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Job Summary: The Clinical Research Associate at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. For those with medical and/or health/life science interest and background who want to explore the research field and be part...

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery,...

Job Advert Posting - ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.- With our patients at the centre of all that we do, we help to...

Social network you want to login/join with:col-narrow-leftClient:ParexelLocation:Job Category:Other-EU work permit required:Yescol-narrow-rightJob Reference:0cb3218a65b7Job Views:4Posted:06.03.2025Expiry Date:20.04.2025col-wideJob Description:When our values align, there's no limit to what we can achieve.Parexel is in the business of improving the world's...

**Funtieomschrijving**: Ben je gebeten door IT en heb jij al enkele jaren ervaring bij het ontwikkelen van applicaties? Ben je een echte teamplayer die samen met de collega’s elke dag het beste van zichzelf geeft? Hou jij van differentiatie binnen een job en en ga jij proactief te werk? Lees dan zeker onze vacature tot het einde en wie weet maak jij straks...

CareForce One is a dynamic, global CRO with over 3000 dedicated colleagues worldwide. We are seeking a Clinical Trials Specialist to optimize and advance the progress of clinical trials.The ideal candidate will have a Master's degree in Life Sciences or equivalent experience. A minimum of three years of proven prior experience in on-site monitoring...

CareForce One is a global CRO with over 3000 dedicated colleagues worldwide. We are seeking a Study Feasibility Coordinator to develop strategic relationships with clinical research sites.In this role, you will maintain internal site databases, refine site identification processes, and create initial lists of potential sites. You will communicate effectively...

We are seeking a Site Development Manager to join our team at CareForce One. As a global CRO, we focus on Phase 2 and 3 clinical trials in various therapeutic areas.In this role, you will be responsible for developing strategic relationships with clinical research sites, refining internal site databases, and participating in improvement strategies for the...

We are in search of a Site Identification Specialist (feasibility). This position is open to candidates with similar experience or as CRA (min 3 years), Study Startup specialist or equivalent. Experience in oncology is required.The hiring company is a dynamic, global CRO with more than 3000 highly dedicated colleagues across the world, mainly focussing on...

Social network you want to login/join with:col-narrow-leftClient:IQVIALocation:Job Category:Other-EU work permit required:Yescol-narrow-rightJob Reference:9a5623a89260Job Views:2Posted:06.03.2025Expiry Date:20.04.2025col-wideJob Description:The RoleAs Local Trial Manager you will be responsible for running international/global studies in all therapeutic...

We are in search of a Site Identification Specialist (feasibility). This position is open to candidates with similar experience or as CRA (min 3 years), Study Startup specialist or equivalent. Experience in oncology is required. The hiring company is a dynamic, global CRO with more than 3000 highly dedicated colleagues across the world, mainly focussing on...

Job Summary: Our clinical activities are growing rapidly, and we are currently seeking a full-time Site Relationship Coordinator to join our vibrant Clinical Operations team. This is a fantastic opportunity to work on pre-award and post-award study feasibilities, build and maintain strategic relationships with our network of sites, and develop key strategies...

Job Summary: - Our clinical activities are growing rapidly, and we are currently seeking a full-time Site Relationship Coordinator to join our vibrant Clinical Operations team. This is a fantastic opportunity to work on pre-award and post-award study feasibilities, build and maintain strategic relationships with our network of sites, and develop key...

My Client who is a very successful, mid-size CRO are currently looking for a Regulatory Submission Manager to join their team in Leuven (Belgium). They are constantly growing, which allows for your personal growth as well as great opportunities to develop & grow your career. Along with that you will receive top quality training which has been voted one of...

Are you currently working in a CRO and looking to move your career forward to Regulatory Affairs ? This is a chance to do so. We are in search of a Regulatory Submissions Manager based in Leuven, Belgium to support this quality multinational CRO's daily operations. The company is focused on hiring the most talented people and are offering a lot of support in...

Social network you want to login/join with:Clinical Research Associate, Flemish BrabantClient:Location:Job Category:OtherEU work permit required:YesJob Reference:819ce21d4f5bJob Views:2Posted:06.03.2025Expiry Date:20.04.2025Job Description:Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High PerformanceAt Boston Scientific, we'll...

Company Description We are the company that cares - for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those...

Social network you want to login/join with:Client:Oxford Global ResourcesLocation:Brussels/ZaventemJob Category:OtherEU work permit required:YesJob Reference:70819c0726aaJob Views:3Posted:06.03.2025Expiry Date:20.04.2025Job Description:The Submission Specialist supports regulatory activities at study start up in assigned region (DACH). The focus is on...

At Terumo, we enhance lifesaving medical technologies for the benefit of society. Are you eager to contribute to people's health and patients' wellbeing? We'll challenge you to become a master in your field of expertise. You can invest your talents in balance with your personal aspirations - live and work in harmony. Built on our Japanese origins; we are...

Job Summary: Responsibilities: Concreet betekent dit dat we het volgende van jou verwachten: - Je verzorgt het databeheer - Je geeft organisatorische/administratieve ondersteuning in de uitvoering van onze diverse projecten - Je hebt contacten met diverse stakeholders - Verder voer je allerhande administratieve taken - Je bent detail-minded - Je bent...