Clinical Research Assistant
Clinical Research Assistant

Clinical Research Assistant

Edinburgh Full-Time 30000 - 42000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Assist with clinical studies, document control, and volunteer recruitment.
  • Company: Join Eurofins, a global leader in life sciences dedicated to safety and sustainability.
  • Benefits: Enjoy enhanced leave, pension plans, healthcare cash plans, and worldwide career opportunities.
  • Why this job: Make a real impact on health and safety while working in a diverse and inclusive environment.
  • Qualifications: GCP awareness, IT skills, attention to detail, and effective communication are essential.
  • Other info: No visa sponsorship available; apply early as positions may close quickly.

The predicted salary is between 30000 - 42000 £ per year.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies.

Unfortunately, we are unable to offer visa sponsorship for this role. 35 Hours per week. Monday - Friday. 9.00am - 5.00pm.

Purpose of The Post: You will be responsible for assisting with the delivery of a portfolio of clinical studies including the adherence to regulatory processes within the department. In addition to clinical/volunteer-based tasks.

  • Document generation and control
  • Study tracking
  • Data collection
  • Ensure relevant documents are available for all research subjects.
  • Complete all documentation relating to volunteer participation.
  • Deal with telephone enquiries from volunteers, external and internal customers.
  • Contact volunteers to recruit them for specific studies, scheduling times for their visits and performing the administration on the database.
  • Interact with study participants in relation to the requirements of the study.
  • Regular communication with relevant Project Managers/Senior Management and immediately on identifying untoward events.
  • Responsible for the testing, preparation, storage and shipping of research samples.
  • Assist with ensuring that all test materials and other consumables are available for the proposed study commencement and to ensure satisfactory disposal of test materials on study completion.
  • Dispensation and preparation of study test materials employing correct sample containers, sample labels, etc in line with standard operating procedures and the study protocol.
  • Identify eligible volunteers for recruitment to participate from volunteer database or screening records.
  • Preparation, assessment and testing of volunteers participating in research, including observations & recording of skin responses, instrument data and other appropriate measurements as required.
  • Instruct study participants on the study procedures and use (where appropriate) of test materials/devices.
  • Assist with ensuring that all aspects of the study schedule are adhered to and that results are available (to other teams) on time.
  • Maintain required records of study activity including case report forms, test material dispensation records, or regulatory forms.
  • Responsible for the monitoring and maintenance of clinical stock levels and clerical store levels, ensuring effective and economic use of resources.
  • Prepare data for reporting and study files for archiving.
  • Assist with responding to QA audits throughout the life cycle of studies including study inspections, data, and report audits.

Qualifications:

  • Awareness of GCP (Good Clinical Practice).
  • IT literate Microsoft Office (Excel, Word)
  • Strong attention to detail to identify errors and refine documents for clarity and precision.
  • Attention to Detail
  • Compliance & Accuracy
  • Problem-Solving
  • Effective communication skills both written and oral.
  • Organised.
  • Excels working in a team but also independently.
  • Good time management and can prioritise.
  • Experience working in a fast-paced, dynamic environment with competing priorities and shifting deadlines.
  • Experience working with cross-functional teams.
  • SCQF Level 4 or above in English

Additional Information:

At Eurofins we are growing, innovating and always learning. We celebrate the achievements of our employees through annual long service awards, recognise our colleagues special life events, and we are committed to charitable causes through global fundraising activities. As a Eurofins employee you will benefit from:

  • Enhanced Annual Leave Entitlement
  • Annual Leave Sellback Scheme
  • Additional Annual Leave at Employees set service dates
  • Company Pension Plan
  • Life Assurance Scheme (4 times annual salary)
  • Healthcare Cash Plan (6+ months service)
  • Enhanced Maternity, Adoption and Paternity Schemes
  • Employee Assistance Programme – 24/7 confidential Health and Wellbeing Programmes
  • Worldwide career opportunities

We also have in place rewards recognising the great work our employees deliver, their dedicated service and celebrating special life events.

What Happens Next: Our people are the backbone of what we do, so it’s incredibly important we find the right individuals to join us. As a potential new recruit you’ll be invited to meet the team in the form of an assessment centre or a staged interview process dependent on the role and its requirements, this will give you the opportunity to see what working for Eurofins is really like and enable us to get to know your key skills and strengths.

Your data: As part of any recruitment process, the company collects and processes personal data relating to job applicants. The company is committed to being transparent about how it collects and uses that data and to meeting its data protection obligations.

Closing Date: We reserve the right to close or extend this position depending on application numbers. Therefore we would urge candidates to submit an application as early as possible. Due to the high volume of applications we receive please be aware that if you do not receive a response within 4 weeks of the vacancy expiry date unfortunately, on this occasion your application has been unsuccessful.

We support your development! Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development.

We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique.

Sustainability matters to us! We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal!

Clinical Research Assistant employer: Eurofins

Eurofins Scientific is an exceptional employer that prioritises employee well-being and professional growth, offering a supportive work culture where diversity, equity, and inclusion are celebrated. With comprehensive benefits such as enhanced annual leave, a robust pension plan, and a commitment to career development, employees can thrive in a dynamic environment dedicated to making the world safer and healthier. Located in a vibrant area, Eurofins provides unique opportunities to engage in meaningful work while contributing to global sustainability efforts.
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Contact Detail:

Eurofins Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Clinical Research Assistant

✨Tip Number 1

Familiarise yourself with Good Clinical Practice (GCP) guidelines, as this knowledge is crucial for a Clinical Research Assistant role. Understanding these regulations will not only help you in interviews but also demonstrate your commitment to maintaining high standards in clinical research.

✨Tip Number 2

Highlight your organisational skills during the interview process. Since the role involves managing multiple studies and ensuring compliance with protocols, showcasing your ability to prioritise tasks and maintain accurate records will set you apart from other candidates.

✨Tip Number 3

Prepare to discuss your experience working in fast-paced environments. The job description mentions dynamic settings with competing priorities, so be ready to share specific examples of how you've successfully managed similar situations in the past.

✨Tip Number 4

Demonstrate your effective communication skills by preparing questions for your interviewers. Engaging them with thoughtful inquiries about the team dynamics or study processes will show your genuine interest in the role and help you make a positive impression.

We think you need these skills to ace Clinical Research Assistant

Knowledge of Good Clinical Practice (GCP)
Document Generation and Control
Data Collection and Management
Attention to Detail
Effective Communication Skills (Written and Oral)
Organisational Skills
Time Management and Prioritisation
Problem-Solving Skills
IT Literacy (Microsoft Office: Excel, Word)
Experience in a Fast-Paced Environment
Teamwork and Collaboration
Ability to Work Independently
Experience with Cross-Functional Teams
Record Keeping and Documentation Skills

Some tips for your application 🫡

Understand the Role: Before applying, make sure you fully understand the responsibilities of a Clinical Research Assistant. Familiarise yourself with the key tasks mentioned in the job description, such as document generation, study tracking, and data collection.

Tailor Your CV: Customise your CV to highlight relevant experience and skills that align with the job requirements. Emphasise your attention to detail, problem-solving abilities, and any previous experience in clinical research or related fields.

Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and your understanding of Eurofins' mission. Mention specific examples of how your skills and experiences make you a great fit for the role.

Proofread Your Application: Before submitting, carefully proofread your application materials. Check for spelling and grammatical errors, and ensure that all information is clear and concise. A polished application reflects your attention to detail.

How to prepare for a job interview at Eurofins

✨Understand Good Clinical Practice (GCP)

Familiarise yourself with the principles of Good Clinical Practice, as this is crucial for a Clinical Research Assistant role. Be prepared to discuss how you would ensure compliance with these standards in your work.

✨Showcase Your Attention to Detail

Highlight your ability to spot errors and refine documents for clarity. Bring examples of past experiences where your attention to detail made a significant impact on a project or task.

✨Demonstrate Effective Communication Skills

Prepare to discuss how you communicate with team members and study participants. Think of specific instances where your communication skills helped resolve an issue or improve collaboration.

✨Be Ready for Problem-Solving Scenarios

Expect questions that assess your problem-solving abilities. Prepare examples of challenges you've faced in previous roles and how you approached finding solutions, especially in fast-paced environments.

Clinical Research Assistant
Eurofins
Location: Edinburgh
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  • Clinical Research Assistant

    Edinburgh
    Full-Time
    30000 - 42000 £ / year (est.)
  • E

    Eurofins

    5000+
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