Clinical Trial Associate (CTA), Perm, Leicester, UK

Clinical Trial Associate (CTA), Senior Clinical Project Administrator - Permanent - Leicester, UKPermanent roleCompetitive salaryGreat benefits packageOpportunity for career progression

A unique opportunity has arisen as CTA for one of one of the country's leading independent providers of services to Pharmaceutical. The CTA will manage all administrative aspects of a number of clinical trials, at every stage of the process and will be expected to prepare, distribute, track and file all clinical trial documents and supporting evidence.

About SRG: We are 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.Role responsibilities:*Set up and maintain clinical investigator files and essential clinical trial documents*Tracking, distributing and filing documents when they are returned*Maintaining the electronic Trial Master File (TMF)*Preparing and sending study materials to investigator sites*Attending study meetings and arranging investigator meeting arrangements*Supporting clinical research associates*Prepare study-related documents and other materials for delivery to archives, at appropriate intervals

Requirements:*University/college degree or certification in a health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology) preferred.*Robust relevant experience in Pharmaceutical or CRO*Project management skills*Excellent organisational skills*Methodical approach to work*Computer literacy for updating spreadsheets, word process documents and search databases*Ability to work in a team

HOW TO APPLY?Click on the "apply" button below. Please contact Arnaud Heroult on +44 (0)203 096 4712 or email if you would like to know more about this opportunity. CVs will be shortlisted and presented for the role in the next 48 hours.Our team at SRG Clinical also cover roles in Clinical Operations (CPM, CRA etc.), Biometrics (Statistics, SAS programming, Data Management), Medical information, Medical affairs, Pharmacovigilance and Regulatory affairs so do not hesitate to call me at +44 (0)203 096 4712.Key Words:CRO, Pharma, Pharmaceutical, Biotechnology, Biotech, Clinical Research Organisation, Medical Device, Permanent, Freelance, Contract, Part-time, Temporary, Clinical Research, Non-interventional, Therapeutic Areas, Indication, Oncology, Respiratory, COPD, Cardiovascular, cardiology, Rheumatology, Diabetes, Ophthalmology, Dermatology, Urology, CNS, Neurology, haematology, orphan diseases, nephrology, musculoskeletal, endocrinology, gastroenterology, vaccines, Clinical Trial Associate, CTA, CTC, Administrator, Assistant, Clinical Project Administrator 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

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.