27 Jobs für Client Support Investigator
Stellenangebote Client Support Investigator Jobs
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
Syneos Health
• AT- 9 Wien
[. .. ] ability to perform activities for assigned sites working with study start-up and regulatory. Conduct of all remote and on-site monitoring activities through all study stages. Routinely reviews [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Investigator Site File (ISF) for accuracy, timeliness and completeness. Reconciles contents of the ISF with the Trial Master File (TMF) . Ensures the investigator/ physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations. Documents activities via confirmation letters, follow-up letters, trip [. .. ] (only as applicable) . Review data using data trend reports and knowledge of site practices. Ensure the resolution of data queries within agreed timelines. Utilize available hardware and software to support efficient study data collection and review. Maintain effective, accurate and timely communication with site staff and project team, and ensure appropriate issue escalation and resolution as per SOPs with a focus on issue prevention. Maintains clinical tracking and management systems. Ensure all assigned sites are trained and compliant with requirements [. .. ] Real World Late Phase study designs as well as Real World Research and relevant regulations including GPP. Excellent customer focus (internal and external) and able to interact professionally with a client organization and study site. Willingness to work within a teamoriented environment. Ability to work in a virtual team setting as well as work independently, seeking guidance as appropriate. Ability to handle multiple tasks (across multiple studies as necessary) and prioritize accordingly to achieve study timelines. Sound problem solving and analytical [. .. ]
Job am 22.02.2026 bei Mindmatch.ai gefunden
Syneos Health, Inc.
CRA Germany or Austria-single-client
• AT- 9 Wien
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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. Applies query resolution techniques remotely and on site, and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelines. Utilizes available hardware and software to support the effective conduct of the clinical study data review and capture. Verifies site compliance with electronic data capture requirements. May perform investigational product (IP) inventory, reconciliation and reviews storage and security. Verifies the IP has been dispensed and administered to subjects/ patients according to the protocol. Verifies issues or risks [. .. ]
Job am 15.01.2026 bei Jobleads gefunden
Führungs-/ Leitungspositionen
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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) with specialist medical training in Ophthalmology and at least 5 years experience in clinical practice. Clinical Trial Expertise: Experience serving on safety data review boards or [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Research Lead Cognitive Modeling Human-AI Systems
• Bremen
Führungs-/ Leitungspositionen
Our
client, an innovation-driven research organization operating at the intersection of AI, cognitive science, and wearable technologies, is seeking a Principal
Investigator to lead its neuroscience and cognitive modeling direction. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] This role combines scientific leadership with hands-on research, focusing on the development of cognitive intelligence systems that transform multimodal wearable and behavioral data into structured models within a knowledge-grounded digital twin framework. The selected candidate will define and advance the [. .. ] data fusion frameworks or benchmarking systems Knowledge of privacy-preserving machine learning, dynamic consent mechanisms, and GDPR-compliant workflows Prior experience leading or coordinating research projects What We Offer Relocation support to Germany, Serbia, Singapore, or other regions where the organization has established offices and research hubs or remote work opportunity A clear and structured academic growth trajectory, with the opportunity to develop toward a professorship-level position Flexible career pathways: the option to combine research with teaching or to focus [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
• Berlin
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] activities of the client. This includes the provision of scientific and medical data on both licensed and unlicensed products and indications as permissible by local laws and regulations. The MSL will act as the medical representative across a large, complex environment with flexibility to support other countries as needed by the organisation. Responsibilities Develop and maintain, in a self-driven manner, outstanding knowledge of cardiometabolic diseases and related areas, including specialised expertise in rare disease such as Familial Chylomicronemia Syndrome (FCS) and Severe Hypertriglyceridemia (SHTG) , along with comprehensive client and competitor product knowledge Understand [. .. ] aligned to strategy within the business Serve 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 Facilitate clear communication between the client and investigators in investigator engagement for both client trials and investigator-sponsored studies and barriers to enrolment for pipeline assets Work to the highest ethical compliance, ethics and safety standards adhering to all local regulations and laws Maintain [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
Medical Science Liaison Rare Disease (m/w/d) Region Nord
• Leipzig, Sachsen
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] activities of the client. This includes the provision of scientific and medical data on both licensed and unlicensed products and indications as permissible by local laws and regulations. The MSL will act as the medical representative across a large, complex environment with flexibility to support other countries as needed by the organisation. Responsibilities Develop and maintain, in a self-driven manner, outstanding knowledge of cardiometabolic diseases and related areas, including specialised expertise in rare disease such as Familial Chylomicronemia Syndrome (FCS) and Severe Hypertriglyceridemia (SHTG) , along with comprehensive client and competitor product knowledge Understand [. .. ] aligned to strategy within the business Serve 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 Facilitate clear communication between the client and investigators in investigator engagement for both client trials and investigator-sponsored studies and barriers to enrolment for pipeline assets Work to the highest ethical compliance, ethics and safety standards adhering to all local regulations and laws Maintain [. .. ]
Job vor 14 Tagen bei Jobleads gefunden
• Köln, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
Overview Responsible for providing strategic leadership and direction to
support global medical imaging project execution, with a strong emphasis on delivering exceptional customer experience. Oversees the imaging project management [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] team to ensure high-quality, timely, and responsive service that aligns with client expectations and evolving needs. As a key member of the medical imaging leadership team, this role drives the development and implementation of customer-centric solutions, service-oriented strategies, and operational best practices. Responsibilities include optimizing project management processes, ensuring regulatory compliance, forecasting resources and financials, and fostering team performance. Success [. .. ] allocation, resource planning, project oversight, training and development, employee engagement, team building, performance management, and succession planning. Represents the imaging project management function as a senior leader in client meetings, investigator sessions, and business development engagements, reinforcing a culture of excellence, partnership, and customer focus. Project and Product Leadership (10-15) Provides strategic oversight and direct involvement in imaging project development, collaborating with Sponsors and functional Directors to negotiate scope, allocate resources, and ensure delivery of high-quality, compliant solutions. Oversees [. .. ]
Job vor 14 Tagen bei Jobleads gefunden
Medical Science Liaison Rare Disease (m/w/d) Region Süd
• Heidelberg, Baden- Württemberg
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] activities of the client. This includes the provision of scientific and medical data on both licensed and unlicensed products and indications as permissible by local laws and regulations. The MSL will act as the medical representative across a large, complex environment with flexibility to support other countries as needed by the organisation. Responsibilities Develop and maintain, in a selfdriven manner, outstanding knowledge of cardiometabolic diseases and related areas, including specialised expertise in rare disease such as Familial Chylomicronemia Syndrome (FCS) and Severe Hypertriglyceridemia (SHTG) , along with comprehensive client and competitor product knowledge Understand and [. .. ] to strategy within the business Serve as an 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 Facilitate clear communication between the client and investigators in investigator engagement for both client trials and investigator-sponsored studies and barriers to enrolment for pipeline assets Work to the highest ethical compliance, ethics and safety standards adhering to all local regulations and laws Maintain [. .. ]
Job am 11.03.2026 bei Jobleads gefunden
Medical Science Liaison Rare Disease (m/w/d) Region Nord
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] activities of the client. This includes the provision of scientific and medical data on both licensed and unlicensed products and indications as permissible by local laws and regulations. The MSL will act as the medical representative across a large, complex environment with flexibility to support other countries as needed by the organisation. Responsibilities Develop and maintain, in a selfdriven manner, outstanding knowledge of cardiometabolic diseases and related areas, including specialised expertise in rare disease such as Familial Chylomicronemia Syndrome (FCS) and Severe Hypertriglyceridemia (SHTG) , along with comprehensive client and competitor product knowledge Understand and [. .. ] to strategy within the business Serve as an 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 Facilitate clear communication between the client and investigators in investigator engagement for both client trials and investigator-sponsored studies and barriers to enrolment for pipeline assets Work to the highest ethical compliance, ethics and safety standards adhering to all local regulations and laws Maintain [. .. ]
Job am 11.03.2026 bei Jobleads gefunden
Medical Science Liaison Rare Disease (m/w/d) Region Süd
• Frankfurt, Hesse
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] activities of the client. This includes the provision of scientific and medical data on both licensed and unlicensed products and indications as permissible by local laws and regulations. The MSL will act as the medical representative across a large, complex environment with flexibility to support other countries as needed by the organisation. Responsibilities Develop and maintain, in a selfdriven manner, outstanding knowledge of cardiometabolic diseases and related areas, including specialised expertise in rare disease such as Familial Chylomicronemia Syndrome (FCS) and Severe Hypertriglyceridemia (SHTG) , along with comprehensive client and competitor product knowledge Understand and [. .. ] to strategy within the business Serve as an 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 Facilitate clear communication between the client and investigators in investigator engagement for both client trials and investigator-sponsored studies and barriers to enrolment for pipeline assets Work to the highest ethical compliance, ethics and safety standards adhering to all local regulations and laws Maintain [. .. ]
Job am 11.03.2026 bei Jobleads gefunden
• Nürnberg, Bayern
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] activities of the client. This includes the provision of scientific and medical data on both licensed and unlicensed products and indications as permissible by local laws and regulations. The MSL will act as the medical representative across a large, complex environment with flexibility to support other countries as needed by the organisation. Responsibilities Develop and maintain, in a selfdriven manner, outstanding knowledge of cardiometabolic diseases and related areas, including specialised expertise in rare disease such as Familial Chylomicronemia Syndrome (FCS) and Severe Hypertriglyceridemia (SHTG) , along with comprehensive client and competitor product knowledge Understand and [. .. ] to strategy within the business Serve as an 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 Facilitate clear communication between the client and investigators in investigator engagement for both client trials and investigator-sponsored studies and barriers to enrolment for pipeline assets Work to the highest ethical compliance, ethics and safety standards adhering to all local regulations and laws Maintain [. .. ]
Job am 11.03.2026 bei Jobleads gefunden
Medical Science Liaison Rare Disease (m/w/d) Region Süd
• München, Bayern
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] activities of the client. This includes the provision of scientific and medical data on both licensed and unlicensed products and indications as permissible by local laws and regulations. The MSL will act as the medical representative across a large, complex environment with flexibility to support other countries as needed by the organisation. Responsibilities Develop and maintain, in a selfdriven manner, outstanding knowledge of cardiometabolic diseases and related areas, including specialised expertise in rare disease such as Familial Chylomicronemia Syndrome (FCS) and Severe Hypertriglyceridemia (SHTG) , along with comprehensive client and competitor product knowledge Understand and [. .. ] to strategy within the business Serve as an 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 Facilitate clear communication between the client and investigators in investigator engagement for both client trials and investigator-sponsored studies and barriers to enrolment for pipeline assets Work to the highest ethical compliance, ethics and safety standards adhering to all local regulations and laws Maintain [. .. ]
Job am 07.03.2026 bei Jobleads gefunden
Medical Science Liaison Rare Disease (m/w/d) Region Süd
• Stuttgart, Baden- Württemberg
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] activities of the client. This includes the provision of scientific and medical data on both licensed and unlicensed products and indications as permissible by local laws and regulations. The MSL will act as the medical representative across a large, complex environment with flexibility to support other countries as needed by the organisation. Responsibilities Develop and maintain, in a selfdriven manner, outstanding knowledge of cardiometabolic diseases and related areas, including specialised expertise in rare disease such as Familial Chylomicronemia Syndrome (FCS) and Severe Hypertriglyceridemia (SHTG) , along with comprehensive client and competitor product knowledge Understand and [. .. ] to strategy within the business Serve as an 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 Facilitate clear communication between the client and investigators in investigator engagement for both client trials and investigator-sponsored studies and barriers to enrolment for pipeline assets Work to the highest ethical compliance, ethics and safety standards adhering to all local regulations and laws Maintain [. .. ]
Job am 07.03.2026 bei Jobleads gefunden
Medical Science Liaison Rare Disease (m/w/d) Region Nord
• Bremen
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] activities of the client. This includes the provision of scientific and medical data on both licensed and unlicensed products and indications as permissible by local laws and regulations. The MSL will act as the medical representative across a large, complex environment with flexibility to support other countries as needed by the organisation. Responsibilities Develop and maintain, in a selfdriven manner, outstanding knowledge of cardiometabolic diseases and related areas, including specialised expertise in rare disease such as Familial Chylomicronemia Syndrome (FCS) and Severe Hypertriglyceridemia (SHTG) , along with comprehensive client and competitor product knowledge Understand and [. .. ] to strategy within the business Serve as an 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 Facilitate clear communication between the client and investigators in investigator engagement for both client trials and investigator-sponsored studies and barriers to enrolment for pipeline assets Work to the highest ethical compliance, ethics and safety standards adhering to all local regulations and laws Maintain [. .. ]
Job am 05.03.2026 bei Jobleads gefunden
Medical Science Liaison Rare Disease (m/w/d) Region Nord
• Berlin
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] activities of the client. This includes the provision of scientific and medical data on both licensed and unlicensed products and indications as permissible by local laws and regulations. The MSL will act as the medical representative across a large, complex environment with flexibility to support other countries as needed by the organisation. Responsibilities: Develop and maintain, in a self-driven manner, outstanding knowledge of cardiometabolic diseases and related areas, including specialised expertise in rare disease such as Familial Chylomicronemia Syndrome (FCS) and Severe Hypertriglyceridemia (SHTG) , along with comprehensive client and competitor product knowledge Understand [. .. ] 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 Facilitate clear communication between the client and investigators in investigator engagement for both client trials and investigator-sponsored studies and barriers to enrolment for pipeline assets Works to the highest ethical compliance, ethics and safety standards adhering to all local regulations and laws Maintains [. .. ]
Job am 05.03.2026 bei Jobleads gefunden
Medical Science Liaison Rare Disease (m/w/d) Region Nord
• Hannover, Niedersachsen
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] activities of the client. This includes the provision of scientific and medical data on both licensed and unlicensed products and indications as permissible by local laws and regulations. The MSL will act as the medical representative across a large, complex environment with flexibility to support other countries as needed by the organisation. Responsibilities Develop and maintain, in a selfdriven manner, outstanding knowledge of cardiometabolic diseases and related areas, including specialised expertise in rare disease such as Familial Chylomicronemia Syndrome (FCS) and Severe Hypertriglyceridemia (SHTG) , along with comprehensive client and competitor product knowledge Understand and [. .. ] to strategy within the business Serve as an 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 Facilitate clear communication between the client and investigators in investigator engagement for both client trials and investigator-sponsored studies and barriers to enrolment for pipeline assets Work to the highest ethical compliance, ethics and safety standards adhering to all local regulations and laws Maintain [. .. ]
Job am 05.03.2026 bei Jobleads gefunden
Medical Science Liaison Rare Disease (m/w/d) Region Nord
• Kiel, Schleswig- Holstein
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] activities of the client. This includes the provision of scientific and medical data on both licensed and unlicensed products and indications as permissible by local laws and regulations. The MSL will act as the medical representative across a large, complex environment with flexibility to support other countries as needed by the organisation. Responsibilities: Develop and maintain, in a self-driven manner, outstanding knowledge of cardiometabolic diseases and related areas, including specialised expertise in rare disease such as Familial Chylomicronemia Syndrome (FCS) and Severe Hypertriglyceridemia (SHTG) , along with comprehensive client and competitor product knowledge Understand [. .. ] 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 Facilitate clear communication between the client and investigators in investigator engagement for both client trials and investigator-sponsored studies and barriers to enrolment for pipeline assets Works to the highest ethical compliance, ethics and safety standards adhering to all local regulations and laws Maintains [. .. ]
Job am 28.01.2026 bei Jobleads gefunden
Join our Talent Pool-Project Management (Europe)
• München, Bayern
[. .. ] is actively monitoring this pool-no black box here About the Role (s) Project Manager As the project lead, will act as primary liaison throughout the project life [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] cycle ensuring client/ sponsor expectations appropriately managed; addressing and resolving queries/ issues, planning and executing all project meetings, assisting with site and patient recruitment strategies and materials, assisting with the development of stakeholder training and by regularly providing sponsor/ client with project status and update reports Manage project budget and initiate, review and [. .. ] years of relevant experience + substantial on-going training. The ideal candidate will have people management experience and possess significant and progressive experience in the management of global, multi-centre, investigator-initiated clinical trials. The successful individual will demonstrate exceptional communication and time management skills Project Director-Applicants should have a minimum of seven years of related work experience with ongoing training, and a three-year College Advance Diploma/ Degree in a relevant field of study, preferable in (Health) Sciences or [. .. ] ensure you feel supported If contacted for an initial call, a member of our TA team will be happy to share more. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us. [. .. ]
Job am 22.01.2026 bei Jobleads gefunden
• Frankfurt, Hesse
Freiberuflich
EPM Scientific are currently partnered with a
client running a global project in Aesthetic Medicine. They are urgently seeking a Freelance Clinical Research Associate to
support their expanding [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical operations team. See a short summary below: Contract Conditions Location: Germany, Remote Project: Medical Device, Aesthetic Medicine Key Responsibilities Conduct site monitoring visits (pre-study, initiation, routine, and close-out) to ensure compliance with protocol, GCP, and regulatory requirements. Serve as the primary point of contact for investigator sites, ensuring high-quality data collection and patient safety. Support site selection, feasibility assessments, and start-up activities. Identify and resolve site-level issues, escalating risks as needed to ensure timely trial delivery. Maintain accurate and timely documentation of monitoring activities and site communications. Contribute to continuous process improvement and [. .. ]
Job am 16.12.2025 bei Jobleads gefunden
Clinical Trial Manager-single sponsor
• München, Bayern
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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/ [. .. ] patient safety or data integrity. Document requested revisions and approvals in CTMS. Ensures these deliverables are provided according to company and/or sponsor specifications, including delivery deadlines. Interacts with the client and other functional departments related to clinical monitoring, central monitoring and site management activities and deliverables. Provides status updates on the clinical deliverables and risks to clients, project management and leadership as per departmental or study agreements. Provides solutions for obstacles in protocol execution and site management. Demonstrates understanding of [. .. ] clinical trial management scope. Oversees CRAs and Central Monitors assigned to the study and routinely assesses studyspecific process and training compliance, CMP compliance, and identifies emerging risks. May develop and support execution of corrective action plans at site and study level. Supports and completes activities 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. Qualifications Bachelors degree or RN [. .. ]
Job vor 3 Tagen bei Neuvoo gefunden
GULP experts united
Medical Science Liaison Uro-Oncology (m/f/d)
• Stuttgart, Baden- Württemberg
We are currently seeking a dedicated Medical Science Liaison Manager (m/f/d) in the field of uro-oncology for our
client in the pharmaceutical industry. In this position, you will make [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a significant contribution to the implementation of medical strategies, promote scientific exchange with leading experts, and support the development of innovative, patient-centered solutions. The area of responsibility includes Baden-Württemberg and Augsburg. The position is initially to be filled for 18 months as part of a temporary staffing arrangement with the option of extension or permanent employment. We look forward to receiving your application Heres what [. .. ] Support in the development of medical strategies and assistance with the market launch of an innovative medical device (including training and presence in the treatment room) Study support: Preparation of investigator meetings as well as processing and presentation of current clinical data and study results Cross-functional collaboration: Close coordination with medical leads, marketing and sales, as well as continuous analysis of scientific literature and the competition. Your profile Qualifications: Completed studies in natural sciences, pharmacy or medicine; a doctorate is [. .. ]
Job vor 3 Tagen bei Neuvoo.com gefunden
Green Life Science
Clinical Research Coordinator
Job Title: Clinical Research Coordinator (CRC) Location: Fully Remote Germany Employment Type: Full-time, Permanent Language Requirement: Native or Fluent German About the Company Our
client is a leading next-generation, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] full-service Contract Research Organization (CRO) transforming how clinical trials are delivered. The company combines a world-class clinical operations team with advanced AI-powered software to run faster, more reliable clinical studies for life sciences organizations. By integrating innovative technology with deep clinical expertise, [. .. ] motivated CRC looking to join a modern, technology-driven CRO environment while contributing to high-impact clinical research. Key Responsibilities Coordinate day-to-day activities related to clinical trial execution Support site management and investigator communication Assist with patient recruitment, screening, and retention activities Maintain accurate and complete study documentation and regulatory files Ensure compliance with study protocols, GCP, and applicable regulatory requirements Assist with data collection, query resolution, and clinical data entry Collaborate closely with clinical operations, monitoring teams, and sponsors Support study start-[. .. ]
Job vor 6 Tagen bei Neuvoo gefunden
GULP experts united
Medical Scientific Liaison Rheumatology (m/f/d) Northeast Region (Berlin/ Rostock)
• Berlin
Homeoffice möglich
[. .. ] leader within our Patient Impact Department. You are passionate about building long-term partnerships and exploring new avenues to sustainably increase patient value. This is a temporary position [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with the client for 14 months as parental leave cover. Heres what our clients offer Meaningful work: A role in which patient value is at the center of every decision. Culture: A highly professional, interdisciplinary team with flat hierarchies and an agile working environment. Flexibility: Independent work in the home office and in the field. Development: Insight into a global pharmaceutical company and the opportunity to make valuable contacts in the medical community. Your tasks Network management: Proactive identification and support of national and international thought leaders (KOLs) as well as other healthcare professionals (HCPs) . Scientific exchange: Conducting discussions on disease patterns, treatment algorithms and study data to support the positioning of our therapies for the right patient groups. Evidence generation: Generation and management of data (e. g. , Investigator Initiated Studies, RWE, audits) as well as support for clinical trials. Internal interface: Close collaboration with R D, Market Access and regulatory departments, as well as presentation of clinical data to decision-makers (e. g. , Formulary Committees) . Innovation: Development and implementation of innovative solutions that create measurable added [. .. ]
Job vor 13 Tagen bei Neuvoo gefunden
Amplity Health
Medical Science Liaison, Rare Disease
Work-Life-Balance
[. .. ] work An environment that empowers and supports colleagues to manage all aspects of their wellbeing by focusing on a holistic approach What youll be doing: In this [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] role you will support activities across both Medical Affairs Clinical Development objectives for the portfolio of pipeline products in rare disease (rare proteinuric kidney disorder, rare metabolic disorder) . You will serve as a key interface with clinical trial sites across all development programs, working closely with Clinical Development and Clinical Operations. Additionally, you [. .. ] and developing enduring relationships with HCPs, patient advocacy groups, professional societies, and institutions, creating constructive cross-functional partnerships with internal and external stakeholders Serving as a primary interface between our client and clinical trial sites across all development programs, working closely with Clinical Development Clinical Operations Advising and participating in the planning and set-up of clinical studies Representing our client at select scientific congresses and professional society meetings Sharing important clinical and scientific insights that you have gathered from fieldwork to cross-functional teams Acting as an internal and external scientific expert Adhering to compliance requirements Supporting investigator-initiated studies What youll need to be successful: An advanced doctoral degree (MD, Ph D, Pharm D) or MSc is preferred Relevant therapeutic area knowledge in the field of rare disease is preferred. Established KOL contacts in metabolic/ genetic disorders is a plus Post graduate therapeutic area experience is preferred Fluency [. .. ]
Job am 14.02.2026 bei Neuvoo gefunden
Thermo Fisher Scientific
Part-Time CRA II-Klinischer Monitor (0.8 FTE) (m/w/d)
• Munich, Bavaria
[. .. ] on now and in the future. Our clinical department defines, develops and delivers clinical programmes. Our global Clinical Operations colleagues within our PPD clinical research services provide [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] end-to-end support for clinical trials from study start up to monitoring through to study close out, across commercial and government contracts. Together, we help clients define and develop clinical programs, minimize delays, and implement high-quality, cost-efficient clinical studies. The role can be home-based, office-based in Munich or Karlsruhe, [. .. ] Develops collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to role are outlined in the task matrix. Travel up to 50-75 A day in the Life: Monitors investigator sites with a risk-based monitoring approach applies root cause analysis (RCA) , critical thinking and problem-solving skills to identify site processes failure and corrective/ preventive actions to bring the site into compliance and decrease risks. Ensures data accuracy through SDR, SDV and CRF review as applicable through on-[. .. ] Clinical Trial Management System, CTMS) . Performs QC check of reports generated from CTMS system where required. Participates in investigator meetings as necessary. Identifies potential investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Ensures trial close out and retrieval of trial materials. Ensures that required essential documents are complete [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Client Support Investigator pro Jahr?
Als Client Support Investigator verdient man zwischen EUR 45.000,- bis EUR 70.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Client Support Investigator Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 27 offene Stellenanzeigen für Client Support Investigator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Client Support Investigator Jobs?
Aktuell suchen 8 Unternehmen nach Bewerbern für Client Support Investigator Jobs.
Welche Unternehmen suchen nach Bewerbern für Client Support Investigator Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Client Support Investigator Stellenangebote:
- GULP experts united (2 Jobs)
- Syneos Health (1 Job)
- Green Life Science (1 Job)
- Amplity Health (1 Job)
- Thermo Fisher Scientific (1 Job)
In welchen Bundesländern werden die meisten Client Support Investigator Jobs angeboten?
Die meisten Stellenanzeigen für Client Support Investigator Jobs werden derzeit in Bayern (4 Jobs), Berlin (3 Jobs) und Baden-Württemberg (3 Jobs) angeboten.
Zu welchem Berufsfeld gehören Client Support Investigator Jobs?
Client Support Investigator Jobs gehören zum Berufsfeld Polizei, Militär, Sicherheit.
