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* Type: Temporary
* Job #25525
Join a Leading Global Biopharma Company: Exciting Opportunity for a Clinical Study Specialist!
Are you passionate about making a real difference in the lives of patients with rare genetic diseases? Our client, a trailblazer in the pharmaceutical industry, is on a mission to develop ground-breaking therapeutics. We’re looking for a dynamic and proactive Clinical Study Specialist to join their Global Study Operations (GSO) team and help drive innovation in clinical research.
Meet the Team:
Nestled in the heart of London, our client’s office is home to 26 passionate professionals, forming an integral part of a global team of around 60 members. Together, they ensure the seamless execution of global studies, upholding the highest standards of quality, timeliness, and budget efficiency.
Your Role:
As a Clinical Study Specialist, you’ll be central to GSO study execution. Your leadership will be crucial in driving cross-functional collaboration and ensuring that every study milestone is achieved. You’ll oversee diverse study teams, manage external vendors, and navigate challenges effectively.
Key Responsibilities:
* Lead the day-to-day execution of GSO studies.
* Act as the primary point of contact within GSO and across departments.
* Ensure all study timelines, budgets, and quality benchmarks are met.
* Manage study teams, vendors, and CROs efficiently.
* Proactively handle risks, issues, and opportunities.
What You Bring:
* Leadership skills to inspire and manage study teams.
* Adaptability and proactive problem-solving abilities.
* Exceptional communication skills for cross-functional collaboration.
Ideal Candidate Profile:
* A degree in life sciences or a related field (BA/BS/BSc).
* At least 7 years of experience in life sciences or related fields, with 4+ years in biopharmaceutical clinical research.
* Experience in compliance, quality data analysis, and interpretation.
* Knowledge of drug development and study design.
* Understanding of complex therapeutic areas and products.
* Experience managing external vendors (e.g., CROs, labs, imaging vendors).
* Proficiency with Microsoft Teams, Office, and Clinical Trial Management Systems.
* Prior industry experience is essential.
Hiring Timeline:
Our client aims to appoint by the end of July, with a start date as soon as possible thereafter.
Conditions:
* Location: London (Hybrid: 2 days in-office, 3 days remote)
* Contract: Temporary PAYE contract
* Pay: £75-100k/year, based on experience
* Contract Length: 6 or 12 months
If you meet these qualifications and are excited about this opportunity, please submit your CV today!
Not the right fit? We have other roles advertised on our website –
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