At a Glance
- Tasks: Lead global study start-up strategies for clinical trials in various therapeutic areas.
- Company: Parexel is a leading provider of clinical research services, supporting major drug trials worldwide.
- Benefits: Enjoy remote work flexibility and the chance to impact patient well-being.
- Other info: This role is perfect for those passionate about healthcare and innovation.
- Why this job: Join a dynamic team and contribute to groundbreaking medical advancements.
- Qualifications: Bachelor’s degree and 5+ years in clinical trial management required.
The predicted salary is between 36000 - 60000 £ per year.
Parexel Uxbridge, England, United Kingdom
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Join to apply for the Global Study Start Up Manager / SSU Manager - Remote - FSP - Register Your Interest role at Parexel
Parexel Uxbridge, England, United Kingdom
2 days ago Be among the first 25 applicants
Join to apply for the Global Study Start Up Manager / SSU Manager - Remote - FSP - Register Your Interest role at Parexel
REGISTER YOUR INTEREST FOR AN UPCOMING OPPORTUNITY
Parexel FSP is starting to recruit in advance of an upcoming need for an experienced Global Study Start Up Manager/ Leader to join one of our key sponsors in the UK.
In this role you will be responsible for defining, developing and delivering the global start up project strategy, you’ll be assigned to one or more interventional studies in one or more therapy areas such as oncology, vaccines, internal medicine, rare disease or inflammation and immunology.
Typically your responsibility ends when all investigative sites are activated and ready to enroll participants, however this can extend further into the participant recruitment period to specifically deliver the implementation of protocol amendments across active sites for selected studies.
Some Specifics About This Advertised Role
- Partner with country / site feasibility specialists to incorporate up to date intelligence for the planned countries and sites into the overall start up strategy and site activation plan.
- Partner and co-ordinate across teams responsible for regulatory submissions (local and country) and start up functions to align country and site activities to form a robust start-up strategy and site activation plan.
- Provide project management of activities directly required to complete all site activations for an assigned study as part of a study management led team to complete all start up activities for a study.
- Act as a key point of escalations for site activation related issues raised by country level start up roles.
- Responsible for the completeness and quality of site activation timeline plans for every site from investigator initiation package sent for first site in study, to site activation complete for last site in study.
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 In This Role
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.
Here are a few requirements specific to this advertised role.
- Bachelor’s Degree or equivalent and 5+ years of experience in clinical trials
- Extensive global start up clinical trial/study management experience is essential
- Excellent verbal, written and interpersonal communication skills in a dynamic and growing organization.
- Working knowledge of clinical trial functions, including clinical operations, regulatory and drug safety.
- Ability to prioritize and manage multiple tasks simultaneously.
Seniority level
Seniority level
Mid-Senior level
Employment type
Employment type
Full-time
Job function
Job function
Research, Analyst, and Information TechnologyIndustries
Pharmaceutical Manufacturing, Biotechnology Research, and Hospitals and Health Care
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#J-18808-LjbffrGlobal Study Start Up Manager / SSU Manager - Remote - FSP - Register Your Interest in Uxbridge employer: Parexel
At Parexel, we pride ourselves on being an exceptional employer, offering a dynamic work culture that prioritises patient well-being and fosters professional growth. Our remote opportunities allow for flexibility while working on impactful clinical trials across diverse therapeutic areas, ensuring that our employees are engaged in meaningful work that contributes to the advancement of healthcare. With a commitment to collaboration and innovation, Parexel provides a supportive environment where your expertise can thrive and make a real difference.
StudySmarter Expert Advice🤫
We think this is how you could land Global Study Start Up Manager / SSU Manager - Remote - FSP - Register Your Interest in Uxbridge
✨Unlock Networking Opportunities
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✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Parexel. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.
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When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what Parexel is looking for. A tailored application can really make you stand out!
We think you need these skills to ace Global Study Start Up Manager / SSU Manager - Remote - FSP - Register Your Interest in Uxbridge
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 Parexel!
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 Parexel that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Parexel!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Parexel, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Parexel
✨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 Parexel that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
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.
✨Know Their Products
Take some time to familiarise yourself with Parexel’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
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.