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ClinTec International is actively recruiting for a Senior Clinical Trials Coordinator to join our expanding global company in Prague – this is a Permanent position, Office based opportunity. By working for ClinTec you can further your career in a dynamic, fast-paced environment and you can be assured of rewarding benefits.
Role Description
Working as a Senior Clinical Trial Coordinator for ClinTec you will be involved in some of the most prestigious drug development projects for a number of leading global pharmaceutical companies with the opportunity to develop progress and travel globally. This is a perfect role for Clinical Trial Coordinator who understands the drug development process, has significant experience within CTC role and is willing to travel as required.The Senior Clinical Trial coordinator will be responsible for Trial and Site Administration, Regulatory and Start-up responsibilities, reviewing budgets and planning meetings. The successful candidate(s) be in charge of Document Management according to study protocol, Standard Operating Procedures, applicable regulations and ICH-GCP guidelines.
Responsibilities of the SCTC:
Tracking and reporting trial documents and ensuring collation and distribution of study tools and documents
Updating clinical trial databases
Management of clinical and non-clinical
Prepare, collate, distribute and archive clinical documents and correspondence
Updating manuals/documents (e.g., patient diaries, instructions) and documenting proper destruction of clinical supplies
Providing and collecting from investigators forms/lists for site evaluation/validation and site start-up
Preparation of submission package for IRB/ERC and support regulatory agencies submissions
Collaboration with finance/budgeting representatives for tracking, reporting of negotiations, contract development, approval, maintenance and payments (investigators, vendors, grants)
Monitor, track adherence and disclosures and budget closeout
Organising meetings, creating and tracking study memos/letters
Supporting and preparing for local investigators meetings
Essential Criteria:
Life Science Degree or equivelant OR equivalent healthcare experience
Fluency in English – verbal and written
Fluency in Czech language – verbal and written
IT skills
Strong organizational and communication skills
Willing and able to work office based in Prague
Company Information:
ClinTec International is a UK-based, dynamic privately owned full service Contract Research Organisation with presence in over 40 countries worldwide. We have been providing clinical research support services to clients in the pharmaceutical, biotechnology and medical device industries and assist in their key product development efforts for over a decade. At ClinTec International, we pride ourselves provides high quality, flexible and professional services and solutions to our clients. ClinTec International has a wealth of experience in managing clinical trials in all major therapeutic areas including oncology, neurology, cardiovascular, psychiatry, infectious disease, rheumatology, immunology, respiratory and gastroenterology.
ClinTec employees can expect to receive expert training and guidance throughout their careers as well as the opportunity to be involved in every aspect of Clinical Trials across the full life-cycle of the drug development process from the CRO perspective. We have strong partnership with some of the world's leading pharmaceutical companies and employees can expect to be involved in some of the most prestigious drug development projects with the opportunity to develop, progress and travel globally. ClinTec International offers a competitive salary and rewards package.
You must be logged in to apply for this position. Log in using the form on the right, at the top of the page beneath the logo, or click here to register.
Please Note: Applications to this vacancy are not made using our website. When you click above, you will be taken to the recruiter's website to complete your application.
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