About the role
As a Clinical Research Coordinator, you will Perform a variety of clinical procedures to collect, record, report and interpret data on patients enrolled and/or seeking enrolment in clinical studies according to the protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP). Assist with daily workload planning.
Tell me more, tell me more…
Our client is currently looking for a recruit in joining their current team, below are the job details for your reference.
You can also ask our friendly recruitment team for any questions you may have about the role, between 09.00am till 17.00pm Monday to Friday.
Shifts: Monday to Friday (37.5 hours)
Roles and Responsibilities:
* Provide clinical research support to investigators to prepare for and execute assigned research studies, including:
* Review study protocols, Case Report Forms (CRFs), other study-specific documents, and electronic data capture systems used to record clinical research data.
* Attend all relevant study meetings.
* Collect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies governing the conduct of clinical research.
* Recruit and screen patients for clinical trials and maintain subject screening logs.
* Orient research subjects to the study, including the purpose of the study, procedures, and protocol issues such as timelines for visits.
* Design and maintain source documentation based on protocol requirements.
* Schedule and execute study visits and perform study procedures.
* Collect, record and maintain research subject study data according to study protocol and SOPs, preserving quality control for content, accuracy and completeness.
* Handle lab testing and analysis, including preparation of specimen collection tubes and lab logistics.
The must haves:
* Bachelor's Degree Req Or High School Diploma or equivalent Req
* 3 years’ relevant work experience in a clinical environment or medical setting, e.g., medical assistant, assistant nurse, laboratory technician; or equivalent combination of education, training and experience Req
* Working knowledge of clinical trials
* Working 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
* Skill in carrying out required clinical procedures such as intravenous catheter insertion and spirometry testing
* Good skill in using MS Windows and Office applications such as Access, Outlook and Word
* Excellent interpersonal skills
* Ability to pay close attention to detail
* Ability to establish and maintain effective working relationships with coworkers, managers and clients
What’s in it for you? –
Our client loves to reward their people for doing a great job.
* This is a 8 Weeks contract
* This role provides a hybrid working access in Belfast (5 days in a week).
* Rate: £20 – £25 per hour through umbrella / PAYE
Next Steps
Once you’ve applied, one of our friendly recruitment consultants will give you a call and talk you through the screening process.
If your application is successful, you’ll be involved in a live virtual interview with one of our client’s hiring managers to get to know you better.
We look forward to speaking to you!