clinical study

Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical...

Lead full scope of Biostatistics conduct for the responsible program within a therapeutic area. Define statistical strategy and ensure appropriate statistical methodologies applied to study design and data analysis for clinical trials and regulatory submissions. Influence and contribute to clinical development plans, collaborate with cross-functional team...

Arcadis is seeking a motivated Clinical Research Associate (CRA) to oversee clinical study sites within a MedTech environment. You will monitor trial activities, ensure GCP compliance, and partner with investigators and operational teams to drive quality data and study delivery.Requirements include a Life Sciences degree (Bachelor/Master), 1–2 years of...

A global Clinical Research Organization is seeking a Start up Specialist to work remotely in Belgium. The ideal candidate should have a bachelor's degree in life-science and at least 1.5 years of experience in Ethics Committee and Competent Authority submissions within a CRO, Pharma, or Biotech. Responsibilities include managing submissions, keeping abreast...

Reading, Berkshire, United Kingdom Belgrade, Serbia Paris, France Warsaw, Poland Amsterdam, Netherlands Madrid, Spain Budapest, Hungary Dublin, Ireland Frankfurt, Hesse, Germany Ljubljana – Dunajska, Slovenia Bucuresti, Romania Brussels, Brussels-Capital Region, Belgium Gothenburg, Sweden Copenhagen, Denmark Bratislava, Slovakia Full time R1503450 Lead...

As Local Trial Manager (LTM) you will be responsible for running international/global studies in all therapeutic areas, managing the operational aspects of projects to meet contractual requirements. You will act as primary point of contact in Belgium to lead, manage and co-ordinate the conduct of clinical trials from study start-up (COLA) to close out at a...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as an Associate Medical Director – Make an Impact at the Forefront of InnovationAt Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to...

About the RoleAre you passionate about healthcare innovation and curious about how new ideas become real-world improvements for patients and healthcare professionals?The Clinical Study Unit (CSU) Belgium, part of Sanofi's North Europe MCO, is looking for a Local Innovation Trainee to join the team for a 6-month internship starting in September 2026.This is...

Arcadis is seeking an experienced Senior Clinical Research Associate to support and monitor clinical studies within a MedTech environment. You will manage multiple study sites, ensure protocol and GCP compliance, and drive data quality and study performance.Applicants should have 4+ years of site monitoring experience, strong communication skills, and...

Reading, Berkshire, United KingdomBelgrade, SerbiaParis, FranceWarsaw, PolandAmsterdam, NetherlandsMadrid, SpainBudapest, HungaryDublin, IrelandFrankfurt, Hesse, GermanyLjubljana – Dunajska, SloveniaBucuresti, RomaniaBrussels, Brussels-Capital Region, BelgiumGothenburg, SwedenCopenhagen, DenmarkBratislava, SlovakiaFull timeR1503450Lead full scope of...

ResponsibilitiesAny additional information you require for this job can be found in the below text Make sure to read thoroughly, then apply.(a) Site management• Study site selection, initiation (SIV) and clinical monitoring.• Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not...

ResponsibilitiesMake sure to apply with all the requested information, as laid out in the job overview below.(a) Site managementStudy site selection, initiation (SIV) and clinical monitoring.Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and...

Responsibilities(a) Site managementStudy site selection, initiation (SIV) and clinical monitoring.Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience.Prepare and conduct SIV to ensure adequate study training for relevant site staff to...

Responsibilities(a) Site managementStudy site selection, initiation (SIV) and clinical monitoring.Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience.Prepare and conduct SIV to ensure adequate study training for relevant site staff to...

Responsibilities(a) Site managementStudy site selection, initiation (SIV) and clinical monitoring.Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience.Prepare and conduct SIV to ensure adequate study training for relevant site staff to...

Responsibilities(a) Site managementStudy site selection, initiation (SIV) and clinical monitoring.Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience.Prepare and conduct SIV to ensure adequate study training for relevant site staff to...

Responsibilities(a) Site managementStudy site selection, initiation (SIV) and clinical monitoring.Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience.Prepare and conduct SIV to ensure adequate study training for relevant site staff to...

Responsibilities(a) Site managementStudy site selection, initiation (SIV) and clinical monitoring.Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience.Prepare and conduct SIV to ensure adequate study training for relevant site staff to...

Responsibilities(a) Site managementStudy site selection, initiation (SIV) and clinical monitoring.Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience.Prepare and conduct SIV to ensure adequate study training for relevant site staff to...

Responsibilities(a) Site managementStudy site selection, initiation (SIV) and clinical monitoring.Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience.Prepare and conduct SIV to ensure adequate study training for relevant site staff to...