Clinical Research Associate Job at Novotech, France | Life Sciences | Apply Now
If you are a recent life sciences graduate or an early-career clinical professional looking to secure a foundational role within a global Contract Research Organization (CRO), this position at Novotech is an exceptional find. Located in the scientific hub of Paris, France, this office-based role embeds you directly within the company’s expanding European Clinical Operations framework. For structured coordinators searching for a high-trajectory Clinical Research Associate Job, this position offers a comprehensive training ground to master international Trial Master File (TMF) auditing, study budget tracking, and clinical systems management. It serves as an elite corporate launchpad for a long-term Novotech Job and stands out as a premier entry point among global Life Science Jobs for Freshers.
- Job Position: Inhouse Clinical Research Associate
- Location: France
- Job ID:
About The Company
Novotech is a global, full-service clinical Contract Research Organization (CRO) that has been partnering with leading biotechnology and pharmaceutical firms since 1997. Operating 30+ offices across the Asia-Pacific region, the United States, and Europe, Novotech is widely recognized for its advanced therapeutic and regulatory expertise. The company boasts an award-winning workplace culture, consistently named an Employer of Choice, Great Place to Work, and Employer of Choice for Gender Equality (EOCGE). Through its employee-centered “NovoLife” flexible benefits framework, Novotech empowers its global workforce with the trust, autonomy, and flexibility required to drive professional satisfaction and maximize client trial results.
Clinical Research Associate Job – Key Responsibilities
As an Inhouse Clinical Research Associate (IHCRA), you will deliver vital in-house operational, administrative, and logistical support to the clinical team, ensuring all trial phases comply with ICH-GCP guidelines, local regulations, and corporate SOPs.
Your day-to-day data, compliance, and coordination duties will include:
- TMF Archive & Quality Control: Coordinating, tracking, and maintaining essential study documentation within the Trial Master File (TMF). You will run routine quality control reviews, handle document translations, and execute final reconciliations to ensure complete audit-readiness.
- CTMS & Database Management: Managing the Clinical Trial Management System (CTMS), auditing site compliance metrics, and monitoring data completeness for site milestones, subject tracking, and Informed Consent Forms (PISCFs).
- Logistics & Investigator Site Files: Creating Investigator Site Files (ISF), coordinating the ordering and dispatch of key trial supplies (such as patient diaries, lab kits, and investigational drug supplies), and generating stock reports.
- Financial & Payment Processing: Taking ownership of the submission and tracking of Investigator and vendor payments within the CTMS, alongside completing financial data reconciliations against site Subject Visit Templates (SVT) and site budgets.
- Ethics & CTA Negotiation Support: Assisting with Institutional Review Board (IRB) and ethics submissions (safety data, line listings, and DSURs). You will also assist in drafting and amending site-specific Clinical Trial Agreements (CTAs) alongside the Legal and Project Management teams.
- CRA & Safety Support: Partnering with field-based CRAs to prepare for on-site monitoring visits, following up on open action items, and tracking study SUSARs/CIOMS to regulatory authorities and sponsors.
Qualifications & Requirements For Clinical Research Associate Job
This entry-to-junior position is explicitly optimized to onboard ambitious analysts who display a quality-minded approach to document tracking.
- Educational Foundation: Relevant qualification or Bachelor’s degree in Life Sciences, or a closely related discipline.
- Experience Range: Entry-level to less than 2 years of experience as an inhouse CRA, clinical administrator, or relevant clinical research role. Previous exposure to a pharmaceutical, healthcare, or CRO environment is highly advantageous.
- Technical Aptitude: Familiarity with basic clinical trial frameworks, Good Documentation Practices (GDP), and ICH-GCP regulatory guidelines.
- Core Competencies: A collaborative, partnership-driven mindset, an ability to handle standard data analysis platforms, and a proactive approach to troubleshooting operational delays.
- Logistics & Schedule: Full-time, office-based position located in Paris, France.
In short, the Inhouse Clinical Research Associate position at Novotech is a definitive route to transitioning your scientific background into a highly marketable asset within the international clinical trials industry. Securing this role allows you to bypass isolated laboratory work and gain comprehensive mastery over CTMS infrastructure, global regulatory filings, and study budget analytics. If you possess a life sciences background, a sharp eye for document compliance, and a passion for biotechnology, apply today to secure this premier Clinical Research Associate Job and advance your Novotech Job trajectory.
