My multinational pharmaceutical client has a fantastic opportunity for a Healthcare professional looking for an exciting new challenge, in the Clinical Research field.
This role would see you work as part of a diverse team who monitor and record all the Clinical Trial activity that the company is engaged in.
You would gain exposure to clinical study start-up activities across the EU and other regions, like the Middle East, Africa and Russia.
You would ensure that the investigator sites meet requirements to enrol study participants into clinical trials and support ongoing activities during site maintenance and closeout.
You would also be responsible for obtaining clinical trial authorizations and ethical approvals, execution of the budget and contract, and activities related to clinical finance records management and site training. The ability to identify, communicate, and resolve issues is also key as well as providing feedback and shared learning experiences for continuous improvement for the team.
- Bachelor’s degree preferably in a scientific or health-related field, two years of clinical research experience or relevant experience preferred
- Understanding of the overall clinical development paradigm and the importance of efficient site initiation
- Applied knowledge of project management processes and skills
- Appreciation of / experience in a compliance-driven environment
This role is permanent and has some fantastic benefits including healthcare, pension and life assurance benefits, subsidised canteen, wellbeing facilities, educational assistance, on-site parking and much more
Please call Leah on 021 4847 135 or send your CV to email@example.com for more information
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