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For Companies At a Glance
- Tasks: Support clinical study teams in executing impactful clinical trials and managing essential documentation.
- Company: Join Parexel, a leader in improving global health through innovative clinical solutions.
- Benefits: Remote work, competitive salary, and opportunities for professional growth.
- Why this job: Make a real difference in patient care while working with a passionate team.
- Qualifications: Bachelor's degree and 2+ years of relevant experience; strong communication and problem-solving skills.
- Other info: Dynamic role with the chance to influence the future of healthcare.
The predicted salary is between 36000 - 60000 £ per year.
Overview
When our values align, there\’s no limit to what we can achieve. At Parexel, we all share the same goal – to improve the world\’s health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we\’re committed to making a difference.
REGISTER YOUR INTEREST IN AN UPCOMING ROLE. Parexel is beginning to search for an experienced Clinical Trial Administrator to join one of our key sponsors in the UK as a Clinical Study Specialist. In this role you will provide technical and administrative support to the clinical study teams responsible for clinical trial execution. The CSS may be assigned to support the execution of one or more studies across a program.
We’ll look for you to be an influential member of the wider team and to contribute to the successful execution of clinical studies.
Responsibilities
- Organizes and delivers reports and metrics to the clinical study lead.
- Schedules and coordinates meetings, prepares agendas, presentation materials and minutes for clinical study team meetings and other study related meetings
- Collates data for assessments such as feasibility and site selection and reviews site usability database.
- Contributes to review of study documents such as informed consent forms, case report forms and facilitates study document reviews per company standard operating procedures.
- Compiles study manuals including but not limited to: study reference binders and manuals and maintains versioning of study reference materials (e.g., regulatory, pharmacy, and laboratory binders).
- Collates materials for training and investigator meetings.
- Tracks site activation, enrolment and monitoring visits to projected plans, and escalate any issues or delays with site activation or deviations from monitoring plan.
- Monitors and updates investigator/site status for the trial, and supports with clinical trial registry postings.
- Performs scheduled reconciliations of study Trial Master File (TMF) with clinical study lead guidance.
About Parexel
Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base. We supported the trials of most of today\\\’s top 50 best-selling drugs, but equally we enable more niche drug developments that are critical to the well-being of many patients. You\\\’ll be an influential member of the wider team.
What we are looking for
For every role, we look for professionals who have the determination and courage always to put patient well-being first. That to us is working with heart.
Qualifications
- Bachelor\\\’s degree (or equivalent) and a minimum of 2+ years\\\’ industry related work experience or an advanced degree in a related field with a minimum of one (1) to two (2) years of relevant work preferred.
- Attention to details for the ability to track information and deliver on assigned study activities
- Good communication and interpersonal skills; ability to build relationships internally and externally
- Ability to be resourceful and to demonstrate problem solving skills
- Demonstrate the ability to proactively assess information and investigate impact on clinical trials
- Technical proficiency in trial management systems and MS applications, including but not limited to Teams, MS Office, Project, CTMS, EDC, IWRS/IVRS.
- Proactive and self-disciplined, ability to meet deadlines, effective use of time, and prioritization
- Basic familiarity with medical terms and clinical drug development
- Awareness of ICH/GCP
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Clinical Study Specialist / Snr CTA - FSP - Remote employer: Parexel
Contact Detail:
Parexel Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Study Specialist / Snr CTA - FSP - Remote
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical trial space on LinkedIn or at industry events. A friendly chat can lead to opportunities that aren’t even advertised yet.
✨Tip Number 2
Prepare for interviews by researching Parexel and their values. Show us how your passion for improving health aligns with our mission. We love seeing candidates who genuinely care about making a difference!
✨Tip Number 3
Practice your responses to common interview questions, especially those related to teamwork and problem-solving. We want to hear how you’ve tackled challenges in past roles and how you can contribute to our team.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows us you’re serious about joining our team at Parexel.
We think you need these skills to ace Clinical Study Specialist / Snr CTA - FSP - Remote
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Study Specialist role. Highlight relevant experience and skills that match the job description, like your attention to detail and communication skills. We want to see how you can contribute to our mission!
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 aligns with our values at Parexel. Show us your enthusiasm for making a difference in patient well-being.
Be Clear and Concise: When filling out your application, keep your language clear and concise. Avoid jargon unless it's relevant to the role. We appreciate straightforward communication, so make it easy for us to see your qualifications!
Apply Through Our Website: Don’t forget to apply 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 serious about joining our team at Parexel!
How to prepare for a job interview at Parexel
✨Know Your Stuff
Make sure you brush up on clinical trial processes and the specific responsibilities of a Clinical Study Specialist. Familiarise yourself with key terms like ICH/GCP, TMF, and EDC. This will show that you're not just interested in the role but also understand the industry.
✨Showcase Your Communication Skills
Since this role involves coordinating meetings and preparing reports, be ready to demonstrate your communication prowess. Prepare examples of how you've effectively communicated with teams or stakeholders in past roles. This will highlight your interpersonal skills and ability to build relationships.
✨Be Proactive in Problem Solving
Think of instances where you've had to troubleshoot issues in previous projects. Be prepared to discuss how you assessed the situation, what steps you took, and the outcome. This will illustrate your resourcefulness and ability to handle challenges head-on.
✨Prepare Questions for Them
Interviews are a two-way street! Prepare thoughtful questions about the team dynamics, study execution strategies, or how they measure success in clinical trials. This shows your genuine interest in the role and helps you gauge if it's the right fit for you.
