SrCRA / CRA2 - home based
Chiltern International AB / Apotekarjobb / Ospecificerad arbetsort
2015-12-17
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hela Sverige Visa alla jobb hos Chiltern International AB i Ospecificerad arbetsort Chiltern is the leading, global mid-sized contract research organization that can deliver customized clinical development solutions. We are looking to expand our Biopharma function across the business. We are now looking for talented clinical development candidates that want to be part of our accelerated growth plans across the globe.
Chiltern is looking to recruit a home based experienced monitor based in Sweden to work in the role of Senior Clinical Research Associate (SrCRA) or CRA2 depending on the qualifications of the selected candidate. These roles offer excellent exposure to all therapeutic indications/Oncology indications types and defined career development.
The SrCRA/CRA2 will provide expert advice, guidance and general supervision to Clinical Monitoring team activities for designated projects, and to monitor specified sites to ensure quality and integrity of data, ensuring study completion on time and within budget. They may be called upon to interact independently with clients not directly involved in their projects, and to assist in some relevant departmental tasks. We encourage the development of SrCRAs into the lead function giving co lead responsibilities where possible and excellent exposure. We also welcome applicants that want to be career monitors.
Job Primary Functions:
The successful applicant will be responsible for coordinating Phase I-IV clinical trials in the Nordics.
Perform all types of site visits including, but not limited to, qualification visits, initiation visits, monitoring visits, motivational visits, audit support visits, and termination visits.
To identify potential sites for a proposed study in conjunction with the Project Team, and conduct feasibility assessment of sites as required
Ensure that all study related communication including e-mail is tracked, printed and filed as required
To track patient recruitment by contacting investigators as specified for the study, and discuss potential study risks and opportunities with the Project Manager and LCRA
To liaise with all other appropriate departments within Chiltern International to ensure the smooth running of the study
To assemble files and ensure documents for the trial master file accurately reflect the progress of the study
SrCRA will also assist with document submissions to local authorities
SrCRA may mentor and train other CRAs
Job Qualifications:
A BSc or BA degree in a biomedical or related life science, or nursing qualification. Previous CRA experience within clinical research of at least 18 months. Good clinical knowledge with an understanding of medical terminology. Understanding of the principles of ICH GCP and regulatory requirements. Experience using a clinical trial management system. Good oral and written communication, organizational skills and personal presentation
Additional Information:
This is a permanent, full time and home based role based in Sweden. Work will require national or international travel and some overnight stays may be required.
To apply please send your application to: Simone Schaefer;
simone.schaefer@chiltern.comPubliceringsdatum2015-12-17KörkortskravB
Varaktighet, arbetstid
Tillsvidare
Heltid
ErsättningFast månads- vecko- eller timlön
Så ansöker duSista dag att ansöka är 2016-01-16
Ansökan kan skickas till e-postadress:
simone.schaefer@chiltern.comFöretagChiltern International AB
AdressChiltern International AB
Box 2024
40311 Göteborg
KontorsadressStora Badhusgatan 18-20
Göteborg
Övriga kontaktuppgifterTelefonnummer: 031-132790
Jobbnummer 2582000
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