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Remote Site Monitor
PPD Czech Republic, s.r.o.
Place of work
Budejovicka alej, Antala Staska 2027/79, 140 00 Praha 4, Prague
Budejovicka alej, Antala Staska 2027/79, 140 00 Praha 4, Prague
Contract type
full-time
full-time
Wage (gross)
Competitive
Competitive
Information about the position
Job description, responsibilities and duties
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.
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.
Requirements for the employee
Candidates with education suit the position
University education (Bachelor's degree)
University education (Master's degree)
University education (Master's degree)
Personality requirements and skills
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
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
Advertiser
Brief description of the company
At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.
Number of employees
1000 and more employees
ID: 3159069
Datum zveřejnění: 16.10.2017
2017-10-16
lokalita: Prague Pozice: Administrative Worker, Official, Clinical Research Associate Společnost: PPD Czech Republic, s.r.o.
Základní složka mzdy (brutto) a další odměny: Competitive