144 Jobs für Clinical Support Investigator
Stellenangebote Clinical Support Investigator Jobs
Job vor 4 Tagen bei StepStone gefunden
Sigmund Freud Privatuniversität Wien
• Wien
[. .. ] future researchers and medical specialists. The mission of medical research at SFU is to foster innovation in healthy aging and preventive medicine across all fields of human [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] medicine. We actively support investigator-initiated clinical studies and translational research within SFU and its partner hospitals, as well as collaborative projects with external senior scientists, always with the goal of translating research outcomes directly into patient care. Our laboratories are equipped with a broad range of state-of-the-art instruments supporting molecular and cellular biology [. .. ]
Job vor 5 Tagen bei StepStone gefunden
Miltenyi Biotec B. V. Co. KG
Lead Medical Writer (m f d)
• Bergisch Gladbach
Führungs-/ Leitungspositionen Homeoffice möglich
Miltenyi Biomedicine is a biopharmaceutical company committed to advancing personalized cell and gene therapies. We are pioneering groundbreaking therapies for serious life-threatening diseases, and reshaping their accessibility for
clinical professionals [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and patients worldwide with the aim to improve and extend patients lives. We are currently focusing on difficult-to-treat hematological cancers using CAR-T and other technologies, while also exploring treatments for other diseases. Our lead candidate, a tandem CAR-T cell product, is currently undergoing pivotal clinical [. .. ] Writer you are part of our Miltenyi biomedicine business and within the Clinical Development team. You will be responsible for the development and oversight of clinical and regulatory documents that support global drug development programs, including preparation, development, review, revision and finalization of clinical documents for submission to regulatory authorities. You lead the development, authoring, and submission of regulatory documents (e. g. , CTD modules, clinical study reports, investigator brochures, INDs/ IMPDs, NDAs/ MAAs, and briefing documents) . Your responsibility includes ensuring that all documents are scientifically sound, strategically aligned, and compliant with global regulatory standards. In addition, you manage document timelines, coordinate internal reviews, and ensure on-time delivery. Collaborating closely within cross-functional teams (clinical, regulatory, biostatistics, [. .. ]
Job am 29.11.2025 bei Mindmatch.ai gefunden
Sigmund Freud Privatuniversität Wien
Professor of Molecular Medicine (m/f/x)
• Vienna
[. .. ] future researchers and medical specialists. The mission of medical research at SFU is to foster innovation in healthy aging and preventive medicine across all fields of human [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] medicine. We actively support investigator-initiated clinical studies and translational research within SFU and its partner hospitals, as well as collaborative projects with external senior scientists, always with the goal of translating research outcomes directly into patient care. Our laboratories are equipped with a broad range of state-of-the-art instruments supporting molecular and cellular biology [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Manager Medical Science Liaison Oncology
• München, Bayern
[. .. ] 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. Qualifications Advanced degree [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
• Hamburg
Führungs-/ Leitungspositionen
TFS Health Science is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire
clinical development journey. Our expertise includes full service-capabilities, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] resourcing and Functional Service (FSP) solutions. About this role As part of our Ophthalmology team you will working alongside passionate and innovative professionals to ensure our customers achieve their goals. Key Responsibilities Expert Guidance : Provide advanced medical input on study design, measurement strategies, and trial protocols, including safety sections and investigator brochures. Comprehensive Safety Oversight : Review safety data such as adverse events, labs, vital signs, ECGs, and clinical trial reports from a medical perspective. Regulatory Risk Support : Conduct senior-level medical reviews of individual cases, cumulative listings, PSURs, PBRERs, DSURs, and Risk Management Plans. Medical Monitoring Signal Detection : Serve as a medical monitor in trials, perform literature reviews, and contribute to signal detection and interpretation. Regulatory Document Contributions : Offer expert medical insight into regulatory [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
Medical Science Liaison Complement-Mediated Diseases
• München, Bayern
[. .. ] stakeholders. Compile, analyse, prepare and deliver high quality medical pharmaceutical and scientific communications in line with defined communication plans. Create and execute stakeholder engagement plans, according to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Sobis high standards. Support country Global Brand team in developing local medical tactics and provide input to Headquarter (HQ) / regional plans if relevant Organise and set up scientific advisory boards with the appropriate key stakeholders, in collaboration with Medical Advisor or Senior Medical Advisor (MA, SMA) . Contribute and support medical scientific aspects [. .. ] various activities locally and regionally. Provide local and regional feedback to HQ when performing Business Development Due Diligence. Deliver inputs to head office led medical programs ahead of launch. Coordinate Investigator Sponsored Studies (ISSs) as appropriate and support studies on the local level Coordinate medical information enquiries in collaboration with MA/ SMA and HQ in Stockholm. Attend relevant local, regional and global congresses and symposia to represent Sobi and interact with appropriate stakeholders and customers. Represent the scientific interests in internal [. .. ] Sc. , D. N. P. , Ph. D. , or M. D. / D. O. ) Consideration will be given to candidates with an advanced health degree and extensive industry or clinical experience. Ability to understand and effectively communicate scientific information; respond to inquiries and address needs of key stakeholders A minimum of 1 year of MSL experience Demonstrated success managing internal/ external stakeholders and leading or influencing cross-functional teams in a matrixed environment including strong teamwork and collaboration Proven track [. .. ]
Job am 07.12.2025 bei Jobleads gefunden
• Cham, Zug
[. .. ] for Abbvie in key academic centers by facilitation of research and educational initiatives, while supporting requests for medical and scientific information on products or areas of therapeutic [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] interest to Abbvie. Support internal teams such as sales and marketing and members of the Affiliate Brand Team to develop their scientific and technical expertise through the delivery of scientific update presentations. Assist in the initiation; oversight and follow up of assigned clinical studies and medical projects initiated within the therapeutic area for which the MSL carries responsibility (e. g. post marketing clinical activities such as registry/ database projects, epidemiological surveys, post-authorization studies (phase IV) . All such activities must comply with applicable local laws, guidelines, codes of practice, SOPs, and Abb Vie R D (GPRD) SOPs. Act as the point of contact with thought leaders to facilitate investigator initiated study (IIS) ideas and requests for support to the local and global medical teams as appropriate. Serve as a point of contact within the Medical Affairs team for thought leaders and external experts within western Switzerland in order to satisfy their needs for scientific knowledge in a therapeutic area [. .. ]
Job am 04.12.2025 bei Jobleads gefunden
Senior/ Medical Director (Ophthalmology)
• München, Bayern
Führungs-/ Leitungspositionen
TFS Health Science is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire
clinical development journey. Our expertise includes full [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] service-capabilities, resourcing and Functional Service (FSP) solutions. About this role As part of our Ophthalmology team you will working alongside passionate and innovative professionals to ensure our customers achieve their goals. Key Responsibilities Expert Guidance : Provide advanced medical input on study design, measurement strategies, and trial protocols, including safety sections and investigator brochures. Comprehensive Safety Oversight : Review safety data such as adverse events, labs, vital signs, ECGs, and clinical trial reports from a medical perspective. Regulatory Risk Support : Conduct senior-level medical reviews of individual cases, cumulative listings, PSURs, PBRERs, DSURs, and Risk Management Plans. Medical Monitoring Signal Detection : Serve as a medical monitor in trials, perform literature reviews, and contribute to signal detection and interpretation. Regulatory Document Contributions : Offer expert medical insight into regulatory [. .. ]
Job am 24.11.2025 bei Jobleads gefunden
• Wien
Führungs-/ Leitungspositionen Homeoffice möglich
[. .. ] as digitally integrated solutions for our patients and clients. To ensure sustainable company growth we continually aim to offer attractive career opportunities for more than 170 employees [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] at our Vienna support of our existing team we are currently looking for : Senior Director Medical Affairs (m/f/d) Responsibilities Oversight of the development and execution of the Medical Affairs strategy for the country based on deep understanding of global regional and local opportunities and requirements Creating and maintaining a high performing [. .. ] D. degree required MPH, Ph. D. , MBA degree in Health Administration or Economics is seen as a plus Proven experience in global biopharmaceutical industry in Medical Affairs and/or Clinical Development Solid people management experience running a large matrix organization of healthcare professionals Experience in one of the following fields : Oncology (strong plus) Infectious Diseases Treatment Vaccines or Specialty care Strong leadership skills demonstrated effective organizational skills including ability to set goals and align priorities Business acumen ethics and [. .. ] recognition bonuses during the year Discounted fitness offer Pharmacy discounts wholesale discounts etc. Required Skills Advisory Board Development Clinical Development Clinical Medicine Decision Making Healthcare Education Healthcare Marketing Infectious Disease Investigator-Initiated Studies (IIS) Job Placement Leadership Management Process Medical Affairs Medical Care Medical Marketing Strategy People Leadership Results Oriented Scientific Communications Specialty Care Stakeholder Engagement Strategic Planning Strategic Thinking Writing Job Descriptions Preferred Skills Current Employees apply HERE Current Contingent Workers apply HERE Job Details Employee Status : Regular Relocation [. .. ]
Job am 23.11.2025 bei Jobleads gefunden
Medical Science Liaison Manager, Nephrology, South
• München, Bayern
[. .. ] within a geographic area. He/ she manages and maintains collegial and professional relationships with KOLs and identifies and facilitates collaboration opportunities with Alexion. He/ she combines strong [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] business acumen and clinical expertise and serves as a peer-to-peer liaison internally and externally. He/ she ensures a close working relationship with all functions in their region, including sales, and market access. You will be responsible for: Develop and maintain peer-to-peer collaborations with key medical experts in nephrology and adjacent [. .. ] medical community with up-to-date medical and scientific information Identify and execute collaboration opportunities between expert KOLs in nephrology and Alexion medical affairs and clinical development such as publications, investigator-initiated trials, regional advisory boards, training and speaker development programs. Communicate experts opinion, feedback on new data and clinical trends to Alexion Medical Affairs, therapeutic area (TA) franchises and translate this information into strategic recommendations to enhance science and advance patient care. Respond to unsolicited medical information requests in the [. .. ] manage questions, liaise with headquarters to ensure proper response has been provided and ensure that data is fair and balanced. In conjunction with clinical operations perform clinical study feasibility and support effective study implementation. Deliver quality medical education presentations in a variety of settings and obtain valuable feedback that can be disseminated throughout the organization e. g. Staff Meetings, Round Tables, Hospital Meeting activities. Serve as an Alexion-internal expert in therapeutic area demonstrating up-to-date and high-level therapeutic [. .. ]
Job am 23.11.2025 bei Jobleads gefunden
• München, Bayern
[. .. ] within a geographic area. He/ she manages and maintains collegial and professional relationships with KOLs and identifies and facilitates collaboration opportunities with Alexion. He/ she combines strong [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] business acumen and clinical expertise and serves as a peer-to-peer liaison internally and externally. He/ she ensures a close working relationship with all functions in their region, including sales, and market access. You will be responsible for: Develop and maintain peer-to-peer collaborations with key medical experts in nephrology and adjacent [. .. ] medical community with up-to-date medical and scientific information Identify and execute collaboration opportunities between expert KOLs in nephrology and Alexion medical affairs and clinical development such as publications, investigator-initiated trials, regional advisory boards, training and speaker development programs. Communicate experts opinion, feedback on new data and clinical trends to Alexion Medical Affairs, therapeutic area (TA) franchises and translate this information into strategic recommendations to enhance science and advance patient care. Respond to unsolicited medical information requests in the [. .. ] manage questions, liaise with headquarters to ensure proper response has been provided and ensure that data is fair and balanced. In conjunction with clinical operations perform clinical study feasibility and support effective study implementation. Deliver quality medical education presentations in a variety of settings and obtain valuable feedback that can be disseminated throughout the organization e. g. Staff Meetings, Round Tables, Hospital Meeting activities. Serve as an Alexion-internal expert in therapeutic area demonstrating up-to-date and high-level therapeutic [. .. ]
Job am 18.11.2025 bei Jobleads gefunden
Medical Science Liaison Oncology
• Stuttgart, Baden- Württemberg
[. .. ] the primary field contact for the companys Medical Affairs. Engage thought leaders in a compliant manner developing strategic engagement plans. Disseminate scientific information accurately and fairly addressing [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] medical inquiries. Manage investigator-initiated research interests and support clinical development activities. Lead advisory board meetings and provide internal/ external training. Represent the company at medical conferences contributing to scientific discussions in Oncology. About you: Degree in life sciences discipline 3 years of medical affairs experience preferably in Oncology/ Hematology. Fluent German good professional English Car driving licence Key Skills [. .. ]
Job am 17.11.2025 bei Jobleads gefunden
• Stuttgart, Baden- Württemberg
[. .. ] Moderation indikationsbezogener Vorträge, wissenschaftlicher Fortbildungen sowie Unterstützung ärztlicher Referenten bei Präsentationen Organisation und Umsetzung regionaler Fortbildungen und Experten-Meetings inklusive Budgetverantwortung Mitarbeit bei klinischen Studienprojekten: Studienunterstützung in Zusammenarbeit [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] mit Global Clinical Operations, Betreuung nicht-interventioneller Studien (NIS) sowie Begleitung von Investigator Initiated Studies (IIS) Teilnahme an Kongressen und Symposien, Erstellung von Kongressberichten und wissenschaftlicher Support vor Ort Bewertung und Diskussion präklinischer und klinischer Projektanträge sowie aktive Mitwirkung an laufenden medizinischen Projekten Identifikation regionaler Versorgungslücken und Ableitung von Maßnahmen zur Verbesserung der Versorgungssituation gemeinsam mit Experten, Fachgesellschaften und Verbänden Planung und Durchführung von Trainings für den Außendienst in Abstimmung mit medizinischer Leitung, Training Development, Sales und [. .. ]
Job am 20.10.2025 bei Jobleads gefunden
Clinical Site Contracts Lead client-based in Munich
• München, Bayern
Führungs-/ Leitungspositionen
Are you ready to take your expertise in
clinical contracts and budgeting to the next level At Fortrea we are looking for a detail-oriented and strategic professional to join [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] our FSP team as a Site Contract Lead. In this role you will be at the forefront of clinical trial execution ensuring that contracts and budgets are aligned with [. .. ] alignment with trial timelines. Maintain accurate records in Clinical Trial Management Systems and contract management platforms. Identify and escape business risks appropriately while supporting internal teams with contract-related guidance. Support payment tracking invoice preparation and financial reconciliation for investigator sites as needed. Required Qualifications Bachelors degree in life sciences business or a related field; equivalent experience may be considered. Minimum of 2 years experience negotiating legal and/or financial agreements preferably in clinical research or the pharmaceutical industry. Strong understanding of ICH-GCP guidelines clinical trial start-up processes [. .. ]
Job am 10.10.2025 bei Jobleads gefunden
• München, Bayern
Firmenwagen 30+ Urlaubstage
[. .. ] innovative global specialty pharma business and a preferred partner for innovator pharma companies, instigating a paradigm shift in the lifecycle management of iconic medicines. We seek to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] extensively engage with clinical communities to communicate product improvements and prioritise environmental, social, and governance considerations across the business and workforce. Pharmanovias therapeutic areas include Cardiovascular, Oncology, Endocrinology and Neurology. About The Role Reporting to the Medical Department, you will be a member of the MSL team, whose primary responsibility is to interact with influential stakeholders and healthcare providers. You will collaborate with physicians and other medical experts to support trial management, realworld evidence initiatives, interact with patient organisations, and ensure that healthcare professionals have the most uptodate information about medical and clinical benefits of Pharmanovias products. Main Responsibilities Duties Setting up strategies to target the most relevant HCPs for Pharmanovias therapeutic efforts and coordinate and align key messages to [. .. ] Identifying, developing, and maintaining professional relationships with national/ regional KOLs, establishing peertopeer collaborations with key medical experts in the therapeutic areas covered by Pharmanovia. Supporting evidence generation initiatives including potential investigator site identification, trial recruitment, registries, and presentation of final approved data, involving experts to generate scientific data including investigatorinitiated trials. Collaborating with physicians on medical affairs initiatives including publication and communication plans, advisory boards, medical education opportunities, webinars, training, and speaker development. Serving as a scientific peertopeer resource to external [. .. ]
Job am 27.06.2025 bei Jobleads gefunden
Senior/ Medical Director (Ophthalmology) 0.5 FTE
Führungs-/ Leitungspositionen
[. .. ] Senior/ Medical Director (Ophthalmology) , 0.5 FTE. TFS Health Science is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] their clinical development journey. Join our team as a Senior/ Medical Director (Ophthalmology) . The Senior/ Medical Director is a key member of the Project Delivery team, working independently to manage safety and medical matters in line with company policies, standard operating procedures (SOPs) , and regulatory requirements. With deep medical expertise, [. .. ] 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 medical monitor in trials, perform literature reviews, and contribute to signal detection and interpretation. Regulatory Document Contributions: Offer expert medical insight into regulatory submissions and safety-[. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
• Wien
[. .. ] Description Sponsor Dedicated Global Senior Project Manager (CTL level role) remote-Austria Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to [. .. ] and central monitoring deliverables with a focus on patient safety, protocol/ GCP/ regulatory compliance and data integrity. Oversees site interactions post activation through site closeout. This may include patient recruitment, investigator payments or other related activities. May be responsible for identification of critical data and process, protocol execution risks and risk mitigations related to completion of the Risk Assessment and Categorization Tool (RACT) . Reviews the study scope of work, budget and protocol content and ensures the clinical project team (CRAs/ [. .. ] clinical trial management scope. Oversees CRAs and Central Monitors assigned to the study and routinely assesses study-specific process and training compliance, CMP compliance, and identifies emerging risks. Develop and support execution of corrective action plans at site and study level. Supports and completes activities to achieve data cut and lock deadlines. Provides feedback to line managers on staff performance including strengths as well as areas for development. May be assigned to larger, more complex trials or may coordinate clinical activities [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Quality Assurance Officer Belgium
[. .. ] position for 12months and we are open to considering candidates who are open to a temporary employment contract (FTC) or freelancers with their own company. The Quality [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Assurance Officer will support distribution activities including administrative batch release and Annual Product Quality Review (APQR) , customer activation, field actions and reporting, in addition to being responsible for the documentation and maintenance of the Quality Management System. Clin Choice is a global full-service CRO with a strong focus on quality, professional development [. .. ] Goods reporting and management. Local Complaint Coordinator. Local Documentation Coordinator, including coordinate implementation at local level of corporate documentation, author and publish SOPs, and SOP periodic review. NCR/ CAPA initiator, investigator or task assignee (as needed) . Support implementation of Field Action. Support training planning and carry out reporting. Support the maintenance and management of the document retention system. Participate in Regulatory Affairs activities as needed. Education, Experience and Skills: Bachelors or Masters degree in a relevant scientific discipline. Prior experience [. .. ] the number of applications we receive, we cannot reply to everyone individually if you are not successful. About Clin Choice Clin Choice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28years of proven high-quality delivery and results across all our services, with over 4000 professionals in more than 20 countries across the Americas, Europe, and Asia Pacific. Our Company Ethos Our mission drives [. .. ]
Job gestern bei Jobleads gefunden
• Frankfurt (Oder) , Brandenburg
Senior CRA ICON plc is a worldleading healthcare intelligence and
clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] join us on our mission to shape the future of clinical development. Role: Clinical Research Associate (12+ months monitoring experience required) Location: Must be based in the UK, ideally in the Midlands [. .. ] corrective actions are implemented within specified timelines. Identify issues at sites, resolve and escalate as appropriate; collaborate with stakeholders to manage data query resolution for accurate data entry. Ensure the Investigator Folder is up to date and maintain TMFs. Negotiate investigator remuneration, prepare financial contracts, and trigger payments to investigational sites. You will need the following: Right to work in the UK. Up to 2years of pharmaceutical industry experience or other relevant experience (NHS or Academic) . Good knowledge of the [. .. ] familys needs. Competitive retirement planning offerings to maximise savings. Global Employee Assistance Programme, TELUS Health, offering 24hour access to a global network of over 80, 000 independent specialised professionals to support your wellbeing. Life assurance. Flexible countryspecific optional benefits: 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: https:/ / careers. iconplc. com/benefits Equal Employment Opportunity At ICON, diversity, inclusion [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
GCP QA Consultant
• Berlin
Beratungs-/ Consultingtätigkeiten
Champion compliance and precision-help deliver life-changing therapies. Proclinical is seeking a GCP QA Consultant to
support quality assurance activities for oncology-focused
clinical trials. This role involves overseeing quality [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] processes for phase 2-3 studies, ensuring compliance with ICH-GCP and regulatory requirements, and managing risk-based quality plans. You will collaborate with internal teams and external partners to maintain high standards of clinical trial execution and inspection readiness. This is a fully remote position, open to candidates located anywhere within Europe. Responsibilities Develop and oversee study quality-related plans, including Oversight Quality and Audit Plans. Collaborate with third parties to formalize Investigator Site Audits (ISA) and agendas. Oversee quality activities for phase 2-3 trials, focusing on risk management and endpoint de-risking. Conduct risk-based reviews of study documents to ensure compliance with protocols, ICH-GCP, and regulatory requirements. Act as the Clinical Quality Assurance Representative in weekly monitor-site meetings. [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
GCP QA Consultant
Beratungs-/ Consultingtätigkeiten
[. .. ] job poster from Proclinical Staffing Connecting top-tier QA talent with groundbreaking life sciences opportunities Champion compliance and precisionhelp deliver lifechanging therapies. Proclinical is seeking a GCP QA [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Consultant to support quality assurance activities for oncologyfocused clinical trials. This role involves overseeing quality processes for phase 23 studies, ensuring compliance with ICHGCP and regulatory requirements, and managing riskbased quality plans. You will collaborate with internal teams and external partners to maintain high standards of clinical trial execution and inspection readiness. This is a fully remote position, open to candidates located anywhere within Europe. Responsibilities Develop and oversee study qualityrelated plans, including Oversight Quality and Audit Plans. Collaborate with third parties to formalize Investigator Site Audits (ISA) and agendas. Oversee quality activities for phase 23 trials, focusing on risk management and endpoint derisking. Conduct riskbased reviews of study documents to ensure compliance with protocols, ICHGCP, and regulatory requirements. Act as the Clinical Quality Assurance Representative in weekly monitorsite meetings. Monitor site performance, ensuring adherence [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Medical Science Liaison, Immunology (IBD) , Germany
• Berlin
Work-Life-Balance
[. .. ] work An environment that empowers and supports colleagues to manage all aspects of their wellbeing by focusing on a holistic approach What Youll Be Doing In this [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] role you will support activities across both Medical Affairs Clinical Development objectives for the portfolio of pipeline products in inflammatory bowel disease. You will serve as a key interface with clinical trial sites across all development programs, working closely with Clinical Development and Clinical Operations. Additionally, you will collaborate with Medical Affairs to identify and engage key opinion leaders within [. .. ] meetings Sharing important clinical and scientific insights that you have gathered from fieldwork to cross-functional teams Acting as an internal and external scientific expert Adhering to compliance requirements Supporting investigator-initiated studies What Youll Need To Be Successful An advanced doctoral degree (MD, Ph D, Pharm D) is preferred Relevant therapeutic area knowledge in the field of immunology or immuno-oncology, experience in gastroenterology is a plus. Post graduate therapeutic area experience is preferred Fluency in English and local language 3+ [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Regional Medical Science Liaison (MSL) - Breast Cancer/ Oncology-Germany
[. .. ] experience. The MSL is a member of a global field-based team of scientific experts who function as an extension of Medical Affairs. The MSL role focuses primarily [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] on providing clinical, scientific, and educational support to healthcare professionals (HCPs) at clinical trial research sites (Principal Investigators PIs and their study teams) , and potential clinical trial sites, in addition to national and regional Key Opinion Leaders (KOLs) who have a key influence in the medical oncology communities. The MSL develops strong relationships within the respective [. .. ] and approved resources If requested, keep up to date with clinical knowledge, published data and trial work for client and competitive product studies If requested, support relevant education at Site Investigator Meetings, including Site Initiation Visits, in line with clinical study plans Develop strong communication links with PIs and study physicians and their teams Ensure requests received from PIs are managed efficiently and effectively, and that the client studies are the primary focus of the study site support teams Act as [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Medical Science Liaison, Immunology (IBD) , Germany
Work-Life-Balance
[. .. ] to work An environment that empowers and supports colleagues to manage all aspects of their wellbeing by focusing on a holistic approach What youll be doing:In this [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] role you will support activities across both Medical Affairs Clinical Development objectives for the portfolio of pipeline products in inflammatory bowel disease. You will serve as a key interface with clinical trial sites across all development programs, working closely with Clinical Development and Clinical Operations. Additionally, you will collaborate with Medical Affairs to identify and engage key opinion leaders within [. .. ] meetings Sharing important clinical and scientific insights that you have gathered from fieldwork to cross-functional teams Acting as an internal and external scientific expert Adhering to compliance requirements Supporting investigator-initiated studies What youll need to be successful: An advanced doctoral degree (MD, Ph D, Pharm D) is preferred Relevant therapeutic area knowledge in the field of immunology or immuno-oncology, experience in gastroenterology is a plus. Post graduate therapeutic area experience is preferred Fluency in English and local language 3+ [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Site Relationship Manager
• Essen, Nordrhein- Westfalen
About this role TFS Health Science is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire
clinical development journey. Our [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] expertise includes full service capabilities, resourcing and Functional Service (FSP) solutions. The Site Relationship Manager (SRM) covers multiple indications within the assigned country throughout the full life cycle of the trial. The key focus areas are to facilitate optimal clinical trial setup, execution, and quality by understanding [. .. ] freelance opportunity at around 0.7FTE. Key Responsibilities Understanding the Local Environment Gain knowledge of the assigned region (treatment standards, healthcare system, regulatory environment, KOLs, site capabilities, etc. ) . Support development of countryspecific plans to engage advocacy groups and enhance recruitment. Attend local medical/ support group meetings and conferences. Collaborate with internal teams and CROs to ensure quality feasibility data and effective site selection. Provide input on sitelevel recruitment targets and strategies. Understand and support compliance with local regulatory and [. .. ] 5 years of experience as a Clinical Research Associate, Monitor, or similar role. Proven clinical research and site management experience within Pharma, Biotech, or CRO settings. Direct experience collaborating with investigator sites and investigators. Strong knowledge of ICH GCP guidelines. Demonstrated ability to build and maintain site relationships both inperson and remotely. Excellent networking, communication, and problemsolving skills. Experience in rare diseases and endocrinology What We Offer We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and [. .. ]
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Häufig gestellte Fragen
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 144 offene Stellenanzeigen für Clinical Support Investigator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Support Investigator Jobs?
Aktuell suchen 15 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:
- wax. (11 Jobs)
- Tubulis GmbH (11 Jobs)
- TFS Health Science (10 Jobs)
- Sobi (2 Jobs)
- Miltenyi Biotec B. V. Co. KG (1 Job)
In welchen Bundesländern werden die meisten Clinical Support Investigator Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Support Investigator Jobs werden derzeit in Bayern (27 Jobs), Nordrhein-Westfalen (20 Jobs) und Baden-Württemberg (12 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Support Investigator Jobs?
Clinical Support Investigator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
