At a Glance
- Tasks: Manage clinical trials, ensuring compliance and safety for participants.
- Company: Syneos Health, a leader in biopharmaceutical solutions.
- Benefits: Competitive salary, travel opportunities, and professional growth.
- Other info: Dynamic role with up to 75% travel and excellent career advancement.
- Why this job: Make a real difference in healthcare by managing impactful clinical trials.
- Qualifications: Bachelor’s degree or RN, with knowledge of clinical practices.
The predicted salary is between 40000 - 55000 € per year.
Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.
Job Responsibilities
- Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiological Practices (GPP) and protocol compliance.
- Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific actions; immediately communicates/escalates serious issues to the project team.
- Verifies that the process of obtaining informed consent has been adequately performed and documented for each subject/patient.
- Assesses factors that might affect subject/patient’s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues.
- For the Clinical Monitoring/Site Management Plan (CMP/SMP): Assesses site processes, conducts Source Document Review, and verifies clinical data entry in the case report form (CRF) is accurate and complete.
- Applies query resolution techniques remotely and on site, driving query resolution to closure within agreed timelines.
- May perform investigational product (IP) inventory, reconciliation and reviews storage and security.
- Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness and reconciles contents with the Trial Master File (TMF).
- Documents activities via confirmation letters, follow-up letters, trip reports, and communication logs.
- Manages site-level activities and communication to ensure project objectives, budgets, and timelines are met.
- Provides guidance at the site and project level towards audit readiness standards.
Qualifications
- Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience.
- Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.
- Must demonstrate good computer skills and be able to embrace new technologies.
- Excellent communication, presentation and interpersonal skills.
- Ability to manage required travel of up to 75% on a regular basis.
Clinical Trial Manager in London employer: Syneos Health
Syneos Health® is an exceptional employer for Clinical Trial Managers, offering a dynamic work environment that fosters innovation and collaboration. With a strong commitment to employee growth, we provide comprehensive training and development opportunities, ensuring our team members are equipped to excel in their roles. Located in the UK, our culture prioritises work-life balance and inclusivity, making it a rewarding place to contribute to meaningful advancements in biopharmaceutical solutions.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Trial Manager in London
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical trial field on LinkedIn or at industry events. We can’t stress enough how personal connections can lead to job opportunities that aren’t even advertised.
✨Tip Number 2
Prepare for interviews by practising common questions and scenarios related to clinical trials. We recommend role-playing with a friend or using mock interview platforms to boost your confidence and refine your answers.
✨Tip Number 3
Showcase your skills through real-life examples during interviews. We want you to highlight your experience with site management, compliance, and problem-solving. Use the STAR method (Situation, Task, Action, Result) to structure your responses.
✨Tip Number 4
Don’t forget to follow up after interviews! A simple thank-you email can set you apart from other candidates. We suggest reiterating your enthusiasm for the role and mentioning something specific from the conversation to keep you fresh in their minds.
We think you need these skills to ace Clinical Trial Manager in London
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Clinical Trial Manager role. Highlight relevant experience and skills that match the job description, like your knowledge of Good Clinical Practice and any site management activities you've performed.
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical trials and how your background makes you a perfect fit for our team. Don't forget to mention your ability to manage site-level activities and ensure compliance.
Showcase Your Communication Skills:Since excellent communication is key in this role, make sure your application reflects your ability to convey information clearly. Use concise language and structure your documents well to demonstrate your interpersonal skills right from the start.
Apply Through Our Website:We encourage you to apply through our website for the best chance of getting noticed. It’s super easy, and you’ll be able to keep track of your application status directly!
How to prepare for a job interview at Syneos Health
✨Know Your GCP Inside Out
Make sure you brush up on Good Clinical Practice (GCP) guidelines and ICH regulations. Being able to discuss these in detail will show that you’re not just familiar with them, but that you can apply them in real-world scenarios.
✨Showcase Your Communication Skills
As a Clinical Trial Manager, communication is key. Prepare examples of how you've effectively communicated with site staff or project teams in the past. This will demonstrate your interpersonal skills and ability to manage site-level activities.
✨Be Ready for Scenario Questions
Expect questions that put you in hypothetical situations, like handling protocol deviations or managing site compliance issues. Think through your past experiences and be ready to explain how you would approach these challenges.
✨Highlight Your Tech Savvy
Since the role requires good computer skills and embracing new technologies, be prepared to discuss any relevant software or tools you’ve used in previous roles. This will show that you can adapt quickly and efficiently to the tech side of clinical trials.
