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Associate Director Clinical Development, Egham
Client:
Location: Egham, United Kingdom
Job Category: Other
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EU work permit required: Yes
Job Views:
3
Posted:
05.05.2025
Expiry Date:
19.06.2025
Job Description:
Clinical Development Associate Director
Essential Pharma is seeking an Associate Director, Clinical Development to lead the clinical development strategy for our Hu14.18 program in high-risk neuroblastoma. This role involves executing clinical trials, regulatory interactions, establishing a KOL management system, and fostering cross-functional collaboration within Essential. Responsibilities include supporting investigator meetings, site visits, regulatory interactions, and stakeholder engagement.
What You Will Do
* Set development strategy for Hu14.18 in high-risk neuroblastoma.
* Lead global clinical trials for Hu14.18.
* Serve as clinical lead on cross-functional teams.
* Provide input on trial design and regulatory submissions.
* Collaborate with investigators, KOLs, and external partners.
* Guide internal teams throughout drug development.
* Assist in preparing INDs, CTAs, regulatory documents, and publications.
* Act as medical monitor, ensuring safety, data integrity, and compliance.
* Engage with investigators and site staff for high-quality study conduct.
* Analyze trial data, monitor safety, and review adverse events.
* Represent the company in scientific and regulatory meetings.
About Essential Pharma
Essential Pharma is an international specialty pharmaceutical company focusing on niche medicines for small patient populations, with a portfolio over 300 medicines across multiple therapeutic areas, treating patients in over 70 countries. We focus on low-volume, difficult-to-manufacture products and late-stage clinical assets, including recent acquisitions like Renaissance Pharmaceuticals. In December 2024, we announced a €900 million recapitalization with partners Gyrus Capital, AlpInvest, and Sixth Street. Our team comprises around 70 employees based in Surrey UK, Malta, France, Spain, and Switzerland.
What You Will Bring
* MD or equivalent medical degree.
* Board-certified (or eligible) in Oncology or Pediatric Oncology preferred.
* Experience in neuroblastoma is highly desirable.
* Strong clinical development experience in pharma or biotech.
* Proven track record in leading global trials and working with FDA, EMA.
* Scientific acumen, clinical judgment, and data interpretation skills.
* Ability to travel 50–60% internationally (EU and US).
* Excellent communication and leadership skills.
What We Offer
* Hybrid working model with flexibility for remote and office work.
* £150 home office allowance.
* Pension scheme (5% employee and employer contributions).
* Life insurance (4x basic salary).
* Enhanced family leave and sick pay.
* 26 days annual leave.
* Discretionary annual bonus.
What To Expect
* Inclusive, agile working culture emphasizing authenticity, autonomy, and responsibility.
* Engaging social events and regular interactions with leadership.
* Focus on employee growth, personalized development, and open communication.
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