the US and one in the Netherlands. The Planners handle medium-high complex clinical studies. This role has narrow scope in a complex logistical environment that is ideal for people without extensive working experience. Your aim is to improve the processes using LEAN and six sigma tools ...
experience - Industry certifications such as CCRA or RAC are preferred - Fluent in English - Clinical / medical devices background is a plus Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Naut van Osnabrugge ...
six years of experience - Very good understanding and experience in clinical study management, monitoring, developing study related documents, associated regulatory, processes and quality requirements - English and Dutch are a must. Are you interested and do want to apply for this
Life Sciences or related field - Awareness of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines - Knowledge of applicable protocol requirements as provided in company training - Available immediately
completeness - Making sure the Clinical Trial Supplies are distributed correctly - Tracking and management of CRFs REQUIREMENTS - Bachelor in Life Sciences or related field - Awareness of applicable clinical research regulatory requirements; i.e., Good Clinical Practice
REQUIREMENTS - Master degree in Biomedical Sciences, Statistics or Comparable - Excellent communication skills in English, Dutch would be a plus - 6+ years' of experience in Clinical Data Management - Previous work experience within a Clinical, Pharma or Biotech environment - Work
clinical research associates' productivity - Contacting client and internal project teams - Planning and executing various recruitment strategies to enhance patient enrollment - Developing and implementing risk management strategies and contingency plans for clinical deliverables
following GCP guidelines. You analyse and report these results to project management. REQUIREMENTS - BSc in a relevant field - 2 years minimum of clinical research experience - Fluent in English and German is required - Detail oriented, precise personality
database(s). Working in a cross-functional, inter-company capacity to ensure compliance is maintained with all Legal and Regulatory requirements pertaining to any and all applicable clinical studies that are sponsored by the AstraZeneca Group of companies. Along with other team members, proactively
Minimum of 8 years Clinical Trial Management - Oncology experience - Willing to travel 1/5 of the time - Start-up to database lock track record. Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Neal Hagen ...
of expertise in clinical monitoring - Knowledge of FDA guidelines, GCPs and applicable Standard Operating Procedures - Skills to mentor and train other monitors in a positive and effective manner - Demonstrated ability to evaluate medical research data and proficient knowledge of medical terminology
Clinical Trial Administrator Warszawa NR REF.: 1092475 Currently our client, a big pharmaceutical company in Warsaw, is looking for an experienced individual who could join their Clinical Trial team as Administrator. Working in Clinical Trial team your duties may include:ensuring that the
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
a Bachelor’s degree or a minimum o - Drug development experience, at least 3 years - Experience in MS Project and/or Planisware is required! - Understanding of clinical development/trial execution required. - Knowledge of project planning, tracking, resource management Are you interested
research. RESPONSIBILITIES - Build the team with a mix of internal personnel and external consultants - Develop strong relationships with the heads of other clinical related fields - Provide leadership for matters both clinical and Neurology related
accurate, complete according to regulations and guidelines. The position consists also of administrative help for panel meetings and support for study supplies. REQUIREMENTS - BSc minimum - Administrative experience for at least one year is a must - Clinical research
managing professional staff in a clinical research environment required - Thorough knowledge of ICH and local regulatory authority regulations regarding drug research and development is required - Read, write, and speak fluent English; fluent in host country language required. Are you
Clinical Data Management Specialist Poznań NR REF.: 1089881 Dla naszego Klienta – producenta sprzętu medycznego, poszukujemy osoby na stanowisko Clinical Data Management Specialist, która będzie odpowiedzialna za tworzenie, rozwój oraz utrzymanie baz danych wykorzystywanych w badaniach