40 Jobs für Client Support Investigator
Stellenangebote Client Support Investigator Jobs
Job vor 11 Tagen bei Jobleads gefunden
• Hamburg
Führungs-/ Leitungspositionen
[. .. ] 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 [...]
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 [. .. ]
Job am 04.12.2025 bei Jobleads gefunden
Senior/ Medical Director (Ophthalmology)
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] 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 [...]
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 [. .. ]
Job am 18.11.2025 bei Jobleads gefunden
• Stuttgart, Baden- Württemberg
Our
client global Leader in the Pharmaceutical Industry is looking for an experienced Medical Science Liaison specialized in Oncology. The role will be based remotely (ideally from Stuttgart) with frequent [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] travelling at a regional level. Your activities will consist in establishing scientific collaborations within the medical/ scientific community engaging with healthcare providers [. .. ] 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 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 [. .. ]
Job am 20.10.2025 bei Jobleads gefunden
Clinical Site Contracts Lead client-based in Munich
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] alignment with trial timelines. Maintain accurate records in Clinical Trial Management Systems and contract management platforms. Identify and escape business risks appropriately while supporting internal teams with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] contract-related guidance. Support payment tracking invoice preparation and financial reconciliation for investigator sites as needed. Required Qualifications Bachelors degree in life sciences business or a related field; equivalent experience may be considered. Minimum of 2 years experience negotiating legal and/or financial agreements preferably in clinical research or the pharmaceutical industry. Strong understanding of ICH-GCP guidelines clinical trial start-up processes [. .. ]
Job am 27.06.2025 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 [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Medical Science Liaison, Immunology (IBD) , Germany
• Berlin
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 inflammatory bowel disease. 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 will collaborate with Medical Affairs to identify [. .. ] 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) is preferred Relevant therapeutic area knowledge in the field of immunology or immuno-oncology, experience in gastroenterology is a plus. Post graduate therapeutic area experience is preferred Fluency in English and local language 3+ [. .. ]
Job gestern bei Jobleads gefunden
Work-Life-Balance
[. .. ] to 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 inflammatory bowel disease. 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 will collaborate with Medical Affairs to identify [. .. ] 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) is preferred Relevant therapeutic area knowledge in the field of immunology or immuno-oncology, experience in gastroenterology is a plus. Post graduate therapeutic area experience is preferred Fluency in English and local language 3+ [. .. ]
Job gestern bei Jobleads gefunden
Regional Medical Science Liaison (MSL) - Breast Cancer/ Oncology-Germany
[. .. ] for all our clients. Through strategic partnerships + deep therapeutic expertise, Amplity transforms how breakthrough treatments reach the people who need them. Regional Medical Science Liaison Oncology/ [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Breast Cancer Germany Client: Biotech, Oncology (Precision Medicine) Reports to: Field Manager at Amplity Health Primary Territory: Germany, Poland, Hungary, Check Republic, Switzerland and Austria Location: Germany RESPONSIBILITIES: Our client is a US based biopharmaceutical company fully dedicated to the research and development of medicines with the aim to improve the lives of patients. [. .. ] a member of a global field-based team of scientific experts who function as an extension of Medical Affairs. The MSL role focuses primarily 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 relationships within the respective [. .. ] 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 6 Tagen bei Jobleads gefunden
• München, Bayern
Beratungs-/ Consultingtätigkeiten
[. .. ] 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 vor 6 Tagen 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 6 Tagen bei Jobleads gefunden
[. .. ] position for 12months and we are open to considering candidates who are open to a temporary employment contract (FTC) or freelancers with their own company. The Quality [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Assurance Officer will support distribution activities including administrative batch release and Annual Product Quality Review (APQR) , customer activation, field actions and reporting, in addition to being responsible for the documentation and maintenance of the Quality Management System. Clin Choice is a global full-service CRO with a strong focus on quality, professional development and supportive culture. As a clientfacing role, we are looking for confident candidates with the ability to work independently whilst establishing a hightrust environment with the client counterparts. Main Job Tasks and Responsibilities: Coordinate with the Qualified Person (QP) the administrative batch releases (files preparation, monthly release register, reconciliation and archives) and Annual Product Quality Reviews. Perform customer qualification (eligibility checks) . Support First Code Activation, Quarantine/ Hold/Returned Goods reporting and management. Local Complaint Coordinator. Local Documentation Coordinator, including coordinate implementation at local level of corporate documentation, author and publish SOPs, and SOP periodic review. NCR/ CAPA initiator, investigator or task assignee (as needed) . Support implementation of Field Action. Support training planning and carry out reporting. Support the maintenance and management of the document retention system. Participate in Regulatory Affairs activities as needed. Education, Experience and Skills: Bachelors or Masters degree in a relevant scientific discipline. Prior experience [. .. ]
Job vor 9 Tagen bei Jobleads gefunden
CRA Germany or Austria-single-client
• München, Bayern
Beratungs-/ Consultingtätigkeiten
Join to apply for the CRA Germany or Austria-single-
client role at Syneos Health 1 day ago Be among the first 25 applicants Join to apply for the CRA Germany [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] or Austria-single-client role at Syneos Health Get AI-powered advice on this job and more exclusive features. Description CRA Germany or Austria-single-client Syneos Health is a [. .. ] each subject/ patient, as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/ patient. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol deviation/ violations and pharmacovigilance issues. Per the Clinical Monitoring/ Site Management Plan (CMP/ SMP) : Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) is accurate and complete. 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 vor 10 Tagen bei Jobleads gefunden
Medical Science Liaison Oncology
• Berlin
Our
client global Leader in the Pharmaceutical Industry is looking for an experienced Medical Science Liaison specialized in Oncology. The role will be based remotely (ideally from Berlin) with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] frequent travelling at a regional level. Your activities will consist in establishing scientific collaborations within the medical/ scientific community engaging with healthcare providers [. .. ] 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 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 [. .. ]
Job vor 14 Tagen bei Jobleads gefunden
Sponsor Dedicated Global Senior Project Manager (CTL level role) remote-Austria
• Wien
[. .. ] 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 [. .. ] for 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. 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 or may coordinate clinical activities [. .. ]
Job am 07.12.2025 bei Jobleads gefunden
[. .. ] activities, including feasibility, pre-study activities and site selection Collect, review and track essential/ regulatory documents Participate in and complete all general and study specific training as required [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Participate in investigator, client and project team meetings; may include presentations Create and implement subject enrollment strategies for assigned study sites Ensure proper storage, dispensation and accountability of all Investigational Product (IP) and trial-related materials Perform site management activities and provide ongoing updates of site status to Clinical Project Manager Conduct remote monitoring [. .. ] spoken and written German and English About CTI Advance Your Career We invest in your professional growth. Our structured mentoring program, leadership development courses, and dedicated training department provide the support you need to excel. We also encourage ongoing education to help you achieve your professional goals. Join an Award-Winning Team Join a global team spanning 60 countries, recognized for its award-winning culture that prioritizes people. We support your worklife balance with hybrid work opportunities. Through our CTI Cares [. .. ]
Job am 07.12.2025 bei Jobleads gefunden
Clinical Operations Specialist
• München, Bayern
[. .. ] Prepares and maintains site manuals, reference tools and other documents Maintains, updates, and inputs clinical tracking information into databases Tracks incoming and outgoing clinical and regulatory documents [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and updates for investigator sites, studies, project team, or client Manages shared mailbox, processes site requests and routes correspondence appropriately Coordinates the ordering, packaging, shipping and tracking of site supplies and materials Assists with coordination of team meetings, attends meetings and prepares accurate meeting minutes and action items May handle receipt, tracking and disposition of Case Report Forms and Queries [. .. ] globally and by region. Collaborates with crossfunctional teams to develop study materials, monitor trial progress, and address any issues that arise during the study. Individual contributors who provide organizational related support or service (administrative or clerical) , as well as roles operating in support of daily business activities (e. g. , technical, production, or craft levels) . The majority of time is spent in the delivery of support services or activities, typically under supervision. Roles do not typically require advanced education [. .. ]
Job am 05.12.2025 bei Jobleads gefunden
• München, Bayern
Beratungs-/ Consultingtätigkeiten
Our
client has a fantastic opportunity for a Senior Medical Science Liaison (MSL) / Regional Medical Advisor to join the Medical team. This role will focus on the Central/ [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Southern part of Germany. This role will support their portfolio of products and relay field-based clinical/ medical insights in order to support the future strategy. This position will provide operational support for activities related to Medical Information and Communication, Medical Education and Training, Investigator Initiated Trials, Key Opinion Leader outreach bringing value via scientific exchange. The position will also provide Research Clinical Development support as needed. The RMA will support the Medical Director in all aspects, i. e. representation of company in scientific presentations, conferences, and support for the Commercial Organisation while ensuring compliance [. .. ]
Job am 05.12.2025 bei Jobleads gefunden
Senior Regional Medical Advisor-Rare Disease (Central/ South)
• Düsseldorf, Nordrhein- Westfalen
Beratungs-/ Consultingtätigkeiten
Our
client has a fantastic opportunity for a Senior Medical Science Liaison (MSL) / Regional Medical Advisor to join the Medical team. This role will focus on the Central/ [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Southern part of Germany. This role will support their portfolio of products and relay field-based clinical/ medical insights in order to support the future strategy. This position will provide operational support for activities related to Medical Information and Communication, Medical Education and Training, Investigator Initiated Trials, Key Opinion Leader outreach bringing value via scientific exchange. The position will also provide Research Clinical Development support as needed. The RMA will support the Medical Director in all aspects, i. e. representation of company in scientific presentations, conferences, and support for the Commercial Organisation while ensuring compliance [. .. ]
Job am 04.12.2025 bei Jobleads gefunden
• Zürich
Medical Science Liaison (MSL) / Medical Affairs Manager Rare Diseases Endocrinology-Swiss Subsidiary position (Ref. 2569) For our
client, the Swiss subsidiary of a rapidly expanding, dynamic, highly innovative biopharmaceutical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] company, we are searching for a: Medical Science Liaison (MSL) / Medical Affairs Manager Rare Diseases Endocrinology-Swiss Subsidiary position (Ref. 2569) The MSL/ Medical Affairs Manager will serve as a critical link between the company and the medical [. .. ] functionally with internal colleagues (e. g. Market Access, Marketing, Sales, PV, Regulatory) by providing medical expertise and to ensure alignment on strategic decision Collaborate with regional Medical Affairs colleagues to support regional deliverables (e. g. , scientific support, internal/ external presentations) Monitor competitive activities and emerging trends within relevant therapeutic areas Provide medical training for commercial Support clinical trial operations to ensure success with planned and ongoing clinical trials to include identifying, supporting, and regularly engaging clinical trial investigators, and sites [. .. ] medical congresses such as participation in clinical data presentations, scientific exchange at the medical affairs booth, and internal or external meetings Engage with external researchers as a primary contact for investigator-initiated trials (IITs) Ensure successful patient access initiatives by managing medical access programs and collaborating on regulatory and market access dossier Your profile Advanced degree (MD, Pharm D, Ph D) in a relevant scientific field Experience as Medical Science Liaison (MSL) and Medical Manager in a Swiss subsidiary of a smaller pharmaceutical [. .. ]
Job am 08.11.2025 bei Jobleads gefunden
Director, Clinical Study Management
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Responsible for providing leadership and oversight to
support the global activities and timelines related to execution of full-service clinical trials, including oversight of project management and project finance teams. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] As part of the senior leadership team, participate in the development and implementation of organizational strategies, technologies and best practices that ensure superior customer service, staff development, quality [. .. ] staff allocation, training and development, employee engagement, team development and performance management (staff evaluation, performance improvement and lost time management) . Acts as senior representative of project operations team at client meetings. Represent project operations at business development meetings including but not limited to bid defenses, general capabilities, and scientific conferences. Attend and present at investigator meetings as needed. Product Service/ Excellence (10-15) Works in collaboration with leadership team to achieve excellence in project services, evaluating and implementing recommendations to minimize organizational risk, meet all regulatory and/or industry standards, while creating and promoting programs that support the Organizations growth as a world class provider [. .. ]
Job am 21.10.2025 bei Jobleads gefunden
Regional Medical Science Liaison (MSL) - Breast Cancer/ Oncology-Germany
[. .. ] for all our clients. Through strategic partnerships + deep therapeutic expertise, Amplity transforms how breakthrough treatments reach the people who need them. Regional Medical Science Liaison Oncology/ [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Breast Cancer Germany Client: Biotech, Oncology (Precision Medicine) Reports to: Field Manager at Amplity Health Primary Territory: Germany, Poland, Hungary, Check Republic, Switzerland and Austria Location: Germany RESPONSIBILITIES: Our client is a US based biopharmaceutical company fully dedicated to the research and development of medicines with the aim to improve the lives of patients. [. .. ] a member of a global field-based team of scientific experts who function as an extension of Medical Affairs. The MSL role focuses primarily 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 relationships within the respective [. .. ] 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 am 15.10.2025 bei Jobleads gefunden
Clinical Site Contracts Lead client-based in Munich
Führungs-/ Leitungspositionen
[. .. ] alignment with trial timelines. Maintain accurate records in Clinical Trial Management Systems and contract management platforms. Identify and escalate business risks appropriately while supporting internal teams with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] contract-related guidance. Support payment tracking, invoice preparation, and financial reconciliation for investigator sites as needed. Required Qualifications: Bachelors degree in life sciences, business, or a related field; equivalent experience may be considered. Minimum of 2 years experience negotiating legal and/or financial agreements, preferably in clinical research or the pharmaceutical industry. Strong understanding of ICH-GCP guidelines, clinical trial start-up processes, [. .. ]
Job am 22.08.2025 bei Jobleads gefunden
Director, Imaging Project Management
• 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 9 Tagen bei Neuvoo gefunden
TFS Health Science
Senior Clinical Research Associate
• Essen, North Rhine- Westphalia
[. .. ] this is a Freelance opportunity for approximately 0.7 FTE with sites in both Germany and Switzerland. Key Responsibilities Monitor clinical trials on-site and remotely in accordance with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] TFS/ client SOPs, FDA regulations, and GCP/ ICH guidelines Review CRFs (paper or electronic) and subject source documentation for validity and accuracy; generate queries to resolve data issues Identify site problems or deficiencies and report them to management through trip reports, memos, and communication with the Project Manager or Lead CRA Initiate [. .. ] collaboration with the CTA and as directed by the Lead CRA/ Project Manager Participate in contract handling and negotiation under direction of the Lead CRA/ Project Manager Set up the Investigator Site File (ISF) and Study Master File (SMF) , or support the CTA in doing so, and distribute materials to investigational sites Collaborate with the study team on SMF maintenance Order, ship, and reconcile clinical investigational supplies for study sites, if applicable Coordinate ordering and shipment of study supplies to sites Prepare and submit status reports as directed by the Lead [. .. ]
Job vor 9 Tagen bei Neuvoo gefunden
TFS Health Science
Senior Clinical Research Associate
• Mainz, Rhineland- Palatinate
[. .. ] this is a Freelance opportunity for approximately 0.7 FTE with sites in both Germany and Switzerland. Key Responsibilities Monitor clinical trials on-site and remotely in accordance with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] TFS/ client SOPs, FDA regulations, and GCP/ ICH guidelines Review CRFs (paper or electronic) and subject source documentation for validity and accuracy; generate queries to resolve data issues Identify site problems or deficiencies and report them to management through trip reports, memos, and communication with the Project Manager or Lead CRA Initiate [. .. ] collaboration with the CTA and as directed by the Lead CRA/ Project Manager Participate in contract handling and negotiation under direction of the Lead CRA/ Project Manager Set up the Investigator Site File (ISF) and Study Master File (SMF) , or support the CTA in doing so, and distribute materials to investigational sites Collaborate with the study team on SMF maintenance Order, ship, and reconcile clinical investigational supplies for study sites, if applicable Coordinate ordering and shipment of study supplies to sites Prepare and submit status reports as directed by the Lead [. .. ]
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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 40 offene Stellenanzeigen für Client Support Investigator Jobs.
In welchen Bundesländern werden die meisten Client Support Investigator Jobs angeboten?
Die meisten Stellenanzeigen für Client Support Investigator Jobs werden derzeit in Bayern (7 Jobs), Nordrhein-Westfalen (6 Jobs) und Hamburg (3 Jobs) angeboten.
Zu welchem Berufsfeld gehören Client Support Investigator Jobs?
Client Support Investigator Jobs gehören zum Berufsfeld Polizei, Militär, Sicherheit.
