38 Jobs für Client Support Investigator
Stellenangebote Client Support Investigator Jobs
Job vor 3 Tagen bei Jooble 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 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 17.01.2026 bei Jooble gefunden
Alira Health
Project Manager Senior
• München
[. .. ] an important member of the Alira Health Clinical team. Manages clinical study functions, which may include investigational supply, IWRS/ IXRS, data management, biostatistics, pharmacovigilance, and central laboratory. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Supervises and provides support to the Clinical team, including Clinical Assistants, In-house Clinical Research Associates, and Clinical Research Associates. Creates and reviews clinical study documents, including protocols, ICF templates, study budgets, site log/ form templates, study manuals and plans, site binders, etc. Presents at project meetings such as investigator meetings and new client meetings. Updates management accurately and regularly through frequent communication. Manages subject accrual, retention, and compliance. Assists in TMF management and manages TMF reviews as needed. Complies with and ensures team compliance with ICH GCP guidelines, FDA regulations, and company SOPs. 3 years of experience in the pharmaceutical/ biotechnology/ CRO industry [. .. ]
Job am 17.01.2026 bei Jooble gefunden
Alira Health
• München
[. .. ] an important member of the Alira Health Clinical team. Manages clinical study functions, which may include investigational supply, IWRS/ IXRS, data management, biostatistics, pharmacovigilance, and central laboratory. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Supervises and provides support to the Clinical team, including Clinical Assistants, In-house Clinical Research Associates, and Clinical Research Associates. Creates and reviews clinical study documents, including protocols, ICF templates, study budgets, site log/ form templates, study manuals and plans, site binders, etc. Presents at project meetings such as investigator meetings and new client meetings. Updates management accurately and regularly through frequent communication. Manages subject accrual, retention, and compliance. Assists in TMF management and manages TMF reviews as needed. Complies with and ensures team compliance with ICH GCP guidelines, FDA regulations, and company SOPs. 3 years of experience in the pharmaceutical/ biotechnology/ CRO industry [. .. ]
Job am 17.01.2026 bei Jooble gefunden
Alira Health
Senior Project Management Officer
• München
[. .. ] an important member of the Alira Health Clinical team. Manages clinical study functions, which may include investigational supply, IWRS/ IXRS, data management, biostatistics, pharmacovigilance, and central laboratory. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Supervises and provides support to the Clinical team, including Clinical Assistants, In-house Clinical Research Associates, and Clinical Research Associates. Creates and reviews clinical study documents, including protocols, ICF templates, study budgets, site log/ form templates, study manuals and plans, site binders, etc. Presents at project meetings such as investigator meetings and new client meetings. Updates management accurately and regularly through frequent communication. Manages subject accrual, retention, and compliance. Assists in TMF management and manages TMF reviews as needed. Complies with and ensures team compliance with ICH GCP guidelines, FDA regulations, and company SOPs. 3 years of experience in the pharmaceutical/ biotechnology/ CRO industry [. .. ]
Job am 17.01.2026 bei Jooble gefunden
Alira Health
• München
[. .. ] study functions, which may include investigational supply, IWRS/ IXRS, data management, biostatistics, pharmacovigilance, and central laboratory. Generates and presents frequent study status updates and reports to sponsor. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Supervises and provides support to the Clinical team, including Clinical Assistants, In-house Clinical Research Associates, and Clinical Research Associates. Supervises and trains Associate PMs. Creates and reviews clinical study documents, including protocols, ICF templates, study budgets, site log/ form templates, study manuals and plans, site binders, etc. Drives and facilitates clinical teamwork and communications to ensure timely attainment of trial milestones. Ensures accuracy of reports and material work product. Provides monthly billing information to finance team. Presents at project meetings such as investigator meetings and new client meetings. Updates management accurately and regularly through frequent communication. Identifies issues and develops problem-solving strategies to ensure study timelines are met. Manages subject accrual, retention, and compliance. Assists in TMF management and manages TMF reviews as needed. Prepares for and participates in third-party audits and FDA inspections. Complies [. .. ]
Job am 17.01.2026 bei Jooble gefunden
Alira Health
Senior Project Director
• München
Führungs-/ Leitungspositionen
[. .. ] an important member of the Alira Health Clinical team. Manages clinical study functions, which may include investigational supply, IWRS/ IXRS, data management, biostatistics, pharmacovigilance, and central laboratory. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Supervises and provides support to the Clinical team, including Clinical Assistants, In-house Clinical Research Associates, and Clinical Research Associates. Creates and reviews clinical study documents, including protocols, ICF templates, study budgets, site log/ form templates, study manuals and plans, site binders, etc. Presents at project meetings such as investigator meetings and new client meetings. Updates management accurately and regularly through frequent communication. Manages subject accrual, retention, and compliance. Assists in TMF management and manages TMF reviews as needed. Complies with and ensures team compliance with ICH GCP guidelines, FDA regulations, and company SOPs. 3 years of experience in the pharmaceutical/ biotechnology/ CRO industry [. .. ]
Job am 17.01.2026 bei Jooble gefunden
Alira Health
• München
[. .. ] an important member of the Alira Health Clinical team. Manages clinical study functions, which may include investigational supply, IWRS/ IXRS, data management, biostatistics, pharmacovigilance, and central laboratory. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Supervises and provides support to the Clinical team, including Clinical Assistants, In-house Clinical Research Associates, and Clinical Research Associates. Creates and reviews clinical study documents, including protocols, ICF templates, study budgets, site log/ form templates, study manuals and plans, site binders, etc. Presents at project meetings such as investigator meetings and new client meetings. Updates management accurately and regularly through frequent communication. Manages subject accrual, retention, and compliance. Assists in TMF management and manages TMF reviews as needed. Complies with and ensures team compliance with ICH GCP guidelines, FDA regulations, and company SOPs. 3 years of experience in the pharmaceutical/ biotechnology/ CRO industry [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Thermo Fisher Scientific
Local Clinical Trial Manager-FSP, Germany-6 month FTC (m/f/d)
• Homeoffice
[. .. ] will improve health outcomes that people and communities depend on now and in the future. 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 execute high-quality, cost-efficient clinical studies. The PPD FSP Solution: PPD s Functional Service Provider division partner with [. .. ] to help customers manage capacity and set programs up for success. Joining within our PPD FSP functional area, allows you to join the renowned PPD CRO and still gain invaluable client dedicated experience. Discover Impactful Work: Accountable for achieving the final clinical deliverable (usually clean data from evaluated patients as specified in the study protocol) within the time period specified in the contract with the customer. Interprets data on project issues and makes good business decisions with support from experienced team [. .. ] required, advises support/ develops and negotiates on contract development with Sites/ CRO/ Vendors ensuring legal input where required and may participate in budget/ contract negotiations with study vendors or clinical investigator sites. As required, selects manages local vendors in accordance with local practices in alignment with overall resourcing strategy for the study; accountable for local vendor management including oversight, agreements, payments, communications issue management. Manages the development of key study documents, plans manuals according to local requirements (monitoring plan, local informed [. .. ]
Job am 14.01.2026 bei Jooble gefunden
ICON
• Homeoffice
Work-Life-Balance
[. .. ] largest most comprehensive clinical research organisation, powered by healthcare intelligence. The Site Engagement Liaison Manager is a field based expert who supports the conduct and the patient [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] recruitment of the client global clinical trials at investigative sites, through local and relational support. What you will be doing: Participate in study-level feasibility activities through providing key country/ regional and site specific knowledge including patient pathways and operational execution. Interface and act as a local client Trial Ops representative, an expert on the clinical trial protocol (s) and SME providing the sites with [. .. ] signature as needed. Proactively work to fully understand all matters that impact the successful patient recruitment and high quality conduct of the clinical trial at each site, eg the Principle Investigator (PI) and site preferences and best practices on clinical trials, standard of care treatments, competing studies etc. Ensure a supportive relationship with clinical sites and trial personnel. Proactively work to fully understand the patient voice, preferences and pathway (s) . Closely work with the client GPA team. Speak to patient [. .. ]
Job vor 3 Tagen bei Jooble gefunden
Medical Science Liaison Rare Disease-Ostdeutschland
• Schwerin
[. .. ] 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 23.01.2026 bei Jooble gefunden
Foundever
• Ausland
[. .. ] fluent with strong English communication skills? Looking to make your career in a multicultural environment in sunny and happy Lisbon ? So we have the perfect opportunity [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] for you Our client is a global leader in insurance broking and risk management, bringing global, national, and industry-specific solutions. As a customer service specialist in this project, your daily responsibilities will include: Provide first contact resolutions to customer queries Offer specialized customer support through written and phone communication Build meaningful relationship, answering customers questions in a courteous, friendly, and professional manner Meet and exceed our customer service quality goals, compliance regulations and productivity targets Create amazing customer experience that people value and we are proud of Be responsible to follow the direction of [. .. ] skills with excellent phone conversation skills, attentive listening and superior writing skills Analytical and problem solving skills with strong attention to detail Desire to learn and advance, be a curious investigator and problem solver Must hold EU citizenship or valid work permit for Portugal Be a local candidate or willing to relocate to Lisbon, Portugal (Work on site) Benefits. Relocation package Competitive wages Paid professional training Employee discounts Private healthcare dental insurance (after six months of employment) Growth opportunities through various [. .. ]
Job am 17.01.2026 bei Jooble gefunden
NUVISAN GmbH
Lab Head (m/f/d) in vitro DMPK
• Berlin
Jobticket
[. .. ] technicians, ensure high assay performance, introduce innovative methodologies, and serve as the DMPK representative in cross-functional drug discovery and development teams, The role combines operational lab leadership, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] scientific excellence, client interaction, and regulatory-quality documentation. Responsibilities Lead and develop a high-performing in vitro DMPK team (2-4 technicians) ; plan, coordinate and optimize day-to-day lab operations and resource allocation Design, execute, troubleshoot, and report routine and advanced in vitro ADME/ DMPK studies, including: Transporter assays (uptake/ efflux, [. .. ] with in vivo PK data to inform project decisions; act as DMPK representative in cross-functional teams Author, edit, and contribute to study reports and regulatory documents (e. g. , Investigator s Brochure, IMPD, IND, CTD) ; maintain compliant quality documentation (SOPs, audit-ready records) Support client interactions: prepare and deliver presentations, host customer visits, and contribute to audits Contribute to budget planning at group project level, monitor spend against plan Ensure compliance with applicable regulations and guidelines (Gx P principles, health and safety, environmental protection, radiation protection as applicable) and with EMA, FDA, and ICH guidance [. .. ]
Neu Job vor 6 Std. bei Mindmatch.ai gefunden
Syneos Health Commercial Solutions
Medical Science Liaison Rare Disease-Ostdeutschland
• AT- 2 Lavamünd
[. .. ] 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 am 20.01.2026 bei Jobleads gefunden
Medical Science Liaison Oncology
• München, Bayern
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 Munich) 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 Key [. .. ]
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 [. .. ]
Neu Job vor 6 Std. bei Jobleads gefunden
Medical Science Liaison Rare Disease-Ostdeutschland
• 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 [. .. ]
Neu Job vor 6 Std. bei Jobleads gefunden
Medical Science Liaison Rare Disease-Ostdeutschland
• Dresden, 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 [. .. ]
Neu Job vor 6 Std. bei Jobleads gefunden
Medical Science Liaison Rare Disease-Ostdeutschland
• Lavamünd, Kärnten Lavamuend
[. .. ] 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 [. .. ]
Neu Job vor 6 Std. bei Jobleads gefunden
Medical Science Liaison Rare Disease-Ostdeutschland
• 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 [. .. ]
Neu Job vor 6 Std. bei Jobleads gefunden
Medical Science Liaison Rare Disease-Ostdeutschland
• Dresden, 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 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 [. .. ]
Neu Job vor 6 Std. bei Jobleads gefunden
Medical Science Liaison Rare Disease-Ostdeutschland
• 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 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 [. .. ]
Neu Job vor 6 Std. bei Jobleads gefunden
Medical Science Liaison Rare Disease-Ostdeutschland
• Brandenburg
[. .. ] 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 [. .. ]
Neu Job vor 6 Std. bei Jobleads gefunden
Medical Science Liaison Rare Disease-Ostdeutschland
• Brandenburg
[. .. ] 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 [. .. ]
Neu Job vor 6 Std. bei Jobleads gefunden
Medical Science Liaison Rare Disease-Ostdeutschland
• 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 [. .. ]
Neu Job vor 6 Std. bei Jobleads gefunden
Medical Science Liaison Rare Disease-Ostdeutschland
• Schwerin, Mecklenburg- Vorpommern Schwerin;Kreisfreie Stadt Schwerin
[. .. ] 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 [. .. ]
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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 38 offene Stellenanzeigen für Client Support Investigator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Client Support Investigator Jobs?
Aktuell suchen 10 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:
- Alira Health (6 Jobs)
- Thermo Fisher Scientific (4 Jobs)
- ICON (1 Job)
- Foundever (1 Job)
- NUVISAN GmbH (1 Job)
- Syneos Health Commercial Solutions (1 Job)
In welchen Bundesländern werden die meisten Client Support Investigator Jobs angeboten?
Die meisten Stellenanzeigen für Client Support Investigator Jobs werden derzeit in Sachsen (4 Jobs), Berlin (3 Jobs) und Bayern (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Client Support Investigator Jobs?
Client Support Investigator Jobs gehören zum Berufsfeld Polizei, Militär, Sicherheit.
