Clinical Trials Officer Stellenangebote


+ Suchfilter (0 aktiv)

17 Jobs für Clinical Trials Officer


Stellenangebote Clinical Trials Officer Jobs


Job gestern bei Jooble gefunden Hlx Life Sciences

Senior Project Management Officer

• Berlin Were working with a CRO whose seeking a Project Manager with 5+ years of CRO project management experience and a strong understanding of the full clinical trial lifecycle. Lead clinical [...]
MEHR INFOS ZUM STELLENANGEBOT[...] trials from study start-up through closeout-Manage sponsor relationships and cross-functional project teams-Coordinate activities across Clinical Operations and must have strong experience in Medical Writing, Data Management, and Quality Assurance-Ensure compliance with ICH-GCP, regulatory requirements, and company SOPs-Drive project success through effective communication, planning, and [. .. ]

▶ Zur Stellenanzeige
Job vor 7 Tagen bei Mindmatch.ai gefunden Teleflex

Clinical Research Associate

• AT- 9 Wien Homeoffice möglich 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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 [. .. ] 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/ [. .. ] Cardiology and/or Peripheral Vascular Intervention is an advantage. Specialized Skills/ Other Requirements Strong working knowledge, understanding and ability to apply MDR, ISO 14155 and ICH/ GCP guidelines governing clinical trials. Strong compliance focus. Demonstrated aptitude and knowledge in relevant therapeutic areas and ability to learn and integrate new therapeutic areas knowledge. Ability to train and mentor Clinical Studies personnel for remote and onsite monitoring visits. Ability to train onsite staff on the protocol, GCPs, data entry and other pertinent regulations. [. .. ]

▶ Zur Stellenanzeige
Job am 22.01.2026 bei Jobleads gefunden

Head of Clinical Operations-ONCOLOGY-HYBRID

• 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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 focus on solid tumours. The Role As Head of Clinical Operations, you will provide handson leadership across global clinical programmes, shaping and executing the clinical operations strategy while remaining close to day-to-day execution. Key responsibilities include: Leading, mentoring, [. .. ]

▶ Zur Stellenanzeige
Job vor 4 Tagen bei Jobleads gefunden

Head of Data Governance, Anonymization and Quality

• Basel, Basel- Stadt Führungs-/ Leitungspositionen [. .. ] Hybrid 3 days/ week in office Internal job title: Head of Data Governance, Anonymization and Quality, Data42 About the Role Data42 is Novartis enterprise data and AI [...]
MEHR INFOS ZUM STELLENANGEBOT[...] platform, bringing together clinical, research, and real world data to power advanced analytics and accelerate the discovery and development of innovative medicines. As part of the Data42 leadership team, the Head of Data Governance, Anonymization and Quality will establish and enforce data governance frameworks, standards, and controls to ensure data integrity, regulatory compliance, and [. .. ] data governance and data quality practices across BR, driving accountability and measurable outcomes Ensure ongoing audit readiness by maintaining robust controls, documentation, and compliance processes Serve as Deputy Enterprise Data Officer (EDO) , providing leadership, guidance, and continuity in data governance and oversight activities Essential Requirements 15+ Years of experience in Data Governance or related field, with strong interest in Governance and Application of AI Ph D or MSc in Statistics, Bioinformatics, Computer Science, Biostatistics, or a related quantitative discipline. Experience in [. .. ] please send an email to and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Skills Desired Clinical Trials Data Architecture Data Governance Data Integration Data Management Data Products Data Quality Data Science Data Strategy Drug Development Global Project Management Operations People Management #J-18808-Ljbffr 96108030 [. .. ]

▶ Zur Stellenanzeige
Job vor 12 Tagen bei Jobleads gefunden

Global Clinical Operations Lead (m/f/d)

• Luzern Führungs-/ Leitungspositionen [. .. ] health. If youre looking to join a successful, global company with real career opportunities, wed love to meet you. About the Role We are seeking an experienced [...]
MEHR INFOS ZUM STELLENANGEBOT[...] and proactive Global Clinical Operations Lead (f/m/d) to manage and oversee clinical trials/ clinical studies/ clinical investigations from initiation to close-out. This role will work closely with GC crossfunctional project teams, investigators, and Contract Research Organizations (CRO) to ensure that studies are conducted in compliance with applicable regulatory requirements, Good Clinical Practice (GCP) , and applicable institutional policies. Key responsibilities include ensuring the protocols are prepared and ensure that endpoints are aligned with the requirements for approval and for feasibility evaluations. Reporting to the Chief Technology (R D) Officer, this role is critical in ensuring the timely execution of clinical trials/ clinical studies/ clinical investigations, the integrity of clinical data and the safety and wellbeing of study participants. This is a global senior individual contributor role with an initial primary focus on Europe, responsible for establishing and overseeing clinical [. .. ]

▶ Zur Stellenanzeige
Job am 10.05.2026 bei Jobleads gefunden

Business Process

• Hamburg Homeoffice möglich [. .. ] the Workplace Coordinator, the Office Services Assistant will provide exceptional customer service to both internal and external customers. To go above and beyond, making our guests feel [...]
MEHR INFOS ZUM STELLENANGEBOT[...] welcome and comfortable. Clinical Trials Assistant 1 (m/w/d) Frankfurt, Hesse, Germany We currently offer the exciting opportunity to join the team as Clinical Trials Assistant 1/ CTA I (m/w/d) in fulltime and work officebased in our Germany headquarter in Frankfurt. Occasional homeoffice is possible after onboarding. Administrative Assistant for the Climate [. .. ] (m/f/d) International Environment. Das bieten wir Ihnen: Organise and coordinate internal meetings as well as interviews and negotiation meetings with bidders in close cooperation with the relevant Contract Officer Monitor attendance confirmations and proactively reschedule meetings where necessary Submit documents to the electronic visa workflow within the Document Management System Monitor document workflows and issue reminders as required Prepare contractual documents for signature following approval Support the Contract Officer in drafting memoranda and standard forms Handle incoming mail Assist [. .. ]

▶ Zur Stellenanzeige
Button Jobabo Nichts verpassen: Jobs per eMail
► Speichern Sie jetzt Ihre Jobsuche!

Job am 28.04.2026 bei Jobleads gefunden

Director (gn) Portfolio Management, Market Analysis Strategic Projects

• Martinsried, Bayern Führungs-/ Leitungspositionen [. .. ] the company is able to span the entire value chain of biosimilar drug development, from market analysis and target definition by protein analytics, to the development of [...]
MEHR INFOS ZUM STELLENANGEBOT[...] production processes, to clinical trials and the regulatory approval process. Our focus is on treatments in ophthalmology and immunology as well as for other key chronic diseases. Formycon is making a major contribution towards providing as many patients as possible with access to vital and affordable medicines. To support our team in Martinsried near Munich, [. .. ] responsibilities Director (gn) Portfolio Management, Market Analysis Strategic Projects with deep expertise in the global biosimilars market to drive strategic decisionmaking at company level. Reporting directly to the Chief Business Officer (CBO) , this role acts as a key strategic partner to the Board and senior leadership, combining portfolio ownership, market intelligence, business case development, and crossfunctional project leadership. Key tasks include: Portfolio Management Identification of new portfolio candidates for our development pipeline based on a variety of criteria including commercial [. .. ]

▶ Zur Stellenanzeige
Job am 12.04.2026 bei Jobleads gefunden

Scientific Founders Associate (Md/Phd/comparable)

• Berlin Tasks About the Role We are looking for a Scientific Founders Associate to work directly with our founders, especially our Chief Medical Officer, on some of the most important [...]
MEHR INFOS ZUM STELLENANGEBOT[...] clinical, scientific, and strategic topics across the company. This is not a classic research role and not a standard clinical operations position. It is a founderadjacent, highownership role at the intersection of: clinical research evidence generation scientific communication product and AI validation strategic company building You will work closely with our [. .. ] inside. Requirements What you will do Work directly with the founders on high-priority clinical, scientific, and strategic projects Support and help shape Noah Labs evidence generation strategy across clinical trials, AI validation, and real-world studies Contribute to protocol design, endpoint definitions, analysis concepts, and interpretation of clinical data Draft and co-author publications, abstracts, conference submissions, and scientific materials Translate clinical and scientific findings into clear internal and external narratives for clinicians, partners, investors, and other stakeholders Collaborate closely [. .. ]

▶ Zur Stellenanzeige
Job am 29.03.2026 bei Jobleads gefunden

Chief Revenue Officer (CRO)

• 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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 fundraising within the next 1218 months. This role represents a rare opportunity to build and scale the entire commercial organization from the ground up and [. .. ]

▶ Zur Stellenanzeige
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 [. .. ] 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/ [. .. ] Cardiology and/or Peripheral Vascular Intervention is an advantage. Specialized Skills/ Other Requirements Strong working knowledge, understanding and ability to apply MDR, ISO 14155 and ICH/ GCP guidelines governing clinical trials. Strong compliance focus. Demonstrated aptitude and knowledge in relevant therapeutic areas and ability to learn and integrate new therapeutic areas knowledge. Ability to train and mentor Clinical Studies personnel for remote and onsite monitoring visits. Ability to train onsite staff on the protocol, GCPs, data entry and other pertinent regulations. [. .. ]

▶ Zur Stellenanzeige
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 [. .. ] the development program, notably those relevant for the German treatment and reimbursement landscape and to address them within the country medical affairs program Knowledge in development and implementation of clinical trials and RWE programs preferred Ability to work independently and effectively in complex, rapidly changing environments Sense of urgency Flexibility, diplomacy, and the ability to manage expectations Interested in new ways of thinking and innovative approaches Ability to travel up to 25 of working time Language: German, English fluent Proficient 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 [. .. ]

▶ Zur Stellenanzeige
Job am 08.02.2026 bei Jobleads gefunden Medical Science Liaison Dermatology (m/f/d) - Münster, Dortmund, Bielefeld [. .. ] communicate medical insights to inform medical strategy and cross-functional decision-making Lead and support advisory board meetings, round table meetings and investigator meetings. Facilitate company sponsored and investigator [...]
MEHR INFOS ZUM STELLENANGEBOT[...] sponsored trials (ISTs) Actively support real-world evidence generation activities, including non-interventional studies (NIS) , registries and collaborative research projects. Closely cooperate and align with KAM-team for all activities related to medical information for external groups. Act as point of contact for unsolicited information requests on company inline products and pipeline. Provide frequent updates on investigative site support by updating medical/ clinical teams with feedback and insights from interactions and discussions with External Experts and investigators. Provide medical/ scientific leadership and expertise to internal and external groups Conduct internal trainings on medically relevant topics. Adhere to corporate SOPs and ensure vigilant compliance with relevant legal and regulatory requirements and guidelines governing scientific [. .. ] 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 79884065 [. .. ]

▶ Zur Stellenanzeige
Job am 08.02.2026 bei Jobleads gefunden Medical Science Liaison Dermatology (m/f/d) - Frankfurt, Kassel, Saarbrücken [. .. ] Liaisons, who are eager to help shape this next phase scientifically and operationally. Job Summary Medical Science Liaisons (MSLs) are a team of field-based, highly trained professionals [...]
MEHR INFOS ZUM STELLENANGEBOT[...] with strong clinical and/or scientific backgrounds and excellent communication skills. They represent the Medical Affairs organization to the broad scientific community. Essential Functions of The Job (Key Responsibilities) Represent the company and lead medical scientific exchanges within the respective community Develop and lead Key External Experts and investigators engagement plans identify, develop [. .. ] communicate medical insights to inform medical strategy and cross-functional decision-making Lead and support advisory board meetings, round table meetings and investigator meetings. Facilitate company sponsored and investigator sponsored trials (ISTs) Actively support real-world evidence generation activities, including non-interventional studies (NIS) , registries and collaborative research projects. Closely cooperate and align with KAM-team for all activities related to medical information for external groups. Act as point of contact for unsolicited information requests on company inline products and [. .. ] 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 79883083 [. .. ]

▶ Zur Stellenanzeige
Job vor 8 Tagen bei Neuvoo gefunden Pfizer Oncology Medical Head, International • Berlin [. .. ] through post-approval value optimization. The role serves as a core member of the global Oncology Medical Affairs leadership team and is a strategic partner to the Chief [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Medical Affairs Officer ( International Commercial Division) , Regional Global Study Site and Operations (CD O) , Global Clinical Development, International Commercial, Access, Public Policy and Country Medical organizations to deliver patient-centered, evidence-driven medical impact globally. This position combines deep oncology clinical and scientific expertise with enterprise leadership to ensure patient-centered, evidence-driven decisions; consistent interpretation and communication of oncology data; and high-quality medical execution [. .. ] meetings (advisory boards, congresses, symposia) and ensure feedback and continuous improvement. Support patient access and public policy initiatives across the international region Lead coordinate international medical support to global clinical trials Establish and track performance indicators (KPIs) for medical plan delivery and outcomes; use data to prioritize, learn, and optimize. F. Leadership, Talent Development Culture Build a high-performing, inclusive team culture that encourages coaching, collaboration, continuous learning, and constructive challenge. Coach colleagues before and after key meetings to elevate performance [. .. ]

▶ Zur Stellenanzeige
Job vor 12 Tagen bei Neuvoo gefunden Allucent Chief Medical Officer Führungs-/ Leitungspositionen Were looking for an experienced Chief Medical Officer to join our A-team (hybrid/remote) . This is a unique opportunity at an innovative full-service global CRO. The role In this [...]
MEHR INFOS ZUM STELLENANGEBOT[...] role, youll be responsible for setting the department strategy and overall utilization and profitability of Allucent Medical Affairs and Pharmacovigilance. This position controls and monitors the [. .. ] according to the organizational chart and reports directly to the Chief Operations Officer. At Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe. Key responsibilities: Identify, develop and implement the business strategy for the Medical Affairs and Pharmacovigilance departments Develop and agree upon annual revenues, sales, profit and operational targets for the Medical Affairs and Pharmacovigilance departments Evaluate and direct the [. .. ]

▶ Zur Stellenanzeige
Job am 14.04.2026 bei Neuvoo gefunden dehaze GmbH Medical Lead • Berlin Führungs-/ Leitungspositionen [. .. ] and make a call under uncertainty. At some point, you realized you could have more impact beyond direct patient and you started building a second dimension alongside [...]
MEHR INFOS ZUM STELLENANGEBOT[...] or after your clinical work. dehaze AI identifies chronic disease risks on already existing health data. Thanks to us, our customers, fully integrated health insurers, save 10 of their yearly health budget. In an industry with relatively low margins, a real game changer. You are the medical authority inside dehaze. But this is not a clinical advisory board seat. You are embedded in the team, working daily with the CEO, CTO, and Chief Scientific Officer. Your core focus is validating our AI outputs and building the clinical evidence base that makes our technology credible to regulators, customers, and the medical community. You bring the physicians judgment that no engineer or data scientist can replicate combined with the analytical and commercial thinking youve developed beyond the [. .. ] degree. Research-literate. You understand clinical study design, outcome measurement, and what it takes to produce evidence that regulators and the medical community take seriously. Whether through academic research, clinical trials, or health outcomes work, you know how to build a clinical evidence base. Analytical and data-literate. You can work with datasets, interpret model outputs, and evaluate whether results make clinical sense. You dont need to write code, but youre comfortable around data and understand enough about AI and machine [. .. ]

▶ Zur Stellenanzeige
Job am 18.03.2026 bei Neuvoo gefunden Avomind (Senior) Clinical Research Scientist-Digital Cardiology and Heart Failure • Berlin [. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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, 000 [. .. ] 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-[. .. ]

▶ Zur Stellenanzeige
Jobs



Häufig gestellte Fragen

Wieviel verdient man als Clinical Trials Officer pro Jahr?

Als Clinical Trials Officer verdient man zwischen EUR 50.000,- bis EUR 75.000,- im Jahr.


Wieviele offene Stellenangebote gibt es für Clinical Trials Officer Jobs bei unserer Jobsuche?

Aktuell gibt es auf JobRobot 17 offene Stellenanzeigen für Clinical Trials Officer Jobs.


Wieviele Unternehmen suchen nach Bewerbern für Clinical Trials Officer Jobs?

Aktuell suchen 7 Unternehmen nach Bewerbern für Clinical Trials Officer Jobs.


Welche Unternehmen suchen nach Bewerbern für Clinical Trials Officer Stellenangebote?

Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Trials Officer Stellenangebote:


  • Hlx Life Sciences (1 Job)
  • Teleflex (1 Job)
  • Pfizer (1 Job)
  • Allucent (1 Job)
  • dehaze GmbH (1 Job)
  • Avomind (1 Job)


In welchen Bundesländern werden die meisten Clinical Trials Officer Jobs angeboten?

Die meisten Stellenanzeigen für Clinical Trials Officer Jobs werden derzeit in Berlin (4 Jobs), Bayern (3 Jobs) und Hamburg (1 Jobs) angeboten.


Zu welchem Berufsfeld gehören Clinical Trials Officer Jobs?

Clinical Trials Officer Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.


Jobs per Email


Verpassen Sie keine Jobs!
Wir informieren Sie kostenfrei über neue Jobangebote!


Datenschutzklärung lesen


Dauer: 0.0518 s., Vers. V.2025-d-2009-Ind-141