This leading international CRO is seeking a SCRA to work onsite with a global pharma sponsor. This is an excellent opportunity to work with a single sponsor on multiple therapy areas. This position can be field or office based nationwide. Career growth and development is readily available with this exciting career opportunity.
Belgium - Home Based (1 day office every 3 weeks)
You'll have 2+ years' independent experience including routine monitoring, maintenance of study files, conduction of pre-study and initiation visits and close-out of clinical sites. You will also have skill in applying applicable research regulatory requirements (GCP - ICH).
Working directly with the sponsor you will implement and monitor trials across a broad spectrum of therapeutic areas, and be responsible for managing the investigator sites in accordance with ICH - GCP guidelines. This position requires you to develop and maintain strong working relationships with investigational sites and client company personnel. You may also be required to provide assistance to less experienced clinical staff from time to time.
This globally known and well renowned CRO currently operates in 20 countries with more than 10,000+ employees. The company works with a large and diverse portfolio of trials including but not limited to Oncology, Cardiovascular, Rare Disease and Orphan Drugs, Neuroscience, Inflammations, Infectious Diseases, and Diabetes.
- Bachelor of Science or Bachelor of Nursing Degree
- 4+ years independent monitoring experience
- In depth therapeutic and protocol knowledge
- Study start up activity experience
- Excellent Salary
- Car or car allowance
- 25 days' annual leave
- 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 Recruitment Consultant Tim Lobley on +44 (0)203907 1986, or email firstname.lastname@example.org. If this role is not suitable, Tim is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
CRA / Clinical Research Associate / CRA II / Senior CRA / SCRA / 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 / England / Scotland / Wales / London / North West England / South West England / North East England / North West England / West Midlands / East Midlands / CRO / Contract Research Organisation / Pharmaceutical / Home Based /