This leading specialty drug development organisation with an international presence is seeking an experienced CRA who has worked with complex studies across a range of therapeutic areas, including but not limited to Cardiovascular, Oncology, Paediatrics, Women's Health, Rare and Orphan Disease, Endocrine and Metabolic, and Neuroscience. This is an excellent opportunity for CRAs with 1.5+ years' experience to work with a global CRO with clear career development and growth.
Poland - home or office based
You'll have two plus years' experience as a CRA working across a range of diverse therapeutic areas. You'll have experience working across study site monitoring including routine monitoring, maintenance of study files, conduction pf pre-study and initiation visits and close-out of clinical sites. You'll have knowledge of, and skill in applying, applicable research regulatory requirements (Good Clinical Practice, and International Conference on Harmonisation guidelines), as well as a sound understanding of the drug development process.
You will be working on a variety of innovative studies, and independently ensuring sites are monitored in accordance with protocol monitoring guidelines, GCP and ICH guidelines. You will be required to carry out site initiation, routine monitoring and close out visits. You will also be required to develop and maintain relationships with investigational sites and client company personnel.
This CRO is a dynamic leader within the pharmaceutical industry, with progression and career development high on their list of priorities. This CRO has a network of 250+ employees and operates across 6 continents. Trials are ongoing in a diverse range of therapeutic areas, including Cardiovascular, Oncology, Paediatrics, Women's Health, Rare and Orphan Disease, Endocrine and Metabolic, and Neuroscience.
- Bachelor of Science or Bachelor of Nursing Degree
- 1.5 years independent monitoring experience
- Experience working in a range of therapeutic areas
- Entitlement to work in Poland
- Sound presentation and communication skills
- Excellent Salary
- Car or car allowance
- Flexi Benefits
ABOUT i-PHARM CONSULTING
i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.
If you would like to discuss this vacancy further, please call Business Manager Ciara Noble on +44 (0)20 31890469, or email firstname.lastname@example.org. If this role is not suitable, Ciara is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
CRA / Clinical Research Associate / Clinical Monitor / Clinical Trials / Phase I / Phase II / Phase III / Phase IV / Good Clinical Practice / GCP / International Conference on Harmonisation guidelines / ICH / Oncology / Neuroscience / Cardiovascular/ Paediatrics / Women's Health / Endocrine & Metabolic / Rare Diseases / Poland / Warsaw / Krakow / CRO / Contract Research Organisation / Pharmaceutical / Home Based /