70 Jobs für Clinical Trials Investigator
Stellenangebote Clinical Trials Investigator Jobs
Job vor 4 Tagen bei Mindmatch.ai gefunden
Novartis
• 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] 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 [. .. ] statistical analysis methodology and good medical/ scientific writing skills Ability to collaborate across boundaries for shared success and resolve issues or understand when to escape Skills Desired Clinical Research, Clinical Trials, Data Integrity, Learning Design, Risk Monitoring J-18808-Ljbffr 03698147 [. .. ]
Job vor 14 Tagen bei Mindmatch.ai gefunden
IQVIA
Site Management Lead
• 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 [...]
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 [. .. ] 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.
• 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] 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 [. .. ] or medical device companies (Director level) At least 10 years of clinical research experience working within pharmaceutical, biotech, or medical device companies (Senior Director level) Demonstrated experience leading global clinical trials or overseeing international clinical study programs across multiple regions Previous experience leading physician teams and managing direct reports (Senior Director level) Strong understanding of the clinical development process, including matrix multidisciplinary teams, regulatory submissions, and data analysis Sound understanding in oncology clinical research, with tumor-based program experience Hands-on [. .. ]
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 [. .. ] 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
• 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 [. .. ] 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
Pharmako-/ Vigilanzmanagerin in klinischen Studien (stellvertretende Fachbereichsleitung) (m/w/d)
• Freiburg im Breisgau, Baden- Württemberg
Führungs-/ Leitungspositionen Abgeschlossenes Studium
Flexible Arbeitszeiten Betriebliche Altersvorsorge Jobticket
[. .. ] Freiburg. Es bietet für Wissenschaft und Industrie umfassenden und professionellen Service bei der Planung, Durchführung und Auswertung von klinischen Studien gemäß geltenden Regularien und der international gültigen [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Qualitätsstandards der Good Clinical Practice (ICH-GCP) . Wir bieten Ihnen: Mitarbeit an Forschungsprojekten zur Beantwortung aktueller patientenorientierter Fragen in der Medizin, eine verantwortungsvolle und abwechslungsreiche Tätigkeit mit abgeschlossenem Studium der Medizin als Hintergrund: Einarbeitung in die Rolle des Physician in Pharmaco-/ Vigilance Einarbeitung in die Rolle des Medical Officer angenehme und kollegiale Arbeitsatmosphäre [. .. ] Bereich Ihr Profil: ein abgeschlossenes Studium der Medizin oder Pharmazie oder vergleichbare Abschlüsse Erfahrung in der Arzneimittelsicherheit und Kenntnisse der relevanten gesetzlichen Vorschriften Kenntnisse in der Planung und Durchführung von Investigator Initiated Trials (IITs) sind von Vorteil sehr gute Kenntnisse der medizinischen Terminologie Erfahrung mit klinischen Kodier- und Klassifikationssystemen versiert im Umgang mit Windows, MS-Office und Datenbankeingabesystemen sehr gute Kommunikationsfähigkeiten in Wort und Schrift, auch in englischer Sprache sehr sorgfältiges und systematisches Arbeiten Teamfähigkeit Die Stelle ist unbefristet zu besetzen. Universitätsklinikum Freiburg [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
• Hamburg
[. .. ] functions. This role represents SWAV as a scientific expert at conferences and internal/ external meetings, supports HEOR and market access initiatives, reviews promotional materials, and partners with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] cross-functional teams (Clinical Affairs, Regulatory, Professional Education, Marketing) . Additionally, the role will actively support investigator-initiated studies (IISs) , facilitating scientific and operational collaborations with investigators, and supporting dissemination and publication of results while ensuring compliance with applicable laws, codes, and company policies. Key Responsibilities Support in development of professional and credible relationships with clinical and scientific thought leaders. Support investigatorinitiated studies (IISs) : Interact [. .. ] information. Support in driving communication and education of internal (e. g. commercial, management) and external (e. g. customers, collaborators, distributors) stakeholder on scientific evidence (out of congresses, adboards, funded/sponsored trials) Be a therapeutic expert and provide scientific support for key regional business partners (Clinical Affairs, Regulatory, Marketing, Professional Education and Market Access and HEOR) . Collaborate with internal stakeholders, including HEOR, to develop summaries of key data, health economic insights and other scientifically relevant information to inform SWAV strategic priorities [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Senior CRA-Germany
[. .. ] organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, youll collaborate with passionate problem [. .. ] each subject/ patient as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/ patient. 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 [. .. ] or applicants to perform the essential functions of the job. Summary Roles within Clinical Monitoring/ CRA job family are responsible for monitoring during clinical research studies to ensure that the trials are being conducted in accordance with widely accepted clinical practices. This includes conducting on-site and remote monitoring, developing tools, procedures, and processes to ensure quality monitoring. Impact and Contribution Individual contributors with responsibility in a professional or technical discipline or specialty, but may manage two or fewer employees. May [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] The specific deliverables being managed can vary and is defined in the contract Amplity holds with the client organisation. CDL Responsibilities Education and Engagement Educate on science, our client, pipeline, trials, disease Assist Clinical Ad-Board coordination and execution for studies Assist and attend National and International Meetings Attend and support Patient Advocacy with sponsored events Study Start-Up Identify KOLs and create a working network for trials Serve as companys ambassador for early phase studies Boots on the ground to [. .. ] 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
(Senior) Medical Science Liaison (m/w/d)
Abgeschlossene Ausbildung
[. .. ] Betreuung Netzwerkarbeit: Sie gestalten den wissenschaftlichen Austausch auf Augenhöhe mit führenden Onkolog:innen, Chefärzt:innen und Key Opinion Leadern und leiten zukunftsweisende Advisory Boards Medical Projects Advisory: Sie betreuen [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] und begleiten eigenverantwortlich Investigator Initiated Trials (IITs/ ISRs) und unterstützen lokale klinische Studienaktivitäten Medical Insights Strategie: Sie erfassen kontinuierlich relevante Insights aus dem Markt und gestalten die regionale wie nationale Medical-Affairs-Strategie aktiv mit Cross-funktionale Zusammenarbeit: Sie agieren als geschätzte Schnittstelle zu Key Account Management, Clinical Operations und Marketing unter strikter Wahrung der wissenschaftlichen Unabhängigkeit Kongresspräsenz: Sie repräsentieren das Unternehmen auf nationalen und internationalen Fachkongressen und Expertenforen Das Anforderungsprofil Ausbildung: Abgeschlossenes naturwissenschaftliches, pharmazeutisches oder medizinisches Studium (Master, Ph D, MD, Pharm D) Industrie-Erfahrung (Must-have) : Zwingend 23 Jahre aktuelle Praxiserfahrung als MSL oder Field-based Medical [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
• 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. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 and develops synergistic relationships with KOLs to expand research, advisory, and educational partnership opportunities Training of the Key Account Management Team [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
Manager Medical Affairs International (m/f/d)
• Hamburg
[. .. ] functions. This role represents SWAV as a scientific expert at conferences and internal/ external meetings, supports HEOR and market access initiatives, reviews promotional materials, and partners with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] cross-functional teams (Clinical Affairs, Regulatory, Professional Education, Marketing) . Additionally, the role will actively support investigator-initiated studies (IISs) , facilitating scientific and operational collaborations with investigators, and supporting dissemination and publication of results while ensuring compliance with applicable laws, codes, and company policies. Key Responsibilities Support in development of professional and credible relationships with clinical and scientific thought leaders. Support investigator-initiated studies (IISs) : [. .. ] information. Support in driving communication and education of internal (e. g. commercial, management) and external (e. g. customers, collaborators, distributors) stakeholder on scientific evidence (out of congresses, adboards, funded/sponsored trials) . Be a therapeutic expert and provide scientific support for key regional business partners (Clinical Affairs, Regulatory, Marketing, Professional Education and Market Access and HEOR) . Collaborate with internal stakeholders, including HEOR, to develop summaries of key data, health economic insights, and other scientifically relevant information to inform SWAV strategic [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
• Genf
Führungs-/ Leitungspositionen
We are looking for a Director,
Clinical Scientific Strategy Precision Oncology to serve as the scientific and clinical backbone of one of our flagship AI-based Sa MD (Software as [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a Medical Device) product lines in the breast cancer space. This is a lifecycle role spanning evidence generation, KOL engagement, and clinical deployment support. This person will be [. .. ] at key congresses and symposia; deliver medical education and facilitate advisory boards Identify clinical champions and research collaborators including cooperative groups, academic institutions, and healthcare systems for clinical validation interventional trials; codevelop investigator-initiated research frameworks Gather and synthesise fieldbased medical insights; systematically feed clinical intelligence back into Product, Portfolio, and R D strategy 4. Crossfunctional Collaboration Collaborate closely with: Medical Affairs, Commercial, VP Pathology, Market Access, R d/Biostatistics, and Marketing Contribute to boardlevel and investorfacing scientific communications as required Support Medical [. .. ]
Job vor 8 Tagen bei Jobleads gefunden
Medical Science Liaison Austria
[. .. ] patients treated with Tumor Treating Fields (TT Fields) . Additional responsibilities includebut are not limited toacting as a scientific interface between the company and HCP communities regarding [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] communication about Novocures clinical development plans as well as other research and development activities. Developing appropriate training materials, supporting external research projects related to marketed or investigational Novocure indications, and participating in field-based activities to advance existing products and introduce new indications are also part of the role. The MSL plays an important [. .. ] Increase therapy awareness among prescribers and non-prescribers Manage the entire Austrian territory and all associated field activities Deliver medical training on Novocure products and disease areas Support and accompany investigator-sponsored trials (ISTs) and other research projects Provide HCP insights and market information to the company Participate in medical (Europe-wide) congresses, and organize and follow up on advisory boards Promote scientific advancement related to TT Fields Support Phase 3 studies in collaboration with clinical teams and researchers Build and maintain relationships [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
• Dresden, Leipzig, Frankfurt, Kassel, Sachsen, Hesse, Hessen
[. .. ] Manager Position type: Field Reporting Line: Medical Director, Germany How will your role help us transform hope into reality? The Medical Science Liaison (MSL) is a field-based [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] scientific and clinical expert who strategically supports the medical objectives of Blueprint Medicines development programs. The MSL is responsible for identifying, developing, and managing peer-to-peer relationships with a variety of healthcare providers, including hematologists, oncologists, pathologists, dermatologists, gastroenterologists, and allergists/ immunologists, as well as basic scientists, in academic and community hospitals. [. .. ] with HCPs. Accurately profile country and define local dynamics related to patient diagnosis and referral for treatment Deliver medical/ scientific presentations to internal external stakeholders Assist with company-sponsored clinical trials and facilitation of investigator-initiated trials (ISTs) Lead planning and execution of regional advisory boards Collaborate with cross functional partners on internal projects and external initiatives Provide educational meeting support at scientific congresses Support training of cross functional teams Adhere to corporate and healthcare compliance guidance in all activities, including those related to clinical [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
(Senior) Medical Science Liaison, Medical Affairs (EU) - Northwest Germany
• 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 [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
• Baar, Zug
Führungs-/ Leitungspositionen
Biogen is seeking a Director, Country Site Operations (CSO) , Europe to lead
clinical country and site operations across European countries, ensuring site performance,
investigator engagement, affiliate collaboration, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and sponsor oversight. You will supervise 5-8 direct reports and 15-25 matrixed resources, guiding strategy and execution for trials. In this role, you will partner with medical, development, QA, CRO/ FSP partners, and affiliates to optimize protocol implementation, recruitment #J-18808-Ljbffr 03320165 [. .. ]
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 development [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
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, consulting, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 our [. .. ] (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 and develops synergistic relationships with KOLs to expand research, advisory, and educational partnership opportunities Training of the Key Account Management Team [. .. ]
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. [. .. ] remote monitoring of trial sites to verify compliance with regulatory requirements and clinical protocols. Utilizes data analytics and risk-based monitoring techniques to identify potential issues and trends, ensuring that trials are conducted in accordance with established clinical practices. Collaborates with site teams to develop and implement tools, procedures, and processes that enhance quality monitoring and support the overall success of clinical trials. Impact and Contribution Individual contributors with responsibility in a professional or technical discipline or specialty, but may manage [. .. ]
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 America, Africa, and Southeast Asia, P95 supports public health agencies, pharmaceutical companies, academic institutions, and global organizations such as WHO and the European Commission. [. .. ] 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. [. .. ] remote monitoring of trial sites to verify compliance with regulatory requirements and clinical protocols. Utilizes data analytics and risk-based monitoring techniques to identify potential issues and trends, ensuring that trials are conducted in accordance with established clinical practices. Collaborates with site teams to develop and implement tools, procedures, and processes that enhance quality monitoring and support the overall success of clinical trials. Impact and Contribution Individual contributors with responsibility in a professional or technical discipline or specialty, but may manage [. .. ]
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 [. .. ] and to grow with a team that values collaboration and impact, we encourage you to apply. Skills Analytical Thinking, Clinical Data Interpretation, Clinical Development, Clinical Pharmacology, Clinical Trial Designs, Clinical Trials Monitoring, Digital Fluency, Drug Regulatory Affairs, Evidence Based Decision Making, Executive Presence, Hematology and Oncology, Learning Agility, Matrix Leadership, Real World Evidence (RWE) , Scientific Presentations If you are based in Cambridge, MA; Waltham, MA; Rockville, MD; or San Francisco, CA, the annual base salary for new hires in this [. .. ]
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 leading global clinical development partner delivering insights driven clinical and consulting solutions to the life sciences industry. With 22, 000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient [. .. ] 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, [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical Trials Investigator pro Jahr?
Als Clinical Trials Investigator verdient man zwischen EUR 60.000,- bis EUR 100.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Trials Investigator Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 70 offene Stellenanzeigen für Clinical Trials Investigator Jobs.
In welchen Bundesländern werden die meisten Clinical Trials Investigator Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trials Investigator Jobs werden derzeit in Baden-Württemberg (10 Jobs), Niedersachsen (8 Jobs) und Bayern (7 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trials Investigator Jobs?
Clinical Trials Investigator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
