93 Jobs für Clinical Trials Investigator
Stellenangebote Clinical Trials Investigator Jobs
Neu Job vor 4 Std. bei Jobleads gefunden
• München, Bayern
[. .. ] and deliver regional medical strategies and engagement activities aligned with global and country plans. Provide timely, evidence-based responses to medical and scientific inquiries from clinicians and healthcare [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] partners. Support investigator-initiated projects and clinical research activities, including site identification and scientific feasibility. Design and deliver medical education, advisory boards and regional congress activities. Collect and share local insights and evidence with cross-functional teams to inform medical strategy and improve patient care. Basic Qualification We are seeking professionals with the following required skills and [. .. ] Qualification If you have the following characteristics, it would be a plus: Field-based experience as a Medical Science Liaison, Regional Medical Affairs Manager or similar role. Experience supporting clinical trials, investigator-initiated studies or study start-up activities. Experience planning medical education, advisory boards and congress activities. Knowledge of the German healthcare system and market access considerations. Proven ability to build and maintain networks with key opinion leaders and investigators. Comfortable using digital engagement tools and omnichannel communication approaches. Weitere [. .. ]
Neu Job vor 4 Std. bei Neuvoo gefunden
Chronos Consulting
Regional Director of Clinical Affairs and CRO Europe based in Germany
• deutschland,
Führungs-/ Leitungspositionen
Job Description Our client is a leading, global medical device company pioneering noninvasive surgical treatments. The Regional Director of
Clinical Affairs will work closely with senior management to translate business [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] commercial objectives into requirements for specific clinical trials and programs. This role is responsible for the successful execution of the EU clinical portfolio as well as the management, growth and development of the clinical staff. Skills and Experience: 1) BS, BA, BSN or RN or higher degree in the Life Sciences or related disciplines 2) Minimum 5+ years [. .. ] will be an advantage. 10) Willing able to travel domestically and internationally, as required (up to 40) Responsibilities: Strategic translation of business objectives into successful clinical requirements for clinical trials, investigator-sponsored studies, publications, etc, and by meeting EU regulatory requirements for clinical evaluations and post-market surveillance Manage and develop global internal team of Clinical Project Managers and outside vendors, as needed Overall responsibility for design of clinical trials including protocol development, clinical trial discussions with EU Competent Authorities, and [. .. ]
Neu Job vor 4 Std. bei Neuvoo gefunden
Chronos Consulting
• deutschland,
Job Description Our client is a global medical device company, a pioneer of the MR-guided focused ultrasound technology which is a game-changing innovation. They are looking for a
Clinical Affairs [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Program Manager Europe. The role is remote with up to 40 travel and based in Europe. As part of the global clinical affairs team, you will be responsible for developing strategies for a successful execution of roadmap clinical trials that demonstrate medical product safety and efficacy. Additional responsibilities include management of clinical trials approvals with local IRBs and/or Competent Authorities. Required Skills and Experience: 1) BS, BA, BSN or RN or higher degree in the Life Sciences or related disciplines 2) Minimum 3+ years in clinical management position [. .. ] abilities to operate independently 11) Willing able to travel domestically and internationally, as required (up to 40) Responsibilities: Collaborate with Company Stakeholders to execute company objectives into successful clinical trials, investigator-sponsored studies, etc. Overall responsibility for design of clinical trials including protocol development, clinical trial discussions with EU Competent Authorities, and development of timeline and budget Manage the process of screening/ qualifying, selecting, and contracting with investigators, sites and vendors required for conduct of clinical trials Direct/ Manage necessary clinical [. .. ]
Job am 25.04.2026 bei StepStone gefunden
Universität Bielefeld
Datenmanagerin (m/w/d) klinische Forschung
• Bielefeld
Homeoffice möglich
Flexible Arbeitszeiten 30+ Urlaubstage
[. .. ] für die translationale Forschung gehört. Diese in Entwicklung begriffene Struktur führt die bereits in Betrieb genommene Forschungsbiobank, das Datenintegrationszentrum für die medizinische Forschung sowie die Biometrie mit [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] der nun aufzubauenden Clinical Research Support Unit (CRSU) eng zusammen. Als zentrale Einrichtung der Universitätsmedizin OWL unterstützt die CRSU zukünftig Forschende bei der Antragstellung, Planung, Vorbereitung, Durchführung und den Abschluss von eigeninitiierten klinischen Studien (IITs) im gesamten Spektrum der patientenorientierten klinischen Forschung. Für das Angebot professioneller Datenmanagementleistungen sowie den Aufbau eines praxis- und prozessorientierten [. .. ] Das wünschen wir uns Kenntnisse in der Programmierung mit Java Kenntnisse der medizinischen Terminologie und Kodierung (Med DRA) Kenntnisse der CDISC Standards Erfahrung in der Planung und Umsetzung von Datenbanken bei Investigator Initiated Trials (IITs) Erfahrungen in der deskriptiven Datenauswertung Erfahrung in der regulativen Beratung bei studiesspezifischen Anfragen Vergütung nach E13 TV-L unbefristet Vollzeit interne und externe Fortbildungsmöglichkeiten Vielzahl von Gesundheits-, Beratungs- und Präventionsangeboten Vereinbarkeit von Familie und Beruf sicherer Arbeitsplatz fester Dienstort (Bielefeld) ohne Reisetätigkeit flexible Arbeitszeiten 30 Tage Urlaub und [. .. ]
Job am 12.04.2026 bei Mindmatch.ai gefunden
Medizinische Universität Wien
• AT- 9 Wien
[. .. ] consequential heart failure, as well as the evaluation and development of therapeutic strategies in structural heart interventions and heart valve medicine. We actively pursue and participate in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] pure academic studies, investigator initiated trials and industry-sposored studys. The research is embedded in a highly active academic and clinical environment with close interaction between clinical cardiology, cardiovascular imaging, heart failure, and interventional structural heart therapy. Participation in clinical research projects in the field of structural heart disease and valvular heart disease Scientific work on phenotyping of valve disease, in particular aortic valve disease and mitral and tricuspid valve disease [. .. ]
Job am 11.03.2026 bei Mindmatch.ai gefunden
Teleflex
Clinical Research Associate
• 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 [...]
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 [. .. ] visit preparation. Conducts monitoring visits per the department SOP, WIs and monitoring plans. Applies MDR, ISO 14155, ICH/ GCP guidelines and Teleflex SOP and WIs to monitoring activities. Completes the Investigator Files with all appropriate documentation. Ensures all required documentation is completed prior to site initiation, during enrollment and followup, and at site close out. Provides findings to site staff, clear directions for resolution, appropriate retraining, and reviews data queries with site staff to ensure they are understood and can be [. .. ] 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. [. .. ]
Job am 06.03.2026 bei Mindmatch.ai gefunden
PSI CRO
• AT- 9 Wien
[. .. ] committed to delivering high-quality, timely services across a wide range of therapeutic areas. Job Description We are in search of an experienced professional dedicated to developing strategic [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] relationships with clinical research sites, with the aim of optimizing and advancing the progress of clinical trials. Hybrid role in Vienna, Austria This is the main responsibility of a site ID specialist. Communicate and build relationship with clinical sites to identify potential centres for clinical trials. Maintain and refine internal site databases in cooperation with Study Startup, Clinical Operations and Process Improvement. Project Responsibilities Conduct site identification [. .. ] recommended investigators or clinical sites. Support the project team throughout study startup and further on, whenever additional rounds of site identification are necessary, and/or additional information on the site/ investigator is needed. Qualifications University/ college degree (Md/Pharm D degree) , or an equivalent combination of education, training and experience. On-site monitoring experience is a plus. Understanding of Good Clinical Practice, local laws and applicable regulations in the region. Demonstrated ability to work in a dynamic environment, under compressed deadlines [. .. ]
Job am 02.03.2026 bei Mindmatch.ai gefunden
IQVIA
Senior Clinical Contracts Negotiator (German/ English)
• AT- 9 Wien
A global provider of
clinical research services is seeking a Contract Specialist in Vienna. In this role, you will be responsible for developing contracts and coordinating
investigator grants [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to support clinical trials. You will need a Bachelors Degree or 5 years of relevant experience, along with strong negotiation and communication skills. Fluency in English and German is required. Join a leading firm dedicated to enhancing patient outcomes globally. J-18808-Ljbffr 82516537 [. .. ]
Job am 25.02.2026 bei Mindmatch.ai gefunden
IQVIA
• AT- 9 Wien
Essential Functions Develop coordinate the development of
investigator grants and estimates, contracting strategies and proposal text to support the proposal development process. Develop contract language, payment language and budget [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] templates as required as applicable to the position. Utilize and maintain contracting systems, tools, processes, and training materials for selected sponsors, studies or multi-protocol programs according to the [. .. ] RSU Management Plan. Provide specialist legal, operational and financial contracting support to the Study Teams, as applicable to site agreements to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements. Ensure overall contracting efficiency and adherence to project timelines and financial goals as applicable to site agreements. Report contracting performance metrics and out of scope contracting activities as required. Work with Quality Management to ensure appropriate contract management and quality standards. Mentor and coach [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Medical Director-Psychiatry (m/w/d)
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Job Overview The Associate Medical Director/ Medical Director will provide medical,
clinical and scientific advisory expertise to all IQVIA divisions as requested. Participate in all aspects of Medical Science [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] involvement on assigned trials. Serve as a medical expert during project delivery lifecycle. Provide therapeutic and medical expertise to business development activities. Essential Functions The role includes predominantly Medical Monitoring responsibilities with Medical Strategic input involvement as requested. Medical Monitoring: # # Primarily serves as Global and/or Regional Medical Advisor on assigned [. .. ] Brochure (IDB) , and/or Case Report Forms (CRFs) . # # Provides therapeutic area/ indication training for the project clinical team. # # Attends and presents at Investigator Meetings. # # Performs review and clarification of trial-related Adverse Events (AEs) . # # May perform medical case review of Serious Adverse Events (SAEs) , including review of case documentation and patient narrative, in collaboration with the Pharmacovigilance department. # # May provide medical support [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
• Bayern
Führungs-/ Leitungspositionen
Job Description Summary Strategic leadership and scientific oversight of a therapeutic area or disease domain across the
clinical development lifecycle. Responsibilities Define and drive the clinical strategy for the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] assigned care area (oncology) . Lead the development of Target Product Profiles (TPPs) , Integrated Evidence Generation Plans (IEGPs) , and clinical development plans. Represent the therapeutic area in governance forums and regulatory interactions. Engage with KOLs and external [. .. ] alignment across Regulatory, Medical Affairs, Commercial, and Clinical Operations. Mentor and guide clinical scientists and medical monitors working within the care area. Provide medical oversight for one or more clinical trials. Review safety data, assess adverse events, and support dose modifications or protocol amendments. Respond to investigator queries and support site engagement. Participate in Data Safety Monitoring Boards (DSMBs) and internal safety reviews. Contribute to clinical study reports (CSRs) , regulatory submissions, and medical writing. Collaborate with Clinical Operations and Pharmacovigilance teams. Qualifications MD or Ph D with deep expertise in the therapeutic area. Extensive experience in clinical [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Clinical Trials Lead Site Coordinator
• Zug
Führungs-/ Leitungspositionen
Overview Milestone One is a Site Enabling Services organization with global headquarters in Zug, Switzerland. We understand what
clinical study sites need and our overall mission is to support [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] sites in stronger study delivery. Job Description Milestone One Site Coordinator supports trial sites in all related activities according to ICH-GCP, protocol requirements within study-specific defined timelines and enrollment goals. Responsibilities Act as the main line of communication [. .. ] of investigational products and clinical supplies. Collect, handle and maintain all site-specific regulatory documents as needed. Facilitate and support the contract and budget negotiations at the site level. Support Investigator and Site payments and processes as needed. Schedule and/or perform study procedures as per study requirements and delegation of responsibilities. Prepare for and participate in onsite study audits or regulatory agency inspections. Build and sustain long-lasting relationships with existing and potential clients (sponsors, CROs, medical institutions) . Qualifications [. .. ] Science, preferably in pharmacy, nursing or lab analytics. Minimum of 2 years of on-the-job experience in a clinical trial environment, where relevant experience has been gained in clinical trials, clinical terminology, and medical research working in the role of a Study Coordinator or similar function. Upper-intermediate level of English, with the ability to work in a global team environment. Experience in Oncology, Renal, or Cardiology clinical studies is a plus. Ability to work in a fast-paced environment, [. .. ]
Job vor 9 Tagen bei Jobleads gefunden
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Job Overview The Associate Medical Director/ Medical Director will provide medical,
clinical and scientific advisory expertise to all IQVIA divisions as requested. They will participate in all aspects of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] medical science involvement on assigned trials, serve as a medical expert during the project delivery lifecycle, and provide therapeutic and medical expertise to business development activities. Essential Functions Primarily responsible for medical monitoring with input into medical strategy as requested. Medical Monitoring Primarily serves as Global and/or Regional Medical Advisor on assigned projects. Serves as [. .. ] review of the protocol, Investigative Drug Brochure (IDB) , and/or Case Report Forms (CRFs) . Provides therapeutic area/ indication training for the project clinical team. Attends and presents at Investigator Meetings. Performs review and clarification of trial-related Adverse Events (AEs) . May perform medical case review of Serious Adverse Events (SAEs) , including review of case documentation and patient narrative, in collaboration with the Pharmacovigilance department. May provide medical support for the Analysis of Similar Events (AOSE) , in [. .. ]
Job am 17.04.2026 bei Jobleads gefunden
Director, Medical Affairs (m/f/d)
• Eschborn, Hessen
Führungs-/ Leitungspositionen
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] product safety processes and procedures for new products and technologies as clinical studies are implemented, worldwide regulatory approvals are obtained and new products are commercialized. Key responsibilities Regionally responsible for Investigator Initiated Study and Research Grant programs Develop the priorities for the Global Abbott HF ISS strategy Responsible for medical affairs contributions to physician level professional education on advanced HF, MCS and hemodynamic management Work with professional societies on increasing awareness and knowledge about advanced HF and hemodynamic management Assists the [. .. ] and delivers internal educational activities related to HF Provide input to R D on all aspects and stages of the product portfolio Support clinical affairs and help drive Abbott led trials and ensure the region is represented in critical evidence generation in the field of HF. Be responsible for off label discussions with clinicians in the OUS region. Assist market access with clinical input to reimbursement processes OUS Represent Abbott HF Medical Affairs in interactions with regulatory bodies Assists investigation teams [. .. ]
Job am 17.04.2026 bei Jobleads gefunden
• Zürich
Führungs-/ Leitungspositionen
Discover Intenarnational is partnered with a Swiss Biotech in their search for an experienced Medical Director Oncology to provide medical and
clinical leadership across a portfolio of innovative oncology [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] assets within a fast-growing biotech group. This role will lead oncology clinical development strategy, provide medical oversight across studies, and work closely with R D and executive leadership to advance novel cancer therapies through clinical development. Key Responsibilities Lead medical strategy for [. .. ] focus on solid tumours and targeted therapies Provide oversight for oncology clinical trial design, protocols, and study execution Act as senior medical lead for safety review, clinical data interpretation, and investigator engagement Support regulatory submissions and health authority interactions Provide scientific leadership to internal teams, KOLs, and external partners Contribute to portfolio assessment and oncology asset strategy Requirements Md/MBBS with significant oncology drug development experience Strong background in clinical oncology trials (Phase IIII) Experience in biotech or pharma clinical development Excellent knowledge of GCP and oncology regulatory requirements Strong leadership and stakeholder management skills #J-18808-Ljbffr 88847617 [. .. ]
Job am 08.04.2026 bei Jobleads gefunden
Sr. Medical Affairs Manager-DACH (w, m, d)
[. .. ] country launch plans for new products, and executes them with excellence. They will have and maintain an indepth understanding of diabetes, the current and future treatment landscape [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] along with ongoing clinical research with a focus on the diabetes device market. This individual has leadership responsibilities to ensure the execution of all above tasks. They will be responsible to lead a team in the development and successful execution of medical strategies and tactics that enhances regulatory approval, customer access and adoption of [. .. ] training with generation and delivery of medical content Inform strategize evidence generation plans, in answer to fulfil market access, regulatory and marketing needs Support the local execution of Insuletsponsored and Investigator Initiated trials Disseminate evidence within local markets Identify and engage with HCP to inform and seek advice on the companys solutions, through the execution of advisory boards, clinical activity, scientific Exchange and educational Events Establish and maintain credible peertopeer scientific relationships with national and regional KOLs Build confidence and advocacy among key [. .. ]
Job am 08.04.2026 bei Jobleads gefunden
• Berlin
Jobticket
[. .. ] aligned with local and European medical affairs priorities. Build and expand relationships/ networks with key medical and scientific experts in the field of breast cancer and/or lung [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] cancer. Support clinical trials by identifying study sites, participating in SIVs (Site Initiation Visits) , assisting with patient enrollment, and ensuring smooth information exchange. Identify research opportunities, including Investigator Initiated Trials, Real World Evidence, and other evidencegeneration studies. Represent the organization at scientific conferences, advisory boards, and educational events, sharing insights and preparing reports for internal stakeholders. Ensure timely documentation of HCP interactions, compliance with local policies, and accurate reporting of insights and safety information. A Good Match: Advanced [. .. ]
Job am 04.04.2026 bei Jobleads gefunden
Medical Monitor (Gastroenterology)
• München, Bayern
[. .. ] to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Job Description PSI Medical Monitors provide medical input [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to global clinical studies and advise the teams and business partners, while always focusing on patients safety and well-being. Hybrid working based in Munich Responsibilities Serve as medical point of contact for internal project team, study sites and study sponsor for medical matters related to the conduct of clinical trials per protocol and per GCP guidelines Advise clients, project teams, sites, regulatory agencies and third-party vendors on medical matters Collaborate with internal departments in the preparation of clinical development plans, protocols, investigator brochures, annual reports, clinical study reports, patient narratives, and scientific presentations Review and analysis of clinical data to ensure the safety of study participants in clinical trials Ensure that the reported trial data is accurate, complete, and verifiable, and that the conduct of the trial is in compliance with the [. .. ]
Job am 24.02.2026 bei Jobleads gefunden
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Overview The IQVIA Cell and Gene Therapy Center of Excellence (CAGT COE) , a hub of CAGT
clinical innovation, is growing We are looking for an exceptional Board-Certified physician [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to join our team as a Medical Strategy Lead to help us expand our CAGT portfolio, with an emphasis on Gene Therapy/ Gene Editing platforms, and advance this dynamic and rapidly expanding area of clinical development. The CAGT Medical Strategy Lead is a subject matter expert with experience in clinical research and clinical trials in CAGT and especially in the areas of Gene Therapy/ Gene Editing, who will be a champion for CAGT across IQVIA. The key remit of the role is drive growth of the IQVIA CAGT portfolio through scientific and clinical expertise. The CAGT Medical Strategy Lead will be charged with using [. .. ] development plan, mining data to address important clinical questions relevant to the study, reviewing the protocol for scientific/ regulatory soundness and feasibility, logistics challenges, identification of target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape. Support preparation of customer and bid defense meetings, e. g. training and preparation of the assigned project team; provide specific content; ensure presentation focus and content effectively conveys CAGT strategy. Attends and presents at customer meeting, or bid defense or [. .. ]
Job am 21.02.2026 bei Jobleads gefunden
Senior Medical Director-Cell and Gene Therapy (m/w/d)
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
[. .. ] locations: Frankfurt, Hesse, Germanytime type: Full timeposted on: Posted Todayjob requisition id: R1529858Job Overview The IQVIA Cell and Gene Therapy Center of Excellence (CAGT COE) , a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] hub of CAGT clinical innovation, is growing We are looking for an exceptional Board-Certified physician to join our team as a Medical Strategy Lead to help us expand our CAGT portfolio, with an emphasis on Gene Therapy/ Gene Editing platforms, and advance this dynamic and rapidly expanding area of clinical development. The CAGT Medical Strategy Lead is a subject matter expert with experience in clinical research and clinical trials in CAGT and especially in the areas of Gene Therapy/ Gene Editing, who will be a champion for CAGT across IQVIA. The key remit of the role is drive growth of the IQVIA CAGT portfolio through scientific and clinical expertise. The CAGT Medical Strategy Lead will be charged with using [. .. ] development plan, mining data to address important clinical questions relevant to the study, reviewing the protocol for scientific/ regulatory soundness and feasibility, logistics challenges, identification of target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape. Support preparation of customer and bid defense meetings, e. g. training and preparation of the assigned project team; provide specific content; ensure presentation focus and content effectively conveys CAGT strategy. Attends and presents at customer meeting, or bid defense or [. .. ]
Job am 15.01.2026 bei Jobleads gefunden
Senior/ Medical Director (Ophthalmology) 0.5 FTE
Führungs-/ Leitungspositionen
[. .. ] Senior/ Medical Director (Ophthalmology) , 0.5 FTE. TFS Health Science is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] their clinical development journey. Join our team as a Senior/ Medical Director (Ophthalmology) . The Senior/ Medical Director is a key member of the Project Delivery team, working independently to manage safety and medical matters in line with company policies, standard operating procedures (SOPs) , and regulatory requirements. With deep medical expertise, [. .. ] and answering complex questions related to medical, legal, and regulatory concerns. Responsibilities Expert Guidance: Provide advanced medical input on study design, measurement strategies, and trial protocols, including safety sections and investigator brochures. Comprehensive Safety Oversight: Review safety data such as adverse events, labs, vital signs, ECGs, and clinical trial reports from a medical perspective. Regulatory Risk Support: Conduct senior-level medical reviews of individual cases, cumulative listings, PSURs, PBRERs, DSURs, and Risk Management Plans. Medical Monitoring Signal Detection: Serve as a medical monitor in trials, perform literature reviews, and contribute to signal detection and interpretation. Regulatory Document Contributions: Offer expert medical insight into regulatory submissions and safety-related documentation. Team Client Engagement: Mentor junior medical staff, support SOP/ tool development, and join Commercial Operations in client meetings and presentations. Qualifications Medical Qualifications: Medical Doctor (MD) [. .. ]
Job am 23.11.2025 bei Jobleads gefunden
Medical Science Liaison Manager, Nephrology, North-West
• München, Bayern
[. .. ] become recognized and educate the medical community with up-to-date medical and scientific information. Identify and execute collaboration opportunities between expert KOLs in nephrology and Alexion medical affairs [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and clinical development such as publications, investigator-initiated trials, regional advisory boards, training and speaker development programs. Communicate experts opinion, feedback on new data and clinical trends to Alexion Medical Affairs, therapeutic area (TA) franchises and translate this information into strategic recommendations to enhance science and advance patient care. Respond to unsolicited medical information requests in the region, manage [. .. ]
Job am 23.11.2025 bei Jobleads gefunden
Medical Science Liaison Manager, Nephrology, South
• München, Bayern
[. .. ] within a geographic area. He/ she manages and maintains collegial and professional relationships with KOLs and identifies and facilitates collaboration opportunities with Alexion. He/ she combines strong [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] business acumen and clinical expertise and serves as a peer-to-peer liaison internally and externally. He/ she ensures a close working relationship with all functions in their region, including sales, and market access. Responsibilities Develop and maintain peer-to-peer collaborations with key medical experts in nephrology and adjacent specialties within the assigned [. .. ] medical community with up-to-date medical and scientific information. Identify and execute collaboration opportunities between expert KOLs in nephrology and Alexion medical affairs and clinical development such as publications, investigator-initiated trials, regional advisory boards, training and speaker development programs. Communicate experts opinion, feedback on new data and clinical trends to Alexion Medical Affairs, therapeutic area (TA) franchises and translate this information into strategic recommendations to enhance science and advance patient care. Respond to unsolicited medical information requests in the region, manage [. .. ]
Neu Job vor 4 Std. bei Jooble gefunden
GSK
Heme Clinical Trial RMAM (m/f/d)
• Deutschland Deutschland, DE
Site Name: Field Worker-DEU (Munich) Posted Date: Apr 21 2026 The Heme
Clinical Trial RMAM is responsible for the successful conduction of all our clinical
trials in Germany [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and is responsible for efficient and compliant management of medical and scientific study activities to generate robust evidence that supports the scientific positioning and the medical care of patients. Responsibilities This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include [. .. ] compliance requirements in the pharmaceutical environment. Preferred Qualification If you have the following characteristics, it would be a plus: Prior experience in oncology, hematology or related therapy areas. Experience supporting investigator-initiated trials or clinical partnerships. Experience designing or delivering omnichannel engagement plans and digital medical communications. Project management or budget management experience. Experience presenting at national or regional scientific meetings. A collaborative mindset and commitment to inclusive working with diverse stakeholders. Weitere Informationen: #EBDE #LI-Vii V #LI-[. .. ]
Job vor 2 Tagen bei Jooble gefunden
Senior CRA Germany Oncology
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern
[. .. ] 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. 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 [. .. ] Lead (COL) , or operational line manager. Qualifications: Bachelors degree or RN in a related field or equivalent combination of education, training and experience Experience as a CRA in oncology trials. Knowledge of Good Clinical Practice/ ICH Guidelines and other applicable regulatory requirements Must demonstrate good computer skills and be able to embrace new technologies Excellent communication, presentation and interpersonal skills. Basic level of critical thinking skills expected. Fluency in German and English Ability to manage required travel of up to [. .. ]
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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 93 offene Stellenanzeigen für Clinical Trials Investigator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trials Investigator Jobs?
Aktuell suchen 15 Unternehmen nach Bewerbern für Clinical Trials Investigator Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Trials Investigator Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Trials Investigator Stellenangebote:
- Biontech (4 Jobs)
- Thermo Fisher Scientific (4 Jobs)
- IQVIA (2 Jobs)
- Incyte Corporation (2 Jobs)
- Chronos Consulting (2 Jobs)
In welchen Bundesländern werden die meisten Clinical Trials Investigator Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trials Investigator Jobs werden derzeit in Bayern (31 Jobs), Niedersachsen (8 Jobs) und Baden-Württemberg (7 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trials Investigator Jobs?
Clinical Trials Investigator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
