At a Glance
- Tasks: Support clinical trials by coordinating meetings, tracking data, and maintaining essential documents.
- Company: Join Regeneron, a leader in developing life-changing medicines through science and innovation.
- Benefits: Enjoy competitive pay, health benefits, remote work options, and career development opportunities.
- Other info: Inclusive workplace culture with excellent growth potential.
- Why this job: Make a real difference in patients' lives while working in a dynamic, science-driven environment.
- Qualifications: Bachelor’s degree or relevant experience; industry experience preferred.
The predicted salary is between 63000 - 77000 £ per year.
Build our future together
At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases.
We are seeking a Clinical Study Specialist to join our Clinical Trial Management team, supporting our clinical trial execution in a hybrid role.
In this role, you will provide technical and administrative study support while collaborating with clinical study teams, sites, and third-party vendors.
This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.
When & where
Uxbridge (Hybrid)
Discover your role
- Deliver analysable study reports and metrics to the Clinical Study Lead.
- Coordinate study meetings, agendas, presentations, minutes, training materials, and investigator meetings.
- Collate feasibility and site-selection data, including site usability database reviews.
- Facilitate document reviews and maintain version-controlled regulatory, pharmacy, and laboratory manuals.
- Track site activation, enrolment, monitoring visits, registry postings, and scheduled compliance reports.
- Reconcile the Trial Master File and track close-out documents, product reconciliation, and CRA visits.
- Maintain Share Point sites, site contacts, BDRM line listings, and third-party vendor oversight.
- You proactively identify issues, elevate delays, and recommend departmental process improvements.
This role requires
- Bachelor’s degree or five years of relevant experience.
- At least two years of industry-related experience.
- An advanced related degree with one to two years of relevant experience is preferred.
We are committed to building a workplace with an inclusive culture.
Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law.
Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.
Where necessary, we disclose salary ranges for roles in all countries in which we operate.
The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience.
In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits.
Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e. g. medical, dental, vision, life and disability), paid time off, and family support benefits.
For additional information about Regeneron benefits in the U.
S., please visit https://careers. regeneron. com/en/working-at-regeneron/total-rewards/.
For other locations, additional information will be provided during the recruitment process.
Please be advised that at Regeneron, we believe we do our best work when we are together.
For that reason, many roles are required to be performed on‑site.
Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.
As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based.
The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.
For jobs in Canada: this posting is for an existing position.
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Clinical Study Specialist in Uxbridge employer: Regeneron Pharmaceuticals, Inc
At Regeneron, we pride ourselves on being an exceptional employer, offering a dynamic and inclusive work culture that fosters innovation and collaboration. As a Senior Manager in our Global Development Quality Assurance team, you will have the opportunity to lead impactful audit strategies while working remotely from the UK or Ireland, benefiting from a comprehensive rewards package that includes competitive bonuses, health and wellness programs, and robust employee growth opportunities. Join us in making a meaningful difference in patients' lives while enjoying a supportive environment that values diversity and professional development.
Contact Details:
Regeneron Pharmaceuticals, Inc Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Study Specialist in Uxbridge
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We think you need these skills to ace Clinical Study Specialist in Uxbridge
Some tips for your application 🫡
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How to prepare for a job interview at Regeneron Pharmaceuticals, Inc
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In health sciences administration, being organised is key. Make sure you can demonstrate your skills in managing schedules, paperwork, and data accurately. Be ready to discuss specific tools you've used, like electronic health record systems or scheduling software, and how they improved efficiency in your past experiences.
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Familiarity with healthcare regulations and compliance is crucial. Brush up on HIPAA, GDPR, or other relevant policies before your interview. We recommend preparing examples of how you've ensured compliance or handled sensitive information in past roles—this will show you're not just knowledgeable but also responsible.
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Interviews for administrative roles often involve scenario-based questions to assess your problem-solving skills. Practice responses to common situations you might face, such as dealing with a challenging patient or managing a sudden schedule change. This will not only demonstrate your ability to think on your feet but also highlight your interpersonal skills.
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