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                          37 results for Clinical Associate jobs in Bierbeek within a 30 km radius

                          Clinical Research Associate (H/F/X) - CDI- 38h/semaine - Bordet

                          H.U.B.
                          Bruxelles
                          Grâce à des infrastructures de pointe et une approche centrée sur le patient, le Clinical Trials Center contribue activement à la mission de l'Institut Jules Bordet : offrir à chaque patient l'accès aux traitements les plus innovants et participer au développement de la médecine de demain.
                          Grâce à des infrastructures de pointe et une approche centrée sur le patient, le Clinical Trials Center contribue activement à la mission de l'Institut Jules Bordet : offrir à chaque patient l'accès aux traitements les plus innovants et participer au développement de la médecine de demain.
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                          JC Invest Vof * VILVOORDE * Vast contract, onbepaalde tijd * Deeltijds, Voltijds - Solliciteer als één van de eersten - Introductie - Ter uitbreiding van onze activiteiten is Medidental Hair CLINIC, gevestigd in Vilvoorde, op zoek naar een technisch medewerker gespecialiseerd in haartransplantaties om ons dynamische en gepassioneerde team te versterken. Jouw verantwoordelijkheden * Voorbereiden van de patiënt en het materiaal vóór de ingreep * Assisteren van de arts tijdens haartransplantatieprocedures (FUE, DHI, enz.) * Nauwkeurig en zorgvuldig uitvoeren van extractie en implantatie van grafts * Basis nazorg en het geven van adviezen aan patiënten * Ervaring binnen het domein van haartransplantatie is een pluspunt, maar gemotiveerde beginners zijn eveneens welkom * Opleiding in schoonheidszorg, verpleegkunde of paramedische richting is een troef
                          JC Invest Vof * VILVOORDE * Vast contract, onbepaalde tijd * Deeltijds, Voltijds - Solliciteer als één van de eersten - Introductie - Ter uitbreiding van onze activiteiten is Medidental Hair CLINIC, gevestigd in Vilvoorde, op zoek naar een technisch medewerker gespecialiseerd in haartransplantaties om ons dynamische en gepassioneerde team te versterken. Jouw verantwoordelijkheden * Voorbereiden van de patiënt en het materiaal vóór de ingreep * Assisteren van de arts tijdens haartransplantatieprocedures (FUE, DHI, enz.) * Nauwkeurig en zorgvuldig uitvoeren van extractie en implantatie van grafts * Basis nazorg en het geven van adviezen aan patiënten * Ervaring binnen het domein van haartransplantatie is een pluspunt, maar gemotiveerde beginners zijn eveneens welkom * Opleiding in schoonheidszorg, verpleegkunde of paramedische richting is een troef
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                          No match yet? There are 35 more jobs that could match your search

                          The Clinical Diabetes Sales Specialist is directly responsible for the promotion and sale of Tandem Diabetes products and clinical services within the assigned territory. He / She is expected to plan and ensure achievement of sales goals through clinical acceptance of Tandem products' insulin pump therapy. * Develop and execute effective strategies to address clinical needs, drive adoption of Tandem Diabetes products and services, and retain existing customer relationships. * Serve as a clinical and educational leader within the territory, with a strong focus on Type 1 diabetes management and insulin pump therapy. * Create value for providers by clearly differentiating Tandem's technology, services, and clinical advantages, particularly versus legacy pump systems, while effectively communicating Tandem's unique market position and competitive strengths.
                          The Clinical Diabetes Sales Specialist is directly responsible for the promotion and sale of Tandem Diabetes products and clinical services within the assigned territory. He / She is expected to plan and ensure achievement of sales goals through clinical acceptance of Tandem products' insulin pump therapy. * Develop and execute effective strategies to address clinical needs, drive adoption of Tandem Diabetes products and services, and retain existing customer relationships. * Serve as a clinical and educational leader within the territory, with a strong focus on Type 1 diabetes management and insulin pump therapy. * Create value for providers by clearly differentiating Tandem's technology, services, and clinical advantages, particularly versus legacy pump systems, while effectively communicating Tandem's unique market position and competitive strengths.
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                          BUSINESS DEVELOPMENT MANAGER, PHARMA, BIOANALYSIS DIVISION

                          SGS Group Belgium
                          Wavre
                          Easy Apply
                          Actively prospecting new customers and new business opportunities worldwide and develop new opportunities with existing clients on Preclinical (GLP) and Clinical (GCLP) Bioanalytical projects. with your extensive knowledge of current market evolutions and conditions you will be responsible for the growth of our Bioanalysis Business with both new and existing customers, with an emphasis on customer satisfaction and repeat business;
                          Actively prospecting new customers and new business opportunities worldwide and develop new opportunities with existing clients on Preclinical (GLP) and Clinical (GCLP) Bioanalytical projects. with your extensive knowledge of current market evolutions and conditions you will be responsible for the growth of our Bioanalysis Business with both new and existing customers, with an emphasis on customer satisfaction and repeat business;
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                          SGS Life Sciences is a leading contract research organization offering Clinical Research Drug Development and Quality Control/Laboratory Testing Services to the pharmaceutical and biopharmaceutical industry.
                          SGS Life Sciences is a leading contract research organization offering Clinical Research Drug Development and Quality Control/Laboratory Testing Services to the pharmaceutical and biopharmaceutical industry.
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                          Microsoft Certified: Power Platform Developer Associate (PL-400) * Microsoft Certified: Power Platform App Maker Associate (PL-100) * Microsoft 365 Certified: Developer Associate (MS-600) * Microsoft Certified: Identity and Access Administrator Associate (SC-300) (Relevant for Entra ID) * Microsoft Certified: Information Protection and Compliance Administrator Associate (SC-400) (Relevant for Purview) * Associate ()
                          Microsoft Certified: Power Platform Developer Associate (PL-400) * Microsoft Certified: Power Platform App Maker Associate (PL-100) * Microsoft 365 Certified: Developer Associate (MS-600) * Microsoft Certified: Identity and Access Administrator Associate (SC-300) (Relevant for Entra ID) * Microsoft Certified: Information Protection and Compliance Administrator Associate (SC-400) (Relevant for Purview) * Associate ()
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                          Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. We are not just about conducting clinical trials; we are about building a community where every team member has the opportunity to thrive and contribute to groundbreaking advancements in the pharmaceutical industry. PSI Medical Monitors provide medical input to global clinical studies and advise the teams and , while always focusing on patients' safety and well-. * Collaborate with internal departments in the preparation of clinical development plans, protocols, investigator brochures, annual reports, clinical study reports, manuscripts, and different scientific presentations * Review and analysis of clinical data to ensure the safety of study participants in clinical studies
                          Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. We are not just about conducting clinical trials; we are about building a community where every team member has the opportunity to thrive and contribute to groundbreaking advancements in the pharmaceutical industry. PSI Medical Monitors provide medical input to global clinical studies and advise the teams and , while always focusing on patients' safety and well-. * Collaborate with internal departments in the preparation of clinical development plans, protocols, investigator brochures, annual reports, clinical study reports, manuscripts, and different scientific presentations * Review and analysis of clinical data to ensure the safety of study participants in clinical studies
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                          PSI Medical Monitors provide medical input to global clinical studies and advise the teams and , while always focusing on patients' safety and well-being. * 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 * Collaborate with internal departments in the preparation of clinical development plans, protocols, investigator brochures, annual reports, clinical study reports, patient narratives, and scientific presentations * 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. * 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 * Collaborate with internal departments in the preparation of clinical development plans, protocols, investigator brochures, annual reports, clinical study reports, patient narratives, and scientific presentations * 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
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                          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.
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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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                          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.
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                          Take a leadership role and make valuable contributions to significant sales opportunities by creating a statement of work (SOW) that outlines the scope of the solution, estimates the associated costs and staffing efforts, and establishes the project timeline.
                          Take a leadership role and make valuable contributions to significant sales opportunities by creating a statement of work (SOW) that outlines the scope of the solution, estimates the associated costs and staffing efforts, and establishes the project timeline.
                          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
                          The above job description is not intended as, nor should it be construed as, exhaustive of all duties, responsibilities, skills, efforts, or working conditions associated with this job.
                          The above job description is not intended as, nor should it be construed as, exhaustive of all duties, responsibilities, skills, efforts, or working conditions associated with this job.
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                          What is the average salary for Clinical Associate in Bierbeek?

                          Average salary per year
                          38.500 €

                          The average salary for a Clinical Associate in Bierbeek is 38.500 €. Clinical Associate in Bierbeek salaries range from 31.000 € to 46.500 €.

                          Frequently Asked Questions

                          How many Clinical Associate jobs are there in Bierbeek?
                          There are 37 Clinical Associate jobs within 20 miles of Bierbeek available on StepStone right now.

                          What other similar jobs are there to Clinical Associate jobs in Bierbeek?
                          As well as Clinical Associate jobs in Bierbeek, you can find IT, Communication, Engineering, amongst many others.

                          Which skills are beneficial for Clinical Associate jobs in Bierbeek?
                          The following skills are useful for Clinical Associate jobs in Bierbeek: Communication, Engineering, Projects, Business, Problem Management.

                          Which industry do Clinical Associate jobs in Bierbeek belong to?
                          Clinical Associate jobs in Bierbeek are part of the Health industry.

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