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- Tasks: Manage and evaluate clinical trial safety data, focusing on HIV treatments.
- Company: Join CY Partners, a dynamic recruitment agency dedicated to healthcare roles.
- Benefits: Enjoy remote work flexibility with a competitive salary of up to £550 per day.
- Why this job: Make a real impact on patient safety while working in a collaborative environment.
- Qualifications: Experience in Clinical Trials and strong knowledge of safety regulations required.
- Other info: This is a 6-month contract role with opportunities for professional growth.
The predicted salary is between 110000 - 150000 £ per year.
Contract Clinical Safety Scientist
Location: Remote
Salary: up to £550 per day
Contract Length: 6 Months
CY Partners is excited to be recruiting on behalf of our client for the role of Contract Clinical Safety Scientist. This is a fantastic opportunity to play a significant role in the management and evaluation of clinical trial safety data with a particular focus on medicines for the treatment and prevention of HIV. The successful candidate will contribute to enhancing patient safety and ensuring compliance with regulatory standards.
Key Responsibilities:
- The role will include conducting routine pharmacovigilance activities, signal detection/evaluation and authoring of key regulatory documents (e.g. DSURs, EU RMPs and PBRERs).
- Throughout delivery of the role, you will ensure that all safety documentation is accurate and available to meet global compliance and regulatory requirements.
- Conduct safety assessments and provide expert input on clinical trial protocols.
- Review, assess, and interpret safety data from clinical trials.
- Collaborate with cross-functional teams to ensure safety data is effectively communicated.
- Assist in the preparation of safety-related documents for regulatory submissions.
- Participate in safety meetings and contribute to risk management strategies.
- Ensure compliance with regulatory requirements and internal policies.
Role Requirements:
- Proven experience in Clinical Trials, with a focus on safety monitoring.
- Strong knowledge of clinical safety regulations and guidelines.
- Excellent communication and interpersonal skills.
- Ability to work collaboratively within a team and across departments.
- Strong analytical and problem-solving capabilities.
If you are an experienced Clinical Safety Scientist looking for your next challenge, we would love to hear from you!
CY Partners is acting as an employment agency/business in relation to this vacancy.
Clinical Safety Scientist employer: CV-Library
Contact Detail:
CV-Library Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Safety Scientist
✨Tip Number 1
Familiarise yourself with the latest regulations and guidelines related to clinical safety, especially those pertaining to HIV treatments. This knowledge will not only boost your confidence but also demonstrate your commitment to the role during interviews.
✨Tip Number 2
Network with professionals in the clinical safety field, particularly those who have experience with pharmacovigilance. Engaging in discussions or attending relevant webinars can provide insights and potentially lead to referrals.
✨Tip Number 3
Prepare to discuss specific examples from your past experiences where you successfully managed safety data or contributed to regulatory submissions. Highlighting these instances will showcase your expertise and problem-solving skills.
✨Tip Number 4
Stay updated on current trends and challenges in clinical trials, particularly those related to safety monitoring. Being knowledgeable about industry developments will help you engage in meaningful conversations during interviews.
We think you need these skills to ace Clinical Safety Scientist
Some tips for your application 🫡
Understand the Role: Before applying, make sure to thoroughly understand the responsibilities of a Clinical Safety Scientist. Familiarise yourself with pharmacovigilance activities and the specific regulatory documents mentioned in the job description.
Tailor Your CV: Highlight your relevant experience in clinical trials and safety monitoring. Emphasise your knowledge of clinical safety regulations and any specific projects you've worked on that relate to HIV treatment or prevention.
Craft a Compelling Cover Letter: In your cover letter, express your passion for enhancing patient safety and compliance with regulatory standards. Mention how your skills align with the key responsibilities outlined in the job description.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any errors. Ensure that all information is clear, concise, and professional, as attention to detail is crucial in this field.
How to prepare for a job interview at CV-Library
✨Know Your Regulations
Familiarise yourself with the key clinical safety regulations and guidelines relevant to the role. Being able to discuss these confidently will demonstrate your expertise and commitment to compliance.
✨Showcase Your Experience
Prepare specific examples from your past work in clinical trials, particularly those involving safety monitoring. Highlight your contributions to pharmacovigilance activities and any regulatory documents you've authored.
✨Communicate Effectively
Since excellent communication is crucial for this role, practice articulating complex safety data clearly and concisely. Be ready to explain how you would collaborate with cross-functional teams to ensure effective communication of safety data.
✨Demonstrate Problem-Solving Skills
Be prepared to discuss scenarios where you've had to analyse safety data and make critical decisions. Show how your analytical skills have contributed to risk management strategies in previous roles.
