At a Glance
- Tasks: Ensure quality control of clinical programming outputs and support documentation processes.
- Company: Join a leading organisation in clinical and statistical programming.
- Benefits: Gain valuable experience, competitive pay, and opportunities for professional growth.
- Other info: Dynamic team atmosphere with opportunities to learn and advance your career.
- Why this job: Make a real difference in clinical projects while developing your skills in a supportive environment.
- Qualifications: Attention to detail, administrative experience, and proficiency in Microsoft Office.
The predicted salary is between 30000 - 40000 £ per year.
The Role As a QC Coordinator I, you will provide quality control and administrative support to the Clinical and Statistical Programming group.
You will play an important role in ensuring the accuracy, consistency and integrity of clinical and statistical programming outputs, helping to maintain compliance with regulatory and Good Clinical Practice (GCP) requirements.
Working closely with Clinical and Statistical Programmers, you will support the review of study outputs, preparation of key study documentation and archiving activities, contributing to the successful delivery of clinical projects.
Key Responsibilities
Perform quality control (QC) reviews of programming output, including tables, figures and listings (TFLs).
Assist with the creation and maintenance of annotated Case Report Forms (a CRFs).
Support the team with study documentation and archiving procedures.
Ensure all activities are conducted in accordance with Standard Operating Procedures (SOPs), regulatory requirements and applicable guidance.
Maintain accurate records and documentation to support study deliverables.
Provide general administrative and operational support to the Clinical and Statistical Programming group.
Undertake additional duties and responsibilities as required by the business.
What You'll Bring
Exceptional attention to detail and a commitment to quality.
Experience undertaking administrative tasks and/or conducting quality control reviews of data or documentation.
Good working knowledge of Microsoft Office applications, particularly Word and Excel.
Strong verbal and written communication skills.
Ability to organise workload effectively and manage multiple priorities.
A proactive and team-oriented approach to work.
Stats, Stats Programming, PK and Medical Writing - QC Coordinator I in Edinburgh employer: Quotient Sciences
Quotient Sciences is an exceptional employer located in Nottingham, offering a dynamic work environment that prioritises volunteer safety and compliance in clinical research. With a strong focus on professional development and leadership opportunities, employees are encouraged to grow their careers while contributing to meaningful advancements in medical solutions. Join us to be part of a collaborative culture that values innovation and excellence in healthcare.
StudySmarter Expert Advice🤫
We think this is how you could land Stats, Stats Programming, PK and Medical Writing - QC Coordinator I in Edinburgh
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We think you need these skills to ace Stats, Stats Programming, PK and Medical Writing - QC Coordinator I in Edinburgh
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Quotient Sciences!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Quotient Sciences that you're not just a fit for the job but also a safety-conscious candidate!
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How to prepare for a job interview at Quotient Sciences
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Quotient Sciences that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
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If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
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In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
