Remote Site Monitor (Ref. No.: 141960)

Náplň práce, pravomoci a zodpovědnosti

Remote Site Monitor, Czech Republic - 141960

Description

PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. With offices in 46 countries and more than 16 000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a firm commitment to quality to help clients and partners bend the cost and time curve of drug development to deliver life-changing therapies that improve health.

Currently, we are looking for professionals who would like to join our Clinical Management team as:

Remote Site Monitor

Responsibilities:
•Performs remote site management activities on assigned project(s) in accordance with FDA and/or local regulations and guidelines, ICH GCPs and PPD procedural documents.
•Reviews study data from various sources remotely.
•Contacts study sites to collect study documentation, resolves issues and requests outstanding information.

HOW TO APPLY:

Please submit your CV in English.

Registration on our website will also give you the opportunity to be considered for other positions if this one is not the most appropriate for your qualifications and experience.

Suitable candidates will be contacted accordingly.

Minimální požadované vzdělání: University education (Master's degree)
Pozici vyhovuje i uchazeč se vzděláním: University education (Bachelor's degree)

Osobnostní předpoklady a dovednosti
Qualifications

Education and Experience:
•Bachelor’s Degree in a life science-related field or relevant/equivalent combination of education, training and experience that provides the individual with the required knowledge, skills, and abilities.

Knowledge, Skills and Abilities:
•Basic medical/therapeutic area knowledge and understanding of medical terminology
•Ability to attain and maintain a working knowledge of FDA and/or local regulation and guidelines, ICH GCPs and PPD procedural documents
•Ability to successfully complete PPD’s Clinical Foundation Training Program (CFP)
•Ability to evaluate medical research data
•Ability to advise, counsel, and motivate investigational sites
•Effective oral and written communication skills with the ability to communicate effectively with medical personnel
•Excellent interpersonal and customer service skills
•Good organizational and time management skills
•Proven flexibility and adaptability
•Strong attention to detail
•Ability to work in a team or independently, as required
•Good computer skills with good knowledge of MS Office (Word, Excel, PowerPoint) and the ability to learn appropriate software
•Ability to extract pertinent information from all study documents, such as protocols, electronic study data systems, CTMS and dashboards
•Excellent English language and grammar skills
•Czech language knowledge is a must

Práce v oboru: Administrativa, Zdravotnictví, farmacie, sociální péče

Lokality: Praha