Wij zijn gespecialiseerd in functies binnen de farmaceutische industrie. Wij bemiddelen starters en ervaren kandidaten met een life science achtergrond.
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Clinical Research Associate I/II


Deze vacature staat offline!
De opdrachtgever
Clinical Research Organisation
De omschrijving
Completes project activities associated with monitoring functions of Phase I-IV clinical research studies while developing an understanding of the drug development process, Good Clinical Practices, and relevant regulations. Performs management of study site activities to ensure the integrity of clinical data, in adherence to all applicable regulatory guidelines and Standard Operating Procedures (SOPs) and Project Specific Operating Procedures (PSOPs).
De eisen
AA, RN, BS/BA or equivalent or experience as follows: The candidate/incumbent should have six months to one year of clinical research monitoring experience; or at least one year experience performing relevant project support in-house functions; or 1-2 years of experience in a related health care or clinical research work experience (e.g. study coordinator). Previous practical experience in conducting clinical pharmaceutical research studies in a hospital setting, pharmaceutical company, or CRO preferred but not required. Experience or education indicates a sound basic knowledge of medical and pharmaceutical terminology. Position requires: Excellent verbal and written communication skills along with excellent organizational, record retention, time management, decision making, customer service, and interpersonal skills. Good command of written and spoken English language. Ability to travel domestically and internationally as required and process visit reports and expense reports effectively. If applicable ability to obtain credit cards for the purpose of paying expenses while traveling. Ability to work independently. Proficient in the use of laptop computer and software systems. Ability to understand basic and complex medical details. Understanding of basic data processing functions preferred. Knowledge of GCP and all applicable regulatory requirements preferred.
Contactinformatie
Voor meer informatie over deze functie kunt u zich wenden tot:

Dr. Arjan van den Wijngaard
FarmaSel Scientific
Consultant R&D
Hullenbergweg 353-367
1101 CP Amsterdam Z-O
tel 020 311 8770
mobiel 06 51784142
Geinteresseerden kunnen hun c.v. rechtstreeks mailen naar info@pharmamediair.nl
NL EN DE pharmamediar.nl