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 development.
- Other info: Dynamic role with up to 75% travel and excellent career growth potential.
- Why this job: Make a real difference in healthcare by managing impactful clinical trials.
- Qualifications: Bachelor’s degree or RN, knowledge of clinical practices, and strong communication skills.
The predicted salary is between 40000 - 50000 € 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. Every role within Corporate is vital to furthering our vision of Shortening the Distance from Lab to Life®.
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 employer: Syneos Health
At Syneos Health, we pride ourselves on being an exceptional employer that fosters a collaborative and innovative work culture. Our commitment to employee growth is evident through comprehensive training programmes and opportunities for advancement within the biopharmaceutical sector. Located in the UK, we offer a dynamic environment where you can make a meaningful impact on patient lives while enjoying a supportive team atmosphere and flexible working arrangements.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Trial Manager
✨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 researching the company and its projects. We recommend practising common interview questions related to clinical trials, so you can showcase your knowledge and experience confidently.
✨Tip Number 3
Follow up after interviews! A quick thank-you email can set you apart from other candidates. We suggest mentioning something specific from your conversation to remind them of your fit for the role.
✨Tip Number 4
Don’t forget to apply through our website! We often have exclusive roles listed there, and it’s a great way to ensure your application gets seen by the right people. Let’s get you that Clinical Trial Manager position!
We think you need these skills to ace Clinical Trial Manager
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 at Syneos Health. Keep it engaging and personal!
Showcase Your Communication Skills:Since excellent communication is key in this role, make sure your application reflects your ability to convey information clearly. Whether it's through your CV or cover letter, demonstrate how you've effectively communicated in past roles.
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining our team!
How to prepare for a job interview at Syneos Health
✨Know Your Stuff
Make sure you brush up on Good Clinical Practice (GCP) and ICH guidelines. Familiarise yourself with the specific responsibilities of a Clinical Trial Manager, like site qualification and monitoring. This will show that you're not just interested in the role but also understand what it entails.
✨Showcase Your Experience
Prepare to discuss your previous experiences in clinical trials. Be ready to share specific examples where you managed site activities or resolved issues. Use the STAR method (Situation, Task, Action, Result) to structure your answers and make them impactful.
✨Ask Smart Questions
Interviews are a two-way street! Prepare thoughtful questions about the company’s approach to clinical trials and how they ensure compliance. This shows your genuine interest in the role and helps you assess if the company is the right fit for you.
✨Be Ready for Scenarios
Expect scenario-based questions where you might need to demonstrate your problem-solving skills. Think about potential challenges in site management and how you would handle them. This will highlight your critical thinking and decision-making abilities.
