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- Tasks: Join us as a Clinical Research Coordinator, performing vital clinical procedures and supporting research studies.
- Company: Be part of a dynamic team in Belfast, dedicated to advancing medical research and patient care.
- Benefits: Enjoy flexible part-time hours, valuable experience, and the chance to make a real impact.
- Why this job: This role offers hands-on experience in clinical trials, a collaborative culture, and opportunities for growth.
- Qualifications: A Bachelor’s degree or High School Diploma with relevant experience in a clinical setting is required.
- Other info: Must be able to travel to our Belfast site; sponsorship is not provided.
The predicted salary is between 36000 - 60000 ÂŁ per year.
Duration: Part-time contract until Sep 2025
Location: The resource must be able to travel to client site in Belfast. The site is in Linenhall Street, Belfast.
IR35 Determination: Inside
RTW: Must hold valid UK RTW, sponsorship not provided
Hours: 24 hours/week
Job Description:
- Perform a variety of clinical procedures to collect, record, report and interpret data on patients enrolled and/or seeking enrollment in clinical studies according to the protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP).
- Assist with daily workload planning.
Essential Functions:
- 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;
- Monitor subject safety and report adverse reactions to appropriate medical personnel;
- Correspond with research subjects and troubleshoot study-related questions or issues;
- Participate in “huddles” to confirm daily study tasks are assigned to team members and are executed to the expected standards;
- Assist with study data quality checking and query resolution.
- Perform a variety of complex clinical research procedures including but not limited to ECG, sample collection, spirometry, vital signs, dose verification, cannulation and cardiac telemetry monitoring.
- Record, report and interpret study findings appropriately to develop a study-specific database.
- Assist investigator in verifying that research study objectives are met on time, within budget and according to applicable protocol requirements, clinical research regulations and quality standards.
- Provide training to new investigator site staff members on study-specific topics and requirements.
- Assist in maintaining adherence to investigator site staff training requirements by auditing and maintaining training records.
- Prepare for and attend study monitoring visits, study audits, and regulatory inspections with clinical research regulatory agencies.
- Assist research site with coverage planning related to staffing and scheduling for research projects.
Qualifications:
- Bachelor’s Degree Required or High School Diploma or equivalent Required
- 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 Required
- 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
- Applicable certifications and licenses as required by company, country, state, and/or other regulatory bodies
Clinical Research Coordinator employer: Unity Systems
Contact Detail:
Unity Systems Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Coordinator
✨Tip Number 1
Familiarise yourself with the specific clinical procedures mentioned in the job description, such as ECG and spirometry testing. Being able to discuss your experience or knowledge of these procedures during an interview can set you apart from other candidates.
✨Tip Number 2
Network with professionals in the clinical research field, especially those who have worked as Clinical Research Coordinators. They can provide insights into the role and may even refer you to opportunities at StudySmarter.
✨Tip Number 3
Stay updated on the latest regulations and guidelines related to Good Clinical Practice (GCP). Showing that you are knowledgeable about current standards can demonstrate your commitment to quality in clinical research.
✨Tip Number 4
Prepare for potential interview questions by practising how you would handle common scenarios in clinical trials, such as patient recruitment and data management. This will help you articulate your problem-solving skills effectively.
We think you need these skills to ace Clinical Research Coordinator
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities and qualifications required for the Clinical Research Coordinator position. Familiarise yourself with clinical research protocols, Good Clinical Practice (GCP), and the specific tasks mentioned in the job description.
Tailor Your CV: Customise your CV to highlight relevant experience in clinical environments or medical settings. Emphasise any specific skills related to clinical trials, patient recruitment, and data management that align with the job requirements.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and your understanding of the role. Mention specific experiences that demonstrate your ability to perform the essential functions listed in the job description.
Proofread Your Application: Before submitting your application, carefully proofread all documents for spelling and grammatical errors. Ensure that your application is clear, concise, and free of mistakes to make a strong impression.
How to prepare for a job interview at Unity Systems
✨Know Your Clinical Research Basics
Make sure you brush up on your knowledge of clinical trials and Good Clinical Practices (GCP). Be prepared to discuss how these principles apply to the role of a Clinical Research Coordinator, as this will show your understanding of the field.
✨Familiarise Yourself with the Job Description
Take time to thoroughly read the job description and understand the essential functions listed. Be ready to provide examples from your past experience that demonstrate your ability to perform these tasks effectively.
✨Prepare for Scenario-Based Questions
Expect to be asked about specific scenarios you might encounter in the role. Think about how you would handle patient recruitment, data collection, or regulatory compliance issues, and be ready to articulate your thought process.
✨Showcase Your Interpersonal Skills
As a Clinical Research Coordinator, you'll need excellent interpersonal skills. Prepare to discuss how you've built relationships with colleagues and patients in the past, and be ready to demonstrate your ability to communicate clearly and effectively.
