13 Jobs für Clinical Trial Officer
Stellenangebote Clinical Trial Officer Jobs
Job am 11.03.2026 bei Mindmatch.ai gefunden
Teleflex
• AT- 9 Wien
Expected Travel: More than 50 Requisition ID: 13617 Position Summary The
Clinical Research Associate (CRA) is responsible for scheduling and conducting on-site and remote monitoring visits in compliance with applicable [...]
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[...] regulatory standards (MDR, ISO 14155, ICH/ GCP guidelines, Teleflex procedures and IRB/ EC policies) . The CRA conducts monitoring visits as identified by the monitoring plan, study team or department needs [. .. ] study team and department management via escalation of issues and/or within the monitoring visit report. The CRA has a minimum of two years of work experience as a clinical trial monitor and assists the Management Team with training needs. Principal Responsibilities Conducts monitoring within timelines and according to the monitoring plan and Teleflex procedures. Works cooperatively with Research Coordinators and Investigators to schedule and conduct monitoring visits including site qualification, site initiation, routine monitoring and site closure visits. Evaluates quality [. .. ] for resolution. Collects necessary documents and contributes to document filing. Ensures compliance with national and local safety reporting requirements. Collects information of local safety reporting requirements and reports to Safety Officer (SO) at predefined timepoints. Prepares national safetyrelated submission documents to EC/ NCA upon request by SO. Acts as contact for national EC (s) and NCA regarding safety reporting upon request by SO. Submits local safety documentation to EC/ NCA upon request by SO. Follows up with study sites on safety/ [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
Führungs-/ Leitungspositionen
[. .. ] is a pioneering Healthtech company dedicated to revolutionizing drug development through the power of AI. We are passionate about accelerating medical advancements and improving patient outcomes. Our [...]
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[...] team comprises seasoned clinical research professionals, data scientists, and AI experts, working collaboratively to bridge the gap between cutting-edge technology and real-world clinical needs. With an unwavering commitment to revolutionize healthcare, we envision a world where all patients benefit from accelerated and cost-effective access to treatments. Biorce is poised to redefine [. .. ] Responsibility for hitting quarterly targets and consistently delivering against ambitious commercial goals. Develop and execute go-to-market strategies tailored to the EU market, in collaboration with the Chief Commercial Officer and Global head of commercial operations. Identify high-value potential clients and decision makers, and cultivate strong, trust based relationships. Represent Biorce at industry events, conferences, and client meetings. Collaborate closely with Marketing, Clinical Solutions, and Product teams to tailor pitches and ensure client success. Provide market intelligence and feedback [. .. ] assigned territory with professionalism and drive. Requirements 5+ years of experience in business development, strategic partnerships, or enterprise sales in the biotech, pharmaceutical or CRO sectors. Deep understanding of clinical trial processes and a strong network in the EU biopharma ecosystem. Proven track record of closing mid-to-large enterprise deals and building long-term relationships with C-level stakeholders. Entrepreneurial mindset with the ability to operate independently in a fast-paced, startup environment. Strong communication and presentation skills; ability to [. .. ]
Job am 17.04.2026 bei Jobleads gefunden
• Eschborn, Hessen
Führungs-/ Leitungspositionen
[. .. ] seeking an experienced Director, Global Medical Affairs to help shape the future of mechanical circulatory support and hemodynamic management worldwide. This strategic leadership role reports directly to [...]
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[...] the Chief Medical Officer/ Divisional Vice President, Global Medical Affairs and will be based in Europe. Why This Role Matters This is a highimpact position at the forefront of advancing innovative therapies for patients living with heart failure. The Director will play a key role in guiding the clinical and scientific strategy across a rapidly evolving portfolio, partnering closely with Clinical Affairs, R D, Market Access, Marketing, and Commercial teams. The role requires a significant global presence (approx. 60 travel) to engage with investigators, clinical sites, and internal stakeholders. This position will manage Clinical Research professionals to provide medical [. .. ] support to maintain focus on product performance and safety, ISS, grants, and scientific activities. In addition, Director will work cross functionally to support the review, implementation and publication of clinical trial results. This role provides input to establish the range plans and goals for clinical science, and is responsible for the implementation and maintenance of the clinical research-related policies, processes and procedures related to their respective functional areas. Director provides leadership and direction to product performance testing and evaluation, use [. .. ]
Job am 22.01.2026 bei Jobleads gefunden
• München, Bayern
Führungs-/ Leitungspositionen
We are partnering with a growing, oncology-focused biotech to appoint a Head of
Clinical Operations at Senior Director or VP level. This is a critical leadership role reporting directly to [...]
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[...] the Chief Medical Officer, based in Munich with a hybrid working model (3 days on site) . This position offers the opportunity to make a meaningful impact at a pivotal stage of the companys development. The organisation is currently running Phase II clinical trials and preparing to advance into Phase III, with a strong [. .. ] with execution. You will bring: Significant experience leading clinical operations in oncology, ideally through latestage development Proven leadership experience managing senior teams and external vendors Strong understanding of global clinical trial delivery A collaborative mindset and the ability to act as a true thought partner to senior leadership A handson approach-comfortable being close to the detail and rolling up your sleeves when needed Personality, communication style, and cultural fit are just as important as technical expertise. This is not a [. .. ]
Job vor 9 Tagen bei Jooble gefunden
Linical
• Deutschland Deutschland, DE
The
Clinical Research Associate is responsible for the feasibility, initiation, monitoring, and close-out of investigative sites. Major responsibilities include ensuring the safety and well-being of study participants at assigned sites, [...]
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[...] ensuring site compliance with Good Clinical Practice (GCPs) , applicable regulations, the protocol and study plans; ensuring data integrity through [. .. ] verification and monitoring process, and ensuring site compliance with all Investigational Product (IP) storage, inventory, dispensing, dosing, and disposition requirements. EU CRAs could have a shared role of Regulatory Affairs Officer (RAO) and CRA. The Regulatory department will oversee the RAO role while the Clinical Operations Manager (COM) will oversee the CRA role. Duties and Responsibilities Participates in the identification of potential investigative sites, conducts site qualification visits, collects, and reviews site regulatory documents, and prepares site qualification visit reports and [. .. ] contact with the site staff, to be aware of patient enrolment, enrolled patients status, IP supply and any further site requests or issues Ensures essential documents are filed in the Trial Master File (TMF) according to the project guidelines Ensures appropriate and timely transmission of clinical data to data management; reviews data queries, and clarifies and/or obtains changes to data as appropriate Conducts site close-out visits to include final IP reconciliation and disposition, review of completeness and accuracy of [. .. ]
Job am 18.04.2026 bei Jooble gefunden
GCP- Service International
• Freie Hansestadt Bremen Bremen, DE
Führungs-/ Leitungspositionen
Location: Bremen, Germany (office-based position) As Team Lead
Clinical Data Manager, you will oversee highquality clinical data management in line with GCP Serviceor Sponsor SOPs, ICH/ GCP guidelines, and [...]
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[...] national regulations. You will lead a team of Clinical Data Managers and manage all data related activities across international clinical studies. Responsibilities Lead, mentor, and provide expert support to the [. .. ] Provide structured, solution-oriented leadership and foster collaboration. Oversee data management activities across multiple studies, ensuring accuracy, consistency, and regulatory compliance. Review and approve data management deliverables as per clinical trial protocols. Supervise the design, testing, and implementation of clinical trial databases and data entry systems. Ensure timely processing, tracking, validation, and reporting of clinical data. Coordinate data submissions and ensure audit and inspection readiness. Act as the primary contact for clients on data management topics. Collaborate with crossfunctional teams to [. .. ] deletion of your personal data, to restrict or object to its processing, and to request data portability. If you have any questions regarding data protection, please contact our Data Protection Officer at We wish you all the best in your job search. Best regards, HR team GCP Service International Location: Bremen, Germany (office-based position) As Team Lead Clinical Data Manager, you will oversee highquality clinical data management in line with GCP Serviceor Sponsor SOPs, ICH/ GCP guidelines, and national regulations. [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Incyte Corporation
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern München, DE
[. .. ] Medical Affairs Inflammation Autoimmunity (IAI) Team and supports the development of the local medical strategy and medical plans within the therapeutic area of dermatology. The role provides [...]
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[...] a bridge between Clinical Development, Medical Affairs and the commercial organization. The (Senior) Medical Manager Dermatology will play a key role in developing and executing the medical and scientific (non-promotional) strategy for the German Immunology portfolio/ therapeutic area and will be involved in a wide range of activities for Incyte IAI drugs both [. .. ] marketing clinical activities such as registry/ database projects, epidemiological surveys, and PMOS studies) . Provide the required oversight to manage review, approval and conduct of IIR studies Collaborate with clinical trial teams and support investigator engagements (e. g. review new clinical study protocols, identifying potential investigators/ sites, conducting feasibility surveys) Supports adaptation of international/ local training and scientific material in collaboration with marketing and other internal stakeholders Supports development of publication plans and covers country data generation needs Provides scientific in-[. .. ] of the personal data we process, how it is shared, where it is stored or transferred to, how long we keep it, and contact information for Incyte, Incytes data protection officer, and your supervisory authority (if applicable) . Please contact if you have any questions or concerns or would like to exercise your rights. 87189988 [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Avomind
• Berlin Berlin, DE
[. .. ] learning to the human voice to detect heart-failure worsening earlier than any existing method, transforming how clinicians monitor and manage their patients. Building on a strong foundation [...]
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[...] of international clinical trials, they are now entering the next chapter: bringing this breakthrough technology to market and expanding the clinical evidence base to establish their technology as the new standard of care. Together with their deployed remote monitoring platform, which is already trusted by more than 200 cardiologists and more than 1, [. .. ] This is not a back office research role. You will be at the center of our mission, connecting clinical research, scientific development, and medical affairs. The position combines hands-on trial execution with high-level strategic and cutting-edge scientific work in a fast-moving start-up environment. Working closely with their Chief Medical Officer and the R D Team, you will help shape their global evidence strategy across pivotal trials, AI validation, and real-world studies. You will collaborate directly with investigators from the most renowned research institutions around the world (Charit Berlin, Mayo Clinic, UCSF, Duke, and many more) as part of multi-[. .. ]
Job vor 7 Tagen bei Jobleads gefunden
Clinical Research Associate-Germany
• München, Bayern
The
Clinical Research Associate is responsible for the feasibility, initiation, monitoring, and close-out of investigative sites. Major responsibilities include ensuring the safety and well-being of study participants at assigned [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] sites, ensuring site compliance with Good Clinical Practice (GCPs) , applicable regulations, the protocol and study plans; ensuring data integrity through [. .. ] verification and monitoring process, and ensuring site compliance with all Investigational Product (IP) storage, inventory, dispensing, dosing, and disposition requirements. EU CRAs could have a shared role of Regulatory Affairs Officer (RAO) and CRA. The Regulatory department will oversee the RAO role while the Clinical Operations Manager (COM) will oversee the CRA role. Duties and Responsibilities Participates in the identification of potential investigative sites, conducts site qualification visits, collects, and reviews site regulatory documents, and prepares site qualification visit reports and [. .. ] contact with the site staff, to be aware of patient enrolment, enrolled patients status, IP supply and any further site requests or issues Ensures essential documents are filed in the Trial Master File (TMF) according to the project guidelines Ensures appropriate and timely transmission of clinical data to data management; reviews data queries, and clarifies and/or obtains changes to data as appropriate Conducts site closeout visits to include final IP reconciliation and disposition, review of completeness and accuracy of files, [. .. ]
Job am 29.03.2026 bei Jobleads gefunden
• Zug
Führungs-/ Leitungspositionen
Chief Revenue
Officer (CRO) Remote (Europe) Life Sciences Saa S Series A Growth Headhunty has been exclusively retained by a Swiss-based life sciences software company to appoint a Chief [...]
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[...] Revenue Officer (CRO) . Our client operates in the clinical research/ CRO technology space, providing a vertical Saa S platform used by pharmaceutical companies, biotech firms, and contract research organizations to manage and optimize clinical trials. The company has already achieved strong productmarket fit and 15M ARR and is now preparing for rapid commercial expansion ahead of a planned Series A [. .. ] from early revenue through scale Strong network within the European life sciences ecosystem Ability to operate as both strategic leader and handson deal closer Preferred Background Experience working in clinical trial software, research platforms, or healthtech Saa S Prior experience supporting venture fundraising or Series A preparation Track record of building revenue through strategic partnerships and alliances Why This Opportunity? Opportunity to build the commercial organization from day one Direct partnership with the CEO and founding team Highgrowth company in the rapidly [. .. ]
Job am 11.03.2026 bei Jobleads gefunden
Clinical Research Associate
• Wien
Expected Travel: More than 50 Requisition ID: 13617 Position Summary The
Clinical Research Associate (CRA) is responsible for scheduling and conducting on-site and remote monitoring visits in compliance with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] applicable regulatory standards (MDR, ISO 14155, ICH/ GCP guidelines, Teleflex procedures and IRB/ EC policies) . The CRA conducts monitoring visits as identified by the monitoring plan, study team or department needs [. .. ] study team and department management via escalation of issues and/or within the monitoring visit report. The CRA has a minimum of two years of work experience as a clinical trial monitor and assists the Management Team with training needs. Principal Responsibilities Conducts monitoring within timelines and according to the monitoring plan and Teleflex procedures. Works cooperatively with Research Coordinators and Investigators to schedule and conduct monitoring visits including site qualification, site initiation, routine monitoring and site closure visits. Evaluates quality [. .. ] for resolution. Collects necessary documents and contributes to document filing. Ensures compliance with national and local safety reporting requirements. Collects information of local safety reporting requirements and reports to Safety Officer (SO) at predefined timepoints. Prepares national safetyrelated submission documents to EC/ NCA upon request by SO. Acts as contact for national EC (s) and NCA regarding safety reporting upon request by SO. Submits local safety documentation to EC/ NCA upon request by SO. Follows up with study sites on safety/ [. .. ]
Job am 28.02.2026 bei Jobleads gefunden
(Senior) Medical Manager Dermatology (m/f/d)
• München, Bayern
[. .. ] Medical Affairs Inflammation Autoimmunity (IAI) Team and supports the development of the local medical strategy and medical plans within the therapeutic area of dermatology. The role provides [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a bridge between Clinical Development, Medical Affairs and the commercial organization. The (Senior) Medical Manager Dermatology will play a key role in developing and executing the medical and scientific (non-promotional) strategy for the German Immunology portfolio/ therapeutic area and will be involved in a wide range of activities for Incyte IAI drugs both [. .. ] marketing clinical activities such as registry/ database projects, epidemiological surveys, and PMOS studies) . Provide the required oversight to manage review, approval and conduct of IIR studies Collaborate with clinical trial teams and support investigator engagements (e. g. review new clinical study protocols, identifying potential investigators/ sites, conducting feasibility surveys) Supports adaptation of international/ local training and scientific material in collaboration with marketing and other internal stakeholders Supports development of publication plans and covers country data generation needs Provides scientific in-[. .. ] of the personal data we process, how it is shared, where it is stored or transferred to, how long we keep it, and contact information for Incyte, Incytes data protection officer, and your supervisory authority (if applicable) . Please contact if you have any questions or concerns or would like to exercise your rights. #J-18808-Ljbffr 82196456 [. .. ]
Job am 16.12.2025 bei Jobleads gefunden
Senior Biostatistician (m/f/d) in Bremen
• Bremen
Beratungs-/ Consultingtätigkeiten
[. .. ] open to taking responsibility for projects and fellow team members alike. The responsibility of a Senior Biostatistician is to manage all statistical aspects which occur in the [...]
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[...] frame of a clinical trial from initial consultation regarding study concepts, to providing input into study protocols and writing SAPs, to conducting the analysis and summarizing the results. In this context, we are looking for a candidate who understand the importance of the following: Statistical aspects throughout the entire course of clinical trials including establishment [. .. ] deletion of your personal data, to restrict or object to its processing, and to request data portability. If you have any questions regarding data protection, please contact our Data Protection Officer at We wish you all the best in your job search. Best regards, HR team GCP-Service International If we have piqued your interest, we look forward to receiving your application. Please address it as follows, stating your salary expectations and the earliest possible starting date: #J-18808-Ljbffr [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Clinical Trial Officer pro Jahr?
Als Clinical Trial Officer verdient man zwischen EUR 55.000,- bis EUR 80.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Trial Officer Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 13 offene Stellenanzeigen für Clinical Trial Officer Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trial Officer Jobs?
Aktuell suchen 6 Unternehmen nach Bewerbern für Clinical Trial Officer Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Trial Officer Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Trial Officer Stellenangebote:
- Teleflex (1 Job)
- Linical (1 Job)
- GCP- Service International (1 Job)
- Incyte Corporation (1 Job)
- Avomind (1 Job)
In welchen Bundesländern werden die meisten Clinical Trial Officer Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trial Officer Jobs werden derzeit in Bayern (4 Jobs), Bremen (2 Jobs) und Sachsen (1 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trial Officer Jobs?
Clinical Trial Officer Jobs gehören zum Berufsfeld Medizinisch-technische Assistenz / MTA.
