65 Jobs für Clinical Trial Investigator
Stellenangebote Clinical Trial Investigator Jobs
Neu Job vor 2 Std. bei StepStone gefunden
PROVIREX Genome Editing Therapies GmbH
• Hamburg
Teilzeit Homeoffice möglich
[. .. ] die weltweit erste Genome-Editing-Therapie zu entwickeln, die HIV funktionell heilen soll. Gemeinsam mit führenden Universitätskliniken in Deutschland bereiten wir derzeit eine erste klinische Prüfung am Menschen vor. [...]
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[...] Als Clinical Trial Assistant unterstützt du unser Team bei der organisatorischen Vorbereitung und Umsetzung der klinischer Studie und trägst dazu bei. unsere Therapie in die klinische Entwicklung zu bringen. Aufgaben Du unterstützt das klinische Studienteam bei administrativen und organisatorischen Aufgaben im Tagesgeschäft. Du unterstützt den Aufbau und die laufende Pflege des elektronischen Trial Master File (e TMF) sowie den Aufbau der Investigator Site Files (el SF) . Du bereitest studienrelevante Unterlagen vor, koordinierst Versand und Ablage und verfolgst fehlende Dokumente nach zum Beispiel Verträge, Kenntnisnahmen und Unterlagen für das e TMF. Du koordinierst Termine und organisierst Meetings inklusive Protokollführung. Du unterstützt die Koordination der Abrechnung mit den Prüfzentren. Du koordinierst und verfolgst den Versand [. .. ]
Job vor 4 Tagen bei Mindmatch.ai gefunden
Novartis
Clinical Scientific Expert I
• AT- 2 Lavamünd
Job Description Summary-Contributes, with appropriate oversight, to all relevant aspects of global
clinical trial (s) activities to deliver study outcomes within schedule, budget, quality/ compliance and performance standards. May lead [...]
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[...] specific aspects of global clinical trial (s) . Core member of the Clinical Trial Team. -Applicable to Clinical Scientific Expert IThe Clinical Scientific Expert I (CSE I) provides clinical and scientific support through all [. .. ] contributing to aggregate reports/ patient narratives, attendance of Safety Monitoring Meetings (SMT) ) , if required. Produce training materials and provide training to i CTT. Support/ present at study level meetings (Investigator Meetings, Data Monitoring Committee (DMC) meetings or others) , as required. Develop subject matter expertise (disease area knowledge, clinical data review tools and/or processes) . Contribute to line function initiatives, local and/or global education and process development projects, as required. Essential Requirements Advanced degree in life sciences/ healthcare [. .. ]
Job vor 14 Tagen bei Mindmatch.ai gefunden
IQVIA
• AT- 9 Wien
Führungs-/ Leitungspositionen
IQVIA
Clinical Functional Service Partnerships (Clinical FSP) department is providing highly skilled professionals to our clients project team to set-up and execute clinical trials. Site Management Lead is a key [...]
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[...] member of global Clinical Trial Team nominated to a specific trial. The STLs are accountable for authoring the monitoring risk assessments and plans, maintaining sponsor oversight, trend analysis, signal detection and delivery of their assigned trials to provide delivery of sponsors pipeline through accurate planning and efficient execution of the Site Monitoring and Site Management [. .. ] CRAs. Independently author and review trial-level documents. Act as subject matter expert on site management and monitoring topics. Join and presents at global/ regional/ local Trial Team meetings and Investigator Meetings. Integrate patient/ site level feedback to the documents ensuring design with a focus on the patient and patient safety. Represent monitoring strategy in global/ regional/ local meetings. Timely responses to Site Management and monitoring questions from external and internal stakeholders (including Regulatory Authority/ Ethics Committee) . Facilitate communication and [. .. ]
Job am 11.09.2026 bei Mindmatch.ai gefunden
Novocure Inc.
Clinical Trial Physician, Oncology
• AT- 2 Schweiz
Select how often (in days) to receive an alert: Create Alert CH Wayne, PA, US, 19087 Portsmouth, NH, US, 03801 As our new
Clinical Trial Physician, Oncology, youll play a [...]
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[...] key part in this mission. As a key member of our multi-disciplinary oncology team, you will serve as a medical expert supporting Tumor Treating Fields (TT Fields) Therapy clinical programs. Depending on experience and level, you will either lead a clinical study or a [. .. ] the safety and efficacy of TT Fields delivered concomitantly with standard therapy in patients with cancer Drive clinical development strategy including protocol authoring, regulatory and ethics committee submissions, study initiation, investigator communication, safety and medical monitoring, data screening and analysis, and publication initiatives Author and oversee key clinical documents including study protocols and Clinical Study Reports (CSRs) , ensuring submission readiness and inspection/ audit preparedness Establish and lead physician teams and key opinion leader relationships to support study execution and overall [. .. ]
Job gestern bei Jobleads gefunden
Site Management Lead
• Wien
Führungs-/ Leitungspositionen
IQVIA
Clinical Functional Service Partnerships (Clinical FSP) department is providing highly skilled professionals to our clients project team to set-up and execute clinical trials. Site Management Lead is a key [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] member of global Clinical Trial Team nominated to a specific trial. The STLs are accountable for authoring the monitoring risk assessments and plans, maintaining sponsor oversight, trend analysis, signal detection and delivery of their assigned trials to provide delivery of sponsors pipeline through accurate planning and efficient execution of the Site Monitoring and Site Management [. .. ] CRAs. Independently author and review trial-level documents. Act as subject matter expert on site management and monitoring topics. Join and presents at global/ regional/ local Trial Team meetings and Investigator Meetings. Integrate patient/ site level feedback to the documents ensuring design with a focus on the patient and patient safety. Represent monitoring strategy in global/ regional/ local meetings. Timely responses to Site Management and monitoring questions from external and internal stakeholders (including Regulatory Authority/ Ethics Committee) . Facilitate communication and [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Site Management Lead
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
IQVIA
Clinical Functional Service Partnerships (Clinical FSP) department is providing highly skilled professionals to our clients project team to set-up and execute clinical trials. Site Management Lead is a key [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] member of global Clinical Trial Team nominated to a specific trial. The STLs are accountable for authoring the monitoring risk assessments and plans, maintaining sponsor oversight, trend analysis, signal detection and delivery of their assigned trials to provide delivery of sponsors pipeline through accurate planning and efficient execution of the Site Monitoring and Site Management [. .. ] CRAs. Independently author and review trial-level documents. Act as subject matter expert on site management and monitoring topics. Join and presents at global/ regional/ local Trial Team meetings and Investigator Meetings. Integrate patient/ site level feedback to the documents ensuring design with a focus on the patient and patient safety. Represent monitoring strategy in global/ regional/ local meetings. Timely responses to Site Management and monitoring questions from external and internal stakeholders (including Regulatory Authority/ Ethics Committee) . Facilitate communication and [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• Baar, Zug
Führungs-/ Leitungspositionen
[. .. ] with high unmet need, grounded in a deep understanding of disease biology and deliberate scientific choices that connect discovery to meaningful impact in the real world. The [...]
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[...] Medical Director, Oncology Clinical Development-GU (Genitourinary) is the physician within the clinical program team, bringing medical expertise, clinical judgement, and a patient-centered perspective to the design, conduct, and interpretation of clinical studies. This role is accountable for medical monitoring and safety oversight, ensuring that patient safety and clinical integrity are maintained throughout [. .. ] ensure that the physician perspective is fully integrated into study delivery. The role serves as a core member of the Clinical Matrix Team (CMT) , contributing to study-level decisions, investigator engagement, and regulatory interactions. For more complex or multi-study programs, the Medical Director may provide medical guidance to other physicians within the program and contribute to broader clinical discussions that inform program-level decisions led by the CDL. In This Role You Will: Serve as the physician within the [. .. ] medical monitoring activities for assigned clinical studies, including real-time clinical decision-making on patient eligibility, protocol-related medical queries, and safety oversight Conduct and oversee medical review of clinical trial data, both directly and through oversight of delegated medical review activities Interpret and contextualize safety data in collaboration with pharmacovigilance, ensuring appropriate signal detection, escalation, and benefit-risk assessment at the study level Participate in safety review forums, including Safety Review Team (SRT) discussions, Independent Data Monitoring Committee (IDMC) data [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Global Medical Director, Oncology
• Baar, Zug
Führungs-/ Leitungspositionen
Position Summary You will lead global medical activities for one or more oncology assets and work closely with research, commercial,
clinical operations, and local medical teams. You will shape evidence [...]
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[...] generation, guide external scientific engagement, and help translate clinical insights into patient impact. We value collaboration, clear scientific judgement, practical leadership, and a focus on improving patient outcomes. This role offers growth, meaningful impact, and the chance to unite science, technology [. .. ] with external experts, patients, payers and regulators to gather insights and shape strategy. Partner with research and development to design and prioritize global and supportive clinical studies, including review of investigator-initiated proposals. Support brand and launch planning by providing medical input to local operating companies and commercial teams. Provide medical governance and review scientific materials to ensure accuracy, compliance and clear communication. Why You? We are seeking people who bring scientific credibility, practical leadership and a collaborative mindset. You will [. .. ] experience in oncology. 5+ years experience in medical affairs, clinical development, or related roles in Oncology. Demonstrated experience leading global medical strategies and evidence generation plans. Strong understanding of clinical trial design and operational experience with global studies. Experience engaging external experts, advisory boards, and congress planning. Excellent written and verbal communication in English and proven ability to present complex data clearly. Preferred Qualifications Deep disease knowledge in lung oncology. Experience with expanded access programs or post-approval study requirements. Prior [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
[. .. ] 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 [...]
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[...] accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, youll collaborate with passionate problem [. .. ] each subject/ patient as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/ patient. Assess factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol deviation/ violations and pharmacovigilance issues. Per the Clinical Monitoring/ Site Management Plan (CMP/ SMP) : Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) is accurate and complete [. .. ] to ensure IP is appropriately (re) labelled, imported and released/returned. Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness. Reconciles contents of the ISF with the Trial Master File (TMF) . Ensures the investigator/ physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations. Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/ Site [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
Team Leader (Player/ Manager) Clinical Development Liaison (CDL) Neuromuscular Diseases-Germany
Führungs-/ Leitungspositionen
Work-Life-Balance
Team Leader (Player/ Manager)
Clinical Development Liaison (CDL) Neuromuscular Diseases Business Unit: Field Operations Reports to: Program Director, Medical, Amplity Location: Germany Territory: Germany and some other countries in [...]
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[...] Europe Role Type: Individual Contributor with Leadership Responsibilities (Player-Coach) About the Role Amplity is partnering with an innovative global biopharmaceutical company dedicated to advancing transformative [. .. ] Clinical Development Liaison (CDL) to support and drive clinical development activities across Germany. This is a strategic field-based role combining scientific leadership, stakeholder engagement, and operational support for clinical trial execution. As a Clinical Development Liaison, you will serve as a key scientific partner to investigators, study sites, and internal stakeholders, supporting study start-up, patient identification, enrollment strategies, and study conduct. In addition, as a Player-Coach, you will provide mentorship, guidance, and leadership to fellow CDL team members, [. .. ] with insights from interactions with Investigators Email updates post-communication to internal ( CRO) stakeholders about outcomes of discussions Handover of interest/ knowledge about publication interest/ pub planning or potential investigator Initiated Trials (IITs) Compliance Operate in a highly ethical manner and comply with all laws, regulations and policies. Complete mandatory training in assigned timelines upon hire as well as when new policies, SOPs, guidance are issued Team Leader Responsibilities Lead/coordinate the activities of small teams or individual field CDLs [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
• Taufkirchen, Bayern
[. .. ] Medical Affairs team. Your focus will be on desmoid tumour treatment (with options to change in the future) . In this field based role, you will drive [...]
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[...] scientific engagement, support clinical development, and shape our medical strategy within your assigned region. You will serve as a trusted scientific expert, build impactful relationships with KOLs, and play a key role in bringing innovative therapies to patients. The focus area within Germany for this position in Mid Germany is Rhein/ Ruhr, Köln, Gießen/ [. .. ] appropriate exchange of scientific information Build and maintain strong scientific relationships with national, regional, and local KOLs Gather and communicate medical insights to inform strategy and improve patient outcomes Support investigator initiated research as primary liaison Provide scientific support at national and European congresses, advisory boards, and medical programs Lead selected national medical projects and initiatives Provide clinical presentations and information in response to unsolicited questions (as appropriate) in academic, non-academic, and healthcare provider settings Collaborate with Clinical Operations to support trial site identification and patient enrollment Develop and execute territory plans aligned with national and regional medical strategy Partner with HEOR/ Market Access to support health economic and outcomes data generation Support Medical Information requests Assist the Country Medical Director in shaping national KOL engagement and medical plans Mentor new or [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
Medical Science Liaison
• Freiburg im Breisgau, Baden- Württemberg
The Regional Medical Science Liaison (MSL) serves as the primary field-based point of contact with healthcare providers (HCPs) including
clinical investigators on a range of clinical and scientific issues. [...]
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[...] 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 Facilitate clear communication between the client and investigators in investigator engagement for both client trials and investigator-sponsored studies and barriers to enrolment for pipeline assets Works to the highest ethical compliance, ethics and safety standards adhering to all local regulations and laws Maintains [. .. ] or rare disease experience preferred or experience in endocrinology or lipidology experience Knowledge of clinical research design and GCP in the cardiology 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 8 Tagen bei Jobleads gefunden
[. .. ] your time focused on customer-facing activities. The position combines scientific exchange, insight gathering, evidence generation, and cross-functional collaboration. Youll work closely with Medical Affairs, Commercial, Market Access, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and Clinical Development teams to support strategic priorities. The role offers exposure to innovative therapies, clinical development, and evolving therapeutic areas. It is an opportunity to build trusted relationships with leading experts while contributing to initiatives designed to improve patient outcomes. Accountabilities Build and maintain trusted relationships with healthcare professionals, researchers, professional [. .. ] plans for key external experts and contribute to speaker development activities. Collect, analyze, and communicate insights from the field to support medical strategy and broader organizational decision-making. Support clinical trial feasibility assessments, investigator-initiated studies, and other evidence-generation initiatives. Maintain strong knowledge of assigned therapeutic areas, pipeline developments, emerging scientific evidence, and the competitive landscape. Collaborate cross-functionally with Medical Affairs, Commercial, Market Access, Clinical Development, and other internal teams. Contribute to product launch preparation and lifecycle management activities across the Nordic [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
Entry-level Clinical Research Associate-Clinical Study Coordinator experience
Clinical Research Coordinators wanted at Medpace Become a CRA and join our growing team This is an exciting opportunity for clinical research professionals with at least one year of [...]
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[...] Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace. Through our PACE Training Program, you will receive the [. .. ] monitoring, and closeout visits at research sites in compliance with the approved protocol Communication with the medical site staff including coordinators, clinical research physicians, and their site staff Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements On-site and virtual/ remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/ deficiencies and corrective/ preventive actions to bring a site back into compliance and mitigate risks moving forward Verification that the investigator is enrolling only eligible subjects Regulatory document review Medical device and/or investigational product/ drug accountability and inventory Verification and review of adverse [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
• Berlin
[. .. ] (60 of working time) . Roles Responsibilities Scientific Expertise: Act as a local expert for Genmabs areas of interest, maintaining up-to-date knowledge of our products, relevant current [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] evolving clinical landscapes, and the competitive environment. Medical/ Scientific Exchange: Establish and maintain enduring relationships with members of the healthcare/ scientific communities who are experts in Genmabs areas of interest. Provide appropriate clinical and scientific information on Genmab products in a fair and balanced manner to healthcare professionals (HCPs) in response to [. .. ] Genmab at selected medical/ scientific conferences. Offer local expertise to inform engagement of health technology agencies/ other payers regarding the value of Genmab products. Engage HCPs to advance advisory boards, investigator meetings, medical education events. Clinical Trials Research: Collaborate with clinical development and clinical operations teams to support company-sponsored studies, including site identification, feasibility, setup, and recruitment. Engage with investigators to advance understanding of company assets and pipeline data. Reactively facilitate investigator-sponsored trial proposals, coordinating submission for internal review. Territory Management: Align and execute a local territory plan in accordance with EUR/ Ro W global MA objectives. Inform local publication planning. Training Education Support training of Genmab colleagues, enhancing their knowledge and understanding of clinical data and our medicines as required. Cross-Functional Collaboration [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
Director, Country Site Operations (CSO) , Europe
• Baar, Zug
Führungs-/ Leitungspositionen
About This Role The Director, Country Site Operations (CSO) , Europe is accountable for leadership and performance across assigned European countries, supporting Biogen
clinical trials across all phases of [...]
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[...] development and therapeutic areas. This role provides strategic and operational leadership to Clinical Country Site Leads (CCSLs) and country/ site operations resources, ensuring strong country delivery, site performance, investigator engagement, affiliate collaboration, and sponsor oversight. The role serves as the senior CSO operational leader for a sub-regional cluster of countries and provides proactive country intelligence, site insights, risk assessment, and operational recommendations to inform protocol planning, country selection, site strategy, enrollment forecasting, and study execution. This position partners closely with Worldwide Medical, Clinical Trial Delivery Units (CTDU) , Clinical Monitoring Leads (CMLs) , Site Managers, FSP partners, CRO partners, and affiliate leadership to support successful delivery of Biogens clinical trial portfolio and implementation of the CSO operating model, including IFm/SCOUT. Leadership scope is expected to include approximately 5-8 direct reports and 15-[. .. ]
Job vor 12 Tagen bei Jobleads gefunden
• München, Bayern
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 12 Tagen bei Jobleads gefunden
Global Study Manager-6-month contract-FSP
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal-to improve the worlds health. From
clinical trials to regulatory, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] consulting, and market access, every clinical development solution we provide is underpinned by something special-a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take [. .. ] We are expanding our team and seeking talented individuals to help drive industry leading innovation, With Heart. Key Accountabilities: Study Management Oversight Leads and coordinates the execution of a clinical trial globally from sourcing strategy and study specification development for requests for proposals to fully outsourced studies and ancillary vendors, study start up through database release and inspection readiness to ensure timely delivery of quality study data. May also provide input to and support compilation of sections to clinical study reports [. .. ] (TMF) setup for study management and country and site level documents Provides input into the risk planning process for the study Coordinates development of study and protocol training and global investigator meetings (IMs) Ensures that local IMs are coordinated by the SOM, if assigned to study Develops and provides key inputs to clinical trial budget (e. g. , per subject costs) Ensures that SOMs are inputting into the budget for local/ country level tasks (if assigned) , and reviews cost variance, [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
Medical Science Liaison
• Hamburg
[. .. ] Hamburg, Lower Saxony, Germany Job ID: 17828-OTHLOC-CVJw Yfw S The Regional Medical Science Liaison (MSL) 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 Facilitate clear communication between the client and investigators in investigator engagement for both client trials and investigator-sponsored studies and barriers to enrolment for pipeline assets Works to the highest ethical compliance, ethics and safety standards adhering to all local regulations and laws Maintains [. .. ] or rare disease experience preferred or experience in endocrinology or lipidology experience Knowledge of clinical research design and GCP in the cardiology 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 12 Tagen bei Jobleads gefunden
Clinical Research Associate-Berlin/ Leipzig/ Dresden
Clinical Research Associate-Berlin/ Leipzig/ Dresden Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act [. .. ] each subject/ patient, as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/ patient. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol deviation/ violations and pharmacovigilance issues. Per the Clinical Monitoring/ Site Management Plan (CMP/ SMP) : Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) is accurate and complete. [. .. ] to ensure IP is appropriately (re) labelled, imported and released/returned. Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness. Reconciles contents of the ISF with the Trial Master File (TMF) . Ensures the investigator/ physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations. Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/ Site [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
Clinical Research Associate Germany (remote, 0.8-1.0 FTE)
About us P95 and Julius
Clinical have recently joined forces, bringing together two highly complementary organizations with a shared mission: advancing global health through highquality epidemiological research and clinical [...]
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[...] trials. P95, founded in 2011 and headquartered in Belgium, is a global leader in epidemiology, vaccines, and infectious disease research. With offices across Europe, North America, South [. .. ] but are not limited to, the following: Performing Site Selection Visits (SSVs) , Site Initiation Visits (SIVs) , Monitoring Visits (MVs) , and Close-Out Visits (COVs) . Monitoring clinical trial sites according to protocol, sponsor requirements, and applicable regulations. Verifying data accuracy through Source Data Verification (SDV) and Source Data Review (SDR) . Reviewing informed consent documentation and ensuring patient safety is maintained. Identifying, documenting, and following up on protocol deviations and study issues. Supporting sites with studyrelated questions and [. .. ] within required timelines. Ensuring essential documents are complete and inspection ready. Contributing to riskbased monitoring activities and study quality oversight. Supporting study startup, recruitment, maintenance, and closeout activities. Participating in investigator meetings, study team meetings, and training activities as required. Experience The ideal candidate will have A Bachelors or Masters degree in Life Sciences, Nursing, Pharmacy, Biomedical Sciences, or a related field. A minimum of 2 years experience as a CRA on clinical trials (preferably with IP) . Solid knowledge of [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
Clinical Research Associate-Berlin/ Leipzig/ Dresden
Clinical Research Associate-Berlin/ Leipzig/ Dresden Updated: Yesterday Location: Remote, Germany Job ID: 25112473 Description Clinical Research Associate-Berlin/ Leipzig/ Dresden Syneos Health is a leading fully-integrated life sciences services organization [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, [. .. ] each subject/ patient, as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/ patient. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol deviation/ violations and pharmacovigilance issues. Per the Clinical Monitoring/ Site Management Plan (CMP/ SMP) : Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) is accurate and complete. [. .. ] to ensure IP is appropriately (re) labelled, imported and released/returned. Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness. Reconciles contents of the ISF with the Trial Master File (TMF) . Ensures the investigator/ physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations. Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/ Site [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
Medical Director-Oncology Clinical Development-GI
• Baar, Zug
Führungs-/ Leitungspositionen
[. .. ] with high unmet need, grounded in a deep understanding of disease biology and deliberate scientific choices that connect discovery to meaningful impact in the real world. The [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Medical Director, Oncology Clinical Development-GI is the physician within the clinical programme team, bringing medical expertise, clinical judgement, and a patientcentred perspective to the design, conduct, and interpretation of clinical studies. This role is accountable for medical monitoring and safety oversight, ensuring that patient safety and clinical integrity are maintained throughout study execution. [. .. ] to ensure that the physician perspective is fully integrated into study delivery. The role serves as a core member of the Clinical Matrix Team (CMT) , contributing to studylevel decisions, investigator engagement, and regulatory interactions. For more complex or multistudy programmes, the Medical Director may provide medical guidance to other physicians within the programme and contribute to broader clinical discussions that inform programmelevel decisions led by the CDL. In This Role You Will: Serve as the physician within the clinical programme [. .. ] Safety Oversight Lead medical monitoring activities for assigned clinical studies, including realtime clinical decisionmaking on patient eligibility, protocolrelated medical queries, and safety oversight Conduct and oversee medical review of clinical trial data, both directly and through oversight of delegated medical review activities Interpret and contextualise safety data in collaboration with pharmacovigilance, ensuring appropriate signal detection, escalation, and benefitrisk assessment at the study level Participate in safety review forums, including Safety Review Team (SRT) discussions, Independent Data Monitoring Committee (IDMC) data reviews, [. .. ]
Job vor 14 Tagen bei Jobleads gefunden
Site Monitoring Lead/Clinical Operations Leader-FSP-Remote
Führungs-/ Leitungspositionen
About Parexel Parexel is a leading global
clinical development partner delivering insights driven clinical and consulting solutions to the life sciences industry. With 22, 000+ employees worldwide, we partner [...]
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[...] with biopharmaceutical companies and research sites to design and deliver patient focused clinical trials that broaden access and make research a care option for anyone, anywhere. Parexel is a [. .. ] of the Clinical Development Operations team, the Site Monitoring Lead plays a critical role in the successful planning, oversight, and delivery of global clinical trials. This position is accountable for trial level site monitoring strategy, risk assessment, operational oversight, and collaboration with CRO partners to ensure high quality execution of clinical studies. The Site Monitoring Lead works closely with global clinical trial teams to drive performance, support inspection readiness, protect study participants, and ensure compliance with study protocols, ICH GCP, sponsor [. .. ] against milestones and key performance indicators. Participate in the development and maintenance of trial level documents, amendments, training materials, and monitoring related procedures. Lead and contribute to trial oversight meetings, investigator meetings, and cross functional study discussions at global, regional, and local levels. Conduct site and monitoring oversight activities, implement follow up actions, and escalation issues when required. Serve as a subject matter expert on site management and monitoring, providing guidance and training to study teams. Support trial close out activities, [. .. ]
Job vor 14 Tagen bei Jobleads gefunden
Medical Science Liaison
• Bremen
Description The Regional Medical Science Liaison (MSL) serves as the primary field-based point of contact with healthcare providers (HCPs) including
clinical investigators on a range of clinical and scientific [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 Facilitate clear communication between the client and investigators in investigator engagement for both client trials and investigator-sponsored studies and barriers to enrolment for pipeline assets Works to the highest ethical compliance, ethics and safety standards adhering to all local regulations and laws Maintains [. .. ] or rare disease experience preferred or experience in endocrinology or lipidology experience Knowledge of clinical research design and GCP in the cardiology 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 [. .. ]
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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 65 offene Stellenanzeigen für Clinical Trial Investigator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trial Investigator Jobs?
Aktuell suchen 5 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:
- PROVIREX Genome Editing Therapies GmbH (1 Job)
- Novartis (1 Job)
- IQVIA (1 Job)
- Novocure Inc. (1 Job)
In welchen Bundesländern werden die meisten Clinical Trial Investigator Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trial Investigator Jobs werden derzeit in Baden-Württemberg (9 Jobs), Bayern (9 Jobs) und Sachsen (8 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trial Investigator Jobs?
Clinical Trial Investigator Jobs gehören zum Berufsfeld Medizinisch-technische Assistenz / MTA.
