Clinical Research Associate Jobs in Brussels, Latest Clinical Research Associate Jobs in Brussels

AL Solutions is currently seeking a highly motivated and experienced Clinical Research Associate to join their global CRO client. As a Clinical Research Associate, you will be responsible for the execution and management of clinical trials, ensuring adherence to study protocols, regulatory requirements, and timelines.Key Responsibilities:Conduct site initiation, monitoring, and close-out visitsEnsure compliance with study protocols, GCP, and applicable regulatory guidelinesPerform source data ve

Chloe O'Shea has a brand new opportunity for CRA’s in Belgium! I am looking for passionate and driven CRA’s who truly want to make a difference in the life sciences industry. My client is a global leading CRO who has demonstrated a commitment to innovation, quality, and collaboration in the clinical research industry. They really encourage career progression and prioritise work life balance.Requirements- Life science degree educated- Independent on-site monitoring experience- 2 Years minimum as

Liam Newton has partnered with a huge, globally recognised Pharmaceutical Company, who are looking to expand their team across Belgium.This is a fantastic opportunity to join a rapidly growing team where last year, they promoted around 48% of their entire CRA team. They can offer a high salary and an incredibly competitive benefits package.They promote a fantastic work-life balance with their flexible working hours schedule, remote working possibility and a low number of site visits.Requirements

Jordan Griffiths is currently representing a start-up CRO, that is looking for an experienced CRA to join their European team. This is a great opportunity, as you will be one of the first CRAs to join this client and you will shape the future for this CRO.Your Responsibilities- Manage trial execution by visiting ~6 sites regularly - Track and report data, ensuring protocol adherence - Perform SIV and initiate sites smoothly - Build partnerships with Belgium study sites RequirementsYou will o

Allucent is a full-service contract research and development organization with international resources dedicated to helping pharmaceutical and biotechnology companies efficiently and expeditiously navigate the regulatory approval process in order to bring new drugs, biologics, and medical devices to the people who need them. Allucent is a non-laboratory environment. At Allucent, our mission is to help bring new therapies to light. When you work at Allucent, that means rolling up your sleeves and

Chloe O'Shea has a great opportunity for Clinical Research Associates II in Belgium! I am looking for passionate and driven CRA’s who truly want to make a difference in the life sciences industry. My client is a small - mid sized CRO who has demonstrated a commitment to innovation, quality, and collaboration in the clinical research industry. They also really encourage career progression as well as work life balance, giving you the flexibility of being in charge of your own calendar.Requirements

AL Solutions have a unique opportunity for a CRA II to join a small fast emerging organisation with very ambitious growth plans over the coming 18-24 months.My client is still in the early stages of their global growth strategy and have an excellent reputation for providing a positive and supportive working environment along with a clear and realistic development structure. As a result, their staff turnover rate has been extremely low over the last two years.If you are looking to move away from

Chloe O'Shea is looking for a highly motivated CRA to join my clients small sized CRO. My client is looking to expand their clinical operations them. The working environment is more like a family, they are a close knit team as they are such a small CRO at the moment. You will be working closely with managers who you will be able to pick their brains and learn so much! Requirements- Strong communication skills to effectively interact with study sites, sponsors, and study team members. - Ability

- Provide functional assistance to the project team members with administrative, logistical and practical issues, including the tracking, collection, distribution and filing study documentation. - Track and supervise collection of ongoing study data for purpose of regular project status reporting as required. - Assist the Clinical Operations Manager in conducting feasibility assessment for potential studies. - Govern minimum quality standards for trial monitoring activities, with respect to

- Provide functional assistance to the project team members with administrative, logistical and practical issues, including the tracking, collection, distribution and filing study documentation. - Track and supervise collection of ongoing study data for purpose of regular project status reporting as required. - Assist the Clinical Operations Manager in conducting feasibility assessment for potential studies. - Govern minimum quality standards for trial monitoring activities, with respect to

CATO SMS and Pharm-Olam, LLC have merged to form Allucent!Allucent is a full-service contract research and development organization with international resources dedicated to helping pharmaceutical and biotechnology companies efficiently and expeditiously navigate the regulatory approval process in order to bring new drugs, biologics, and medical devices to the people who need them. Allucent is a non-laboratory environment. The Clinical Research Associate (CRA ) under our CRA Academy program per

CATO SMS and Pharm-Olam, LLC have merged to form Allucent!Allucent is a full-service contract research and development organization with international resources dedicated to helping pharmaceutical and biotechnology companies efficiently and expeditiously navigate the regulatory approval process in order to bring new drugs, biologics, and medical devices to the people who need them. Allucent is a non-laboratory environment. We are currently recruiting for a Clinical Research Associate II based i

The Senior Clinical Research Associate (CRA) is part of Clinical Operations within TFS Develop and will function operationally as a member of a Project Team and is responsible for the initiation, onsite and remote monitoring and termination of investigative sites during study conduct, according to company policies, SOPs and regulatory requirements. The CRA may conduct all stages of site monitoring (feasibility, pre-study, initiation, interim, and close-out). Key responsibilities: - Monitor on