115 Jobs für Clinical Trials Investigator
Stellenangebote Clinical Trials Investigator Jobs
Job gestern bei Jobleads gefunden
• München, Bayern
[. .. ] and deliver regional medical strategies and engagement activities aligned with global and country plans. Provide timely, evidence-based responses to medical and scientific inquiries from clinicians and healthcare [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] partners. Support investigator-initiated projects and clinical research activities, including site identification and scientific feasibility. Design and deliver medical education, advisory boards and regional congress activities. Collect and share local insights and evidence with crossfunctional teams to inform medical strategy and improve patient care. Basic Qualifications University degree in medicine, pharmacy, life sciences or a related field. [. .. ] Willingness and ability to travel within the region and nationally. Preferred Qualifications Field-based experience as a Medical Science Liaison, Regional Medical Affairs Manager or similar role. Experience supporting clinical trials, investigator-initiated studies or study startup activities. Experience planning medical education, advisory boards and congress activities. Knowledge of the German healthcare system and market access considerations. Proven ability to build and maintain networks with key opinion leaders and investigators. Comfortable using digital engagement tools and omnichannel communication approaches. GSK is [. .. ]
Job vor 12 Tagen bei Neuvoo gefunden
Rhythm Pharmaceuticals
Scientific Affairs Manager-Germany (North East)
• Hamburg
[. .. ] 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 vor 13 Tagen bei Neuvoo gefunden
Parexel
• Berlin
[. .. ] experienced oncology CRAs in Germany for an expected expansion of one of our key sponsors. This role is responsible for the site management, site monitoring and close-out [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of assigned clinical trials investigator sites to ensure patient safety and quality study execution Some specifics about this advertised role Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan and applicable prevailing laws, Good Clinical Practices. Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from [. .. ]
Job am 12.05.2026 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 10.05.2026 bei Neuvoo gefunden
Chronos Consulting
• deutschland,
Job Description Our client is a global medical device company, a pioneer of the MR-guided focused ultrasound technology which is a game-changing innovation. They are looking for a
Clinical Affairs [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Program Manager Europe. The role is remote with up to 40 travel and based in Europe. As part of the global clinical affairs team, you will be responsible for developing strategies for a successful execution of roadmap clinical trials that demonstrate medical product safety and efficacy. Additional responsibilities include management of clinical trials approvals with local IRBs and/or Competent Authorities. Required Skills and Experience: 1) BS, BA, BSN or RN or higher degree in the Life Sciences or related disciplines 2) Minimum 3+ years in clinical management position [. .. ] abilities to operate independently 11) Willing able to travel domestically and internationally, as required (up to 40) Responsibilities: Collaborate with Company Stakeholders to execute company objectives into successful clinical trials, investigator-sponsored studies, etc. Overall responsibility for design of clinical trials including protocol development, clinical trial discussions with EU Competent Authorities, and development of timeline and budget Manage the process of screening/ qualifying, selecting, and contracting with investigators, sites and vendors required for conduct of clinical trials Direct/ Manage necessary clinical [. .. ]
Job am 08.04.2026 bei Neuvoo gefunden
GSK
Senior Regional Medical Affairs Manager Center North (SRMAM) (m/f/d)
[. .. ] and deliver regional medical strategies and engagement activities aligned with global and country plans. Provide timely, evidence-based responses to medical and scientific inquiries from clinicians and healthcare [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] partners. Support investigator-initiated projects and clinical research activities, including site identification and scientific feasibility. Design and deliver medical education, advisory boards and regional congress activities. Collect and share local insights and evidence with cross-functional teams to inform medical strategy and improve patient care. Basic Qualification We are seeking professionals with the following required skills and [. .. ] Qualification If you have the following characteristics, it would be a plus: Field-based experience as a Medical Science Liaison, Regional Medical Affairs Manager or similar role. Experience supporting clinical trials, investigator-initiated studies or study start-up activities. Experience planning medical education, advisory boards and congress activities. Knowledge of the German healthcare system and market access considerations. Proven ability to build and maintain networks with key opinion leaders and investigators. Comfortable using digital engagement tools and omnichannel communication approaches. Weitere [. .. ]
Job am 07.04.2026 bei Neuvoo gefunden
582 Glaxo Smith Kline GmbH Co. KG
Senior Regional Medical Affairs Manager Center North (SRMAM) (m/f/d)
[. .. ] and deliver regional medical strategies and engagement activities aligned with global and country plans. Provide timely, evidence-based responses to medical and scientific inquiries from clinicians and healthcare [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] partners. Support investigator-initiated projects and clinical research activities, including site identification and scientific feasibility. Design and deliver medical education, advisory boards and regional congress activities. Collect and share local insights and evidence with cross-functional teams to inform medical strategy and improve patient care. Basic Qualification We are seeking professionals with the following required skills and [. .. ] Qualification If you have the following characteristics, it would be a plus: Field-based experience as a Medical Science Liaison, Regional Medical Affairs Manager or similar role. Experience supporting clinical trials, investigator-initiated studies or study start-up activities. Experience planning medical education, advisory boards and congress activities. Knowledge of the German healthcare system and market access considerations. Proven ability to build and maintain networks with key opinion leaders and investigators. Comfortable using digital engagement tools and omnichannel communication approaches. Weitere [. .. ]
Neu Job vor 3 Std. bei XING gefunden
SJP Biotec GmbH
Chief Medical Officer/ SVP Clinical Development (m/f/d)
• 8001 Zürich
Führungs-/ Leitungspositionen
Stellenbeschreibung Introduction About SJP Biotec SJP Biotec Gmb H is a
clinical-stage precision oncology company pioneering a first-in-class Selective Translation Regulatory Inhibitor (STRI) platform powered to overcome treatment resistance [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in refractory cancers. Founded in 2024, SJP targets RAS-driven, hormone-receptor-positive, and immune-refractory tumors with a novel pipeline of small molecules developed in our lab and ready to proceed with regulatory-grade trials. Backed by a Scientific Advisory Board that includes world-leading authorities in RAS and breast cancer biology, and immuno-oncology, SJP has established clinical partnerships with leading medical centers world-wide including UCSF, NCI, MD Anderson, Baylor College of Medicine, MSKCC, and Mc Gill, to name a few. Chief Medical [. .. ] Ar M, FDA, and EMA Develop and implement biomarker-driven patient selection strategies Build and manage relationships with leading academic and clinical sites across Germany, the EU, and the US Oversee Investigator Initiated Trials and partnerships, providing scientific leadership and interactions as required Lead regulatory strategy, developing approaches for Fast Track Designation, Breakthrough Therapy Designation, and accelerated approval pathways as applicable Support pharmaceutical partnering activities-prepare clinical data packages and respond to due diligence for potential licensing and out-licensing transactions Build [. .. ]
Job am 06.06.2026 bei Stellen-Online.de gefunden
Universität zu Köln- Medizinische Fakultät
• Köln, 50667
Teilzeit
Universität zu Köln Medizinische Fakultät Professur für
Clinical Computational Cancer Biology (W3) (w/m/d) Die Universität zu Köln ist eine der größten und forschungsstärksten Hochschulen Deutschlands mit einem vielfältigen Fächerangebot. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Sie bietet mit ihren sechs Fakultäten und ihren interfakultären Zentren ein breites Spektrum wissenschaftlicher Disziplinen und international herausragender Profilbereiche. Das Deutsche Krebsforschungszentrum (DKFZ) ist eines der größten [. .. ] zwischen DKFZ, exzellenten Partnern in der Universitätsmedizin und weiteren herausragenden Forschungspartnern an verschiedenen Standorten in Deutschland. Die zentrale Aufgabe des NCT besteht darin, aus der Forschung heraus innovative klinische Studien (Investigator Initiated Trials, IIITs) zu entwickeln, durchzuführen sowie bundesweit Patientinnen und Patienten zugänglich zu machen. Ihre Aufgaben Im Rahmen dieser Professur leiten Sie eine DKFZ-Forschungsabteilung im Rahmen des NCT. Sie werden umfassende und hochwertige Datensätze analysieren und Algorithmen für das NCT-IIT-Programm entwickeln. Insbesondere sollen Machine Learning-Methoden zum besseren Verständnis [. .. ]
Neu Job vor 3 Std. bei Mindmatch.ai gefunden
Syneos Health
Global Senior Project Specialist (Sponsor Dedicated) Germany
• AT- 9 Wien
[. .. ] organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Job Responsibilities Setup, maintain and/or close out project files and study information (e. g. , regulatory documents, Trial Master [. .. ] reapprovals, data queries) on a variety of databases and systems. Attend, participate, prepare and distribute meeting minutes and action items for both internal and external meetings (sponsor, trusted process, functional, investigator meetings) . Follow up with team members on action items to closure. Maintain timely and effective communication among team members and site staff. Keep Project Leadership and Clinical Research Associates (CRAs) fully apprised of sites and study status. May contact site staff as needed for critical information. Provide administrative support [. .. ] delivery of all the materials, documentation and information needed to set up, execute and deliver the assigned trial (s) ; independently take care for complex technical systems to manage clinical trials; oversight of trial supplies, documentation, submissions, and other operational parameters. The Senior Project Specialist is responsible for maintaining and coordinating the logistical aspects of clinical projects, and provides overall support to functional leads to ensure the successful completion of project deliverables. The Senior Project Specialists supports the Project Lead (PL) [. .. ]
Job vor 6 Tagen bei Mindmatch.ai gefunden
Merck Healthcare
• AT- 9 Wien
[. .. ] for patients with rare tumors. You will define and execute the local medical strategy, drive evidence generation initiatives, build lasting relationships with key opinion leaders and patient [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] organizations, and support clinical development activitiesall while ensuring the highest standards of scientific integrity and regulatory compliance. Key Responsibilities Medical Strategy Scientific Expertise Define and lead the local medical strategy for your therapeutic area, aligned with global and regional objectives. Serve as the internal expert on disease biology, treatment landscape, and evolving standards of [. .. ] Advocacy Director to align countrylevel PAO strategy and tactics. Analyze the local patient advocacy landscape and represent the company externally at relevant meetings. Clinical Development Evidence Generation Support companysponsored clinical trials across all phases, from site identification and initiation through to completion, including patient enrollment support and investigator engagement. Act as primary liaison to investigators interested in developing and conducting investigatorinitiated research (IIS) ; coordinate between investigators and internal stakeholders. Drive realworld evidence (RWE) generation and lead/support local medical studies; contribute to site selection for clinical projects in collaboration with Clinical Operations. Partner with crossfunctional teams, including [. .. ]
Job vor 8 Tagen bei Mindmatch.ai gefunden
Teleflex
Clinical Research Associate
• AT- 9 Wien
Homeoffice möglich
Expected Travel: More than 50 Requisition ID: 13617 Position Summary The
Clinical Research Associate (CRA) is responsible for scheduling and conducting on-site and remote monitoring visits in compliance with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] applicable regulatory standards (MDR, ISO 14155, ICH/ GCP guidelines, Teleflex procedures and IRB/ EC policies) . The CRA conducts monitoring visits as identified by the monitoring plan, study team or department needs [. .. ] visit preparation. Conducts monitoring visits per the department SOP, WIs and monitoring plans. Applies MDR, ISO 14155, ICH/ GCP guidelines and Teleflex SOP and WIs to monitoring activities. Completes the Investigator Files with all appropriate documentation. Ensures all required documentation is completed prior to site initiation, during enrollment and followup, and at site close out. Provides findings to site staff, clear directions for resolution, appropriate retraining, and reviews data queries with site staff to ensure they are understood and can be [. .. ] Cardiology and/or Peripheral Vascular Intervention is an advantage. Specialized Skills/ Other Requirements Strong working knowledge, understanding and ability to apply MDR, ISO 14155 and ICH/ GCP guidelines governing clinical trials. Strong compliance focus. Demonstrated aptitude and knowledge in relevant therapeutic areas and ability to learn and integrate new therapeutic areas knowledge. Ability to train and mentor Clinical Studies personnel for remote and onsite monitoring visits. Ability to train onsite staff on the protocol, GCPs, data entry and other pertinent regulations. [. .. ]
Job am 31.05.2026 bei Mindmatch.ai gefunden
IQVIA
• AT- 9 Wien
Führungs-/ Leitungspositionen
[. .. ] the Sponsors requirements. Sponsor Requirements Budget building within France and UK. Global contracts experience within Germany, Austria, Nordics, Poland, Italy and or Spain. Essential Functions Develop Coordinate [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 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. Assist with the creation and/or review of core scientific, technical and administrative documentation to support business development and enable study initiation and maintenance, as required. Contribute to the collection, interpretation, analysis and dissemination of accurate contracting intelligence to support assigned studies and the [. .. ]
Job am 29.05.2026 bei Mindmatch.ai gefunden
IQVIA
Contract Negotiator
• AT- 9 Wien
[. .. ] the Sponsors requirements. Sponsor Requirements Budget building within France and UK. Global contracts experience within Germany, Austria, Nordics, Poland, Italy and or Spain. Essential Functions Develop Coordinate [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 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. Assist with the creation and/or review of core scientific, technical and administrative documentation to support business development and enable study initiation and maintenance, as required. Contribute to the collection, interpretation, analysis and dissemination of accurate contracting intelligence to support assigned studies and the [. .. ]
Job am 29.05.2026 bei Mindmatch.ai gefunden
IQVIA Argentina
• AT- 9 Wien
Führungs-/ Leitungspositionen
Vienna, Austria Full time Home-based R1546726 To lead Local Study Teams (LSTs) at country level to deliver committed components of
clinical studies according to agreed resources, budget and timelines [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] complying with Sponsor Procedural Documents, international guidelines such as ICHGCP as well as relevant local regulations. In addition to leading LST (s) , the Local Study Associate Director may perform site monitoring as needed to support the flexible capacity model. The Local [. .. ] on country study level: proactively manages sites, stakeholders, local and global vendors and customers to ensure risks are timely identified, mitigated and managed. Communicates and coordinates regularly with National Coordinating Investigator/ National Lead Investigator on recruitment and other study matters, if applicable. Plans and leads National Investigator meet Ensures that all study documents are ready for final archiving and completion of local part of the e TMF. Plans and leads activities associated with audits and regulatory inspections in liaison with CQAD and [. .. ] Affairsled or Academicled studies) . Good knowledge of international guidelines ICH GCP as well as relevant local regulations. Proven ability to lead and motivate cross functional teams to deliver clinical trials according to or ahead of time plan, budget and with required quality. Good medical knowledge of Oncology, Rare Diseases, cardiology, hematology, CVRM Therapeutic Areas. Good knowledge of the Drug Development Process. Excellent understanding of the Clinical Study Process including monitoring. Very good understanding of the Study Drug Handling Process and [. .. ]
Job am 29.05.2026 bei Mindmatch.ai gefunden
IQVIA Argentina
Local Study Associate Director
• AT- 9 Wien
Führungs-/ Leitungspositionen
Vienna, Austria Full time Home-based R1546726 To lead Local Study Teams (LSTs) at country level to deliver committed components of
clinical studies according to agreed resources, budget and timelines [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] complying with Sponsor Procedural Documents, international guidelines such as ICHGCP as well as relevant local regulations. In addition to leading LST (s) , the Local Study Associate Director may perform site monitoring as needed to support the flexible capacity model. The Local [. .. ] on country study level: proactively manages sites, stakeholders, local and global vendors and customers to ensure risks are timely identified, mitigated and managed. Communicates and coordinates regularly with National Coordinating Investigator/ National Lead Investigator on recruitment and other study matters, if applicable. Plans and leads National Investigator meet Ensures that all study documents are ready for final archiving and completion of local part of the e TMF. Plans and leads activities associated with audits and regulatory inspections in liaison with CQAD and [. .. ] Affairsled or Academicled studies) . Good knowledge of international guidelines ICH GCP as well as relevant local regulations. Proven ability to lead and motivate cross functional teams to deliver clinical trials according to or ahead of time plan, budget and with required quality. Good medical knowledge of Oncology, Rare Diseases, cardiology, hematology, CVRM Therapeutic Areas. Good knowledge of the Drug Development Process. Excellent understanding of the Clinical Study Process including monitoring. Very good understanding of the Study Drug Handling Process and [. .. ]
Job am 25.05.2026 bei Mindmatch.ai gefunden
IQVIA Argentina
• AT- 9 Wien
[. .. ] the Sponsors requirements. Sponsor Requirements Budget building within France and UK. Global contracts experience within Germany, Austria, Nordics, Poland, Italy and Spain. Essential Functions Develop and coordinate [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the creation of investigator grants and estimates, contracting strategies, and proposal text to support the proposal development process. Develop contract language, payment language, and budget templates as required. Utilize and maintain contracting systems, tools, processes, and training materials for selected sponsors, studies or multi-protocol programs according to the Scope of Work and Project [. .. ] 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. Assist with the creation and/or review of core scientific, technical and administrative documentation to support business development and enable study initiation and maintenance, as required. Contribute to the collection, interpretation, analysis and dissemination of accurate contracting intelligence to support assigned studies and the [. .. ]
Job am 25.05.2026 bei Mindmatch.ai gefunden
IQVIA Argentina
German-Speaking Contract Negotiator Remote (Clinical Trials)
• AT- 9 Wien
IQVIA Argentina is hiring a Contract Negotiator 2 in Vienna. In this role, you will develop and coordinate
investigator grants and contracting strategies while ensuring compliance with regulatory requirements. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Qualified candidates will have a Bachelors Degree or 5 years relevant experience, strong negotiation and communication skills, and be fluent in both English and German. The position offers a full-time home-based role with opportunities for professional growth. J-[. .. ]
Job am 25.05.2026 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 92572870 [. .. ]
Job am 25.05.2026 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 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. 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 [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
Medical Science Liaison Manager, Nephrology, North-West
• München, Bayern
[. .. ] become recognized and educate the medical community with up-to-date medical and scientific information. Identify and execute collaboration opportunities between expert KOLs in nephrology and Alexion medical affairs [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and clinical development such as publications, investigator-initiated trials, regional advisory boards, training and speaker development programs. Communicate experts opinion, feedback on new data and clinical trends to Alexion Medical Affairs, therapeutic area (TA) franchises and translate this information into strategic recommendations to enhance science and advance patient care. Respond to unsolicited medical information requests in the region, manage [. .. ]
Job am 05.05.2026 bei Jobleads gefunden
Clinical Trials Lead Site Coordinator
• Zug
Führungs-/ Leitungspositionen
Overview Milestone One is a Site Enabling Services organization with global headquarters in Zug, Switzerland. We understand what
clinical study sites need and our overall mission is to support [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] sites in stronger study delivery. Job Description Milestone One Site Coordinator supports trial sites in all related activities according to ICH-GCP, protocol requirements within study-specific defined timelines and enrollment goals. Responsibilities Act as the main line of communication [. .. ] of investigational products and clinical supplies. Collect, handle and maintain all site-specific regulatory documents as needed. Facilitate and support the contract and budget negotiations at the site level. Support Investigator and Site payments and processes as needed. Schedule and/or perform study procedures as per study requirements and delegation of responsibilities. Prepare for and participate in onsite study audits or regulatory agency inspections. Build and sustain long-lasting relationships with existing and potential clients (sponsors, CROs, medical institutions) . Qualifications [. .. ] Science, preferably in pharmacy, nursing or lab analytics. Minimum of 2 years of on-the-job experience in a clinical trial environment, where relevant experience has been gained in clinical trials, clinical terminology, and medical research working in the role of a Study Coordinator or similar function. Upper-intermediate level of English, with the ability to work in a global team environment. Experience in Oncology, Renal, or Cardiology clinical studies is a plus. Ability to work in a fast-paced environment, [. .. ]
Job am 08.04.2026 bei Jobleads gefunden
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 Initiation Visits) , assisting with patient enrollment, and ensuring smooth information exchange. Identify research opportunities, including Investigator Initiated Trials, Real World Evidence, and other evidencegeneration studies. Represent the organization at scientific conferences, advisory boards, and educational events, sharing insights and preparing reports for internal stakeholders. Ensure timely documentation of HCP interactions, compliance with local policies, and accurate reporting of insights and safety information. A Good Match: Advanced [. .. ]
Job am 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) [. .. ]
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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 115 offene Stellenanzeigen für Clinical Trials Investigator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trials Investigator Jobs?
Aktuell suchen 23 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 (6 Jobs)
- IQVIA Argentina (4 Jobs)
- Thermo Fisher Scientific (4 Jobs)
- Bei Gene (3 Jobs)
- Alexion Pharmaceuticals (3 Jobs)
- 582 Glaxo Smith Kline GmbH Co. KG (3 Jobs)
In welchen Bundesländern werden die meisten Clinical Trials Investigator Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trials Investigator Jobs werden derzeit in Bayern (21 Jobs), Niedersachsen (10 Jobs) und Berlin (9 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trials Investigator Jobs?
Clinical Trials Investigator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
