92 Jobs für Clinical Trial Investigator
Stellenangebote Clinical Trial Investigator Jobs
Job vor 9 Tagen bei Jobleads gefunden
• Biberach an der Riß, Baden- Württemberg
[. .. ] Authority regulations, the BI Code of Conduct, Corporate Medicine SOPs and major industry association codes is expected. First experience with ICHGCP and relevant regulatory guidance is valuable; [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] experience as a clinical trial investigator is an additional asset. Strong ability to set direction, innovate, and communicate in a global environment with diverse internal and external stakeholders. Proven ability to build strong relationships, combined with experience using data visualization and IT systems, strong communication skills, analytical thinking, structured working style, and fluency in English. [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
Study Physician
• Biberach an der Riß, Baden- Württemberg
[. .. ] Authority regulations, the BI Code of Conduct, Corporate Medicine SOPs and major industry association codes is expected First experience with ICHGCP and relevant regulatory guidance is valuable; [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] experience as a clinical trial investigator is an additional asset Strong ability to set direction, innovate, and communicate in a global environment with diverse internal and external stakeholders Proven ability to build strong relationships, combined with experience using data visualization and IT systems, strong communication skills, analytical thinking, structured working style, and fluency in English [. .. ]
Neu Job vor 3 Std. bei XING gefunden
SJP Biotec GmbH
• 8001 Zürich
Führungs-/ Leitungspositionen
Stellenbeschreibung Introduction About SJP Biotec SJP Biotec Gmb H is a
clinical-stage precision oncology company pioneering a first-in-class Selective Translation Regulatory Inhibitor (STRI) platform powered to overcome treatment resistance in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] refractory cancers. Founded in 2024, SJP targets RAS-driven, hormone-receptor-positive, and immune-refractory tumors with a novel pipeline of small molecules developed in our lab and ready [. .. ] Ar M, FDA, and EMA Develop and implement biomarker-driven patient selection strategies Build and manage relationships with leading academic and clinical sites across Germany, the EU, and the US Oversee Investigator Initiated Trials and partnerships, providing scientific leadership and interactions as required Lead regulatory strategy, developing approaches for Fast Track Designation, Breakthrough Therapy Designation, and accelerated approval pathways as applicable Support pharmaceutical partnering activities-prepare clinical data packages and respond to due diligence for potential licensing and out-licensing transactions Build [. .. ] needed. Profile Essential Qualifications MD, with specialization in medical oncology and hematology 10+ years of experience in oncology clinical development within pharma, biotech, or CRO settings with hands-on clinical trial leadership Demonstrated track record of successful INd/CTA submissions Leadership of interactions with FDA and/or EMA Experience with biomarker-driven trial design and companion diagnostic development Expertise in breast cancer, NSCLC, and KRAS-mutant tumor biology Strong understanding of the competitive treatment landscape in clinical oncology Proven ability to [. .. ]
Neu Job vor 3 Std. bei Mindmatch.ai gefunden
Syneos Health
Global Senior Project Specialist (Sponsor Dedicated) Germany
• AT- 9 Wien
[. .. ] 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. Job Responsibilities Setup, maintain and/or close out project files and study information (e. g. , regulatory documents, Trial Master File (TMF) , enrollment, Adverse Events (AE) / Serious Adverse Events (SAE) , site supplies, Institutional Review Board reapprovals, data queries) on a variety of databases and systems. Attend, participate, prepare and distribute meeting minutes and action items for both internal and external meetings (sponsor, trusted process, functional, investigator meetings) . Follow up with team members on action items to closure. Maintain timely and effective communication among team members and site staff. Keep Project Leadership and Clinical Research Associates (CRAs) fully apprised of sites and study status. May contact site staff as needed for critical information. Provide administrative support [. .. ]
Job vor 6 Tagen bei Mindmatch.ai gefunden
Alimentiv
• AT- 9 Wien
[. .. ] quite matches what youre looking for, or not ready to make a move yet? Let us know We are proactively inviting qualified candidates to join our talent [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 vor 8 Tagen bei Mindmatch.ai gefunden
Teleflex
Clinical Research Associate
• AT- 9 Wien
Homeoffice möglich
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 31.05.2026 bei Mindmatch.ai gefunden
IQVIA
• AT- 9 Wien
Führungs-/ Leitungspositionen
[. .. ] the Sponsors requirements. Sponsor Requirements Budget building within France and UK. Global contracts experience within Germany, Austria, Nordics, Poland, Italy and or Spain. Essential Functions Develop Coordinate [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 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. Assist with the creation and/or review of core scientific, technical and administrative documentation to support business development and enable study initiation and maintenance, as required. Contribute to the collection, interpretation, analysis and dissemination of accurate contracting intelligence to support assigned studies and [. .. ] negotiator. Equivalent combination of education, training and 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. Knowledge and ability to apply GCP/ ICH and applicable regulatory guidelines. Knowledge of applicable regulatory requirements, SOPs and companys Corporate Standards. Strong understanding of particular Sponsor or stakeholder need and ability to share this knowledge effectively with others. Ability to utilize metrics and [. .. ]
Job am 29.05.2026 bei Mindmatch.ai gefunden
IQVIA
Contract Negotiator
• AT- 9 Wien
[. .. ] the Sponsors requirements. Sponsor Requirements Budget building within France and UK. Global contracts experience within Germany, Austria, Nordics, Poland, Italy and or Spain. Essential Functions Develop Coordinate [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 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. Assist with the creation and/or review of core scientific, technical and administrative documentation to support business development and enable study initiation and maintenance, as required. Contribute to the collection, interpretation, analysis and dissemination of accurate contracting intelligence to support assigned studies and [. .. ] negotiator. Equivalent combination of education, training and 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. Knowledge and ability to apply GCP/ ICH and applicable regulatory guidelines. Knowledge of applicable regulatory requirements, SOPs and companys Corporate Standards. Strong understanding of particular Sponsor or stakeholder need and ability to share this knowledge effectively with others. Ability to utilize metrics and [. .. ]
Job am 29.05.2026 bei Mindmatch.ai gefunden
IQVIA Argentina
• AT- 9 Wien
Führungs-/ Leitungspositionen
Vienna, Austria Full time Home-based R1546726 To lead Local Study Teams (LSTs) at country level to deliver committed components of
clinical studies according to agreed resources, budget and timelines [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] complying with Sponsor Procedural Documents, international guidelines such as ICHGCP as well as relevant local regulations. In addition to leading LST (s) , the Local Study Associate Director may perform site monitoring as needed to support the flexible capacity model. The Local [. .. ] Consent Form (MICF) and subsequent site level ICFs, as required, including any relevant translations, and in line with relevant Sponsor SOPs and local regulations. Ensures all country and site level trial essential documents required by ICHGCP prior to study start have been collected and verified for correctness, prior to setting sites ready to enrol, and in line with Sponsor SOPs. Plans and coordinates applicable local drug activities (from local purchase or reimbursement to drug destruction) . Sets up and maintains the [. .. ] on country study level: proactively manages sites, stakeholders, local and global vendors and customers to ensure risks are timely identified, mitigated and managed. Communicates and coordinates regularly with National Coordinating Investigator/ National Lead Investigator on recruitment and other study matters, if applicable. Plans and leads National Investigator meet Ensures that all study documents are ready for final archiving and completion of local part of the e TMF. Plans and leads activities associated with audits and regulatory inspections in liaison with CQAD and [. .. ]
Job am 29.05.2026 bei Mindmatch.ai gefunden
IQVIA Argentina
Local Study Associate Director
• AT- 9 Wien
Führungs-/ Leitungspositionen
Vienna, Austria Full time Home-based R1546726 To lead Local Study Teams (LSTs) at country level to deliver committed components of
clinical studies according to agreed resources, budget and timelines [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] complying with Sponsor Procedural Documents, international guidelines such as ICHGCP as well as relevant local regulations. In addition to leading LST (s) , the Local Study Associate Director may perform site monitoring as needed to support the flexible capacity model. The Local [. .. ] Consent Form (MICF) and subsequent site level ICFs, as required, including any relevant translations, and in line with relevant Sponsor SOPs and local regulations. Ensures all country and site level trial essential documents required by ICHGCP prior to study start have been collected and verified for correctness, prior to setting sites ready to enrol, and in line with Sponsor SOPs. Plans and coordinates applicable local drug activities (from local purchase or reimbursement to drug destruction) . Sets up and maintains the [. .. ] on country study level: proactively manages sites, stakeholders, local and global vendors and customers to ensure risks are timely identified, mitigated and managed. Communicates and coordinates regularly with National Coordinating Investigator/ National Lead Investigator on recruitment and other study matters, if applicable. Plans and leads National Investigator meet Ensures that all study documents are ready for final archiving and completion of local part of the e TMF. Plans and leads activities associated with audits and regulatory inspections in liaison with CQAD and [. .. ]
Job am 25.05.2026 bei Mindmatch.ai gefunden
IQVIA Argentina
• AT- 9 Wien
[. .. ] the Sponsors requirements. Sponsor Requirements Budget building within France and UK. Global contracts experience within Germany, Austria, Nordics, Poland, Italy and Spain. Essential Functions Develop and coordinate [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the creation of investigator grants and estimates, contracting strategies, and proposal text to support the proposal development process. Develop contract language, payment language, and budget templates as required. Utilize and maintain contracting systems, tools, processes, and training materials for selected sponsors, studies or multi-protocol programs according to the Scope of Work and Project [. .. ] 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. Assist with the creation and/or review of core scientific, technical and administrative documentation to support business development and enable study initiation and maintenance, as required. Contribute to the collection, interpretation, analysis and dissemination of accurate contracting intelligence to support assigned studies and [. .. ] regional experience acting as a contract negotiator. Good negotiating and communication skills with the ability to challenge. Strong legal, financial and/or technical writing skills. Strong understanding of regulated clinical trial environment and knowledge of the drug development process. Knowledge of and ability to apply GCP/ ICH and applicable regulatory guidelines. Knowledge of applicable regulatory requirements, SOPs and the companys Corporate Standards. Strong understanding of particular sponsor or stakeholder needs and the ability to share this knowledge effectively with others. Ability [. .. ]
Job am 25.05.2026 bei Mindmatch.ai gefunden
Syneos Health, Inc.
On-site monitor open to diverse EMEA countries
• 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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, [. .. ]
Job am 25.05.2026 bei Mindmatch.ai gefunden
IQVIA
• 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 am 05.05.2026 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 am 08.04.2026 bei Jobleads gefunden
• 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 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 3 Std. bei Jobleads gefunden
• Wien
[. .. ] 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. Job Responsibilities Setup, maintain and/or close out project files and study information (e. g. , regulatory documents, Trial Master File (TMF) , enrollment, Adverse Events (AE) / Serious Adverse Events (SAE) , site supplies, Institutional Review Board reapprovals, data queries) on a variety of databases and systems. Attend, participate, prepare and distribute meeting minutes and action items for both internal and external meetings (sponsor, trusted process, functional, investigator meetings) . Follow up with team members on action items to closure. Maintain timely and effective communication among team members and site staff. Keep Project Leadership and Clinical Research Associates (CRAs) fully apprised of sites and study status. May contact site staff as needed for critical information. Provide administrative support [. .. ]
Neu Job vor 3 Std. bei Jobleads gefunden
Chief Scientific Officer (80-100)
• Bern
Führungs-/ Leitungspositionen
The Swiss Cancer Institute is the national network for
clinical cancer research in Switzerland. Since 1965, we have been committed to improving cancer treatment for the Swiss population as [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a non-profit organization. Guided by our vision Clinical research for a cure tomorrow, we conduct oncology clinical trials and serve as a key partner for authorities, professional associations, and the [. .. ] precision medicine, AI in oncology) , initiate and support collaborations for innovative research projects and strengthen interdisciplinarity, contribute to efficiency of the organization in terms of speed and costs of trial development Networking Partnerships: Build strong relationships with research group leadership, core teams and contribute to the development of a strong research network across cancer types, build and expand national and international research collaborations (e. g. , National Partners and platforms, international research groups, pharma and biotech partners, ) , represent [. .. ] without hierarchy) University degree in medicine (MD) , natural or pharmaceutical sciences (Ph D) or a related field Proven track record in oncology/ hematology or related life sciences, with experience in Investigator Initiated Trials (Academic track record in leading clinical research is a strong plus) Strong background in clinical research, translational science and interdisciplinary collab-oration Strong strategic mindset, entrepreneurial attitude and solution-oriented thinking. Excellent project management expertise Very good communication, representation and negotiating skills Excellent written and oral communication skills [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• Berlin
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 [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Senior Medical Science Liaison (field-based) Hematology South Germany (Munich, Augsburg, Stut. . .
[. .. ] upon request of Healthcare Professionals. Facilitate responses to unsolicited requests for medical information, often in collaboration with Be One Medical Information Services personnel. Present data on Be [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] One products, including clinical, development, and publication data, and data outside the scope of marketing authorization during adhoc field engagements or scientific meetings. Support, attend, and follow up on local, national, regional, and international scientific congresses and events. Support enterprise activities such as booth duty, session coverage, and insight gathering and participate in the [. .. ] to or conduct monitoring on developments in the therapeutic area landscape and standards of care. In collaboration with clinical operations, participate in site feasibility assessments, planning and onboarding of clinical trial sites, and continuous followup of sites and ongoing trials in the assigned region. Serve as the primary territory liaison for the receipt, preliminary review, and submission of Investigator Sponsored Research proposals, facilitating the process from concept submission through publication. Medical Insights Strategic Input Collect, analyze, and communicate fieldbased medical insights to internal stakeholders. Provide scientific input and fieldbased feedback to define, update, and support medical affairs strategies. Identify unmet medical needs and emerging trends in the therapeutic area. [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Manager Clinical Trial Payments
• Berlin
[. .. ] person is considered as an individual. At Johnson Johnson, we respect the diversity and dignity of our employees and recognize their merit. Job Function R D Operations [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Job Sub Function Clinical Trial Project Management Job Category Professional All Job Posting Locations Beerse, Antwerp, Belgium, Berlin, Germany, Issy-les-Moulineaux, France, Madrid, Spain, Prague, Czechia, Warsaw, Masovian, Poland Job Description Global Clinical Operations (GCO) Manager, Payments (CCS) Position Summary As the Manager, Regional Payments Lead you are responsible to run the local region [. .. ] Acts as liaison among colleagues within CCS and study teams to assist with complex issue resolution and/or guidance, as needed. Responsible for the management of the end-to-end investigator/ site payment processes and payment calculations, including populating CTMS visit templates, suppliers, purchase orders, payment and clinical trial payments. Principal Responsibilities The focus of the job owner is to take on Process Ownership for all processes regarding CCS and drive continuous improvement. Ability to shape processes to develop deep insights. [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Medical Science Liaison/ Senior Medical Science Liaison-Eastern Europe
• München, Bayern
[. .. ] any such changes as a condition of employment. Medical Science Liaison Essential Duties and Responsibilities: Contribute to development and refinement of medical strategy through field insights and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] HCP, KME, and investigator engagement. Develop and execute territory plans aligned with organizational priorities and data milestones. Develop and manage a defined territory of KME and HCP relationships within the I I therapeutic area identifying, mapping, and engaging scientific thought leaders, clinical investigators, and academic centers relevant to Beelines pipeline under the direction of Medical Affairs leadership. Lead segmentation (Tier 1/ 2/ 3) development, strategic engagement plans and longitudinal relationship ownership with HCPs, KMEs, and investigators. Conduct peer-topeer scientific exchange with KMEs, HCPs, and clinical investigators sharing clinical and preclinical data, presenting pipeline updates, and discussing unmet medical needs in I I in a balanced, compliant, and scientifically rigorous manner. Support clinical trial awareness and site identification efforts by engaging with potential investigators and academic institutions, facilitating scientific discussions that may support site initiation and patient enrollment for organizations I I programs. Serve as the key resource for scientific exchange as the face of the sponsor with clinical site investigators from site startup [. .. ]
Job vor 8 Tagen bei Jobleads gefunden
Associate Director CMC Regulatory
Führungs-/ Leitungspositionen
[. .. ] with a strong nonclinical focus, supporting faculty and staff on product development and regulatory strategy. The Associate Director, CMC Regulatory provides expert guidance on regulatory requirements for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] animal studies and clinical applications, prepares and supports submissions to health authorities, and partners closely with clinical research teams to advance innovative therapies, including gene therapies and biologics. The position offers the opportunity to work as part of an internal clinical research organization, gain broad exposure across multiple therapeutic areas, and contribute to cutting-[. .. ] to inquiries, and submission follow-up. Develop, review, and maintain regulatory documentation such as protocols, IND sections, and supporting technical reports. Ensure regulatory strategies and submissions comply with FDA clinical trial regulations and guidance, including GMP, GLP, GVP, and GCP. Collaborate with internal clinical research units, including compliance, regulatory support, contracting, operations, and finance, to facilitate successful clinical trial execution. Provide internal consultation on regulatory pathways for investigator-initiated and industry-sponsored clinical trials across multiple therapeutic areas. Work independently on assigned projects, managing timelines, deliverables, and communication with stakeholders. Contribute to ongoing education and training initiatives related to regulatory requirements and best practices. Participate in regular internal meetings and training sessions to stay current on evolving regulatory [. .. ]
Job vor 9 Tagen bei Jobleads gefunden
Senior Site Contract Manager
• Neuss, Nordrhein- Westfalen
[. .. ] seeking a Senior Site Contract Manager (CCS) to join our team located in Germany. In this role you will be responsible for the development and analysis of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] contractual relationships including investigator grants and may be involved with contract negotiations, providing support to the clinical team in pricing, planning, execution, and control of grants and contracts. Principal Responsibilities Prepare, negotiate, and finalize clinical trial agreements and ancillary agreements for company-sponsored and/or investigator-initiated studies through direct negotiation or oversight of a Clinical Research Organization. Responsible for delivery on established targets/ measurements. Responsible for analyzing contract requests/ needs from operating companies and translating into appropriate contracts/ budgets for company-sponsored and investigator-initiated [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
R D Quality Manager Senior Auditor (m/f/d)
• Frankfurt, Hesse
[. .. ] 6 months, with the option of permanent employment. Location: Frankfurt am Main, with 23 days of remote work per week. This role is responsible for quality oversight [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and support for clinical development projects and the R D Quality Management System. It includes an independent review of the planning, conduct, reporting and documentation of clinical activities and the computer systems used, on the basis of the relevant medical device and pharmaceutical legislation, regulations, standards and guidelines. Audit Programs Planning and performance of various clinical medical devices and medicinal products project audits (e. g. investigator site audits, process audits, TMF audits, CSP/ CSR audits) against Gx P and local regulatory requirements. Creating audit plans for studies based on risk assessments/ analyses. Planning and performance of internal process and vendor audits. Quality Issue Management Lead the evaluation and management of clinical sitespecific escalations related to persistent or [. .. ] Qualifications Masters degree in natural science, pharmacy, or medicine. Prior experience developing riskbased quality management programs across clinical development. Experience working and communicating within crossfunctional teams. Knowledge of overall clinical trial management process, including protocols and other trial plans. Critical thinking and analytical skills for understanding and analyzing complex data and providing insights into risk reports, trends, and outliers. #J-18808-Ljbffr 94818582 [. .. ]
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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 92 offene Stellenanzeigen für Clinical Trial Investigator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trial Investigator Jobs?
Aktuell suchen 23 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:
- IQVIA (4 Jobs)
- IQVIA Argentina (3 Jobs)
- Thermo Fisher Scientific (3 Jobs)
- Bei Gene (2 Jobs)
- Rhythm Pharmaceuticals (2 Jobs)
- Novocure (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 (13 Jobs), Berlin (8 Jobs) und Niedersachsen (7 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trial Investigator Jobs?
Clinical Trial Investigator Jobs gehören zum Berufsfeld Medizinisch-technische Assistenz / MTA.
