Job Detail
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Offered Salary 0
Job Description
Qualifications
- Medical degree from a recognized institution
- Prior experience in clinical practice is required
- Familiarity with clinical research and development in the biopharmaceutical industry
- Strong understanding of clinical development, regulations, and adverse event management
- Excellent project management and leadership skills
- All applicants must have the relevant authorisation to live and work in the UK / EU as applicable
- Dis Ability Confident
- We are proud to be a Disability Confident Employer and we encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments necessary to support your application and future career
Responsibilities
- As part of the Clinical Development and Operations (CD&O) team, you will ensure the medical and scientific integrity of studies and the wellbeing of patients in clinical trials
- You will design and execute high-quality clinical studies, collaborate with cross-functional teams, and contribute to continuous improvement initiatives
- Maintain compliance with standards and manage emerging clinical issues
- Deliver governance-approved protocols efficiently
- Provide clinical input for data collection and analysis
- Support country and site selection, develop training, and participate in investigator meetings
- Author and manage Informed Consent Documents (ICDs) and protocol amendments
- Review safety data and manage serious adverse events (SAEs)
- Interpret and communicate clinical trial data
- Act as a medical monitor, e.g. answer relevant medical questions from investigators and team members
Apply Now
Application ends in 15d 5h 20min