5 Jobs für Clinical Trial Investigator
Stellenangebote Clinical Trial Investigator Jobs
Job am 27.07.2026 bei Mindmatch.ai gefunden
Novocure Inc.
• AT- 2 Schweiz
Führungs-/ Leitungspositionen
Based in either Haifa, Israel or Baar, Switzerland offices. At Novocure, every role contributes to extending the lives of people living with cancer. As our new Senior Director,
Clinical Regulatory [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Affairs, youll play a key part in this mission. This is a highly visible global leadership role at the intersection of clinical development, oncology science, regulatory strategy, and commercialization readiness. This position is designed for a strategic leader who can shape how innovative Class IIb/ III medical technologies are [. .. ] Affairs, Medical Affairs, R D, Marketing, Legal, Quality, and Regulatory Operations to align regulatory strategy with clinical and business objectives. Provide strategic regulatory guidance for clinical study design, protocol development, investigator brochures, informed consent documentation, and overall study execution. Lead and support interactions with global health authorities, including FDA, EMA and Notified Bodies, serving as the primary regulatory contact for clinical and strategic matters. Prepare and lead teams through critical regulatory engagements including pre-submission meetings, advisory panels, inspections, and regulatory negotiations. Author, review, and oversee high-quality regulatory documentation including IDEs, PMAs, EU clinical trial applications, and related clinical regulatory submissions. Interpret and apply complex global regulatory requirements to support development programs involving novel technologies and breakthrough device opportunities. Support global product launch readiness, labeling strategy, and promotional review activities in alignment with evolving regulatory expectations. Contribute to internal governance discussions, risk assessments, and strategic [. .. ]
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 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 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 [. .. ] on medically relevant questions emerging during study execution Develops presentation materials for advisory boards, investigator meetings, protocol training meetings or other clinical events as required. Supports ongoing review of clinical trial safety data, analysis, and interpretation in collaboration with global development team members Provides medical input in development of TPPs and other relevant documents. Supports development team on medical/ scientific aspects of data review, SSRM, coding, edit checks, CRF, DMC, and other study documents. Advises investigators and/or CROs on medically [. .. ]
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] Consent Form (MICF) and subsequent site level ICFs, as required, including any relevant translations, and in line with relevant Sponsor SOPs and local regulations. Ensures all country and site level trial essential documents required by ICHGCP prior to study start have been collected and verified for correctness, prior to setting sites ready to enrol, and in line with Sponsor SOPs. Plans and coordinates applicable local drug activities (from local purchase or reimbursement to drug destruction) . Sets up and maintains the [. .. ] 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 [. .. ]
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] Consent Form (MICF) and subsequent site level ICFs, as required, including any relevant translations, and in line with relevant Sponsor SOPs and local regulations. Ensures all country and site level trial essential documents required by ICHGCP prior to study start have been collected and verified for correctness, prior to setting sites ready to enrol, and in line with Sponsor SOPs. Plans and coordinates applicable local drug activities (from local purchase or reimbursement to drug destruction) . Sets up and maintains the [. .. ] 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 [. .. ]
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 5 offene Stellenanzeigen für Clinical Trial Investigator Jobs.
In welchen Bundesländern werden die meisten Clinical Trial Investigator Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trial Investigator Jobs werden derzeit in Schleswig-Holstein (0 Jobs), Thüringen (0 Jobs) und Berlin (0 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trial Investigator Jobs?
Clinical Trial Investigator Jobs gehören zum Berufsfeld Medizinisch-technische Assistenz / MTA.
