Services is a group within EDS focusing on early-phase clinical trials in patient populations. With management offices in Germany, and clinical operations in several cities across Central Europe, we now have an opening for a RESEARCH PHYSICIAN (Early Phase Clinical Research) for our Warsaw office in
REQUIREMENTS - At least 2 years of experience in (international) clinical study management (i.e. lead CRA, senior CRA, Clinical Study Manager). - Experience with Ethical Committee submission - Knowledge of ICH-GCP guidelines - Experience with site preparation, management and monitoring ...
THE COMPANY Our client is a professional Clinical Research organization, based in Noord-Brabant Netherlands. The company is a CRO that delivers services in the Medical Devices, Pharmaceutical and Biotechnology industries. They specialize in early phase
into the next phase of their research. ROLE DESCRIPTION You are in charge of all clinical trials in terms of managing and overseeing all projects of the clinical department. This position will be needed for at least a half year as the current
into the next phase of their research. ROLE DESCRIPTION You are in charge of all clinical trials in terms of managing and overseeing all projects of the clinical department. This position will be needed for at least a half year as the
- Bachelor, but preferably a Masters in Life Sciences related field - 3-5 years of experience as a project manager in clinical trials - ICH-GCP - ISO 14155 - Excellent English and Dutch knowledge Are you interested and do want to apply for this role, please fill out your
position is office based but the client is flexible with working from home. REQUIREMENTS - MSc degree in (bio) medical sciences - At least 6 years of relevant experience in clinical trials - Biotech/Pharma experience is a plus - Oncology experience is required ...
- Überprüfung der Qualitätsstandards REQUIREMENTS - abgeschlossenes Hochschulstudium der Naturwissenschaften oder verwandter Fachbereiche - min 3+ Jahre Berufserfahrung in einer ähnlichen Qualitätsfunktion - Umfassende Kenntnisse der Good Clinical Practice und
SIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced ...
THE COMPANY Our client is a professional Biotechnology, Clinical Research and Pharmaceutical organization, based in Netherlands. They are a global research organization which strives for quality and has offices in almost 50 countries. They provide
team analysis. The position is needed for 6 months at 32 hours per week (0,8 FTE). RESPONSIBILITIES You assist the Clinical Program Manager where you provide critical path analysis, cross functional project plans and provide strategies and schedules to keep all
design, execute and coordinate clinical trials. You will be supervised by a project manager. RESPONSIBILITIES - Monitor on-site and remotely clinical trials - Make sure the clinical trials are compliant with ICH-GCP - Execute clinical trials according to SOPs
You will coordinate the operational part of the clinical studies RESPONSIBILITIES - Generates program reports and communications to ensure team and program alignment of deliverable expectations. - Provide regular reports and analysis on resource demand and