109 Jobs für Clinical Trials Investigator
Stellenangebote Clinical Trials Investigator Jobs
Job am 22.02.2026 bei Jobleads gefunden
• Berlin
[. .. ] Proactively communicate and educate healthcare professionals on disease states where cortisol modulation may play a role. Provide responsive support for appropriate requests and engage in scientific exchange [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] on Corcepts non-clinical and clinical trial data, as well as the clinical development plan Develop and maintain strong working relationships with thought leaders, patient advocacy organisations, and oncology associations (e. g. , ESMO, ESGO, and other regional bodies) within the oncology community Capture, analyse, and communicate insights and intelligence from the medical and scientific community in a compliant manner to inform Corcepts decision-making. Ensure communications clearly and effectively frame insights for practical use Support company-sponsored clinical trials, investigator-initiated studies (IIS) , scientific communications, publications, clinical and scientific education, advisory boards, and congresses Maintain the highest standards of scientific, clinical, and technical expertise in relevant therapeutic areas Demonstrate teamwork and collaboration within Medical Affairs and cross-functionally with Clinical Development, Clinical Operations, Market Access, Marketing, Commercial, and other [. .. ]
Job am 22.10.2025 bei Neuvoo gefunden
Rhythm Pharmaceuticals
Scientific Affairs Manager-Germany (Southwest)
• Munich, Bavaria
[. .. ] internal colleagues. He/ she will support the local Hospital Affairs Lead (HAL) and will be responsible for building peer to peer relationships with external experts and other [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] stakeholders to provide clinical, scientific, and medical education in the territory. The SAM will support research initiatives, advisory boards, and other compliant scientific exchange activities to support Rhythm s strategically aligned Medical Affairs Plan aimed at identifying and addressing the unmet needs of people living with rare genetic disorders of obesity. Responsibilities and Duties [. .. ] networks to aid experts in uncovering people with rare genetic disease of obesity. Closely collaborate with Global Clinical Development and Operations on interactions with investigators participating in Rhythm s clinical trials, investigator meetings and advisory boards. Support clinical trial execution attending to the needs of investigators. Triage pressure points that may impede progress of clinical studies to the cross functional team for timely resolution. Assist in identification and education of referral sites for clinical trials and investigators to drive trial enrolment. Develop [. .. ]
Job am 20.10.2025 bei Neuvoo gefunden
Chronos Consulting
• 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 [. .. ]
Job am 20.10.2025 bei Neuvoo gefunden
Chronos Consulting
Clinical Affairs Program Manager Germany
• 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 vor 2 Tagen bei StepStone gefunden
Dr. Falk Pharma GmbH
• Freiburg
Führungs-/ Leitungspositionen Homeoffice möglich
[. .. ] firmly believe that medical progress can only be achieved by working together. That is why we are looking for: Your tasks Serves as medical lead (ML) for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the company-sponsored clinical trials and development programs. Responsible for guiding the clinical development strategy and ensuring the scientific integrity of clinical trials. ML collaborates with Clinical Research teams and serves as a key liaison between Clinical Research and Global Safety teams. ML manages all medical aspects of clinical trials and contributes to the development [. .. ] medical expertise in the review of adverse events and safety issues, as requested Provides support in the review of scientific publications (abstracts, presentations, and manuscripts) Supports review of concepts for investigator-initiated studies Contributes to company-internal process improvement initiatives (e. g. SOP updates) Your qualification Physician/ medical license holder A minimum of 5 years of clinical development research, or related clinical research experience within the industry (pharmaceutical, biotech, CRO) at an international (Europe, USA, Australia) level is required Knowledge in [. .. ]
Job vor 3 Tagen bei StepStone gefunden
Universität Bielefeld
Klinischer Studienkoordinatorin (m/w/d) / Study Nurse (m/w/d) für Investigator Initiated Trials-AG Translationale Pharmakologie
• Bielefeld
Homeoffice möglich Abgeschlossenes Studium
Flexible Arbeitszeiten
[. .. ] grundsätzlich auch eine Besetzung in Teilzeit erfolgen. In der Medizinischen Fakultät OWL ist die folgende Position zu besetzen: Klinischer Studienkoordinatorin (m/w/d) / Study Nurse (m/w/d) für
MEHR INFOS ZUM STELLENANGEBOT
[...] class=highlight_text>Investigator Initiated
Trials-AG Translationale Pharmakologie Kennziffer: Tech26019 Start: nächstmöglich Vollzeit Vergütung je nach Qualifikation und Aufgabenübertragung bis zu E10 TV-L befristet Aufbau und regulatorische Leitung einer Studienambulanz (25 ) Mitarbeit bei der Anbahnung und Planung von Investigator Initiated Trials (wissenschaftsgetriebener klinischer Studien) in einem multidisziplinären Team organisatorische Leitung der regulatorischen Angelegenheiten [. .. ] Schrift) sichere Kenntnisse im Umgang mit MS Office Interesse an international vernetztem, wissenschaftlichem Arbeiten Das wünschen wir uns zertifizierte Qualifizierung zur Study Nurse/ Studienassistentin/ Studien Koordinatorin zertifizierte Weiterbildung in Good
Clinical Practice Erfahrung in der Vorbereitung von Genehmigungsverfahren von klinischen Studien Qualifizierung zur venösen Blutentnahmen EDV-Kenntnisse (z. B. Klinische Studien Dokumentation) englische Sprachkenntnisse in Wort und Schrift weitere Sprachkenntnisse in Wort und Schrift Gefahrgutschulung (IATA) Vergütung je nach Qualifikation und Aufgabenübertragung bis zu E10 TV-L befristet auf 2 Jahre [. .. ]
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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
Syneos Health
CRA single sponsor-Germany
• AT- 9 Wien
Description CRA single sponsor-Germany Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and commercial insights into [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to [. .. ] 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. For 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. [. .. ] conducting remote monitoring of trial sites to verify compliance with regulatory requirements and clinical protocols. Utilizes data analytics and riskbased monitoring techniques to identify potential issues and trends, ensuring that trials are conducted in accordance with established clinical practices. Collaborates with site teams to develop and implement tools, procedures, and processes that enhance quality monitoring and support the overall success of clinical trials. Impact and Contribution Individual contributors with responsibility in a professional or technical discipline or specialty, but may manage [. .. ]
Job am 02.03.2026 bei Mindmatch.ai gefunden
IQVIA
• 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
Contract Negotiator 2-FSP-German speaker
• 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 am 22.02.2026 bei Mindmatch.ai gefunden
Syneos Health, Inc.
• AT- 9 Wien
[. .. ] 9, 2025 Location: Vienna, 1, Austria Job ID: 25104265-OTHLOC-3538-2DR Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to [. .. ] 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. [. .. ] conducting remote monitoring of trial sites to verify compliance with regulatory requirements and clinical protocols. Utilizes data analytics and riskbased monitoring techniques to identify potential issues and trends, ensuring that trials are conducted in accordance with established clinical practices. Collaborates with site teams to develop and implement tools, procedures, and processes that enhance quality monitoring and support the overall success of clinical trials. Discover what our more than 29, 000 employees already know: work here matters everywhere. We work hard, and [. .. ]
Job am 22.02.2026 bei Mindmatch.ai gefunden
Syneos Health, Inc.
CRA single sponsor-Germany
• AT- 9 Wien
Updated: Yesterday Location: Vienna, 1, Austria Job ID: 25105750-OTHLOC-3538-2DR Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to [. .. ] 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. [. .. ] remote monitoring of trial sites to verify compliance with regulatory requirements and clinical protocols. Utilizes data analytics and risk-based monitoring techniques to identify potential issues and trends, ensuring that trials are conducted in accordance with established clinical practices. Collaborates with site teams to develop and implement tools, procedures, and processes that enhance quality monitoring and support the overall success of clinical trials. Impact and Contribution: Individual contributors with responsibility in a professional or technical discipline or specialty, but may manage [. .. ]
Job am 22.02.2026 bei Mindmatch.ai gefunden
IQVIA
• AT- 9 Wien
Führungs-/ Leitungspositionen
The IQVIA Dermatology Center of Excellence, a hub of Dermatology
clinical innovation, is looking for exceptional Board-Certified physicians to join our team as a Medical Strategy Lead to help [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] us expand our Dermatology portfolio and advance this dynamic and rapidly expanding area of clinical development. The Dermatology Medical Strategy Lead is a subject matter expert with experience in clinical research and clinical trials who will be a champion for dermatology trials across IQVIA. The key remit of the role is drive growth of the IQVIA Dermatology portfolio through scientific and clinical expertise. The Medical Strategy Lead will be charged with using his/ her clinical, scientific, and operational knowledge to harness the vast IQVIA [. .. ] design/ clinical development plan, mining data to address important clinical questions relevant to the study, reviewing the protocol for scientific/ regulatory soundness and feasibility, 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 strategy. Attends and presents at customer meeting, or bid defense or partnership [. .. ]
Job am 19.01.2026 bei Mindmatch.ai gefunden
IQVIA
Senior Director, Medical Strategy Lead-Cardiologist
• AT- 9 Wien
Führungs-/ Leitungspositionen
The IQVIA Cardiovascular Center of Excellence, a hub of Cardiovascular
clinical innovation, is looking for an exceptional Board-Certified cardiologist to join our team as a Medical Strategy Lead to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] help us expand our Cardiovascular portfolio and advance this dynamic and rapidly expanding area of clinical development. The Cardiovascular Medical Strategy Lead is a subject matter expert with experience in clinical research and clinical trials who will be a champion for Cardiovascular across IQVIA. The key remit of the role is to drive growth of the IQVIA Cardiovascular portfolio through scientific and clinical expertise. The Medical Strategy Lead will be charged with using his/ her clinical, scientific, and operational knowledge to harness the vast IQVIA [. .. ] design/ clinical development plan, mining data to address important clinical questions relevant to the study, reviewing the protocol for scientific/ regulatory soundness and feasibility, 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 Cardiovascular strategy. Attends and presents at customer meeting, or bid defense or [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• Zug
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 sites [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in stronger study delivery. Please submit CV in English. Job Description Milestone One Site Coordinator supports trial sites in all related activities according to ICHGCP, protocol requirements within studyspecific defined timelines and enrollment goals. Act as the main line [. .. ] reconciliation of investigational products and clinical supplies. Collect, handle and maintain all sitespecific 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 longlasting relationships with existing and potential clients (sponsors, CROs, medical institutions) . Qualifications College [. .. ] 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. Upperintermediate 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 fastpaced environment, with short [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Director, Medical Affairs
• 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 vor 7 Tagen bei Jobleads gefunden
• 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 10.03.2026 bei Jobleads gefunden
Senior Director, Medical Strategy Lead-Cardiologist
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
The IQVIA Cardiovascular Center of Excellence, a hub of Cardiovascular
clinical innovation, is looking for exceptional Board-Certified cardiologist to join our team as a Medical Strategy Lead to help [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] us expand our Cardiovascular portfolio and advance this dynamic and rapidly expanding area of clinical development. The Cardiovascular Medical Strategy Lead is a subject matter expert with experience in clinical research and clinical trials who will be a champion for Cardiovascular across IQVIA. The key remit of the role is drive growth of the IQVIA Cardiovascular portfolio through scientific and clinical expertise. The Medical Strategy Lead will be charged with using his/ her clinical, scientific, and operational knowledge to harness the vast IQVIA data [. .. ] design/ clinical development plan, mining data to address important clinical questions relevant to the study, reviewing the protocol for scientific/ regulatory soundness and feasibility, 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 Cardiovascular strategy. Attends and presents at customer meeting, or bid defense or [. .. ]
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 02.02.2026 bei Jobleads gefunden
Senior Director, Medical Strategic Lead-Psychiatrist
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Overview The IQVIA CNS Center of Excellence, a hub of CNS
clinical innovation, is looking for an exceptional Board-Certified psychiatrist to join our team as a Medical Strategy Lead [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to help us expand our CNS portfolio and advance this dynamic and rapidly expanding area of clinical development. The CNS Medical Strategy Lead is a subject matter expert with experience in clinical research and clinical trials who will be a champion for CNS indications across IQVIA. The key remit of the role is driving growth of the IQVIA CNS portfolio through scientific and clinical expertise. The Medical Strategy Lead will be charged with using his/ her clinical, scientific, and operational knowledge to harness the vast IQVIA [. .. ] design/ clinical development plan, mining data to address important clinical questions relevant to the study, reviewing the protocol for scientific/ regulatory soundness and feasibility, 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 CNS strategy. Attends and presents at customer meeting, or bid defense or [. .. ]
Job am 19.01.2026 bei Jobleads gefunden
Senior Director, Medical Strategy Lead-Cardiologist
• Wien
Führungs-/ Leitungspositionen
The IQVIA Cardiovascular Center of Excellence, a hub of Cardiovascular
clinical innovation, is looking for an exceptional Board-Certified cardiologist to join our team as a Medical Strategy Lead to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] help us expand our Cardiovascular portfolio and advance this dynamic and rapidly expanding area of clinical development. The Cardiovascular Medical Strategy Lead is a subject matter expert with experience in clinical research and clinical trials who will be a champion for Cardiovascular across IQVIA. The key remit of the role is to drive growth of the IQVIA Cardiovascular portfolio through scientific and clinical expertise. The Medical Strategy Lead will be charged with using his/ her clinical, scientific, and operational knowledge to harness the vast IQVIA [. .. ] design/ clinical development plan, mining data to address important clinical questions relevant to the study, reviewing the protocol for scientific/ regulatory soundness and feasibility, 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 Cardiovascular 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 13.01.2026 bei Jobleads gefunden
Senior Director, Medical Strategy Lead-Cardiologist
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Senior Director, Medical Strategy Lead-Cardiologist Join the IQVIA Cardiovascular Center of Excellence, a hub of cardiovascular
clinical innovation. This role seeks a Board Certified cardiologist to expand our cardiovascular [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] portfolio and advance this dynamic area of clinical development. The Medical Strategy Lead is a subject matter expert with experience in clinical research and trials, championing cardiovascular across IQVIA. Key remit: drive growth of the IQVIA cardiovascular portfolio through scientific and clinical expertise, using clinical, scientific, and operational knowledge to develop datadriven, patientcentered solutions for cardiovascular trials. The Lead provides senior clinical and scientific expertise to IQVIA divisions, collaborates with indicationspecific teams to develop integrated [. .. ] operational advice to internal stakeholders developing proposals: strategy to protocol design/ clinical development plan, mining data, reviewing protocol for scientific/ regulatory soundness and feasibility, 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, training and preparation of the assigned project team; provide specific content; ensure presentation focus and content effectively conveys cardiovascular strategy; attend and present at customer meetings, bid defense or partnership meetings. Participate [. .. ]
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 [. .. ]
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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 109 offene Stellenanzeigen für Clinical Trials Investigator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trials Investigator Jobs?
Aktuell suchen 22 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:
- IQVIA (9 Jobs)
- Thermo Fisher Scientific (3 Jobs)
- Dr. Falk Pharma GmbH (2 Jobs)
- PSI CRO (2 Jobs)
- Alexion Pharmaceuticals (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 (18 Jobs), Baden-Württemberg (13 Jobs) und Berlin (11 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trials Investigator Jobs?
Clinical Trials Investigator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
