6 Jobs für Clinical Trials Investigator
Stellenangebote Clinical Trials Investigator Jobs
Job vor 2 Tagen bei Mindmatch.ai gefunden
Mini Med Group
• AT- 2 Schweiz
About the Role Lead the EMEA Regulatory Reimbursement
Trials to launch Flex/ Vivera in FY28 OUS. At Mini Med, our mission is to transform the lives of people living with [...]
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[...] diabetes through innovative technologies, services, and solutions. We are looking for a Senior Clinical Research Manager to lead a team of clinical research professionals responsible for generating and communicating high-quality clinical evidence that demonstrates the safety, efficacy, and value of Mini Med diabetes technologies. As a senior member of the Clinical Research team, you will provide strategic and operational leadership across clinical studies [. .. ] Build and maintain organisational clinical and scientific expertise through engagement with scientific literature, professional conferences, healthcare professionals, and internal stakeholders. Ensure effective planning and delivery of clinical study team training, investigator meetings, and education for hospital and study-site personnel. Oversee the medical and scientific review of promotional and educational materials to support compliant, accurate, and evidence-based claims. Establish and maintain strategic relationships with investigators, key opinion leaders, research institutions, and other external partners. Drive strong cross-functional collaboration with [. .. ]
Job vor 10 Tagen bei Mindmatch.ai gefunden
Novocure Inc.
• AT- 2 Schweiz
Select how often (in days) to receive an alert: Create Alert At Novocure, every role contributes to extending the lives of people living with cancer. As our new
Clinical Research [...]
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[...] Scientist, youll play a key role in advancing our global clinical development programs and bringing innovative therapies closer to patients. Reporting to the Senior Clinical Research Scientist within Global Clinical Development, this is an opportunity to shape the scientific direction and execution of innovative oncology clinical trials evaluating Tumor Treating Fields (TT Fields) . This role offers a unique blend of scientific leadership and direct engagement with investigators and clinical sites. Beyond contributing to protocol development, clinical strategy, and data interpretation, youll build meaningful partnerships with investigators, participate in study-related site activities, and help ensure the [. .. ] coding review, and identification of emerging clinical insights. Contribute to statistical analysis planning and review outputs to ensure robust clinical interpretation and alignment with study objectives. Prepare scientific materials for investigator meetings, Data Monitoring Committees (DMCs) , Steering Committees, and senior leadership presentations. Build strong, trusted relationships with investigators, key opinion leaders, and clinical research professionals, serving as a scientific partner throughout the lifecycle of clinical studies. Participate in site initiation visits, investigator interactions, scientific meetings, congresses, advisory committees, and other [. .. ]
Job am 27.07.2026 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 [...]
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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 [. .. ] 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 am 19.07.2026 bei Mindmatch.ai gefunden
Galderma Pharma S. A
• AT- 2 Schweiz
Führungs-/ Leitungspositionen
[. .. ] create an unparalleled, direct impact. Position Summary In collaboration with global development teams, the Head of Medical Experts, Therapeutic Dermatology is responsible for providing lead medical input [...]
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[...] and expertise to clinical development programs conducted for Therapeutic Dermatology products. Acting on the responsibility, the Head of Medical Experts, Therapeutic Dermatology, secures that clinical development is conducted in accordance with the Galderma quality management system, international standards and regulatory requirements. Essential Functions Leadership and Management Member of the Clinical Science Leadership Team Lead [. .. ] global clinical studies to meet regulatory requirements and budget targets. Provides clinical/ medical strategy (e. g. , scientific rationale, objectives, endpoints) to clinical development plans, Target Product Profiles, , protocols, investigator brochures, briefing packages, CTDs, draft labels, and other documents. Serves as lead Therapeutic Dermatology clinical/ medical expert interacting with external stakeholders (e. g. , regulatory authorities, CROs, key opinion leaders, advisory boards, patient advocacy groups) , and internal stakeholders (e. g. , Research, Global Medical Affairs, Global Product Strategy) Advises [. .. ] Dermatology and knowledge in clinical development preferred Minimum of 10 years of drug development experience in Therapeutic Dermatology Minimum of 5 years of demonstrated leadership, management, and accomplishment conducting clinical trials in Therapeutic Dermatology Excellent knowledge of international guidelines ICH/ GCP, basic knowledge of GMP/ GDP Experience with regulatory submissions and health authority interactions is required Proven ability to interpret and present efficacy and safety data derived from clinical trials in Therapeutic Dermatology Demonstrated technical knowledge of methodology of study designs [. .. ]
Job am 09.07.2026 bei Mindmatch.ai gefunden
IQVIA Argentina
• AT- 9 Wien
Führungs-/ Leitungspositionen
Vienna, Austria Full time Home-based R1546726 To lead Local Study Teams (LSTs) at country level to deliver committed components of
clinical studies according to agreed resources, budget and timelines complying [...]
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[...] with Sponsor Procedural Documents, international guidelines such as ICHGCP as well as relevant local regulations. In addition to leading LST (s) , the Local Study Associate Director may perform site monitoring as needed to support the flexible capacity model. The Local [. .. ] on country study level: proactively manages sites, stakeholders, local and global vendors and customers to ensure risks are timely identified, mitigated and managed. Communicates and coordinates regularly with National Coordinating Investigator/ National Lead Investigator on recruitment and other study matters, if applicable. Plans and leads National Investigator meet Ensures that all study documents are ready for final archiving and completion of local part of the e TMF. Plans and leads activities associated with audits and regulatory inspections in liaison with CQAD and [. .. ] Affairsled or Academicled studies) . Good knowledge of international guidelines ICH GCP as well as relevant local regulations. Proven ability to lead and motivate cross functional teams to deliver clinical trials according to or ahead of time plan, budget and with required quality. Good medical knowledge of Oncology, Rare Diseases, cardiology, hematology, CVRM Therapeutic Areas. Good knowledge of the Drug Development Process. Excellent understanding of the Clinical Study Process including monitoring. Very good understanding of the Study Drug Handling Process and [. .. ]
Job am 09.07.2026 bei Mindmatch.ai gefunden
IQVIA Argentina
• AT- 9 Wien
Führungs-/ Leitungspositionen
Vienna, Austria Full time Home-based R1546726 To lead Local Study Teams (LSTs) at country level to deliver committed components of
clinical studies according to agreed resources, budget and timelines [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] complying with Sponsor Procedural Documents, international guidelines such as ICHGCP as well as relevant local regulations. In addition to leading LST (s) , the Local Study Associate Director may perform site monitoring as needed to support the flexible capacity model. The Local [. .. ] on country study level: proactively manages sites, stakeholders, local and global vendors and customers to ensure risks are timely identified, mitigated and managed. Communicates and coordinates regularly with National Coordinating Investigator/ National Lead Investigator on recruitment and other study matters, if applicable. Plans and leads National Investigator meet Ensures that all study documents are ready for final archiving and completion of local part of the e TMF. Plans and leads activities associated with audits and regulatory inspections in liaison with CQAD and [. .. ] Affairsled or Academicled studies) . Good knowledge of international guidelines ICH GCP as well as relevant local regulations. Proven ability to lead and motivate cross functional teams to deliver clinical trials according to or ahead of time plan, budget and with required quality. Good medical knowledge of Oncology, Rare Diseases, cardiology, hematology, CVRM Therapeutic Areas. Good knowledge of the Drug Development Process. Excellent understanding of the Clinical Study Process including monitoring. Very good understanding of the Study Drug Handling Process and [. .. ]
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 6 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 Schleswig-Holstein (0 Jobs), Thüringen (0 Jobs) und Berlin (0 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trials Investigator Jobs?
Clinical Trials Investigator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
