Clinical Research Nurse II
Clinical Research Nurse II
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Salary Not Disclosed
1 Vacancy
Job Description
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
TrialMed is apremier global clinical site network offering comprehensive services for clinical trials from early to latephases (Phase I toPhase IV). As a unified brand TrialMed consolidates all clinical trial offerings under one global name ensuring a seamless experience for stakeholders.
Access to over 250 sites worldwide and apatient database of 20 million individuals ensuring robust and diverse trial enrollments.
Apatient-centric approach with capabilities for home trial services allowingpatients toparticipate in clinical trials from their homes or communities.
Comprehensive service offerings including early development CRO services consulting services and clinicalpharmacology services.
Join TrialMed and bepart of a dynamic team dedicated to advancing medical research and improvingpatient care through innovative clinical
Are you passionate about improving patients lives for the better
We are currentlylooking to recruita Clinical Research Nurse for our Synexus Clinical Research site in Birmingham United Kingdom
Working days Monday to Friday 37 hours a week the main priority will always be patient safety. The Clinical Research Nurse conducts multiple ongoing clinical trials involving patients or healthy volunteers/subjects. Completes all paperwork required to capture all data as specified by a study protocol and for ensuring subject safety understanding and cooperation during the study process. Interacts with the research site team and other interdepartmental staff. Engages in the entire site operations process which includes recruitment enrollment and retention of study participants.
Key responsibilities for a Clinical Research Nurse are as follows:
- Conducts clinical studies according to FDA/GCP and ICH regulations and guidelines.
- Provides medical care to patients always ensuring patient safety comes first.
- Schedules subject visits within protocol windows ensuring scheduling capacity is maximized.
- Performs all defined study activities (i.e. informed consent screening and protocol procedures which include but not limited to vital signs pregnancy tests height weight ECGs etc.).
- Records all patient information and results from tests as per protocol on required forms.
- Where required may complete IP accountability logs and associated information.
- Reports suspected non-compliance to relevant site staff.
- Ensures that IRB approval is obtained prior to study initiation and IRB requirements are met throughout the study.
- Promotes the company and builds a positive relationship with patients to ensure retention.
- Attends site initiation meetings and all other relevant meetings to receive training on protocol.
- May be required to call patients do patient bookings and follow-up calls to confirm bookings or provide information or results.
- Logs/completes information on sponsor systems and ensures all information provided is accurate (i.e. case report forms EDC etc.) and ensures it is completed within timeframe.
- Gathers and maintains source documents updates patient files and notes always ensuring relevant and most up to date information is recorded.
- Adheres to company COP/SCOP.
- May be required to dispose of waste according to standards and assist in keeping a general neat appearance of the facility.
To be considered for this exciting opportunity you will require the following skills and experience:
- Solid understanding of the clinical research process (i.e. GCP SOPs informed consent safety monitoring etc.)
- Capable of working independently analyzing and working with attention to detail processing and prioritizing sensitive complex information and problem solving
- Demonstrated ability to exercise discretion and sound judgement
- Good decision-making negotiation and influencing skills Good communication skills and English fluency will be an advantage
- Good organizational skills
- Good proficiency in basic computer applications
- Good interpersonal skills to work in a team environment
Our Mission is to enable our customers to make the world healthier cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100000 colleagues we share a common set of values - Integrity Intensity Innovation and Involvement - working together to accelerate research solve complex scientific challenges drive technological innovation and support patients in need. #StartYourStory with PPD part of Thermo Fisher Scientific where diverse experiences backgrounds and perspectives are valued.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race color religion sex sexual orientation gender identity national origin protected veteran status disability or any other legally protected status.
Employment Type
Full-Time
