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                          28 results for Clinical Trial Liaison jobs in Hoeilaart within a 30 km radius

                          Clinical Trial Liaison

                          Psi Cro Belgium BV
                          Leuven
                          As a Clinical Trial Liaison, you will help clinical sites identify and recruit patients more efficiently by providing protocol‑focused support. Acting as the face of PSI on-site, you will be a key contributor to the success of our clinical trials and a trusted resource for site teams. * At least 5 years of relevant clinical practice experience, including patient‑enrolment strategies for clinical trials * Full working proficiency in English, Dutch and French * Serve as a specialized liaison to support sites with a protocol‑tailored strategy that enhances patient identification and recruitment efficiency. * Guide clinical sites in developing and implementing effective patient enrolment techniques.
                          As a Clinical Trial Liaison, you will help clinical sites identify and recruit patients more efficiently by providing protocol‑focused support. Acting as the face of PSI on-site, you will be a key contributor to the success of our clinical trials and a trusted resource for site teams. * At least 5 years of relevant clinical practice experience, including patient‑enrolment strategies for clinical trials * Full working proficiency in English, Dutch and French * Serve as a specialized liaison to support sites with a protocol‑tailored strategy that enhances patient identification and recruitment efficiency. * Guide clinical sites in developing and implementing effective patient enrolment techniques.
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                          No match yet? There are 27 more jobs that could match your search

                          Om de groeiambitie verder vorm te geven, zijn we op zoek naar een Medical Science Liaison Benelux. Als Medical Science Liaison binnen Intensive Care ben jij het medisch-wetenschappelijke gezicht van AOP Health in de Benelux.
                          Om de groeiambitie verder vorm te geven, zijn we op zoek naar een Medical Science Liaison Benelux. Als Medical Science Liaison binnen Intensive Care ben jij het medisch-wetenschappelijke gezicht van AOP Health in de Benelux.
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                          Preferable 5 years of experience working in the (bio)pharmaceutical industry preferred, with a minimum of 3 years in the research, clinical development or Pharmacovigilance domain.
                          Preferable 5 years of experience working in the (bio)pharmaceutical industry preferred, with a minimum of 3 years in the research, clinical development or Pharmacovigilance domain.
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                          Regulatory Liaison Experience: Proven ability to engage with regulatory authorities (i.e. EMA, ECHA, NCAs), draft regulatory responses, facilitate audits, and for the company in policy discussions.
                          Regulatory Liaison Experience: Proven ability to engage with regulatory authorities (i.e. EMA, ECHA, NCAs), draft regulatory responses, facilitate audits, and for the company in policy discussions.
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                          NEW
                          Ensure appropriate documentation (URS, validation packages, data flows) is in place for external systems supporting clinical studies and activities. * Work with Computer System QA team and Clinical Operations to ensure that DI controls (including ALCOA+ principles, metadata management, audit trails, system-to-system data transfer checks, and dataflow mapping) are embedded across the full data lifecycle.
                          Ensure appropriate documentation (URS, validation packages, data flows) is in place for external systems supporting clinical studies and activities. * Work with Computer System QA team and Clinical Operations to ensure that DI controls (including ALCOA+ principles, metadata management, audit trails, system-to-system data transfer checks, and dataflow mapping) are embedded across the full data lifecycle.
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                          Smals * Brussel * Vast contract, onbepaalde tijd * Thuiswerken mogelijk, Voltijds - Solliciteer als één van de eersten - Smals realiseert innovatieve ICT-projecten in e-government en e-health voor instellingen uit de sociale zekerheid en de gezondheidszorg. 'ICT for society' is voor Smals meer dan een slogan: alle projecten hebben een positieve maatschappelijke impact. Zo bouwt Smals mee aan het portaal van de sociale zekerheid en het eHealth-platform. Jouw verantwoordelijkheden - Als Infrastructure Scrum Master maak je deel uit van de afdeling IT infrastructuur en zal je één of meerdere agile teams ondersteunen. Je rapporteert aan de . In deze functie faciliteer en stimuleer je de samenwerking binnen de teams en zorg je ervoor dat Scrum-evenementen (sprint planning, reviews, retrospectives, …) correct verlopen en afgestemd zijn op de infrastructuuromgeving (incidenten, changes, ...
                          Smals * Brussel * Vast contract, onbepaalde tijd * Thuiswerken mogelijk, Voltijds - Solliciteer als één van de eersten - Smals realiseert innovatieve ICT-projecten in e-government en e-health voor instellingen uit de sociale zekerheid en de gezondheidszorg. 'ICT for society' is voor Smals meer dan een slogan: alle projecten hebben een positieve maatschappelijke impact. Zo bouwt Smals mee aan het portaal van de sociale zekerheid en het eHealth-platform. Jouw verantwoordelijkheden - Als Infrastructure Scrum Master maak je deel uit van de afdeling IT infrastructuur en zal je één of meerdere agile teams ondersteunen. Je rapporteert aan de . In deze functie faciliteer en stimuleer je de samenwerking binnen de teams en zorg je ervoor dat Scrum-evenementen (sprint planning, reviews, retrospectives, …) correct verlopen en afgestemd zijn op de infrastructuuromgeving (incidenten, changes, ...
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                          However, a significant part of your time will be spent collaborating with technical and commercial colleagues located at the Baytown Technology and Engineering Complex (BTEC), in Baytown, TX, as well as occasionally traveling internationally to support customer trials.
                          However, a significant part of your time will be spent collaborating with technical and commercial colleagues located at the Baytown Technology and Engineering Complex (BTEC), in Baytown, TX, as well as occasionally traveling internationally to support customer trials.
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                          Legal Recruiter/HR Specialist for a leading firm!

                          EXCEL CAREERS
                          Bruxelles
                          Partially remote
                          Easy Apply
                          Act as a key liaison for candidates and internal stakeholders, ensuring a seamless recruitment experience.
                          Act as a key liaison for candidates and internal stakeholders, ensuring a seamless recruitment experience.
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                          Serve as medical point of contact for internal project team, study sites and study sponsor for medical matters related to the conduct of clinical trials per protocol and per GCP guidelines * Review and analysis of clinical data to ensure the safety of study participants in clinical trials * Ensure that the reported trial data is accurate, complete, and verifiable, and that the conduct of the trial is in compliance with the currently approved protocol/amendments - PSI Medical Monitors provide medical input to global clinical studies and advise the teams and , while always focusing on patients' safety and well-being. * Collaborate with internal departments in the preparation of clinical development plans, protocols, investigator brochures, annual reports, clinical study reports, patient narratives, and scientific presentations * Address safety issues across the trial from sites and the study team
                          Serve as medical point of contact for internal project team, study sites and study sponsor for medical matters related to the conduct of clinical trials per protocol and per GCP guidelines * Review and analysis of clinical data to ensure the safety of study participants in clinical trials * Ensure that the reported trial data is accurate, complete, and verifiable, and that the conduct of the trial is in compliance with the currently approved protocol/amendments - PSI Medical Monitors provide medical input to global clinical studies and advise the teams and , while always focusing on patients' safety and well-being. * Collaborate with internal departments in the preparation of clinical development plans, protocols, investigator brochures, annual reports, clinical study reports, patient narratives, and scientific presentations * Address safety issues across the trial from sites and the study team
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                          Liaison avec les fournisseurs : Aider à la communication avec les vendeurs et les fournisseurs, y compris l'échange de documents, le traitement des demandes et les négociations préliminaires.
                          Liaison avec les fournisseurs : Aider à la communication avec les vendeurs et les fournisseurs, y compris l'échange de documents, le traitement des demandes et les négociations préliminaires.
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                          Ensure compliance with regulatory and quality standards relevant to multiple geographies, products and industries including biopharmaceuticals, clinical diagnostics, and direct to consumer sales.
                          Ensure compliance with regulatory and quality standards relevant to multiple geographies, products and industries including biopharmaceuticals, clinical diagnostics, and direct to consumer sales.
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                          NEW
                          It is also one of the market leaders in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in biopharma contract development and manufacturing. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
                          It is also one of the market leaders in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in biopharma contract development and manufacturing. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
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                          NEW
                          It is also one of the market leaders in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in biopharma contract development and manufacturing. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
                          It is also one of the market leaders in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in biopharma contract development and manufacturing. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
                          more
                          It is also one of the market leaders in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in biopharma contract development and manufacturing. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
                          It is also one of the market leaders in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in biopharma contract development and manufacturing. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
                          more
                          NEW
                          It is also one of the market leaders in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in biopharma contract development and manufacturing. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
                          It is also one of the market leaders in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in biopharma contract development and manufacturing. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
                          more
                          Ensure compliance with regulatory and quality standards relevant to multiple geographies, products and industries including biopharmaceuticals, clinical diagnostics, and direct to consumer sales.
                          Ensure compliance with regulatory and quality standards relevant to multiple geographies, products and industries including biopharmaceuticals, clinical diagnostics, and direct to consumer sales.
                          more
                          Easy Apply
                          It is also one of the market leaders in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in biopharma contract development and manufacturing. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
                          It is also one of the market leaders in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in biopharma contract development and manufacturing. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
                          more
                          It is also one of the market leaders in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in biopharma contract development and manufacturing. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
                          It is also one of the market leaders in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in biopharma contract development and manufacturing. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
                          more
                          It is also one of the market leaders in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in biopharma contract development and manufacturing. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
                          It is also one of the market leaders in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in biopharma contract development and manufacturing. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
                          more
                          It is also one of the market leaders in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in biopharma contract development and manufacturing. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
                          It is also one of the market leaders in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in biopharma contract development and manufacturing. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
                          more

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                          What is the average salary for Clinical Trial Liaison in Hoeilaart?

                          Average salary per year
                          40.500 €

                          The average salary for a Clinical Trial Liaison in Hoeilaart is 40.500 €. Clinical Trial Liaison in Hoeilaart salaries range from 33.900 € to 49.900 €.

                          Frequently Asked Questions

                          How many Clinical Trial Liaison jobs are there in Hoeilaart?
                          There are 28 Clinical Trial Liaison jobs within 20 miles of Hoeilaart available on StepStone right now.

                          What other similar jobs are there to Clinical Trial Liaison jobs in Hoeilaart?
                          As well as Clinical Trial Liaison jobs in Hoeilaart, you can find Management, Communication, Business, amongst many others.

                          Which skills are beneficial for Clinical Trial Liaison jobs in Hoeilaart?
                          The following skills are useful for Clinical Trial Liaison jobs in Hoeilaart: Communication, Business, Engineering, Networks, Finance.

                          Which industry do Clinical Trial Liaison jobs in Hoeilaart belong to?
                          Clinical Trial Liaison jobs in Hoeilaart are part of the Science industry.

                          How many temporary and part-time Clinical Trial Liaison jobs are available in Hoeilaart?
                          There are 0 temporary Clinical Trial Liaison jobs and 1 part-time Clinical Trial Liaison jobs available in Hoeilaart at the moment.