119 Jobs für Clinical Trial Investigator
Stellenangebote Clinical Trial Investigator Jobs
Job vor 4 Tagen bei Jobleads gefunden
• München, Bayern
[. .. ] aligned with local and European medical affairs priorities. Build and expand relationships/ networks with key medical and scientific experts in the field of breast cancer and/or lung [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] cancer. Support clinical trials by identifying study sites, participating in SIVs (Site Inviations Visits) , assisting with patient enrollment, and ensuring smooth information exchange. Identify research opportunities, including Investigator-Initiated Trials, Real-World Evidence, and other evidence-generation studies. Represent the organization at scientific conferences, advisory boards, and educational events, sharing insights and preparing reports for internal stakeholders. Ensure timely documentation of HCP interactions, compliance with local policies, and accurate reporting of insights and safety information. Qualifications Advanced degree [. .. ] Germany. Minimum 3 years of experience and an established network in Breast Cancer and/or Lung Cancer therapeutic areas, ideally within a pharmaceutical company. Strong expertise in GCP-compliant clinical trial support, with a solid understanding of trial design and execution. Exceptional ability to process, communicate, and present complex medical and scientific information effectively. Proven self-management and project management skills to independently plan and execute stakeholder engagement. Highest ethical standards with knowledge of clinical regulations, industry standards, and German codes [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
Senior/ Medical Director (Ophthalmology)
• 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 : [. .. ]
Job am 04.12.2025 bei Jobleads gefunden
• 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 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 : [. .. ]
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 our [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 operational goals and regulatory standards. This role offers a hybrid model (50 at clients office in Munich) . Key Responsibilities Serve as the primary point of contact for study teams on all matters related to clinical trial budgets and contracts. Prepare [. .. ] 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 position [. .. ] 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, [. .. ] 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 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/ Ce Ms) is aware of the contractual obligations and parameters. Uses prior clinical experience, operational data, metrics and reports to identify risks to clinical trial management deliverables. Escalates to the project manager any risks to clinical trial management deliverables (timeline, quality and budget) and any activities and requests which are out of contracted scope. Employs strategic thinking and problem-solving skills to propose and implement risk mitigations. Participates and presents in key meetings such as [. .. ]
Job gestern bei Jobleads gefunden
Clinical Research Associate-12 months monitoring experience required
• 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 drug development process, specifically clinical trial/ research. Knowledge of international standards (GCP/ ICH, FDA, EMEA) . 12+ months monitoring experience required. Ability to travel domestically (and possibly internationally) as needed to study sites, training, and meetings. Minimum of 50 overnight travel may be required. What ICON can offer you: In addition to a competitive salary, ICON [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• 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 processes [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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
[. .. ] top-tier QA talent with groundbreaking life sciences opportunities Champion compliance and precisionhelp deliver lifechanging therapies. Proclinical is seeking a GCP QA Consultant to support quality assurance activities [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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
• Berlin
Work-Life-Balance
[. .. ] supports colleagues to manage all aspects of their wellbeing by focusing on a holistic approach What Youll Be Doing In this role you will support activities across [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 the medical community to communicate non-promotional scientific, and medical information regarding disease state and/or pipeline products. What Your Day-to-[. .. ] 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 oncology community and collects impactful insights to [. .. ] 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
[. .. ] and supports colleagues to manage all aspects of their wellbeing by focusing on a holistic approach What youll be doing:In this role you will support activities across [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 the medical community to communicate non-promotional scientific, and medical information regarding disease state and/or pipeline products. What your day-to-[. .. ] 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 the local environment, creating and maintaining strong, longterm relationships with sites, and supporting applicable Sponsor Teams in CRO and Sponsor site oversight activities. As part of our SRS/ FSP team, you will be dedicated [. .. ] 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 [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
Job Description Including, but not limited to the following : Shape and develop the
clinical development plans, while adhering to the highest scientific and ethical standards Design, conduct and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] report Sobi-sponsored studies in close collaboration with the rest of the clinical development team, the clinical study teams, regulatory, safety and other cross-functional teams, as applicable Act as Study Physician responsible for Sobi-sponsored studies if required : responsible for the development of clinical study synopsis and protocols, contribute to the statistical analysis plans, perform medical monitoring, participate in Investigator meetings and other study-related activities and provide input/ review of other main clinical study documents, as needed and appropriate Interact and consult with key opinion leaders and patient representatives, and lead advisory boards to define the clinical development stratetgy and inform the clinical trial design Provide strategic and operational clinical development expertise in interactions with regulatory and reimbursement authorities. Contribute with high-quality scientific and medical input to delivery of clinical parts of submissions and other regulatory documents as well as to responses to Health Authoritys questions to support e. g. , scientific advice, [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
(Junior-) Field Medical Advisor-Rare Oncology South
• München, Bayern
Absolventen, Einsteiger, Trainees
[. .. ] gifted cultivator of new and exciting opportunities grounded in science? The (Junior-) Field Medical Advisor serves as the primary field-based point of contact with healthcare providers (HCPs) [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] including clinical investigators on a range of clinical and scientific issues. The primary role is to deliver and facilitate medical education and communications, research, and scientific insight gathering activities of the client. This includes the provision of scientific and medical data on both licensed and unlicensed products and indications as permissible by [. .. ] aligned to strategy within the business Serves as external, credible scientific expert on disease area and client products at HCP field meetings, key medical and scientific conferences, advisory boards, clinical investigator meetings and patient advocacy group meetings Identify key field insights related to client products, activities and the disease area and effectively disseminate and collaborate with cross-functional partners Facilitate clear communication between the business and investigators in investigator engagement for both client trials and investigator-sponsored studies and barriers to [. .. ] Pharm D Demonstrable experience in an MSL function with oncology desired Knowledge of clinical research design and GCP in the oncology/ immune oncology area Demonstrate a strong understanding of clinical research trial design and study analysis including cost effectiveness and other high-level HEOR evidence approaches Demonstrate ability to develop trust and maintain integrity with KOLs/ External Clinical and Scientific Experts, investigators, HCPs, and institutions; as well as with peers, and others Ability to convey complex scientific concepts and information appropriately tailored [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
• Hamburg
[. .. ] Relationship Manager role at TFS Health Science. 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 entire clinical development journey. Our expertise includes full service capabilities, resourcing and Functional Service (FSP) solutions. About This Role 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 the local environment, creating and maintaining strong, longterm relationships with sites, supporting applicable Sponsor Teams in CRO and Sponsor site oversight activities. As part of our SRS/ FSP team, you will be dedicated to [. .. ] 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 [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Medical Science Liaison NM-Asia Pacific
• Gemeinde Au, Vorarlberg
[. .. ] involved in care of patients. Generate and execute tactical regional plans to provide needs based, value-added support of the medical and scientific community in line with company [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] goals. Support clinical development initiatives including investigator-initiated research (IIR) and Liva Nova-sponsored clinical studies and registries (e. g. , site identification, trial recruitment, and presentation of final approved data) . Collaborate with key internal and external stakeholders on Medical Affairs-led initiatives including publications, advisory boards, medical education (e. g. , CME) opportunities, training, and speaker development. Identify, profile, prioritize and map thought leaders in line with strategic initiatives and goals. Support [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
• Hamburg
[. .. ] their potential. With us, every single employee puts patients first. Make an impact in advancing Cell Therapy by ensuring the highest standards of quality and compliance. We [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] are seeking a Clinical Quality Manager (CQM) (m/f/d) - Cell Therapy to join our Cell Therapy Clinical Operations (CTCO) team. In this role, you will collaborate with the Business Processes, Quality Learning (BPQL) team to provide expert guidance and coaching, enabling the successful delivery of Cell Therapy studies by the Site Management [. .. ] SMM; develop and implement compliance improvement initiatives. Provide country-level consultation during RIST, inspections, and audits; act as audit coordinator for internal audits and serve as SME during sponsor and investigator site inspections. Act as a key member throughout the inspection process, including consultation for inspection responses. Analyze quality metrics and trends to improve performance and proactively manage issues. Participate in regional CT SMM leadership teams and facilitate quality review meetings. Identify, track, and elevate compliance risks; support risk mitigation activities [. .. ] and external partners. Excellent written and verbal communication skills, with the ability to influence, negotiate, collaborate, solve problems, present effectively, mentor others, and manage conflicts. Strong knowledge of international clinical trial regulations and guidelines (ICH GCP, FDA, EMA) and internal standards across functions. Ability to engage and collaborate across boundaries, influence effectively, and maintain a problem-solving focus. Capacity to manage multiple competing priorities, demonstrating innovation, ownership, accountability, and a growth mindset. A strong professional reputation within the business and industry. [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
(Senior) Director Clinical Development
• München, Bayern
Führungs-/ Leitungspositionen
Company Description The (Senior) Director
Clinical Development is responsible for shaping, developing and executing the clinical development strategy for the assigned product. Specific responsibilities include design of clinical trials [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] across all phases (including phase IV) , clinical protocol development, medical monitoring, analysis of study data, and contribution to clinical study reports, registration dossier modules and briefing [. .. ] teams, regulatory, safety and other crossfunctional teams. Act as study physician for Sobi-sponsored studies: develop study synopsis and protocols, contribute to statistical analysis plans, perform medical monitoring, participate in investigator meetings and review other key clinical documents. Interact with key opinion leaders and patient representatives, lead advisory boards to define clinical strategy and inform trial design. Provide strategic and operational clinical development expertise in interactions with regulatory and reimbursement authorities. Contribute highquality scientific and medical input to regulatory submissions, responses to Health Authority questions, and support scientific advice, IND applications and marketing authorisations across multiple geographies. Represent the clinical function in meetings with Health Authorities. [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
MSL Radioligand Therapy
• Rotkreuz, Zug
[. .. ] with Medical Experts and Key Stakeholders. The role strategically supports the development, launch, and commercialization of Novartis products through scientific exchange, soliciting external insights, responding to unsolicited [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] requests, and implementing clinical and educational strategies. This position reports directly to the National MSL Lead. Major Accountabilities Engage with Medical Experts (MEs) to educate on medical/ scientific information Ensure appropriate identification/ mapping of MEs and Key Accounts and identify opportunities to involve MEs when specific medical needs arise Develop and execute ME engagement [. .. ] effective delivery of medical information and insights Develop, plan, implement, and timely execute field medical tactics and engagement plans, aligned with the brand strategy Support Novartis clinical research programs, optimize trial execution, and provide scientific educational support to potential and actual study sites in collaboration with clinical operations Facilitate Investigator Initiated Trial (IIT) process upon investigator request Serve as a medical resource to field matrix colleagues Qualifications MD, Pharm D or Ph D in health/ life sciences with a solid background in the relevant scientific area Business fluent in German and English; knowledge of French is an asset; other languages are a [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Manager Medical Science Liaison Oncology
• Berlin
Jobticket
[. .. ] aligned with local and European medical affairs priorities. Build and expand relationships/ networks with key medical and scientific experts in the field of breast cancer and/or lung [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] cancer. Support clinical trials by identifying study sites, participating in SIVs (Site Inviations Visits) , assisting with patient enrollment, and ensuring smooth information exchange. Identify research opportunities, including Investigator-Initiated Trials, Real-World Evidence, and other evidence-generation studies. Represent the organization at scientific conferences, advisory boards, and educational events, sharing insights and preparing reports for internal stakeholders. Ensure timely documentation of HCP interactions, compliance with local policies, and accurate reporting of insights and safety information. Qualifications Advanced degree [. .. ] Germany. Minimum 3 years of experience and an established network in Breast Cancer and/or Lung Cancer therapeutic areas, ideally within a pharmaceutical company. Strong expertise in GCP-compliant clinical trial support, with a solid understanding of trial design and execution. Exceptional ability to process, communicate, and present complex medical and scientific information effectively. Proven selfmanagement and project management skills to independently plan and execute stakeholder engagement. Highest ethical standards with knowledge of clinical regulations, industry standards, and German codes of [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Site Relationship Manager
• Kassel, Hessen
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 the local environment, creating and maintaining strong, longterm relationships with sites, and supporting applicable Sponsor Teams in CRO and Sponsor site oversight activities. As part of our SRS/ FSP team, you will be dedicated [. .. ] 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 [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
Clinical Trial Project Manager
Our Mandant, an innovative biotech company in the
clinical Phase 2 stage, is seeking a Clinical
Trial Project Manager to oversee the execution of international clinical trials in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the field of neurodegenerative and ophthalmologic diseases. Your Responsibilities Drafting and reviewing clinical trial documents, including study protocols, patient information, investigator brochures, study plans, manuals, and reports End-to-end execution of clinical trials, including comprehensive monitoring activities from study start-up through close-out Development of deviation plans; defining and assessing protocol deviations at patient, site, and study level, and recommending follow-up actions Providing clinical expertise and conducting risk/ [. .. ]
Job vor 8 Tagen bei Jobleads gefunden
Clinical Trial Manager-single sponsor
• München, Bayern
Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and commercial insights into outcomes to address modern [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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/ Central Monitors) is aware of the contractual obligations and parameters. Uses prior clinical experience, operational data, metrics and reports to identify risks to clinical trial management deliverables. Escalates to the project manager any risks to clinical trial management deliverables (timeline, quality and budget) and any activities and requests which are out of contracted scope. Employs strategic thinking and problemsolving skills to propose and implement risk mitigations. Participates and presents in key meetings such as Kick [. .. ]
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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 119 offene Stellenanzeigen für Clinical Trial Investigator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trial Investigator Jobs?
Aktuell suchen 10 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:
- Tigermed (22 Jobs)
- Veeda Lifesciences (11 Jobs)
- Tubulis GmbH (11 Jobs)
- TFS Health Science (5 Jobs)
- Proclinical (1 Job)
- Astra Zeneca (1 Job)
In welchen Bundesländern werden die meisten Clinical Trial Investigator Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trial Investigator Jobs werden derzeit in Nordrhein-Westfalen (21 Jobs), Bayern (21 Jobs) und Sachsen (10 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trial Investigator Jobs?
Clinical Trial Investigator Jobs gehören zum Berufsfeld Medizinisch-technische Assistenz / MTA.
