Quotient Sciences is a leading drug development and manufacturing accelerator that helps biotech and pharma companies bring new medicines to patients faster. We have a fantastic opportunity to join our medical team in Nottingham as a Clinical Research Physician.
Requirements
- Act as a medically qualified person responsible for medical aspects of Phase I and II activities
- Manage the process by which a volunteer is screened for a specific study, to determine their eligibility to take part in the study
- Take medical responsibility for the everyday running of studies including the welfare of volunteers under the direction of the Principal Investigator
- Liaise with the Principal Investigators, Lead Scientists and members of the study teams about any medical and/or safety issues arising from a study
- Support the corporate goals by working closely with the Medical Science, Business Development and Marketing Departments
- Comply & adhere to GXP guidelines and regulations as required of this role
- Ensure study data is collected to a high quality in accordance with Good Clinical Practice (GCP) standards
- Performing a full physical examination for each volunteer
- Conducting or assisting clinical staff in the conduct of other study specific screening activities
- Reviewing all information gathered at pre study visit and confirming volunteer’s eligibility to take part in a study by signing the CRF
- Assisting the Senior Research Physician / Principal Investigator with ward duties
- Ensuring the volunteers health and welfare takes priority
- Providing study specific training and support to the Operations team prior to, during and after study days (as appropriate to the study) in order to ensure efficient execution of the study and acquisition of quality data
- Working closely with the PI to understand the rationale for study design to facilitate the planning and delivery of individual studies
- Production/review of the protocol, volunteer information and consent form, safety summary and any other documentation in conjunction with the Principal Investigator and other relevant personnel
- Acting as study physician on selected studies
- Supporting the Principal Investigator in discussions with clients
- Participating in the on-call rota once has sufficient experience
- Responsible for the development and implementation of Standard Operating Procedures as required
Benefits
- Competitive salary
- Additional remuneration for overnight medical cover and weekend morning cover
- Opportunity to work with a leading drug development and manufacturing accelerator
