ProPharma
5001 - 10000 employees
Founded 2001
đź’Š Pharmaceuticals
🧬 Biotechnology
⚕️ Healthcare Insurance
đź’° $8.6M Venture Round on 2020-10
Pharmaceuticals • Biotechnology • Healthcare Insurance
ProPharma is a leading research consulting organization in the life sciences industry. The company specializes in providing custom solutions across the full product lifecycle, from early discovery to post-market monitoring. ProPharma's services include regulatory sciences, clinical research solutions, quality and compliance services, pharmacovigilance, medical information, and R&D technology. Known for its deep domain expertise, ProPharma assists clients in the pharmaceuticals, biotechnology, and medical device sectors with regulatory support, clinical development, and quality management. ProPharma's global team supports a wide range of therapeutic areas including oncology, cardiovascular, and rare diseases, among others, ensuring effective and efficient delivery of life-saving therapies.
Principal Analytical Consultant
🔥 3 minutes ago
🇬🇧 United Kingdom – Remote
⏳ Contract/Temporary
đź”´ Lead
đź’Ľ Consultant
🇬🇧 UK Skilled Worker Visa Sponsor
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ProPharma
5001 - 10000 employees
Founded 2001
đź’Š Pharmaceuticals
🧬 Biotechnology
⚕️ Healthcare Insurance
đź’° $8.6M Venture Round on 2020-10
Pharmaceuticals • Biotechnology • Healthcare Insurance
ProPharma is a leading research consulting organization in the life sciences industry. The company specializes in providing custom solutions across the full product lifecycle, from early discovery to post-market monitoring. ProPharma's services include regulatory sciences, clinical research solutions, quality and compliance services, pharmacovigilance, medical information, and R&D technology. Known for its deep domain expertise, ProPharma assists clients in the pharmaceuticals, biotechnology, and medical device sectors with regulatory support, clinical development, and quality management. ProPharma's global team supports a wide range of therapeutic areas including oncology, cardiovascular, and rare diseases, among others, ensuring effective and efficient delivery of life-saving therapies.
đź“‹ Description
• Design, implement and manage the analytical strategy for a pegylated enzyme therapeutic program. • Work across the team as an SME to provide key guidance across the project. • Lead and support SEC-HPMC method development and validation for Phase 3 registration activities. • Assess analytical risks and develop mitigation strategies to support program objectives. • Key participation within project/scientific teams and offer sound advice/guidance on analytical development strategies. • Overall support the client as and when directed.
🎯 Requirements
• Ideally educated to a PhD level in a scientific discipline or at least a MSc with substantial experience linked to the project. • Must have a proven SME level in analytical development in the above area. • Hands on experience of SEC-HPLC method development is a must at Phase 3. • 10-15 years experience overall working in the industry (more would also be suitable). • Proven track record in supporting unlicensed medicines through troubleshooting phases to FDA registration. • Fluent in English.
🏖️ Benefits
• We celebrate our differences and strive to create a workplace where each person can be their authentic self. • We are committed to diversity, equity, and inclusion. • Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. • With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.
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