Description
A global CRO who are looking for a Clinical Research Nurse, to join their team ASAP for a 3 month contract in LONDONPURPOSE:
Coordinate and participate in Phase I/II a clinical research studies ensuring that studies are carried out according to protocol, standard operating procedures and applicable guidelines and regulations.
RESPONSIBILITIES:
- Coordinate and participate in clinical research studies conducted by a supervising investigator to ensure that data collected on study volunteers adhere to study protocol; may assist in screening volunteers for inclusion in study based on pre-determined criteria.
- Administer investigational drug to volunteers according to study protocol.
- Record volunteer clinical data in case report forms (CRFs). Collaborate closely with study investigator informing on relevant adverse events and serious adverse events according to procedures outlined in the protocol
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES:
- Good knowledge of Phase I clinical trials
- In-depth knowledge of the principles of Good Clinical Practices (GCP)
- In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
This is a Temp contract for 3 months initially, with the potential to extend for another 3 months.
Training and Skills:
Immediate Life Support (ILS)
Venepuncture and cannulation
Full training will be provided This is an excellent opportunity to work for a fast moving organisation offering £35-£40 per hour. If this is of interest to you and or anyone you know, please get in touch for more information. This will be a fast turnaround with a start in the next couple of weeks should you be immediately available. .
To find out more about Real please visit www.realstaffing.com
Real Staffing, a trading division of SThree Partnership LLP | Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales