AL Solutions

www.alsolutions.co.uk

2 Jobs

40 Employees

About the Company

AL Solutions are a niche Life Science Talent Solutions business that operate across the EMEA, USA, and APAC region. We support the Biotech, Pharmaceutical, Medical Device, CRO, and CDMO sector through various staffing solutions. Our three pillars are:

Executive Search – Strategic hires from VP through to C-Suite and Board level appointments.

Staffing Arm – Permanent and Contract hires across Clinical Operations/Development, Biometrics, HEOR/RWE, Regulatory, Quality, Commercial and CMC/Tech Ops.

Business Consultancy – Staff Retention Strategy, Salary Benchmarking, Outsourcing Solutions, RPOs/MSPs, and other areas of Business Advisory.

As a business, we were founded in 2018 and have since then grown our company substantially. We now operate across x3 offices; London, Manchester, and Miami – giving us an international footprint and agility for global timezones.

We have been able to scale and become a reputable company due to our extensive in-depth market knowledge. Everyone within our business has a specific niche focus that enables them to understand the ins and outs of the sector and to really provide the right advice, support, and hiring strategy to clients worldwide.

Our mission is to provide top tier candidates to top tier clients. We establish and build long-term partnerships with our clients and provide more than just staffing solutions. Every client and candidate of ours will regularly receive market updates, insights, competitor analyses, salary surveys and more - to ensure that you keep an edge on your competitors.

Whether you’re a Life Science professional looking for that next step in your career, or an employer looking to identify top talent, we will have a specialist consultant here to advise you.

Listed Jobs

Company Name: AL Solutions
Job Title: Clinical Research Associate
Job Description: Job Title: Clinical Research Associate II Role Summary: Conducts and oversees late‑phase oncology clinical trials, managing site qualification, monitoring, and close‑out activities, ensuring adherence to ICH‑GCP, local regulations, and sponsor SOPs, while maintaining robust site relationships and documentation. Expectations: Provide independent monitoring and site management for late‑phase oncology studies within a single‑sponsor, home‑based environment; maintain compliance and quality standards; support study progress and regulatory commitments. Key Responsibilities: - Lead qualification, initiation, monitoring, and close‑out visits independently. - Ensure compliance with ICH‑GCP, French regulations, and sponsor SOPs. - Perform source data verification, investigational product accountability, and accurate site documentation. - Build and maintain strong relationships with site staff, offering guidance and support. - Identify and resolve site‑level challenges proactively. - Maintain complete trial documentation in CTMS, eTMF, and EDC systems. Required Skills: - Independent monitoring experience (minimum 2 years) in CRO or pharmaceutical environments. - Strong knowledge of ICH‑GCP and French clinical trial regulations. - Experience with late‑phase oncology studies preferred. - Excellent communication, relationship‑building, and organisational skills. - Proficiency with clinical trial management systems (CTMS), electronic trial master file (eTMF), and electronic data capture (EDC). Required Education & Certifications: - Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related field.

Company Name: AL Solutions
Job Title: Principle Clinical Research Associate
Job Description: **Job Title** Principle Clinical Research Associate **Role Summary** Senior Clinical Research Associate responsible for managing Cell & Gene Therapy trial sites, ensuring compliance with ICH‑GCP, local regulations, and sponsor SOPs, and maintaining accurate documentation across CTMS, eTMF, and EDC systems. **Expectations** - Serve as the primary contact for investigative sites. - Assume ownership of site qualification, initiation, monitoring, and close‑out activities. - Identify and resolve site‑level challenges to keep studies on schedule. - Mentor junior staff and support a high‑performance monitoring team. **Key Responsibilities** - Independently conduct site qualification, initiation, monitoring, and close‑out visits for advanced therapy studies. - Verify source data, ensure investigational product accountability, and maintain compliant site documentation. - Build and sustain productive relationships with site investigators and study teams. - Escalate issues, coordinate corrective actions, and support risk mitigation. - Input and audit trial data in CTMS, eTMF, and EDC platforms. **Required Skills** - Advanced monitoring experience in Cell & Gene Therapy. - Deep knowledge of ICH‑GCP and Belgian clinical trial regulations. - Proficiency with CTMS, eTMF, EDC, and related study management systems. - Strong written and verbal communication; bilingual in English and French (Dutch a plus). - Excellent organizational, problem‑solving, and stakeholder‑management skills. **Required Education & Certifications** - Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related field. - Proven experience as a Senior or Principal Clinical Research Associate. ---

Belgium

Remote

22-12-2025