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Job Details

CRA

Company: SRG Clinical
Location: Edinburgh
Reference: J26961
Closing Date: 27 Jun 18
Type: Permanent
Salary (£): Negotiable
Benefits: Negoitable

Job Summary:

Scottish based CRA either near Glasgow or Edingburgh Permanat role with exciting new med device companyThis role can be home/fieldbased

Requirements:

Scottish based CRA either near Glasgow or Edingburgh Permanat role with exciting new med device company Role Description Working as part of the Product Assurance team you will be responsible for conducting all Regulatory Clinical Studies for In Vitro Diagnostic products on the our clients. Studies will range from single site to international multi-centre so some travel will be required. The role will plan, implement, monitor and review studies in line with our Business plan whilst meeting all ethical, regulatory and scientific needs.Key ResponsibilitiesTechnicalWork with project teams to agree the study design.Identify appropriate clinical sites and manage effective clinical relationships.Prepare and submit clinical documentation according to study needs Work with Clinical Teams to ensure studies are implemented, monitored and reported according to all business processes.Maintain the highest ethical, clinical and scientific standards ensuring both the safety and well-being of study participants.Excellent communication skills, especially written and verbal to ensure all stakeholders are kept current and effective relationships (both internally and externally) are built.Training of clinical users on the our clients and products.Prepare, monitor and report clinical study budgets.ComplianceComply with appropriate ICH GCP standards and relevant sections of the IVD Directive and US Code of Federal regulations, Title 21 (21 CFR).Update Business Processes and Clinical Procedures to meet regulatory and business needs.Essential SkillsAn HND in Life Sciences, Health Sciences or related field, or professional qualification such as nursing, or equivalent experience.Significant experience as a CRA preferably with Medical Devices Experience in implementing clinical studies with good working knowledge of applicable regulatory requirements. Excellent communication skills. Receptive to working in a fast-paced, constantly changing work environment.To apply please send your CV or +44(0)203 0964713. (Only UK/EU nationals may apply - sponsorship not offered)SRG is the market leading supplier of Clinical and Drug development recruitment services to the Life Sciences industries. By putting people at the heart of what we do we are the catalyst that connects the best talent with organisations in the pursuit of ‘Creating Tomorrow’s World’& helping patients world-wide.
Pharma, Pharmaceutical, Biotechnology, Biotech, Clinical Research Organisation, Medical Device, Clinical Research, Administrator, Assistant, CTA, , Senior, Clinical Research Associates, CRA, SCRA, Clinical Monitoring, Site Monitor, Site Manager, CPM, Diagnostics, Reagents, Non-interventional, Therapeutic Areas, Indication, Oncology, Respiratory, Cardiovascular, cardiology, Rheumatology, Diabetes, Ophthalmology, Dermatology, Urology, CNS, Pain Neurology, haematology, orphan diseases, nephrology, musculoskeletal, endocrinology, gastroenterology,The recruiter has stated that all applicants for this job should be able to prove they are legally entitled to work in the EU. SRG is a trading name of Science Recruitment Group Ltd an Employment Business/Agency.The recruiter has stated that all applicants for this job should be able to prove they are legally entitled to work in the EU/UK. SRG is a trading name of Science Recruitment Group Ltd an Employment Business/Agency.

Apply for this job: CRA

Contact Information:

Address:  Head Office
SRG Clinical 9 Devonshire Square London United Kingdom
EC2M 4HP
England
Tel:  +44 (0)203 096 4700
Website:  Visit Our Web Site

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