136 Jobs für Clinical Trials Investigator
Stellenangebote Clinical Trials Investigator Jobs
Job vor 9 Tagen bei Jobleads gefunden
• Zug
Führungs-/ Leitungspositionen
[. .. ] accelerating significant assets that meet patients needs and have the highest probability of success. Were uniting science, technology, and talent to get ahead of disease together. The [...]
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[...] Medical Director Oncology Clinical Development, Breast and Gynecologic Cancerswill report to the Executive Medical Director, Clinical Development Lead (CDL) , Oncology Clinical Development. The Medical Director will be responsible for clinical research activities pertaining to advancing the development of GSKs clinical portfolio and will also have responsibility for engaging in medical dialogues with relevant [. .. ] (Warsaw) campuses. Key Responsibilities Collaborate with physicians, scientists, regulatory professionals, biostatisticians, regulatory, executive staff and others in a complex matrix environment to develop and execute phase 1-3 interventional clinical trials Ensure high quality protocol development aligned with the Clinical Development Plan to effectively determine a medicines potential efficacy, safety profile, key areas of product differentiation and value to patient in the shortest possible timeframe. Use medical expertise to contribute to the end to end (protocol concept to final study report) [. .. ] industry; clinical academic medicine or clinical medical practice settings in the field of oncology or gynecologic oncology. Oncology clinical drug development process experience in the conduct/ participation of clinical trials (investigator initiated, company sponsored or cooperative group trials) and their subsequent publications. Regulatory experience to support registration and GCP principle Robust knowledge of diseasespecific research priorities, public health needs, competitor landscape, clinical practice trends and treatment guidelines evolution If you are based in Cambridge, MA; Waltham, MA; Rockville, MD; or San [. .. ]
Job am 29.10.2025 bei Jobleads gefunden
Scientific Affairs Manager-Germany (Southwest)
• 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 [...]
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[...] 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 vor 5 Tagen bei StepStone gefunden
Miltenyi Biotec B. V. Co. KG
• Bergisch Gladbach
Führungs-/ Leitungspositionen Homeoffice möglich
Miltenyi Biomedicine is a biopharmaceutical company committed to advancing personalized cell and gene therapies. We are pioneering groundbreaking therapies for serious life-threatening diseases, and reshaping their accessibility for
clinical professionals [...]
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[...] and patients worldwide with the aim to improve and extend patients lives. We are currently focusing on difficult-to-treat hematological cancers using CAR-T and other technologies, while also exploring treatments for other diseases. Our lead candidate, a tandem CAR-T cell product, is currently undergoing pivotal clinical trials on a global scale. Join our highly professional team in bringing new medicines to the market. As a Medical Writer you are part of our Miltenyi biomedicine business and within the Clinical Development team. You will be responsible for the development and oversight of clinical and regulatory documents that support [. .. ] review, revision and finalization of clinical documents for submission to regulatory authorities. You lead the development, authoring, and submission of regulatory documents (e. g. , CTD modules, clinical study reports, investigator brochures, INDs/ IMPDs, NDAs/ MAAs, and briefing documents) . Your responsibility includes ensuring that all documents are scientifically sound, strategically aligned, and compliant with global regulatory standards. In addition, you manage document timelines, coordinate internal reviews, and ensure on-time delivery. Collaborating closely within cross-functional teams (clinical, regulatory, biostatistics, [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Manager Medical Science Liaison Oncology
• München, Bayern
[. .. ] 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 Inviations Visits) , assisting with patient enrollment, and ensuring smooth information exchange. Identify research opportunities, including Investigator-Initiated Trials, Real-World Evidence, and other evidence-generation 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. Qualifications Advanced degree [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
• Hamburg
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 service-capabilities, [...]
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[...] 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 am 06.12.2025 bei Jobleads gefunden
Chief Scientific Officer (CSO) Switzerland, 80 100 (Ref. 2605) - Member of the executive Board
• Bern
Führungs-/ Leitungspositionen
[. .. ] of the Executive Board role at Auriga Vision AG. Our client is the Swiss Cancer Institute (former SAKK) , a non-profit organization focused on the development and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] implementation of clinical trials in oncology based in Berne, Switzerland. As part of the teams expansion, we are looking for a Member of the executive Board. Responsibilities Leadership : Leading the Clinical Science team (Senior Scientific Director, Head of Clinical Development, Medical Science Liaison) , approximately 10 Clinical Scientists and Medical Advisors; active member [. .. ] Proven leadership experience (with direct reports) . Knowing how to collaborate in the field of public health, industry and development/ research. Proven track record in oncology/ hematology, with experience in Investigator Initiated Trials (academic record in leading clinical research is a strong plus) . Experience in setting up and handling clinical trials in Switzerland. Fluent in English plus German and/or French. Susanne Rietiker is looking forward to receiving your application documents via our job portal (CV, diploma, reference letters; no [. .. ]
Job am 04.12.2025 bei Jobleads gefunden
Senior/ Medical Director (Ophthalmology)
• 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 service-capabilities, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 am 24.11.2025 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 am 23.11.2025 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 [...]
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[...] 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 23.11.2025 bei Jobleads gefunden
Medical Science Liaison Manager, Nephrology, North-West
• 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 14.11.2025 bei Jobleads gefunden
Medical Science Liaison (mwd) Immunologie
• Düsseldorf, Nordrhein- Westfalen
Abgeschlossenes Studium
Firmenwagen Flexible Arbeitszeiten 30+ Urlaubstage
[. .. ] Markterfolg innovativer Therapien bei. Deine Aufgaben Aufbau und Pflege von Beziehungen zu Key Opinion Leaders (KOLs) Studienzentren und medizinischen Fachgesellschaften Präsentation wissenschaftlicher Daten und Studienergebnisse zu immunologischen [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Therapien Unterstützung von Investigator Initiated Trials (IITs) und klinischen Studienprogrammen Durchführung wissenschaftlicher Schulungen für interne Teams (z. B. Vertrieb Marketing Medical Affairs) Beobachtung und Bewertung aktueller Forschungsergebnisse Trends und Publikationen im Bereich Immunologie Teilnahme an medizinischen Kongressen Symposien und Advisory Boards Unterstützung der medizinisch-wissenschaftlichen Kommunikation im Rahmen von Markteinführungen Das bringst du mit Abgeschlossenes Studium [. .. ] einem dynamischen forschungsnahen Umfeld Interesse Dann sende uns deinen CV an Oder melde dich direkt über Linked In wir freuen uns auf den Austausch 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 69377191 [. .. ]
Job am 10.10.2025 bei Jobleads gefunden
• München, Bayern
Firmenwagen 30+ Urlaubstage
[. .. ] innovative global specialty pharma business and a preferred partner for innovator pharma companies, instigating a paradigm shift in the lifecycle 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 the MSL team, whose primary responsibility is to interact with [. .. ] Identifying, developing, and maintaining professional relationships with national/ regional KOLs, establishing peertopeer 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 investigatorinitiated 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 peertopeer resource to external disease experts and internal stakeholders. Supporting the medical community with uptodate medical information, robust disease expertise, and product information. Communicating [. .. ]
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
• Wien
[. .. ] Description Sponsor Dedicated Global Senior Project Manager (CTL level role) remote-Austria Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We [...]
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[...] translate unique 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 [. .. ] and central monitoring deliverables with a focus on patient safety, protocol/ GCP/ regulatory compliance and data integrity. Oversees site interactions post activation through site closeout. This may include patient recruitment, investigator payments or other related activities. May be responsible for identification of critical data and process, protocol execution risks and risk mitigations related to completion of the Risk Assessment and Categorization Tool (RACT) . Reviews the study scope of work, budget and protocol content and ensures the clinical project team (CRAs/ [. .. ] to achieve data cut and lock deadlines. Provides feedback to line managers on staff performance including strengths as well as areas for development. May be assigned to larger, more complex trials or may coordinate clinical activities for a team of CTMs across a portfolio of projects May coach and mentor CTMs regarding functional clinical delivery, evaluation of project risks, and action implementation. Qualifications Bachelors degree or RN in a related field or equivalent combination of education, training, and experience Demonstrated ability [. .. ]
Job gestern bei Jobleads gefunden
Clinical Research Associate-12 months monitoring experience required
• Frankfurt (Oder) , Brandenburg
Senior CRA ICON plc is a worldleading healthcare intelligence and
clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to [...]
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[...] join us on our mission to shape the future of clinical development. Role: Clinical Research Associate (12+ months monitoring experience required) Location: Must be based in the UK, ideally in the Midlands [. .. ] have the opportunity to build your career in a customerfocused environment that supports creativity, collaboration and performance. Your responsibilities include, but are not limited to: Allocation, initiation and conduct of trials: conduct site selection, recommend sites, and act as the frontline liaison between ICON and sites to ensure successful collaboration and meet milestone and delivery expectations. Manage assigned study sites and networks, conduct phase IIV protocols according to the monitoring plan and client procedures, perform Site Initiation Visits, and ensure personnel is [. .. ] corrective actions are implemented within specified timelines. Identify issues at sites, resolve and escalate as appropriate; collaborate with stakeholders to manage data query resolution for accurate data entry. Ensure the Investigator Folder is up to date and maintain TMFs. Negotiate investigator remuneration, prepare financial contracts, and trigger payments to investigational sites. You will need the following: Right to work in the UK. Up to 2years of pharmaceutical industry experience or other relevant experience (NHS or Academic) . Good knowledge of the [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• Berlin
Beratungs-/ Consultingtätigkeiten
Champion compliance and precision-help deliver life-changing therapies. Proclinical is seeking a GCP QA Consultant to support quality assurance activities for oncology-focused
clinical trials. This role involves overseeing quality processes for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] phase 2-3 studies, ensuring compliance with ICH-GCP and regulatory requirements, and managing risk-based quality plans. You will collaborate with internal teams and external partners to maintain high standards of clinical trial execution and inspection readiness. This is a fully remote position, open to candidates located anywhere within Europe. Responsibilities Develop and oversee study quality-related plans, including Oversight Quality and Audit Plans. Collaborate with third parties to formalize Investigator Site Audits (ISA) and agendas. Oversee quality activities for phase 2-3 trials, focusing on risk management and endpoint de-risking. Conduct risk-based reviews of study documents to ensure compliance with protocols, ICH-GCP, and regulatory requirements. Act as the Clinical Quality Assurance Representative in weekly monitor-site meetings. [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
GCP QA Consultant
Beratungs-/ Consultingtätigkeiten
[. .. ] top-tier QA talent with groundbreaking life sciences opportunities Champion compliance and precisionhelp deliver lifechanging therapies. Proclinical is seeking a GCP QA Consultant to support quality assurance activities [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] for oncologyfocused clinical trials. This role involves overseeing quality processes for phase 23 studies, ensuring compliance with ICHGCP and regulatory requirements, and managing riskbased quality plans. You will collaborate with internal teams and external partners to maintain high standards of clinical trial execution and inspection readiness. This is a fully remote position, open to candidates located anywhere within Europe. Responsibilities Develop and oversee study qualityrelated plans, including Oversight Quality and Audit Plans. Collaborate with third parties to formalize Investigator Site Audits (ISA) and agendas. Oversee quality activities for phase 23 trials, focusing on risk management and endpoint derisking. Conduct riskbased reviews of study documents to ensure compliance with protocols, ICHGCP, and regulatory requirements. Act as the Clinical Quality Assurance Representative in weekly monitorsite meetings. Monitor site performance, ensuring adherence [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
[. .. ] experience. The MSL is a member of a global field-based team of scientific experts who function as an extension of Medical Affairs. The MSL role focuses primarily [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] on providing clinical, scientific, and educational support to healthcare professionals (HCPs) at clinical trial research sites (Principal Investigators PIs and their study teams) , and potential clinical trial sites, in addition to national and regional Key Opinion Leaders (KOLs) who have a key influence in the medical oncology communities. The MSL develops strong [. .. ] oncology community and collects impactful insights to enhance the clients strategic objectives. This role will closely collaborate with the clients Clinical Operations team supporting ongoing and future company-sponsored clinical trials. Strong experience and pre-existing advanced knowledge of working in oncology are expected breast cancer experience is preferred. ACCOUNTABILITIES: Deliver client company, compound and protocol education to specific physicians and their support staff (developing clients presence in country) to optimize study performance to agreed timelines Provide accurate, non-promotional scientific [. .. ] and approved resources If requested, keep up to date with clinical knowledge, published data and trial work for client and competitive product studies If requested, support relevant education at Site Investigator Meetings, including Site Initiation Visits, in line with clinical study plans Develop strong communication links with PIs and study physicians and their teams Ensure requests received from PIs are managed efficiently and effectively, and that the client studies are the primary focus of the study site support teams Act as [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
(Junior-) Field Medical Advisor-Rare Oncology South
• München, Bayern
Absolventen, Einsteiger, Trainees
[. .. ] gifted cultivator of new and exciting opportunities grounded in science? The (Junior-) Field Medical Advisor serves as the primary field-based point of contact with healthcare providers (HCPs) [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] including clinical investigators on a range of clinical and scientific issues. The primary role is to deliver and facilitate medical education and communications, research, and scientific insight gathering activities of the client. This includes the provision of scientific and medical data on both licensed and unlicensed products and indications as permissible by [. .. ] aligned to strategy within the business Serves as external, credible scientific expert on disease area and client products at HCP field meetings, key medical and scientific conferences, advisory boards, clinical investigator meetings and patient advocacy group meetings Identify key field insights related to client products, activities and the disease area and effectively disseminate and collaborate with cross-functional partners Facilitate clear communication between the business and investigators in investigator engagement for both client trials and investigator-sponsored studies and barriers to enrolment for pipeline assets Advanced Degree MD, Ph D, Pharm D Demonstrable experience in an MSL function with oncology desired Knowledge of clinical research design and GCP in the oncology/ immune oncology area Demonstrate a strong understanding of clinical research trial design and study analysis [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Clinical Quality Manager (m/f/d) - Cell Therapy
• Hamburg
[. .. ] their potential. With us, every single employee puts patients first. Make an impact in advancing Cell Therapy by ensuring the highest standards of quality and compliance. We [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] are seeking a Clinical Quality Manager (CQM) (m/f/d) - Cell Therapy to join our Cell Therapy Clinical Operations (CTCO) team. In this role, you will collaborate with the Business Processes, Quality Learning (BPQL) team to provide expert guidance and coaching, enabling the successful delivery of Cell Therapy studies by the Site Management [. .. ] CTCO Process Owners to ensure all established SMM processes align with global quality standards. Leading or contributing to quality-related initiatives and continuous improvement programs that enhance compliance within CTCO trials and processes. Collaborating actively with the Director, Cell Therapy Quality Management to strengthen quality culture and compliance across the organization. Typical Responsibilities Assess training compliance of local SMM teams as part of quality oversight activities; deliver onboarding and ad hoc training on quality and compliance topics. Share global process updates [. .. ] SMM; develop and implement compliance improvement initiatives. Provide country-level consultation during RIST, inspections, and audits; act as audit coordinator for internal audits and serve as SME during sponsor and investigator site inspections. Act as a key member throughout the inspection process, including consultation for inspection responses. Analyze quality metrics and trends to improve performance and proactively manage issues. Participate in regional CT SMM leadership teams and facilitate quality review meetings. Identify, track, and elevate compliance risks; support risk mitigation activities [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
(Senior) Director Clinical Development
• München, Bayern
Führungs-/ Leitungspositionen
Company Description The (Senior) Director
Clinical Development is responsible for shaping, developing and executing the clinical development strategy for the assigned product. Specific responsibilities include design of clinical
MEHR INFOS ZUM STELLENANGEBOT
[...] class=highlight_text>trials across all phases (including phase IV) , clinical protocol development, medical monitoring, analysis of study data, and contribution to clinical study reports, registration dossier modules and briefing books for Health Authority interactions. The Director will represent and defend the clinical strategy during regulatory review processes (MAA) across multiple geographies and [. .. ] teams, regulatory, safety and other crossfunctional teams. Act as study physician for Sobi-sponsored studies: develop study synopsis and protocols, contribute to statistical analysis plans, perform medical monitoring, participate in
investigator meetings and review other key clinical documents. Interact with key opinion leaders and patient representatives, lead advisory boards to define clinical strategy and inform trial design. Provide strategic and operational clinical development expertise in interactions with regulatory and reimbursement authorities. Contribute highquality scientific and medical input to regulatory submissions, responses [. .. ]
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Job vor 6 Tagen bei Jobleads gefunden
Manager Medical Science Liaison Oncology
• 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 Inviations Visits) , assisting with patient enrollment, and ensuring smooth information exchange. Identify research opportunities, including Investigator-Initiated Trials, Real-World Evidence, and other evidence-generation 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. Qualifications Advanced degree [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
Clinical Trial Project Manager
Our Mandant, an innovative biotech company in the
clinical Phase 2 stage, is seeking a Clinical Trial Project Manager to oversee the execution of international clinical
trials in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the field of neurodegenerative and ophthalmologic diseases. Your Responsibilities Drafting and reviewing clinical trial documents, including study protocols, patient information, investigator brochures, study plans, manuals, and reports End-to-end execution of clinical trials, including comprehensive monitoring activities from study start-up through close-out Development of deviation plans; defining and assessing protocol deviations at patient, site, and study level, and recommending follow-up actions Providing clinical expertise and conducting risk/ [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
Arzt/ Ärztin (Allgemeinmedizin oder Innere Medizin) für unser innovatives Studienzentrum in Berl. . .
• Berlin
30+ Urlaubstage
[. .. ] von Patientinnen zur Studienteilnahme Medizinische Betreuung der Teilnehmenden im Rahmen klinischer Studien Zusammenarbeit im multidisziplinären Team mit Study Nurses, Koordinatorinnen und Projektmanagerinnen Dokumentation studienrelevanter Daten gemäß GCP-Richtlinien [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Teilnahme an Investigator Meetings und internen Fortbildungen Ihr Profil Gültige Approbation als Arzt/ Ärztin in Deutschland Facharztanerkennung in Allgemeinmedizin, Innerer Medizin oder einem verwandten Gebiet Interesse an klinischer Forschung und Bereitschaft zur Einarbeitung in neue Indikationen Empathischer Umgang mit Patientinnen und ausgeprägte Kommunikationsfähigkeit Teamorientierte Arbeitsweise und hohe Eigenverantwortung Gute Englischkenntnisse in Wort und [. .. ] Patientinnen-Rekrutierung und -Retention einsetzt. Wir glauben, dass klinische Forschung eine Behandlungsmöglichkeit für alle Patienten sein sollte und unsere Prüferinnen verfügen über umfassende Erfahrung in der Durchführung von General-Medicine-Clinical-Trials. Future Meds ist ein Netzwerk modern eingerichteter, dedizierter Forschungssites, das sowohl Site-Management als auch Patientinnen-Rekrutierungsdienstleistungen für Pharmaunternehmen und Vertragspflegeforschungsorganisationen bietet. Unser Fokus liegt auf der Sicherheit und Gesundheit unserer Patienten und durch die Nutzung innovativer Technologie maximieren wir den Pool von Patienten, die an Studien teilnehmen möchten, und [. .. ]
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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 136 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 (22 Jobs)
- Veeda Lifesciences (11 Jobs)
- wax. (11 Jobs)
- Tubulis GmbH (11 Jobs)
- TFS Health Science (5 Jobs)
- Barrington James (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 (26 Jobs), Bayern (19 Jobs) und Berlin (11 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trials Investigator Jobs?
Clinical Trials Investigator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
