Apsida Life Science

www.apsida.co.uk

2 Jobs

37 Employees

About the Company

Founded in 2019, Apsida Life Science is a specialist recruitment business Headquartered in Surrey, with offices in London UK, Boston USA and Pretoria, SA.

Leveraging our inch-wide, mile-deep networks we’re expertly placed to support your hiring needs across the CRO, Pharmaceutical, Biotechnology, Medical Device, CDMO, eClinical, Patient Recruitment & DCT space.

We recognised the opportunity to provide a recruitment service that delivers genuine value and exceptional experiences through bespoke, cost-effective solutions grounded in quality and integrity.

We build lasting relationships by earning trust through transparency and consistency, utilising our expansive network and deep industry knowledge. Rather than focusing solely on transactions, we guide clients and candidates through every stage of the hiring process, offering strategic insights and tailored support.

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Listen to Apsida Insights Podcast on Spotify, Apple Podcasts & watch on YouTube.

The podcast that takes you inside the world of life science. We bring you exclusive conversations with industry leaders, deep dives into market trends, and discuss career growth, hiring strategies, and international expansion.

Listed Jobs

Company Name: Apsida Life Science
Job Title: Clinical Research Associate
Job Description: **Job Title:** Clinical Research Associate **Role Summary:** Conduct independent clinical trial monitoring across the UK, ensuring compliance with GCP, protocol, and regulatory requirements. Perform source data verification, maintain audit‑ready documentation, support clinical sites, and manage a focused portfolio with structured site visits while operating remotely. **Expactations:** * Navigate and monitor complex Phase I‑IV studies across diverse therapeutic areas. * Execute rigorous source data verification and site documentation. * Demonstrate autonomy in scheduling and completing monitoring visits. * Maintain audit readiness and compliance with GCP and sponsor procedures. **Key Responsibilities:** 1. Plan, coordinate, and conduct monitoring visits for assigned studies. 2. Perform source data verification and identify data discrepancies. 3. Review and maintain study documents, ensuring completeness and regulatory readiness. 4. Provide on‑site support to investigators and study sites. 5. Report site progress, safety events, and protocol deviations to the sponsor and CRO. 6. Travel nationally within the UK to perform visits, while working remotely for administrative duties. **Required Skills:** * Strong knowledge of GCP and clinical trial methodology. * Independent monitoring experience with proven analytical and problem‑solving skills. * Effective communication and report‑writing abilities. * Familiarity with electronic data capture (EDC) and medical device/cell‑therapy trials preferred. * Ability to work autonomously, manage time efficiently, and meet deadlines. **Required Education & Certifications:** * Master’s degree in Life Sciences, Pharmacology, Nursing, or related field. * Minimum 2 years of independent clinical monitoring experience in CRO or pharma sponsors. * UK right to work (UK residency) and valid driver’s licence for travel.

Company Name: Apsida Life Science
Job Title: Senior Clinical Research Associate
Job Description: **Job Title:** Senior Clinical Research Associate **Role Summary:** Lead and oversee clinical study activities across multiple sites for medical device and combination product trials. Conduct site monitoring visits, ensure compliance with GCP, SOPs, and regulatory requirements, and manage patient safety and data integrity to achieve regulatory milestones. **Expectations:** - High travel volume (≈80%) due to multi‑site responsibilities. - 12‑month contract with potential for renewal. - Deliver on study timelines, safety requirements, and regulatory submissions. - Maintain effective collaboration with Investigators, IRBs/ECs, and vendors. **Key Responsibilities:** - Manage day‑to‑day clinical study operations for multiple projects. - Conduct site visits, monitoring, and review of source data. - Verify safety and welfare of study participants. - Ensure adherence to study protocols, GCP, SOPs, and regulatory regulations. - Support patient recruitment and retention strategies. - Maintain Investigator Site Files in compliance with regulations and company procedures. - Coordinate with Investigators, IRBs/ECs, and external vendors as needed. **Required Skills:** - Four years (Bachelor’s) or two years (Master’s/PhD/MD) experience in clinical research with medical device monitoring. - Strong knowledge of medical device and combination product regulations. - Leadership, communication, and organizational skills to manage multiple simultaneous tasks. - Ability to travel extensively (up to 80%). - Proficiency in GCP, SOP implementation, and regulatory compliance documentation. - Problem‑solving, critical‑thinking, and data‑driven decision‑making. **Required Education & Certifications:** - Bachelor’s Degree in Life Science, Nursing, or related field (preferred). - Advanced degrees (MA, PhD, MD) acceptable with at least two years of relevant experience. - Industry certifications preferred: CCRA, RAC, CDE.

Flemish region, Belgium

On site

Senior

25-02-2026