Pharmiweb ChannelsAll | PharmaCo | Clinical Research | R&D/BioTech | Sales/Mktg | Healthcare | Recruitment | Pharmacy | Medical Comms

Pharmiweb.com RSS Feed Pharmiweb.com RSS Feeds

Pharmiweb.com RSS Feed PharmiWeb Candidate Blog

Pharmiweb.com RSS Feed PharmiWeb Client Blog

Job Details

Clinical Research Associate - Sweden

Company: Chiltern
Location: Home or office based - Sweden
Reference: NC899916
Closing Date: 24 Aug 17
Type: Full Time
Salary (£): Negotiable
Benefits:

Job Summary:

• Clinical Research Associate – Sweden • Employed or freelance • Home or office based

Requirements:

Job Background

The source department of Chiltern acts in a similar way to that of a staffing solutions provider.  Our client a leading Pharmaceutical company are looking for a Clinical Research Associate to join their team in the Sweden to monitor Cardiovascular/Haematology studies. Candidates can either be employed by Chiltern to work directly for our client or work full time on a freelance basis. 

Job Summary
• Performs/participates in study site selection visits in the investigational sites
• Performs Primary CRA function for eCRF studies during the set-up phase
• Prepares/collects all study site essential documents needed prior to study initiation in collaboration with the Clinical Project Assistant (CPA) and Start-Up/Regulatory Team
• Facilitates negotiation of site Clinical Trial Agreements (CTA) prepared by the Regional/Local Clinical Project leader (RCPL) or Start-Up/Regulatory Team
• Ensures that sites apply for and receive hospital/practice/institution approval (e.g. R&D).
• Organises/participates in study initiation meetings in which are provided scientific and technical knowledge concerning the study procedures and its organisation
• Works with RCPL, Lead CRA and CPA to prepare, organise and participate in investigator meetings.
• Assists the RCPL/CPA in maintaining and ensuring the completeness of the local study files, checking the country-level (when Lead CRA for studies with regional CPL) and centre-specific files at regular intervals and reconciling with the investigator study files

Job Qualifications

Candidates must be an experienced CRA
Experience of Cardiovascular or Haematology studies is an advantage
Appropriate education (life science degree / nursing qualification)
Knowledge of and experience with GCP and other regulations in force; ability to learn and apply SOPs
Good IT skills in, e.g. MS Office, are essential, for planning, tracking, communicating and reporting


To apply for this position please email your CV to nicky.cooke@chiltern.com or for a confidential discussion please call Nicky on + 44 1753 216 729

Please note that if your experience does not mirror that of the requirements for this role you may not receive a response.

Candidates must be eligible to work in Sweden and be fluent in the Swedish language.

Keywords:  CRA, Clinical Research Associate, Clinical Trials, freelance, Sweden

 

 

Apply for this job: Clinical Research Associate - Sweden

Contact Information:

Address:  London, UK
171 Bath Road Slough Berkshire
SL1 4AA, UK
England
Tel:  +44 (0) 1753 512000
Fax:  +44 (0) 1753 511116
Website:  Visit Our Web Site

Advertising
Share | | |
Site Map | Privacy & Security | Cookies | Terms and Conditions

PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.