124 Jobs für Clinical Trials Investigator
Stellenangebote Clinical Trials Investigator Jobs
Job am 15.06.2025 bei Jobleads gefunden
• Düsseldorf, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] and Switzerland (CH) region. You will have the opportunity to: Participate in scientific meetings to engage Senior KOLs, healthcare providers and customers. Demonstrate conceptual and practical expertise [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in infectious disease, clinical microbiology, and basic knowledge of related disciplines. Serve as a resource to the medical/ scientific community including emergency and infectious disease clinicians, OB/ GYNs, laboratory personnel, infection control, pharmacists and researchers. Develop and maintain a working understanding of the Global Health environment relevant to diagnostic needs. Establish and maintain a [. .. ] problems. Gain expertise in the best application of molecular diagnostics. Maintain knowledge in relevant scientific literature including clinical practice guidelines and emerging healthcare trends. Identify research gaps, support sponsored clinical trials, investigator-initiated research, Advisory Boards and Focus Groups to assist Marketing in requirements for the product pipeline. Communicate insights from the medical/ scientific community about unmet clinical or diagnostic needs and provide scientific expertise on product design, development and implementation. The essential requirements of the job include: Medical Degree (MD) with [. .. ]
Job am 17.11.2025 bei Jobleads gefunden
Clinical Affairs Program Manager Europe
[. .. ] 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 [...]
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[...] a Clinical Affairs 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 29.10.2025 bei Jobleads gefunden
• München, Bayern
[. .. ] 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 Rhythms 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 Responsible [. .. ] treatment 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 Rhythms 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 gestern bei Mindmatch.ai gefunden
Novocure
Medical Science Liaison m/w/d-Austria
• AT- 9 Wien
[. .. ] patients treated with Tumor Treating Fields (TT Fields) . Additional responsibilities includebut are not limited toacting as a scientific interface between the company and HCP communities regarding [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] communication about Novocures clinical development plans as well as other research and development activities. Developing appropriate training materials, supporting external research projects related to marketed or investigational Novocure indications, and participating in field-based activities to advance existing products and introduce new indications are also part of the role. The MSL plays an important [. .. ] Responsibilities Increase therapy awareness among prescribers and nonprescribers Manage the entire Austrian territory and all associated field activities Deliver medical training on Novocure products and disease areas Support and accompany investigator Sponsored Trials (ISTs) and other research projects Provide HCP insights and market information to the company Participate in medical (Europewide) congresses, and organize and follow up on advisory boards Promote scientific advancement related to TT Fields Support Phase 3 studies in collaboration with clinical teams and researchers Build and maintain relationships with [. .. ]
Job vor 11 Tagen bei Mindmatch.ai gefunden
MSD
• AT- 9 Wien
Führungs-/ Leitungspositionen Homeoffice möglich
[. .. ] D. degree required MPH, Ph. D. , MBA degree in Health Administration or Economics is seen as a plus Proven experience in global biopharmaceutical industry in Medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Affairs and/or Clinical Development Solid people management experience running a large matrix organization of healthcare professionals Experience in one of the following fields : Oncology (strong plus) Infectious Diseases Treatment Vaccines or Specialty care Strong leadership skills demonstrated effective organizational skills including ability to set goals and align priorities Business acumen ethics and [. .. ] recognition bonuses during the year Discounted fitness offer Pharmacy discounts wholesale discounts etc. Required Skills Advisory Board Development Clinical Development Clinical Medicine Decision Making Healthcare Education Healthcare Marketing Infectious Disease Investigator-Initiated Studies (IIS) Job Placement Leadership Management Process Medical Affairs Medical Care Medical Marketing Strategy People Leadership Results Oriented Scientific Communications Specialty Care Stakeholder Engagement Strategic Planning Strategic Thinking Writing Job Descriptions Preferred Skills Current Employees apply HERE Current Contingent Workers apply HERE Job Details Employee Status : Regular Relocation [. .. ] date. Required Experience : Exec Key Skills : EMR Systems, Post Residency Experience, Occupational Health Experience, Clinical Research, Managed Care, Primary Care Experience, Medical Management, Utilization Management, Clinical Development, Clinical Trials, Leadership Experience, Medicare Employment Type : Full-Time Experience : years Vacancy : 1 J-18808-Ljbffr 70404421 [. .. ]
Job vor 11 Tagen bei Mindmatch.ai gefunden
Blueprint Medicines, a Sanofi company
Field Medical Advisor, Alpine (Temporary)
• AT- 9 Wien
Homeoffice möglich
[. .. ] role in driving the success of Blueprints mission to improve and extend the lives of as many patients as possible through precision therapy. You will be a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] reliable bridge between clinical research market access and commercialization and within the overall organization building strong relationships and collaboration with external and internal stakeholders. As a Field Medical Advisor you will be living and sharing our core values and will be driven by the pursuit of new ideas new innovations and new ways of [. .. ] information officer for the corresponding indication and of clinical trial treatment plans and protocols of Phase IV projects in line with local compliance regulations. Supports interventional and non-Interventional clinical trials in close collaboration with with Clinical development Clinical Operations and Global Medical Affairs teams. Ensures a strategic approach to such programs and the development of clinical data to support the appropriate use of the Companys products. Works with colleagues of Blueprint Medicines International headquarter in Zug and other countries in the international region to ensure consistency of clinical programs from a medical perspective. Ensures that Investigator Initiated Research studies are in line with the global strategy. Helps to detect need for and enables Real World Evidence generation when required for advancing therapeutic area a/ o for access needs. Collaborates closely with market access for HEOR access required information What minimum qualifications do we require Advanced Clinical/ [. .. ]
Job vor 11 Tagen bei Mindmatch.ai gefunden
bio Mrieux
• AT- 9 Wien
[. .. ] understand patient care pathways and their needs in terms of unmet medical needs, medical information and medical education. Contribute to evidence generation by participating in company-sponsored postmarket [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] studies, supporting Investigator Initiated Trials (IITs) in line with global strategy and according to Medtech requirements and bio Mrieux SOPs, and supporting clinical development initiatives including site identification, trial recruitment, registry and presentation of final approved data. Provide operational and medical support to marketing and sales teams (Account Managers, Clinical Education Managers, Business Developers) . Qualifications Academic degree in Medicine or Pharmacology. Advanced scientific degree (MD, Ph D, Pharm D) with relevant industry experience is [. .. ]
Job am 17.11.2025 bei Mindmatch.ai gefunden
Syneos Health
Experienced CRA Austria
• AT- 9 Wien
Experienced CRA Austria Syneos Health Application open. Position sought for Experienced
Clinical Research Associate in Austria. Description Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model places the customer and the patient at the center of [. .. ] provide recommendations, communicate/ escalate serious issues, and develop action plans. Verify informed consent procedures are performed and documented for each subject, protecting confidentiality and assessing safety and data integrity at investigator sites. Based on the Clinical Monitoring/ Site Management Plan, assess site processes, conduct source document review, verify CRF data accuracy, resolve queries remotely or onsite, support data capture and electronic data capture compliance. Perform IP inventory, reconciliation, storage and security review, and confirm correct dispensing and administration of study product. [. .. ] a centralized location. They conduct remote and onsite monitoring, automate data analytics and riskbased monitoring, and collaborate with site teams to implement effective quality monitoring processes that support successful clinical trials. Employment Details Seniority level: Mid Senior level Employment type: Fulltime Job function: Research, Analyst, and Information Technology Referrals increase your chances of interviewing at Syneos Health by 2x. Get notified about new Clinical Research Associate jobs in Vienna, Vienna, Austria. EEO Statement The Company is committed to compliance with the [. .. ]
Job am 03.11.2025 bei Mindmatch.ai gefunden
Takeda
• AT- 9 Wien
Homeoffice möglich
[. .. ] drive advocacy. Ensure scientific accuracy and compliance of promotional and non-promotional materials in line with Takeda standards and regulations. Support evidence generation initiatives, including real-world evidence (RWE) [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and investigator-initiated studies, and identify opportunities to close data gaps. Deliver medical training to internal teams and provide scientific input into marketing strategies and pricing/ reimbursement dossiers. Oversee medical affairs activities, including budget management, internal knowledge transfer, and support for clinical trials and regulatory functions. What you bring: A scientific degree (MD, Pharmacy, or Life Sciences) or equivalent; relevant certifications and a valid driving license. Preferably over 2 years of experience in Medical Affairs or related roles, ideally with product launch exposure. Very good knowledge of English and German. Proven Medical Affairs [. .. ]
Job am 14.10.2025 bei Mindmatch.ai gefunden
Syneos Health
CRA Austria
• AT- 9 Wien
2 days ago Be among the first 25 applicants Description CRA Austria Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique [...]
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[...] 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. [. .. ] 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. Induvidual contributors with responsibility in a professional or technical discipline or specialty, but may manage two or fewer [. .. ]
Job gestern bei Jobleads gefunden
• München, Bayern
Führungs-/ Leitungspositionen
TFS Health Science is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire
clinical development journey. Our expertise includes full [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] service-capabilities, resourcing and Functional Service (FSP) solutions. About this role As part of our Ophthalmology team you will working alongside passionate and innovative professionals to ensure our customers achieve their goals. Key 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 : [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
Senior Director Medical Affairs (mfd)
• Wien
Führungs-/ Leitungspositionen Homeoffice möglich
[. .. ] D. degree required MPH, Ph. D. , MBA degree in Health Administration or Economics is seen as a plus Proven experience in global biopharmaceutical industry in Medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Affairs and/or Clinical Development Solid people management experience running a large matrix organization of healthcare professionals Experience in one of the following fields : Oncology (strong plus) Infectious Diseases Treatment Vaccines or Specialty care Strong leadership skills demonstrated effective organizational skills including ability to set goals and align priorities Business acumen ethics and [. .. ] recognition bonuses during the year Discounted fitness offer Pharmacy discounts wholesale discounts etc. Required Skills Advisory Board Development Clinical Development Clinical Medicine Decision Making Healthcare Education Healthcare Marketing Infectious Disease Investigator-Initiated Studies (IIS) Job Placement Leadership Management Process Medical Affairs Medical Care Medical Marketing Strategy People Leadership Results Oriented Scientific Communications Specialty Care Stakeholder Engagement Strategic Planning Strategic Thinking Writing Job Descriptions Preferred Skills Current Employees apply HERE Current Contingent Workers apply HERE Job Details Employee Status : Regular Relocation [. .. ] date. Required Experience : Exec Key Skills : EMR Systems, Post Residency Experience, Occupational Health Experience, Clinical Research, Managed Care, Primary Care Experience, Medical Management, Utilization Management, Clinical Development, Clinical Trials, Leadership Experience, Medicare Employment Type : Full-Time Experience : years Vacancy : 1 #J-18808-Ljbffr 70394789 [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
• 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. You will be responsible for: Develop and maintain peer-to-peer collaborations with key medical experts in nephrology and adjacent [. .. ] 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 [. .. ]
Job vor 12 Tagen 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. You will be responsible for: Develop and maintain peer-to-peer collaborations with key medical experts in nephrology and adjacent [. .. ] 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 [. .. ]
Job am 18.11.2025 bei Jobleads gefunden
• Stuttgart, Baden- Württemberg
[. .. ] the primary field contact for the companys Medical Affairs. Engage thought leaders in a compliant manner developing strategic engagement plans. Disseminate scientific information accurately and fairly addressing [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] medical inquiries. Manage investigator-initiated research interests and support clinical development activities. Lead advisory board meetings and provide internal/ external training. Represent the company at medical conferences contributing to scientific discussions in Oncology. About you: Degree in life sciences discipline 3 years of medical affairs experience preferably in Oncology/ Hematology. Fluent German good professional English Car driving licence Key Skills Presentation Skills, Time Management, Clinical Research, Communication skills, GCP, Infusion Experience, Managed Care, Hospice Care, Conflict Management, Clinical Trials, Research Experience, Home Care Employment Type: Full Time Experience: years Vacancy: 1 #J-18808-Ljbffr 69875149 [. .. ]
Job am 15.11.2025 bei Jobleads gefunden
Medical Director-Oncology, Home-Based (m/w/d)
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Job Overview The medical department consists of a Chief Medical Officer, Medical Directors, Sr Medical Directors, Medical Writers, and Safety Associates. The Medical Director provides medical and scientific support to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical research programs, study teams and investigators. The Medical Director also provides review, advice, and leadership for potentially or awarded clinical research programs. The Medical Director role is a team member participant role and functions in a matrix report to project teams much like other members of the project teams. The primary role of Medical Director is to provide medical oversight for clinical trials by serving as Medical Monitor for studies conducted by IQVIA Biotech Clinical on behalf of sponsor companies. The principal function of a Medical Monitor is to serve as primary contact for the sponsor medical team and to serve as front line medical resource to support the project team. The Medical [. .. ] as project team member: Provides medical and scientific input to clinical research programs including review of new business proposals, preclinical and/or clinical data, study protocols, training materials, informed consent, Investigator Drug Brochures, e CRFs, analysis plan designs, clinical study reports, regulatory approval submissions, serious and non-serious adverse event evaluation, and reporting. Ensures medical activities run according to GCP and operate with highest efficiency. Establishes and maintains a network of medical/ scientific consultants, etc. Supervises and manages Medical Director activities. Clinical [. .. ]
Job am 05.11.2025 bei Jobleads gefunden
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Job Overview The medical department consists of a Chief Medical Officer, Medical Directors, Sr Medical Directors, Medical Writers, and Safety Associates. The Medical Director provides medical and scientific support to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical research programs, study teams and investigators. The Medical Director also provides review, advice, and leadership for potentially or awarded clinical research programs. The Medical Director role is a team member participant role and functions in a matrix report to project teams much like other members of the project teams. The primary role of Medical Director is to provide medical oversight for clinical trials by serving as Medical Monitor for studies conducted by IQVIA Biotech Clinical on behalf of sponsor companies. The principal function of a Medical Monitor is to serve as primary contact for the sponsor medical team and to serve as front line medical resource to support the project team. The Medical [. .. ] as project team member: Provides medical and scientific input to clinical research programs including review of new business proposals, preclinical and/or clinical data, study protocols, training materials, informed consent, Investigator Drug Brochures, e CRFs, analysis plan designs, clinical study reports, regulatory approval submissions, serious and non-serious adverse event evaluation, and reporting. Ensures medical activities run according to GCP and operate with highest efficiency. Establishes and maintains a network of medical/ scientific consultants, etc. Supervises and manages Medical Director activities. Clinical [. .. ]
Job am 20.10.2025 bei Jobleads gefunden
Medical Director Oncology, Home-Based (mwd)
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
[. .. ] Job Overview The medical department consists of a Chief Medical Officer Medical Directors Sr Medical Directors Medical Writers and Safety Associates. The Medical Director provides medical and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] scientific support to clinical research programs study teams and investigators. The Medical Director also provides review advice and leadership for potentially or awarded clinical research programs. The Medical Director role is a team member participant role and functions in a matrix report to project teams much like other members of the project teams. The primary role of Medical Director is to provide medical oversight for clinical trials by serving as Medical Monitor for studies conducted by IQVIA Biotech Clinical on behalf of sponsor companies. The principal function of a Medical Monitor is to serve as primary contact for the sponsor medical team and to serve as front line medical resource to support the project team. The Medical [. .. ] as project team member: Provides medical and scientific input to clinical research programs including review of new business proposals preclinical and/or clinical data study protocols training materials informed consent Investigator Drug Brochures e CRFs analysis plan designs clinical study reports regulatory approval submissions serious and non-serious adverse event evaluation and reporting. Ensures medical activities run according to GCP and operate with highest efficiency. Establishes and maintains a network of medical/ scientific consultants etc. Supervises and manages Medical Director activities. Clinical [. .. ]
Job am 12.10.2025 bei Jobleads gefunden
Medical Director-Oncology, Home-Based (m/w/d)
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Job Overview The medical department consists of a Chief Medical Officer, Medical Directors, Sr Medical Directors, Medical Writers, and Safety Associates. The Medical Director provides medical and scientific support to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical research programs, study teams and investigators. The Medical Director also provides review, advice, and leadership for potentially or awarded clinical research programs. The Medical Director role is a team member participant role and functions in a matrix report to project teams much like other members of the project teams. The primary role of Medical Director is to provide medical oversight for clinical trials by serving as Medical Monitor for studies conducted by IQVIA Biotech Clinical on behalf of sponsor companies. The principal function of a Medical Monitor is to serve as primary contact for the sponsor medical team and to serve as front line medical resource to support the project team. The Medical [. .. ] as project team member: Provides medical and scientific input to clinical research programs including review of new business proposals, preclinical and/or clinical data, study protocols, training materials, informed consent, Investigator Drug Brochures, e CRFs, analysis plan designs, clinical study reports, regulatory approval submissions, serious and non-serious adverse event evaluation, and reporting. Ensures medical activities run according to GCP and operate with highest efficiency. Establishes and maintains a network of medical/ scientific consultants, etc. Supervises and manages Medical Director activities. Clinical [. .. ]
Job am 10.10.2025 bei Jobleads gefunden
Medical Science Liaison
• München, Bayern
Firmenwagen 30+ Urlaubstage
[. .. ] global specialty pharma business and a preferred partner for innovator pharma companies, instigating a paradigm shift in the life cycle management of iconic medicines. We seek to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] extensively engage with clinical communities to communicate product improvements and prioritise environmental, social, and governance considerations across the business and workforce. Pharmanovias therapeutic areas include Cardiovascular, Oncology, Endocrinology and Neurology. About the role: Reporting to the Medical Department, you will be a member of MSL team, whose primary responsibility is to interact with influential [. .. ] and maintaining professional relationships with national/ regional KOLs, establishing peer-to-peer collaborations with key medical experts in the therapeutic areas covered by Pharmanovia Supporting evidence generation initiatives including potential investigator site identification, trial recruitment, registries, and presentation of final approved data, involving experts to generate scientific data including investigator-initiated trials Collaborating with physicians on medical affairs initiatives including publication and communication plans, advisory boards, medical education opportunities, webinars, training, and speaker development Serving as a scientific peer-to-peer resource to external disease experts and internal stakeholders Supporting the medical community with up-to-date medical information, robust disease expertise, [. .. ]
Job am 08.10.2025 bei Jobleads gefunden
Medical Science Liaison Manager, Amyloidosis, North-Eastern Germany (Rostock, Berlin, Leipzig, . . .
• 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. This Is What You Will Do The Medical Science Liaison (MSL) is a field-based scientific expert that strategically supports [. .. ] educate the medical community with up-to-date medical and scientific information Identify and execute collaboration opportunities between expert KOLs 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 [. .. ]
Job am 16.09.2025 bei Jobleads gefunden
Associate Medical Director, Cardiology-Metabolic Diseases and Nephrology Experience (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 Medical Monitoring: Primarily serves as Global Medical Advisor on assigned projects. Serves as Scientific Advisor and provides guidance to Project Leaders on the medical and scientific aspects of assigned projects. [. .. ] 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 27.06.2025 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) [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Senior Regional Medical Advisor-Rare Disease (Central/ South)
• München, Bayern
Beratungs-/ Consultingtätigkeiten
[. .. ] Medical Advisor to join the Medical team. This role will focus on the Central/ Southern part of Germany. This role will support their portfolio of products and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] relay field-based clinical/ medical insights in order to support the future strategy. This position will provide operational support for activities related to Medical Information and Communication, Medical Education and Training, Investigator Initiated Trials, Key Opinion Leader outreach bringing value via scientific exchange. The position will also provide Research Clinical Development support as needed. The RMA will support the Medical Director in all aspects, i. e. representation of company in scientific presentations, conferences, and support for the Commercial Organisation while ensuring compliance with all [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Senior Regional Medical Advisor-Rare Disease (Central/ South)
• Düsseldorf, Nordrhein- Westfalen Duesseldorf
Beratungs-/ Consultingtätigkeiten
[. .. ] Medical Advisor to join the Medical team. This role will focus on the Central/ Southern part of Germany. This role will support their portfolio of products and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] relay field-based clinical/ medical insights in order to support the future strategy. This position will provide operational support for activities related to Medical Information and Communication, Medical Education and Training, Investigator Initiated Trials, Key Opinion Leader outreach bringing value via scientific exchange. The position will also provide Research Clinical Development support as needed. The RMA will support the Medical Director in all aspects, i. e. representation of company in scientific presentations, conferences, and support for the Commercial Organisation while ensuring compliance with all [. .. ]
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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 124 offene Stellenanzeigen für Clinical Trials Investigator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trials Investigator Jobs?
Aktuell suchen 13 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:
- Tigermed (32 Jobs)
- wax. (11 Jobs)
- Tubulis GmbH (11 Jobs)
- Syneos Health (2 Jobs)
- Barrington James (2 Jobs)
- Alimera (2 Jobs)
In welchen Bundesländern werden die meisten Clinical Trials Investigator Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trials Investigator Jobs werden derzeit in Nordrhein-Westfalen (25 Jobs), Bayern (15 Jobs) und Baden-Württemberg (9 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trials Investigator Jobs?
Clinical Trials Investigator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
