical development strategy, provide medical oversight across studies, and work closely with R D and executive leadership to advance novel cancer therapies through clinical development. Key Responsibilities Lead medical strategy for oncology programmes, with a focus on solid tumours and targeted therapies Provide oversight for oncology clinical trial design, protocols, and study execution Act as senior medical lead for safety review, clinical data interpretation, and investigator engagement Support regulatory submissions and health authority interactions Provide scientific leadership to internal teams, KOLs, and external partners Contribute to portfolio assessment and oncology asset strategy Requirements Md/MBBS with significant oncology drug development experience Strong background in clinical oncology trials (Phase IIII) Experience in biotech or pharma clinical development [. .. ]
Job am 08.04.2026 bei Jobleads gefunden
Medical Science Liaison Oncology
• Berlin
Jobticket
[. .. ] share and discuss evidencebased medical and scientific information about our oncology portfolio. You act as the field subject matter expert in oncology, while planning and executing stakeholder [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] engagement and informing trial sites as needed. Your Contribution: Act as a field medical expert, delivering continuous medical education to HCPs (Healthcare professionals) in Germany and gathering actionable insights to inform strategy. Build and maintain scientific partnerships with key opinion leaders, Cooperative Study Groups, medical associations, and research organizations in oncology. Develop and execute [. .. ] 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 cancer. Support clinical trials by identifying study sites, participating in SIVs (Site Initiation Visits) , assisting with patient enrollment, and ensuring smooth information exchange. Identify research opportunities, including Investigator Initiated Trials, Real World Evidence, and other evidencegeneration 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. A Good Match: Advanced [. .. ]
Job am 04.04.2026 bei Jobleads gefunden
• München, Bayern
[. .. ] to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Job Description PSI Medical Monitors provide medical input [...]
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[...] to global clinical studies and advise the teams and business partners, while always focusing on patients safety and well-being. Hybrid working based in Munich Responsibilities Serve as medical point of contact for internal project team, study sites and study sponsor for medical matters related to the conduct of clinical trials per protocol and per GCP guidelines Advise clients, project teams, sites, regulatory agencies and third-party vendors on medical matters Collaborate with internal departments in the preparation of clinical development plans, protocols, investigator brochures, annual reports, clinical study reports, patient narratives, and scientific presentations Review and analysis of clinical data to ensure the safety of study participants in clinical trials Ensure that the reported trial data is accurate, complete, and verifiable, and that the conduct of the trial is in compliance with the currently approved protocol/ amendments Address safety issues across the trial from sites and the study team Provide support for medical data review Participate in bid defense meetings and proposal activities Assist in [. .. ]
Job am 24.02.2026 bei Jobleads gefunden
Senior Medical Director-Cell and Gene Therapy (m/w/d)
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Overview The IQVIA Cell and Gene Therapy Center of Excellence (CAGT COE) , a hub of CAGT
clinical innovation, is growing We are looking for an exceptional Board-Certified physician [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to join our team as a Medical Strategy Lead to help us expand our CAGT portfolio, with an emphasis on Gene Therapy/ Gene Editing platforms, and advance this dynamic and rapidly expanding area of clinical development. The CAGT [. .. ] through scientific and clinical expertise. The CAGT Medical Strategy Lead will be charged with using his/ her clinical, scientific, and operational knowledge to harness the vast IQVIA data and clinical trial resources to develop innovative, data-driven, and patient-centered solutions for CAGT trials. The CAGT Medical Strategy Lead will provide clinical and scientific expertise to all IQVIA divisions as requested and will collaborate closely with indication-specific teams to develop integrated strategies for CAGT clinical trials and studies. The CAGT [. .. ] development plan, mining data to address important clinical questions relevant to the study, reviewing the protocol for scientific/ regulatory soundness and feasibility, logistics challenges, identification of target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape. Support preparation of customer and bid defense meetings, e. g. training and preparation of the assigned project team; provide specific content; ensure presentation focus and content effectively conveys CAGT strategy. Attends and presents at customer meeting, or bid defense or [. .. ]
Job am 21.02.2026 bei Jobleads gefunden
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
[. .. ] locations: Frankfurt, Hesse, Germanytime type: Full timeposted on: Posted Todayjob requisition id: R1529858Job Overview The IQVIA Cell and Gene Therapy Center of Excellence (CAGT COE) , a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] hub of CAGT clinical innovation, is growing We are looking for an exceptional Board-Certified physician to join our team as a Medical Strategy Lead to help us expand our CAGT portfolio, with an emphasis on Gene Therapy/ Gene Editing platforms, and advance this dynamic and rapidly expanding area of clinical development. The CAGT [. .. ] through scientific and clinical expertise. The CAGT Medical Strategy Lead will be charged with using his/ her clinical, scientific, and operational knowledge to harness the vast IQVIA data and clinical trial resources to develop innovative, data-driven, and patient-centered solutions for CAGT trials. The CAGT Medical Strategy Lead will provide clinical and scientific expertise to all IQVIA divisions as requested and will collaborate closely with indication-specific teams to develop integrated strategies for CAGT clinical trials and studies. The CAGT [. .. ] development plan, mining data to address important clinical questions relevant to the study, reviewing the protocol for scientific/ regulatory soundness and feasibility, logistics challenges, identification of target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape. Support preparation of customer and bid defense meetings, e. g. training and preparation of the assigned project team; provide specific content; ensure presentation focus and content effectively conveys CAGT strategy. Attends and presents at customer meeting, or bid defense or [. .. ]
Job am 15.01.2026 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 [. .. ]
Neu Job vor 4 Std. bei Jooble gefunden
GSK
• Deutschland Deutschland, DE
Site Name: Field Worker-DEU (Munich) Posted Date: Apr 21 2026 The Heme
Clinical Trial RMAM is responsible for the successful conduction of all our clinical trials in Germany and is [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] responsible for efficient and compliant management of medical and scientific study activities to generate robust evidence that supports the scientific positioning and the medical care of patients. Responsibilities This role will provide YOU the [. .. ] compliance requirements in the pharmaceutical environment. Preferred Qualification If you have the following characteristics, it would be a plus: Prior experience in oncology, hematology or related therapy areas. Experience supporting investigator-initiated trials or clinical partnerships. Experience designing or delivering omnichannel engagement plans and digital medical communications. Project management or budget management experience. Experience presenting at national or regional scientific meetings. A collaborative mindset and commitment to inclusive working with diverse stakeholders. Weitere Informationen: #EBDE #LI-Vii V #LI-[. .. ]
Job vor 2 Tagen bei Jooble gefunden
Senior CRA Germany Oncology
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern
[. .. ] organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, youll collaborate with passionate problem [. .. ] 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 vor 3 Tagen bei Jooble gefunden
Biontech
Associate Director Audit Management
• Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz Mainz, DE
Führungs-/ Leitungspositionen
As Associate Director Audit Management, you will play a pivotal role in ensuring the quality and compliance of Bio NTechs
clinical trials and processes. As part of the Global [...]
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[...] Development Quality Assurance team, you will lead audits across Good Clinical Practice (GCP) , Good Laboratory Practices (GLP) , Good Pharmacovigilance Practice (GVP) , and Information Technology (IT) domains. Your work will directly contribute to advancing Bio NTechs mission by ensuring adherence to regulatory standards and fostering continuous improvement in clinical development activities. Your Contribution: Lead global audits with a focus on clinical investigator sites and vendor audits in the EU, UK, and surrounding regions Ensure audit objectives align with risk-based strategies to uphold quality standards Coordinate and oversee audits conducted by contracted auditors, including scheduling, resource selection, and report reviews Execute audits as the lead auditor for non-contracted audits (remote or [. .. ] Drive continuous improvement initiatives within audit management processes A Good Match: Academic degree in Life Sciences; advanced degree preferred (e. g. , Masters level) At least 10 years of clinical trial experience, including 6 years in clinical auditing within the region Proven leadership experience managing teams or projects for at least 3 years Deep knowledge of global GCP regulations and quality audit methodologies; oncology experience is an advantage Proficient in Microsoft Office software, Veeva, Share Point; excellent English communication skills (written [. .. ]
Job vor 4 Tagen bei Jooble gefunden
Indero
Project Manager II (Germany)
• Unstrut- Hainich- Kreis; Thüringen Thueringen
Description The project manager II has the overall responsibility for the successful initiation, planning, execution, monitoring, controlling and closure of assigned
clinical trials. The project manager II oversees and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] coordinates study resources to ensure compliance with the study budget, project scope and timelines and in accordance with applicable standard operating procedures (SOPs) , good clinical practices, regulatory and study-specific requirements. Project Manager II acts as the main line of communication to [. .. ] in an environment where you can grow your career alongside the company IMPACT AND RESPONSIBILITIES Client interactions Serve as primary contact for the Sponsor Provide efficient and timely updates on trial progress Lead client calls effectively Project planning Oversee and actively participates in the preparation of project deliverables such as; study plans, protocol, informed consent form, electronic case report form (e CRF) , tables/ listings/ figures (TLFs) , clinical study report. Participate in the planning and conduct of the Investigator s Meeting. Ensure that each site has the necessary material to adequately perform the study (e. g. , investigational product, study supplies, special equipment, safety lab kits, etc. ) . Lead study start-up activities including trial kick-off, TMF setup, site selection and activation, vendor set-up timelines, and [. .. ]
Job vor 5 Tagen bei Jooble gefunden
CRA II Germany-eastern Germany (Leipzig, Halle, Berlin)
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern
[. .. ] organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, youll collaborate with passionate problem [. .. ] 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 vor 9 Tagen bei Jooble gefunden
Biontech
Associate Director Translational Sciences (Infectious Diseases)
• Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz Mainz, DE
Führungs-/ Leitungspositionen
Jobticket
[. .. ] cross-functional Translational sub-team you will collaborate with a Translational Lead on the development and implementation of program-specific, integrated biomarker strategies from Ph1 to licensure, in alignment with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical development objectives through contributing to the translation of preclinical results and approaches to clinical biomarker strategies supporting efficient clinical development of the assigned infectious disease assets. Your main responsibilities are: Contributing to the translation of preclinical results and approaches to clinical biomarker strategies supporting efficient clinical development of the assigned [. .. ] strategy and assist in its execution Provides biomarker and translational contributions to the integrated development plan, clinical development plan, and to regulatory study-or program-related documents such as clinical trial protocols, and-reports, investigator brochures, briefing documents, and market authorization applications Contributes to the execution of the translational and biomarker strategy in the assigned development program (s) What you have to offer: Ph D, Pharm D, or Md/Ph D in Immunology, Biology, Biochemistry, Molecular Medicine, Virology or a related field with Minimum of 2-3 years [. .. ]
Job vor 9 Tagen bei Jooble gefunden
Linical
Clinical Research Associate-Germany
• Deutschland Deutschland, DE
The
Clinical Research Associate is responsible for the feasibility, initiation, monitoring, and close-out of investigative sites. Major responsibilities include ensuring the safety and well-being of study participants at assigned [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] sites, ensuring site compliance with Good Clinical Practice (GCPs) , applicable regulations, the protocol and study plans; ensuring data integrity through [. .. ] in the final selection of investigative sites Conducts site initiation visits; trains site personnel on Client and regulatory requirements for study conduct; participates in and/or conducts site meetings and investigator meetings, and prepares site initiation visit reports and associated documentation Conducts site monitoring visits and follow-up to identify significant problems and issues, and to ensure that all clinical aspects of studies are being carried out in accordance with study plans, GCPs, and applicable regulations; prepares monitoring visit reports and [. .. ] contact with the site staff, to be aware of patient enrolment, enrolled patients status, IP supply and any further site requests or issues Ensures essential documents are filed in the Trial Master File (TMF) according to the project guidelines Ensures appropriate and timely transmission of clinical data to data management; reviews data queries, and clarifies and/or obtains changes to data as appropriate Conducts site close-out visits to include final IP reconciliation and disposition, review of completeness and accuracy of [. .. ]
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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 88 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:
- Biontech (5 Jobs)
- Thermo Fisher Scientific (4 Jobs)
- ICON (2 Jobs)
- Chronos Consulting (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 (26 Jobs), Baden-Württemberg (8 Jobs) und Berlin (7 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trial Investigator Jobs?
Clinical Trial Investigator Jobs gehören zum Berufsfeld Medizinisch-technische Assistenz / MTA.
